Adherence, persistence, and medication discontinuation in patients with attention-deficit/hyperactivity disorder - a systematic literature review.

Untreated attention-deficit/hyperactivity disorder (ADHD) can lead to substantial adverse social, economic, and emotional outcomes for patients. The effectiveness of current pharmacologic treatments is often reduced, due to low treatment adherence and medication discontinuation. This current systematic literature review analyzes the current state of knowledge surrounding ADHD medication discontinuation, focusing on: 1) the extent of patient persistence; 2) adherence; and 3) the underlying reasons for patients' treatment discontinuation and how discontinuation rates and reasons vary across patient subgroups. We selected 91 original studies (67 with persistence/discontinuation results, 26 with adherence results, and 41 with reasons for discontinuation, switching, or nonadherence) and 36 expert opinion reviews on ADHD medication discontinuation, published from 1990 to 2013. Treatment persistence on stimulants, measured by treatment duration during the 12-month follow-up periods, averaged 136 days for children and adolescents and 230 days for adults. Owing to substantial study heterogeneity, comparisons across age or medication type subgroups were generally inconclusive; however, long-acting formulations and amphetamines were associated with longer treatment duration than short-acting formulations and methylphenidates. The medication possession ratio, used to measure adherence, was <0.7 for all age groups and medication classes during a 12-month period. Adverse effects were the most commonly cited reason for discontinuation in all studies. Original research studies reported the lack of symptom control as a common discontinuation reason, followed by dosing inconvenience, social stigma associated with ADHD medication, and the patient's attitude. In summary, although there was a lack of consistency in the measurement of adherence and persistence, these findings indicate that drug adherence and persistence are generally poor among patients with ADHD. Clinicians may be able to help improve adherence and persistence to ADHD treatment by educating caregivers and patients on treatment goals, administering long-acting medications, and following-up with patients to verify if medication is still effective and well-tolerated.

Introduction

Attention-deficit/hyperactivity disorder (ADHD) is a common psychiatric disorder characterized by hyperactivity, impulsivity, and difficulty maintaining sustained attention.1 Approximately 5.3% of children and adolescents are affected by ADHD worldwide,2 of whom 60% continue to demonstrate notable ADHD symptoms throughout life.3

Pharmacologic treatment is a key component of evidence-based care for patients with ADHD and has been shown to be a cost-effective therapeutic option.4 Currently, there are two main classes of medications with proven efficacy for ADHD – stimulants and nonstimulants. Stimulants, such as amphetamines (AMPHs) and methylphenidates (MPHs), have been the mainstay of ADHD pharmacotherapy.5 For patients with contraindications, or those who are averse or nonresponsive to stimulants, nonstimulants, such as guanfacine extended release (GXR), atomoxetine (ATX), and clonidine hydrochloride extended release, are alternative treatment options.

Owing to the chronic nature of ADHD symptoms, patients with ADHD typically require long-term pharmacotherapy. Despite the demonstrated effectiveness of current ADHD medications, treatment discontinuation is fairly common. One-half of all patients fail to adhere to treatment guidelines6 or discontinue treatment within 2–3 years of starting pharmacologic therapy.7,8 Such behaviors may be associated with suboptimal control of ADHD symptoms,9 increasing the likelihood of serious deleterious effects that can accrue and escalate over time.10 These include social and academic difficulties, behavioral problems such as substance abuse, delinquency, accidental injury,11,12 and poor economic, social, and emotional well-being.12,13 Such consequences impact patients as well as their families and communities.

The decision to discontinue treatment can be associated with a variety of factors, including patient characteristics, patient or caregiver choice, medication-related factors (eg, duration of action, risk–benefit profile, etc), and practitioner-related or health system-related factors.14,15 Although the literature exists on reasons for ADHD treatment discontinuation, a comprehensive review of these studies synthesizing the underlying issues surrounding discontinuation (particularly for specific ADHD populations, medication classes, and geographic locations) could facilitate the design of programs to improve treatment adherence and subsequent patient health outcomes, and would benefit both researchers and providers. This study aimed to meet this need by conducting a systematic literature review of real-world observational studies and review articles of expert opinions on medication discontinuation among patients with ADHD. In particular, the study sought to accomplish three objectives: 1) to explore the extent of patient persistence on (or discontinuation of) ADHD treatment; 2) to examine patient adherence to various ADHD medications; and 3) to evaluate the underlying reasons for patients’ treatment discontinuation. Variations of discontinuation rates, adherence, and reasons for treatment discontinuation were analyzed across subgroups of patients by age group, geographic location, and medication class.

Materials and methods

Systematic literature search

A systematic literature review was performed on October 11, 2013, by searching four main electronic databases via the OvidSP16 interface: MedLine17 (including In-Process and Other Non-Indexed Citations, January 1990–September 2013); EMBASE18 (January 1990–September 2013); PsycINFO19 (January 1990–September 2013); and Cochrane Database of Systematic Reviews20 (January 2005–July 2013). The four sets of search terms used were: disease of interest (terms for “attention- deficit hyperactivity disorder”); selected medication treatments (terms listed in Table S1); treatment discontinuation (terms for discontinuation, adherence, or persistence); and eligible study types (terms for retrospective or observational studies). Publications retrieved from the search were screened using the inclusion and exclusion criteria detailed in Table 1, and this review followed the reporting guidelines recommended by Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA).21

Table 1

Selection criteria of systematic review

Inclusion criteria	Publication type
	• Full-text primary publications of real-world studies
	• Treatment guidelines for US, Canada, UK, Germany, France, Spain, Italy, Sweden, and the Netherlands – as well as any general European guidelines
	• Editorials and commentaries
	• Reviews (systematic and nonsystematic) and meta-analyses of real-world studies
	Study design of real-world studies
	• Observational studies based on real-world data (cohort studies, including both prospective and retrospective designs, cross-sectional studies, and case-control studies)
	• Phase IV clinical trials
	Population
	• At least 80% of study population (children, adolescents, or adults) have ADHD as the primary disorder
	Interventions
	• ADHD drug treatment approved as of September 2013 by a regulatory agency in North America or Europe for ADHD in monotherapy or in combination therapy, ie:
	○ Stimulants: MPH, AMPH/dexamphetamine, and lisdexamfetamine
	○ Nonstimulants: ATX, GXR, and clonidine extended release
	• Two off-label medications commonly used in ADHD:
	○ GIR and CIR
	Outcomes
	• Reported discontinuation/switching results, or
	• Reported reasons for discontinuation/switching of ADHD drug treatment
	Language: English
	Publication date: During or after 1990
Exclusion criteria	Publication type
	• Nonprimary publications of real-world studies (eg, a publication that has less data than the primary publication to report the same outcomes)
	• Conference abstracts or posters
	• Congress proceedings
	• Books/chapters/addresses/bibliographies/biographies/lectures
	• Case reports
	• Letters
	• Treatment guidelines for countries other than: US, Canada, UK, Germany, France, Spain, Italy, Sweden, and the Netherlands
	• Reviews/meta-analyses not of real-world studies
	Study design
	• Preclinical studies
	• Clinical trials (Phase I–Phase III)
	• Prognostic studies
	• Genetic studies
	Population
	• Nonhuman subjects
	• Not ADHD patients
	• <80% of study population have ADHD as the primary disorder
	Intervention
	• No drug treatment
	• Drug treatment not listed in the inclusion criteria
	Outcomes
	• Does not report discontinuation/continuation results, and
	• Does not report reasons for ADHD medication discontinuation
	Language: Non-English
	Publication date: Before 1990

Abbreviations: ADHD, attention-deficit/hyperactivity disorder; MPH, methylphenidate; AMPH, amphetamine; ATX, atomoxetine; GXR, guanfacine extended release; GIR, guanfacine immediate release; CIR, clonidine immediate release.

Publications were screened at two levels. At the level I screening, inclusion/exclusion criteria were applied at the title/abstract level. At the level II screening, the full text of each article was reviewed against the selection criteria. The reason for its exclusion was recorded for each article failing level I or level II screening. To ensure complete capture of all relevant studies, the bibliographies of all reviews and meta-analysis articles were examined during level II screening to identify any additional original studies previously not included (via the snowballing technique).22 Reviews and meta-analyses were included for data extraction if they reported expert opinions and/or were not based on original studies. Two researchers conducted the level I and level II screenings independently; a third researcher was consulted to arbitrate disagreements over study inclusions when needed.

Multiple publications (kin studies) arising from the same research study (primary publications) were identified based on the study sample, research team, analytical method, and results, and linked to avoid duplication. Information was extracted from the primary study and, if available, additional information from the kin studies was also extracted and combined with the primary study. Because we sought to understand the nature of all of the available literature on these topics, the scientific quality of the published studies was not assessed in this systematic literature review.

Data extraction

For original research articles meeting the selection criteria, study-level specifics, methodology, and discontinuation data were extracted. Study-level specifics consisted of publication details, study type, data source, participant characteristics, medications of interest, and the geographic location of the study population. Methodology-related data included the patient selection criteria and the time frame for outcome measurement in each specific study. Discontinuation data included definitions of measures, estimates, and reasons (including nonadherence and switching), if available.

For publications reporting expert opinions (reviews, meta-analyses, editorials/commentaries, and treatment guidelines), geographic location, study population, treatment(s) of interest, and reasons and recommendations for medication discontinuation were recorded.

Data synthesis

Data were synthesized for the following three outcomes: 1) persistence/discontinuation; 2) adherence; and 3) reasons for discontinuation (including nonadherence and switching). Persistence was evaluated for patients remaining on therapy and was defined as the time between treatment initiation and discontinuation, while adherence was generally defined based on the proportion of time a patient took a prescribed ADHD medication according to its dosage schedule.

A qualitative summary was constructed for persistence/discontinuation studies based on pharmacy refill records/databases, as well as on patient and parent/caregiver surveys. A quantitative analysis was performed using data that originated from the subset of persistence/discontinuation studies that implemented comparable measure definitions and follow-up periods. For various patient subgroups, pooled estimates of treatment duration were calculated as the weighted average across studies by sample size. These pooled estimates were then compared by patient age group, medication class (stimulants versus nonstimulants), formulation (long-acting [LA] versus short-acting [SA]), and stimulant type (AMPH versus MPH).

A qualitative summary was constructed for the adherence studies (pharmacy refill records/databases, patient and parent/caregiver surveys, and physician assessments) using the level or percentage of patients classified as adherent to ADHD medications. For the subset of adherence studies using comparable measure definitions and follow-up periods, a quantitative analysis was conducted by computing average adherence rates for patient subgroups weighted by sample size. Pooled treatment durations were then compared by age group, medication class, formulation, and stimulant type.

It should be noted that, when interpreting persistence and adherence to medication in the child/adolescent population, drug holidays, which refers to being temporarily off the prescribed medication during nonschool days, should be taken into consideration. Persistence and adherence might be underestimated when their measures were defined without considering drug holidays.

Qualitative summaries were constructed to display the treatment discontinuation reasons extracted from original research and expert opinion articles. Reasons for discontinuation were reported from the patients’, parent/caregivers’, and clinicians’ perspectives and were compared by age group, medication class, and geographic location. The summary encompassed a broad range of discontinuation-related information, including type of discontinuation (permanent or temporary), motivation for switching, and reasons for nonadherent behavior. The reasons for discontinuation were ranked based on reporting frequency across the final set of studies. The ability to conduct quantitative comparisons using these data was limited, owing to differences in discontinuation reason descriptions and heterogeneity across study populations.

Results

The initial literature search yielded 1,384 citations. Following the level I screening, 452 publications and an additional eleven studies identified through the citation search were included for full text review. The full text screening identified 127 publications meeting all selection criteria (Figure 1). The final lists of publications are shown in Table S2 (original research studies) and Table S3 (expert opinion articles). Study-level specifics, methodology, and detailed persistence/discontinuation, and/or adherence information were extracted and analyzed for all 127 publications. Details of the number of studies conducted, stratified by age, medication class, and geographic location are summarized in Table 2.

Figure 1

PRISMA diagram of the literature selection criteria.

Notes: aNonrelevant publication type: 1) nonprimary publications of the real-world studies (eg, a publication that has less data than the primary publication to report the same outcomes); 2) conference abstracts or posters; 3) Congress proceedings; 4) books/chapters/addresses/bibliographies/biographies/lectures; 5) case reports; letters; or 6) treatment guidelines for countries other than: US, Canada, UK, Germany, France, Spain, Italy, Sweden, and the Netherlands. bNonrelevant study design: preclinical studies; clinical trials; prognostic studies; genetic studies; nonpopulation-based interview studies; economic studies; reviews/meta-analyses not of real-world studies. cNonrelevant population: nonhuman subjects; not ADHD patients; <80% of the study population have ADHD as the primary disorder. dNonrelevant intervention: no drug treatment; drug treatment not of interest: stimulants (methylphenidate, amphetamine: amphetamine/dexamphetamine and lisdexamfetamine), nonstimulants (atomoxetine, guanfacine immediate/extended release, and clonidine immediate/extended release). eNonrelevant outcome: 1) does not report discontinuation/continuation results; and 2) does not report reasons for ADHD drug discontinuation. fFor expert opinions (reviews, meta-analysis, editorials/commentaries, treatment guidelines), all the relevant citations for ADHD medication adherence or discontinuation were reviewed, and original papers were screened for inclusion. Reviews and meta-analyses were included for data extraction if they reported expert opinions that were not based on original studies. gExpert opinions refer to reviews, meta-analysis, editorials/commentaries, treatment guidelines.

Abbreviations: PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses; ADHD, attention-deficit/hyperactivity disorder.

Table 2

Number of studies reporting results for subgroups

	# of studies
	Original study (n=91)	Expert opinion (n=36)
Outcome
Persistence/discontinuation	67	NA
Based on retrospective database	52
Based on patient and parent/caregiver surveys	15
Adherence	26
Based on retrospective database	13
Based on patient and parent/caregiver surveys	10
Based on physician surveys	3
Reasons for discontinuation/nonadherence	41	36
Population
Children and adolescents	62	24
Adults	7	1
Combined age group of children, adolescents, adultsa	22	11
Drug class
Stimulants	56	18
Nonstimulants	7	0
ADHD treatment including stimulants, nonstimulantsb	28	18
Geographic location
North America	45	25
Europe	33	7
Other parts of the world	13	4

Notes:

Studies conducted in combined age group can report stratified results for children/adolescents or adults.

Studies that included ADHD treatment can report stratified results for stimulants or nonstimulants.

Abbreviations: NA, not applicable; ADHD, attention-deficit/hyperactivity disorder.

Persistence/discontinuation

A total of 67 studies reported findings on persistence/discontinuation: 52 were retrospective database analyses (based on health insurance claims, registries, or patient chart data) and 15 were patient or parent/caregiver surveys.

Database studies

Within the 52 retrospective database studies, three types of persistence measures were reported: discontinuation or continuation/persistence rate; treatment duration; and switching rate. Discontinuation of the index medication was generally defined as a gap, typically 30 days or more, in refill activity after the theoretical end date of the previous prescription.

Considerable heterogeneity existed across methodologies and reported outcomes in the persistence/discontinuation literature, with the most significant differences occurring in the definition of discontinuation, where gap length varied from 15 to 180 days, 23–25 and study length varied from 60 days to 6 years.26,27 Given that persistence declines with time, reliable comparisons of discontinuation rate, treatment duration, or switching rate across studies with different study period lengths were not feasible.

Discontinuation or continuation/persistence rate

Thirty-seven studies reported discontinuation or continuation/persistence rates, defined as the proportion of patients who discontinued their index medication or the proportion of patients who continued treatment as prescribed. Of these studies, eleven reported discontinuation rates among combined groups of children, adolescents, and adults, one study focused on adults only,28 and 25 studies focused on children and adolescents only. Three studies29–31 reported results separately for those patients who were 18 years and under and for those >18 years of age.

Substantial differences in target medication classes existed across the persistence/discontinuation studies. Six studies examined discontinuation rates among nonstimulant users (ATX; guanfacine immediate release [GIR]; GXR; or clonidine users), while 16 studies reported discontinuation rates for stimulants only. Fifteen studies reported rates for both stimulants and nonstimulants. Four studies8,29,32,33 reported results separately for stimulants and nonstimulants.

ADHD treatment discontinuation rates were reported in ten studies with a follow-up period of 12 months. Discontinuation rates for stimulants ranged from 19.1% for LA stimulant users of all ages29 to 99% for SA MPH pediatric (6–12 years old) users.34 Discontinuation rates for nonstimulants, reported from two studies on the use of ATX, ranged from 26.0% for 6–17 year old Italian patients33 to 38.3% for 2.5–90 year old Canadians (in Quebec).29

Treatment duration

Thirteen studies reported treatment duration as the time during which patients remained on initial ADHD therapy until they discontinued. Of these, five studies35–39 (Table 3) employed the same definition of treatment duration – the number of days that a patient remained on his or her initial therapy during a 12-month follow-up period – and termination, which was defined as a gap of at least 30 days in prescription-filling activity. Of these studies, only four were used to create a pooled estimate (Table 4), because two studies38,39 were kin studies. As Christensen et al38 reported additional results for AMPH, this study was chosen to be used for the analysis of treatment duration. Pooling of persistence estimates was only feasible for the children and adolescents population. Persistence ranged from 93.0 days (for SA stimulants) to 166.5 days (for AMPH). Only one study38 examined treatment duration among adults, reporting a range from 182.9 days (for MPH) to 252.7 days (for AMPH). The range of treatment duration reported for the overall age group was from 154.3 days (for nonstimulant ATX) to 254.2 days (for stimulants).

Table 3

Studies included in quantitative analysis for persistence

First author (year)	Persistence measure	Definition	Age group	Treatment
Barner (2011)37	Treatment duration	Persistence was defined as number of days of continuous therapy (without a specified gap period) during the postindex period (12 months). Gap period was 30 days.	Children and adolescents	Stimulants (LA, SA; MPH, AMPH) and nonstimulants; results reported separately
Palli (2012)35	Treatment duration	Persistence in terms of time to discontinuation of index medication; switching from one type of preparation within the stimulant class was allowed, but switching to another class was defined as discontinuation of index stimulant. All stimulant recipients were uniformly followed for 1 year (365 days). Gap period was 30 days.	Children and adolescents	Stimulants (LA, SA); results reported separately
Hodgkins (2011)39,a	Treatment duration	Persistence was defined as number of days (out of 366; follow-up period defined as index day plus 365 days) patient remained on initial therapy. Gap period was 30 days.	Combined age group of children, adolescents, adults; results reported separately	Stimulants (LA MPH; SA MPH); results reported separately
Christensen (2010)38	Treatment duration	Persistence was calculated as number of days out of 366 (follow-up period defined as index day plus 365 days) that patient remained on index therapy. Gap period was 30 days.	Combined age group of children, adolescents, adults; results reported separately	Stimulants (LA, SA; MPH, AMPH) and nonstimulant (ATX); results reported separately
Marcus (2005)36	Treatment duration	Duration of MPH treatment episode for each patient was calculated by sequentially counting unduplicated continuous prescriptions using date of prescription and number of days of medications supplied. Episodes of treatment were considered to have terminated if a gap of 30 or more days occurred from end of last prescription supply and start of subsequent prescription.	Children and adolescents	Stimulants (LA MPH; SA MPH); results reported separately

Note:

Hodgkins et al (2011)39 was excluded from the quantitative summary because it reported fewer results than Christensen (2010) and they both reported results from the same study.

Abbreviations: LA, long acting; SA, short acting; MPH, methylphenidate; AMPH, amphetamine; ATX, atomoxetine.

Table 4

Persistence results (reported as mean treatment duration, in days) from quantitative analysis

Age group	First author (year)	Stimulants		Nonstimulants		LA		SA		MPH		AMPH
		Treatment duration	Sample size	Treatment duration	Sample size	Treatment duration	Sample size	Treatment duration	Sample size	Treatment duration	Sample size	Treatment duration	Sample size
Children and adolescents	Barner (2011)37	134.98	53,838	153.30	8,516	143.70	44,118	95.40	9,720	135.76	33,852	133.57	19,986
	Palli (2012)35	97.83	46,135	NA	NA	104.96	33,561	79.97	8,260	NA	NA	NA	NA
	Christensen (2010)38	232.39	21,386	NA	NA	232.39	21,386	NA	NA	234.40	11,077	230.23	10,309
	Marcus (2005)36	114.42	11,537	NA	NA	140.30	3,444	103.40	8,093	114.42	11,537	NA	NA
	Pooled	135.97	132,896	153.30	8,516	149.41	102,509	92.99	26,073	150.75	56,466	166.46	30,295
Adults	Barner (2011)37	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Palli (2012)35	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Christensen (2010)38	229.63	10,906	NA	NA	229.63	10,906	NA	NA	182.90	3,604	252.70	7,302
	Marcus (2005)36	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Pooled	229.63	10,906	NA	NA	229.63	10,906	NA	NA	182.90	3,604	252.70	7,302
Combined age group of children, adolescents, adults	Barner (2011)37	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Palli (2012)35	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Christensen (2010)38	254.20	47,018	154.30	12,992	239.50	32,292	186.70	10,069	219.20	23,862	240.60	23,156
	Marcus (2005)36	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Pooled	254.20	47,018	154.30	12,992	239.50	32,292	186.70	10,069	219.20	23,862	240.60	23,156

Notes: Treatment duration is defined as the number of days patients stayed on their initial therapy. All four studies use a gap period of 30 days.

Abbreviations: LA, long acting; SA, short acting; MPH, methylphenidate; AMPH, amphetamine; NA, not applicable.

Switching

Switching to another medication was reported in 19 studies as either the rate of switching or the time to medication switch. Of these, six studies23,38–42 used a follow-up length of 12 months; the rate of switching in these studies ranged from 3.7% for patients <18 years old (switching from stimulants to nonstimulants)38 to 59% for children aged 6–12 years (switching from SA MPH to an unspecified ADHD medication).23

Patient and parent/caregiver surveys

Fifteen studies used patient or parent/caregiver interviews and surveys to assess persistence on ADHD medication. Of these, one study43 examined stimulant use among adults, while the remainder focused on ADHD pharmacotherapy among children and adolescents.

Discontinuation or continuation/persistence rates were reported in 13 of the studies. Among children and adolescents, discontinuation rates ranged from 11.1% for 8–18 year old patients, who stopped stimulant use following an average treatment duration of 3.3 years,44 to 96.4% for 4–17 year old Puerto Ricans taking stimulants, and who were observed over a 1-year period.45 Treatment duration was reported in three survey-based studies46–48 and ranged from 79 days to 2.5 years; however, each study had a different follow-up length. Treatment switching was reported in one parent survey of Taiwanese children; the study found that 57% of patients classified as poor adherents switched from SA to LA MPH.49

Adherence

A total of 26 studies reported adherence results, of which 13 were retrospective database analyses, ten were patient or parent/caregiver surveys, and three were physician surveys.

Twelve database studies used health insurance claims data from North American sources; only one study was conducted outside this region.32 Overall, six studies examined adherence in combined populations of children, adolescents, and adults,29,30,38,39,42,50 while the remaining seven focused on adherence among children and adolescents only. Seven studies presented adherence results for both stimulants and nonstimulants, with each reported separately. Five studies assessed adherence to stimulant medications only (AMPH or MPH),24,30,50–52 and one study examined adherence to nonstimulants only (ie, GIR and GXR).53

All studies evaluated adherence as the number of days of medication supplied during a prespecified period. Ten studies defined adherence based on medication possession ratios (MPRs: the ratio of the number of days with medication supply to the total number of days in a defined period), while three studies employed days in possession ratio (DPR),30 annualized prescribed days,54 and proportion of days covered (PDC).42 MPR was reported as a continuous measure of adherence in six studies and as a categorical variable (adherence defined by a given threshold value) in six studies. Of the latter, four studies defined being adherent as having an MPR of >0.8,29,37,39,50 while two employed an adherence threshold of 0.7.51,52

Similar to the persistence/discontinuation studies, the length of study period varied across the 13 database studies, ranging from 3 months to >2 years. The most commonly used study period was 12 months (six studies),32,37–39,42,54 followed by 6 months (three studies)24,30,53 (Table 5). As patients’ adherence levels may change over longer study periods, results were interpreted in the context of their observation length.

Table 5

Studies included in quantitative analysis for adherence

First author (year)	Adherence measure	Definition	Age group	Treatment
12 months
Hodgkins (2011)39,a	MPR	Ratio of number of days of initial therapy (sum of days supplied for all filled prescriptions while index therapy persisted, excluding days of supply of the fill that terminated persistence) to total number of days persistent. Observational period was 12 months.	Children and adolescents	Stimulants (LA, SA; MPH, AMPH) and nonstimulant (ATX); results reported separately
Hodgkins (2011)32	MPR	Ratio of total number of days for which the medication was supplied to total number of days supplied in that year. Observational period was 12 months.	Combined age group of children, adolescents, adults; results reported separately	Stimulants (LA MPH; SA MPH); results reported separately
Christensen (2010)38	MPR	Ratio of number of days of initial therapy (sum of days supplied for all filled prescriptions while index therapy persisted, excluding days of supply of the fill that terminated persistence) to total number of days persistent. Observation period was 12 months.	Combined age group of children, adolescents, adults; results reported separately	Stimulants (LA, SA; MPH, AMPH) and nonstimulant (ATX); results reported separately
Studies excluded owing to inconsistent measures of MPR
Barner (2011)37	MPR	Ratio of sum of days of supply to 365 days.	–	–
Saloner (2013)54	APD	Ratio of days with prescribed medications multiplied by 365 to total days after first prescription. Observation period was 2 years.	–	–
Setyawan (2013)42	PDC	Ratio of number of days covered by prescribed index medication to 365 days.	–	–
6 months
Sikirica (2013)53	MPR	Ratio of sum of days of supply to days in 6-month study period.	Children and adolescents	Nonstimulant (GIR, GXR)
Lawson (2012)30	DPR	Ratio of number of days in which patient possessed medication to 180 day postindex period.	Combined age group of children, adolescents, adults; results reported separately	Stimulants (LA, SA; MPH, AMPH); results reported separately
Studies excluded owing to inconsistent measures of MPR
Sanchez (2005)24	MPR	Ratio of days of supply from index prescription to last prescription of study period to number of days patient optimally should have received medication. Observation period was 6 months.	–	–

Notes:

Hodgkins (2011)39 was excluded from the quantitative summary, because it reported fewer results than Christensen (2010). They both reported results from the same study.

Abbreviations: MPR, medication possession ratio; LA, long acting; SA, short acting; MPH, methylphenidate; AMPH, amphetamine; ATX, atomoxetine; APD, annualized prescribed days; PDC, proportion of days covered; GIR, guanfacine immediate release; GXR, guanfacine extended release; DPR, days in possession ratio.

A quantitative pooling of MPR results was conducted in which comparable study measures were determined for each of the following groups – children and adolescents, adults, and the combined age group (Table 6). Among the six studies measuring adherence during a 12-month period, only two unique studies used the same adherence definition, calculating MPR as the ratio of supply days to the total number of persistent days during the follow-up period.32,38,39 For the three studies using a 6-month period to measure adherence,24,30,53 only two studies used the same MPR definition30,53 – the ratio of supply days to a fixed postindex period of 180 days (Table 5). No pooled results could be estimated using these two studies, however, owing to the lack of a common treatment arm (each study examined a different medication class) (Table 6).

Table 6

Adherence results (mean MPR) from quantitative analysis

Age group	First author (year)	Stimulants		Nonstimulants		LA		SA		MPH		AMPH
		MPR	Sample size	MPR	Sample size	MPR	Sample size	MPR	Sample size	MPR	Sample size	MPR	Sample size
Study period of 12 monthsa
Children and adolescents	Hodgkins (2011)32	0.64	4,801	0.67	81	0.66	419	0.64	4,382	0.64	4,775	0.56	26
	Christensen (2010)38	0.56	21,386	NA	NA	0.56	21,386	NA	NA	0.55	11,077	0.56	10,309
	Pooled	0.57	26,187	0.67	81	0.56	21,805	0.64	4,382	0.58	15,852	0.56	10,335
Adults	Hodgkins (2011)32	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Christensen (2010)38	0.59	10,906	NA	NA	0.59	10,906	NA	NA	0.52	3,604	0.62	7,302
	Pooled	0.59	10,906	NA	NA	0.59	10,906	NA	NA	0.52	3,604	0.62	7,302
Combined age group of children, adolescents, adults	Hodgkins (2011)32	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Christensen (2010)38	0.57	47,018	0.49	12,992	0.56	32,292	0.43	10,069	0.53	23,862	0.57	23,156
	Pooled	0.57	47,018	0.49	12,992	0.56	32,292	0.43	10,069	0.53	23,862	0.57	23,156
Study period of 6 months
Children and adolescents	Sikirica (2013)53	NA	NA	0.61	3,087	NA	NA	NA	NA	NA	NA	NA	NA
	Lawson (2012)30	0.49	14,457	NA	NA	0.50	13,108	0.40	1,349	0.49	10,440	0.49	4,017
	Pooled	0.49	14,457	0.61	3,087	0.50	13,108	0.40	1,349	0.49	10,440	0.49	4,017
Adults	Sikirica (2013)53	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Lawson (2012)30	0.49	586	NA	NA	0.47	450	0.56	136	0.45	267	0.53	319
	Pooled	0.49	586	NA	NA	0.47	450	0.56	136	0.45	267	0.53	319
Combined age group of children, adolescents, adults	Sikirica (2013)53	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA	NA
	Lawson (2012)30	0.49	15,055	NA	NA	0.50	13,570	0.41	1,485	0.49	10,707	0.49	4,348
	Pooled	0.49	15,055	NA	NA	0.50	13,570	0.41	1,485	0.49	10,707	0.49	4,348

Note:

For 12-month studies, the MPR was defined as the ratio of number of days for which the medication was supplied to the total number of days persistent during a 12-month follow-up period.

Abbreviations: MPR, medication possession ratio; LA, long acting; SA, short acting; MPH, methylphenidate; AMPH, amphetamine; NA, not applicable.

Children and adolescents

A total of 12 studies reported adherence results for patients aged ≤18 years. For the eight studies in this group using MPR, PDC, or DPR, adherence ranged from 0.28 for treatment-experienced patients receiving SA MPH for 12 months to 0.76 for patients receiving LA MPH for 6 months.24,42 For studies using an MPR cut-off of 0.8, the rate of adherence ranged from 9.8% (for patients using SA stimulants for 12 months) to 64% (for patients receiving stimulants and/or nonstimulants for 12 months).32,37

From the studies using a 12-month period, the pooled MPR for children and adolescents ranged from 0.56 for LA stimulants and AMPH to 0.67 for a nonstimulant (ATX). For the studies using a 6-month period, the pooled MPR ranged from 0.40 for SA stimulants to 0.61 for nonstimulants (GXR and GIR) (Table 6). Similar to the persistence analysis, the quantitative analysis for adherence was limited by the small number of studies sharing the same follow-up period and measure definitions.

Adults

Five studies reported adherence results for adults separately, using MPR, PDC, or DPR.29,30,38,39,42 Among the four studies that presented continuous measures of adherence,30,38,39,42 adherence ranged from 0.30 for treatment-experienced patients receiving SA MPH for 12 months42 to 0.62 for patients receiving LA AMPH for 12 months.38 Pooling MPR results across adult ADHD studies was not feasible due to a lack of comparability of MPR definitions and study period lengths (Table 6).

A total of ten studies conducted surveys and/or interviews to elicit assessments on medication adherence from patients with ADHD and their parents/caregivers. Two studies assessed adherence among adult patients with ADHD,43,55 while the remaining eight focused on child and adolescent populations. Compared with database studies on adherence, patient and parent/caregiver surveys were conducted over a wider geographic area: two in the US;56,57 three in Taiwan;49,58,59 and the remaining five in Norway,43 India,60 Spain,55 Canada,61 and Saudi Arabia.62 Two studies reported combined adherence on both stimulants and nonstimulants,60,62 while the remainder looked only at stimulants. While all ten studies yielded similar adherence trends, multiple differences existed in study design and execution, limiting cross-comparison of results.

Of the ten survey studies, three compared adherence between LA and SA stimulants.43,49,55 Among these three studies, LA stimulants were found to have better adherence (ranging between 74.3% and 97.1%)49,55 than SA stimulants (ranging between 42.9% and 60.0%).43,49 Definitions of adherence varied widely across these studies.

Physician surveys

Three studies used physician-estimated measures for adherence and treating physicians were asked to rate patient adherence on a questionnaire. Definitions of adherence varied widely across all three studies (eg, physicians’ belief on whether patients were consistently compliant;63 identification of patients who were >80% adherent to treatment during weekdays and >50% adherent during weekends and holidays;64 or application of a 6-point scale to rate adherence65). Thus, adherence rates ranged between 57.1% (African–American youths in the US rated as consistently compliant to stimulants over 2 years)63 and 71.4% (for 6–17 year old western European patients with ADHD evaluated for a minimum of 2 years postdiagnosis).64 As with prior adherence assessments, this analysis was limited by the heterogeneity of methodologies across studies and by small sample sizes.

Reasons for treatment discontinuation

The literature search identified 41 original real-world studies (Table S2) and 36 expert opinion articles (Table S3) reporting reasons for treatment discontinuation. Among the 41 original studies, 30 (73%) reported reasons for discontinuation, seven (17%) reported reasons for nonadherence, and seven (17%) reported reasons for switching. Among the 36 expert opinion articles, 19 (53%) reported reasons for discontinuation, while 24 (67%) reported reasons for nonadherence, along with strategies to improve adherence. The following analysis of the reasons for discontinuation encompassed a broad range, including the type of discontinuation (permanent discontinuation of a medication or temporary discontinuation, such as a drug holiday), motivation for switching, and reasons for nonadherent behavior.

Reasons for discontinuation from original research studies

The most common reasons for discontinuing ADHD medications were adverse effects (reported in 30 out of 41 studies) and ineffective symptom control/suboptimal response (in 27 out of 41 studies) (Table 7). The studies were classified by age group and then analyzed by medication class, geographic region, and perspective for each age group.

Table 7

Most frequently reported reasons for treatment discontinuation in original studies

All original studies (41 studies)			Children and adolescents (31 studies)			Adults (five studies)			Children, adolescents, young adults (five studies)
Reason	na	%b	Reason	na	%b	Reason	na	%b	Reason	na	%b
Adverse effects	30	73	Ineffectiveness/suboptimal response	21	68	Ineffectiveness/suboptimal response	4	80	Adverse effects	5	100
Ineffectiveness/suboptimal response	27	66	Adverse effects	21	68	Adverse effects	4	80	Ineffectiveness/suboptimal response	2	40
Poor adherence	8	20	Poor adherence	7	23	Patient decision	2	40	Dislike of medication	1	20
Parent/caregiver decision	7	17	Parent/caregiver decision	6	19	Symptom relief	2	40	Lack of education	1	20
Symptom relief	7	17	Symptom relief	5	16	Misuse of medication	1	20	Parent/caregiver decision	1	20
Patient attitude	3	7	Patient attitude	3	10	Patient attitude	0	0	Poor adherence	1	20
Dislike of medication	3	7	Dosing inconvenience	3	10	Difficulties in swallowing	0	0	Social stigma	1	20
Dosing inconvenience	3	7	Dislike of medication	2	6	Dislike of medication	0	0	Symptom relief	1	20
Patient decision	3	7	Dosing inconvenience/social stigma	2	6	Dosing inconvenience	0	0	Patient attitude	0	0
Dosing inconvenience/social stigma	2	5	Health care provider decision	2	6	Dosing inconvenience/social stigma	0	0	Difficulties in swallowing	0	0
Health care provider decision	2	5	Patient decision	2	6	Drug holiday	0	0	Dosing inconvenience	0	0
Social stigma	2	5	Difficulties in swallowing	1	3	Forgetting	0	0	Dosing inconvenience/social stigma	0	0
Difficulties in swallowing	1	2	Drug holiday	1	3	Health care provider decision	0	0	Drug holiday	0	0
Drug holiday	1	2	Forgetting	1	3	Ineffectiveness/suboptimal response/adverse effects	0	0	Forgetting	0	0
Forgetting	1	2	Ineffectiveness/suboptimal response/adverse effects	1	3	Lack of access to medication	0	0	Health care provider decision	0	0
Ineffectiveness/suboptimal response/adverse effects	1	2	Lack of access to medication	1	3	Lack of education	0	0	Ineffectiveness/suboptimal response/adverse effects	0	0
Lack of access to medication	1	2	Misdiagnosed	1	3	Misdiagnosed	0	0	Lack of access to medication	0	0
Lack of education	1	2	Parent education	1	3	Parent education	0	0	Misdiagnosed	0	0
Misdiagnosed	1	2	Parent/health care provider decision	1	3	Parent/caregiver decision	0	0	Misuse of medication	0	0
Misuse of medication	1	2	Safety concern	1	3	Parent/health care provider decision	0	0	Parent education	0	0
Parent education	1	2	School factor	1	3	Poor adherence	0	0	Parent/health care provider decision	0	0
Parent/health care provider decision	1	2	Social stigma	1	3	Safety concern	0	0	Patient decision	0	0
Safety concern	1	2	Lack of education	0	0	School factor	0	0	Safety concern	0	0
School factor	1	2	Misuse of medication	0	0	Social stigma	0	0	School factor	0	0

Notes:

Number of studies reported specified reason for discontinuation.

Frequency of reporting specified reason for discontinuation, estimated as number of studies reporting specific reason for discontinuation divided by total number of studies in specified group.

Thirty-one (76%) studies focused on reasons for discontinuing treatment among children and adolescents. The two most frequently reported discontinuation reasons for children and adolescents were adverse effects and treatment ineffectiveness/suboptimal response (each reported in 21 out of 31 studies). Children and adolescents also frequently discontinued treatment due to poor adherence, parent/caregiver’s decision to discontinue, and feeling that treatment was not needed due to symptom relief. Other reported reasons included patient attitude/dislike of medication, inconvenience of dosing, and the social stigma associated with ADHD and psychiatric medication, all of which are relevant in a school environment and might potentially explain children and adolescents’ difficulty remaining on the medication.

Discontinuation reasons for children and adolescents treated with stimulants were extracted from 18 studies. The frequently cited reasons were: adverse effects; treatment ineffectiveness/suboptimal response; and poor adherence (each reported in more than five out of 18 studies). Other factors – such as symptom control, parent/caregiver’s decision to discontinue, dislike of medication, and dosing inconvenience – were reported less frequently. Discontinuation reasons for children and adolescents treated with nonstimulants were detailed in only four studies.66–69 All four of these studies cited treatment ineffectiveness/suboptimal response, three cited adverse effects, and one cited poor adherence to treatment as reasons for discontinuation. For both medication classes, patient attitude was also a reason for discontinuation, although it was not frequently reported. For children and adolescents living in North America (ten studies), the primary reason for discontinuation was experiencing adverse effects (reported in seven out of ten studies), followed by treatment ineffectiveness/suboptimal response, dislike of medication, symptom relief, and the parent/caregiver’s decision to discontinue (each reported in more than two out of ten studies). In Europe (15 studies), treatment ineffectiveness/suboptimal response was the main reason for discontinuation (reported in 14 out of 15 studies), followed by adverse effects, poor adherence, symptom control, and dosing inconvenience. Among the studies reporting discontinuation reasons from both the patient’s and the parent/caregiver’s perspective (14 studies), the top three discontinuation reasons were adverse effects, treatment ineffectiveness/suboptimal response, and parent/caregiver’s decision to discontinue (each reported in more than four out of 14 studies). Studies reporting discontinuation reasons from the physician’s perspective (14 studies) recounted the same top two reasons, and added poor patient adherence as the third most common reason.

Five of the 41 discontinuation studies (12%) reported discontinuation reasons for children, adolescents, and young adults who were <23 years old. The overall results for this age group were similar to the patterns observed in children and adolescents, but one study reported lack of information about ADHD as the reason for discontinuation. All five studies focused on stimulants as a class or on MPH only. Owing to the small number of studies, information on other subgroups based on geographic region and perspective was sparse.

Only five (12%) discontinuation studies covered treatment discontinuation reasons in adults. Of these studies, four focused on stimulants.28,36,43,70 The most common reasons for discontinuation were adverse effects and treatment ineffectiveness/suboptimal response (reported in three out of four studies). Other reported reasons included: achievement of symptom relief; misuse of medication; and the patient’s decision to discontinue medication. Due to the small number of studies, information on other subgroups based on geographic region and perspective were sparse.

Reasons for discontinuation based on expert opinions

The literature review identified 36 expert opinion articles on ADHD treatment discontinuation (Table S3). The five most frequently encountered reasons for discontinuation were: adverse effects; dosing inconvenience; social stigma associated with ADHD and psychiatric medication; patient attitude; and treatment ineffectiveness/suboptimal response (Table 8).

Table 8

Most frequently reported reasons for treatment discontinuation in expert opinions

All studies with expert opinions (36 studies)			Children and adolescents (24 studies)			Adults (one study)			Children, adolescents, adults (eleven studies)
Reason	na	%b	Reason	na	%b	Reason	na	%b	Reason	na	%b
Adverse effects	24	67	Adverse effects	15	63	Dosing inconvenience	1	100	Adverse effects	8	73
Dosing inconvenience	14	39	Dosing inconvenience	10	42	Adverse effects	1	100	Dosing inconvenience	3	27
Social stigma	10	28	Patient attitude	8	33	Social stigma	1	100	Forgetting	3	27
Patient attitude	9	25	Social stigma	8	33	Patient attitude	0	0	Ineffectiveness/suboptimal response	3	27
Ineffectiveness/suboptimal response	7	19	Patient–physician communication	5	21	Clinician’s disparity	0	0	Patient attitude	2	18
Patient–physician communication	5	14	Disorder-related factor	4	17	Patient–physician communication	0	0	Difficulties in swallowing	1	9
Disorder-related factor	4	11	Inadequate monitoring	4	17	Comorbidity	0	0	Education	1	9
Forgetting	4	11	Ineffectiveness/suboptimal response	4	17	Difficulties in swallowing	0	0	Social stigma	1	9
Inadequate monitoring	4	11	Comorbidity	2	8	Disorder-related factor	0	0	Clinician’s disparity	0	0
Difficulties in swallowing	3	8	Difficulties in swallowing	2	8	Drug holiday	0	0	Patient–physician communication	0	0
Education	3	8	Education	2	8	Education	0	0	Comorbidity	0	0
Comorbidity	2	6	Lack of access to medication	2	8	Forgetting	0	0	Disorder-related factor	0	0
Lack of access to medication	2	6	Patient characteristics	2	8	Inadequate monitoring	0	0	Drug holiday	0	0
Patient characteristics	2	6	Clinician’s disparity	1	4	Ineffectiveness/suboptimal response	0	0	Inadequate monitoring	0	0
Clinician’s disparity	1	3	Drug holiday	1	4	Lack of access to medication	0	0	Lack of access to medication	0	0
Drug holiday	1	3	Forgetting	1	4	Logistic difficulties	0	0	Logistic difficulties	0	0
Logistic difficulties	1	3	Logistic difficulties	1	4	Patient characteristics	0	0	Patient characteristics	0	0
Poor adherence	1	3	Poor adherence	1	4	Poor adherence	0	0	Poor adherence	0	0
Self-esteem	1	3	Self-esteem	1	4	Self-esteem	0	0	Self-esteem	0	0
Symptom relief	1	3	Symptom relief	1	4	Symptom relief	0	0	Symptom relief	0	0

Notes:

Number of studies reported specified reason for discontinuation.

Frequency of reporting specified reason for discontinuation, estimated as number of studies reporting specific reason for discontinuation divided by total number of studies in specified group.

When discontinuation reasons were analyzed by age group, children and adolescents (67% of expert opinion studies) were shown to have similar reasons as those for the overall population analysis – adverse effects, dosing inconvenience, patient attitude, social stigma, and patient–physician communication. Commonly cited reasons for discontinuation of stimulant use by children and adolescents (12 studies) included: adverse effects, patient attitude, dosing inconvenience, social stigma, and patient–physician communication (each reported in more than three out of 12 studies). Other reasons included: difficulties in swallowing, disorder-related factors, inadequate monitoring, and treatment ineffectiveness/suboptimal response. No study reported discontinuation reasons for nonstimulants. The top five discontinuation reasons cited by experts in North America (17 studies) were: adverse effects, dosing inconvenience, patient attitude, social stigma, and patient–physician communication. Experts in Europe (five studies)71–75 provided similar reasons, with communication being replaced by inadequate monitoring.

In the only study from North America providing data on adult patients with ADHD (3%),76 adverse effects, social stigma, and dosing inconvenience were listed as the reasons for discontinuation.

In the combined age group (30% of expert opinion studies), six studies focused on stimulant discontinuation,65,77–81 and adverse effects were cited as a discontinuation reason in five of them.77–81 Other reasons given by experts for discontinuing stimulants included: treatment ineffectiveness/suboptimal response; difficulties in swallowing; dosing inconvenience; forgetfulness; and social stigma. No study provided discontinuation reasons for nonstimulants. Adverse effects and treatment ineffectiveness/suboptimal response were consistently referred to as the main reasons for discontinuation in the combined age group of children, adolescents, and adults by experts in North America (seven studies) and Europe (two studies).65,77 Experts from North America also cited: dosing inconvenience; forgetfulness; patient attitude, difficulties in swallowing, and social stigma as reasons for discontinuation. No additional reasons were provided by experts in Europe.

Discussion

This literature review examined persistence and adherence to pharmacologic treatment for ADHD and summarized reasons for treatment discontinuation. Where feasible, the analyses were also stratified across subgroups of patients by age group, geographic location, and medication class. Overall, findings from this study indicate that persistence and adherence to ADHD treatment were generally low and that tolerability was cited as an important reason for treatment discontinuation.

In our review of persistence studies, we observed that there was significant heterogeneity in measures of persistence in studies using patient/caregiver and physician surveys. The issue also affected retrospective database analyses, although to a lesser extent. Most of these studies measured persistence as time to a predefined prescription gap. However, variation in gap lengths and follow-up periods still exists. Rates of treatment persistence varied (between 0.1% and 89.9%), depending on definitions across studies. Despite the variations, higher persistence was observed in patients using LA than SA stimulants.

Definitions of adherence were largely based on the number of days of medication supply. For all three types of studies examined – database studies, patient and parent/caregiver surveys, and physician surveys – adherence measure definitions and follow-up periods varied widely. Most studies reported rates of <80% (or a mean MPR of <0.8),82 indicating a low treatment adherence for the ADHD population. From a societal perspective, it is often important to compare adherence across chronic diseases to help payers and policymakers understand how the adherence and its potential impact in one condition is relative to other similar conditions of interest. In general, adherence to ADHD medication was comparable with estimates reported for other psychiatric (schizophrenia, bipolar disorder)83–85 and nonpsychiatric chronic disorders (hyperlipidemia, diabetes, hypertension, etc)82,86,87 with low adherence. There was no clear evidence that any subgroups (by age or medication class) experienced higher adherence than the others, but, in general, children and adolescents seemed to display higher adherence to nonstimulant than to stimulant medications. Adult adherence rates to various stimulant subcategories,30,38 as measured by MPR, suggest that patients on AMPH may have had higher adherence than those taking MPH; however, more comparable studies are needed to validate these results. The adherence estimates were not influenced by the length of the observation periods (eg, 6 months or 12 months).

This systematic literature review identified numerous reasons for discontinuation of ADHD medication. The most commonly cited reason for discontinuation in original research studies and expert opinion reviews was experiencing some adverse effects from the ADHD medication, regardless of age group, medication class, region, prior treatment status, and reporting perspective. Other reasons for discontinuation were generally similar across these two study types, although some differences were worth noting. Ineffectiveness/suboptimal response was one of the most commonly reported reasons in the original studies, but it was reported less frequently in the expert opinion reviews (although it was still within the top five discontinuation explanations). Similarly, poor adherence was a commonly cited reason in the original studies but not in expert opinion reviews. In contrast, dosing inconvenience and social stigma were among the top five reasons in the expert opinion articles, but they were rarely reported in the original studies. Among adults, symptom relief, concerns over drug misuse, and desire to terminate treatment were frequent motivators. Among children and adolescents, discontinuation often occurred due to symptom relief, but also as a result of poor adherence or the parent/caregiver’s decision to discontinue.

This study observed a number of limitations in the existing body of evidence. First, due to the heterogeneity of study designs and methodology, the scope of a quantitative synthesis of persistence and adherence was limited. In the final quantitative analysis, the selection of eligible articles was narrowed down to a small list of directly comparable studies, which limited the generalizability of our conclusions. Second, the majority of original studies discussed reasons for discontinuation without reporting the proportion of patients affected by each reason; therefore, the rank of discontinuation reasons was based on frequencies of being reported in published studies. It was unclear whether most patients discontinued treatment due to the most frequently reported reasons in the literature. Third, reporting bias may exist as this study did not assess scientific quality of the included studies. Another limitation is related to the adverse effects that were reported to be the main reason for discontinuation across studies. The majority of studies did not provide details on the specific adverse effects that led to discontinuation. Hence, it was not clear if a particular side effect was responsible for a patient’s unwillingness to continue treatment or if generally experiencing some unexpected or unpleasant side effect was sufficient to prompt treatment discontinuation.

Among the 91 original observational studies, only eleven studies reported adherence or discontinuation results for the adult ADHD population and, of these, only five original studies provided information on the underlying reasons for treatment discontinuation. Reasons for discontinuation for adults were provided in only one expert opinion article. This limited information on adherence and persistence in adults is one of the key findings and a call for action for further research to understand the adherence and persistence in the adult population.

Another important aspect of ADHD treatment is drug holidays (scheduled temporary suspensions of pharmacologic treatment). In this analysis, drug holidays were not always considered in studies of children and adolescents with ADHD. Stimulant-treated minors are often advised to take drug holidays during their school holidays or, sometimes, even weekends. Thus, observational database studies using persistence and adherence measures based on commonly used treatment gaps of 30 days may not have taken drug holidays into consideration and may have overestimated the rate of discontinuation – a type of attribution bias. Similarly, database studies measuring adherence as MPRs considered drug holidays as nonadherent days and, therefore, the adherence was underestimated in these studies.

Treatment adjustment is a common phenomenon with ADHD medication, and it should be taken into account when studying adherence and persistence measures. For example, the lower adherence and persistence with SA versus LA stimulants observed in the study could be attributed to a dose titration process. Patients initiating ADHD treatment are often started with low doses and then they titrate to an optimal dosage over time, to maximize medication effectiveness and minimize adverse effects.88,89 SA stimulants may be used for the first titration90 and, then, if the duration of effect of the optimized dosage is not adequate, patients are typically switched to LA formulations.

Over the past few decades, as ADHD knowledge has advanced, the use of alternative treatment modalities, such as the use of nonstimulants as adjunctive therapies to the core stimulant regimen for patients with suboptimal response to stimulant monotherapy, has increased. As ADHD care has evolved, so too should research into the adherence/persistence of these alternative treatment approaches.91 Two nonstimulants have been approved in the US and Canada for adjunctive use.92,93 However, no observational study was identified in this systematic review evaluating persistence/discontinuation and adherence of nonstimulants as adjunctive therapies; these newer treatment modalities may have different usage and outcome patterns compared with ADHD monotherapy.

Finally, differences in treatment settings (specialist versus generalist care) could not be considered in the scope of this review, as it was not reported consistently. Such differences could influence the reporting of specific discontinuation reasons across varying study types. For example, expert opinions may have been written by experienced child psychiatrists, who are more familiar with pharmacological treatment of ADHD – and in particular with stimulants.94 In addition, they may also have access to multiprofessional teams, facilitating patient management through multimodal treatment options, including continuous psychoeducation, cognitive behavioral therapy, parent training, etc. Thus, these practitioners may be less concerned about ineffectiveness/suboptimal response, as observed in our review. In contrast, physician survey studies could potentially include primary care physicians and pediatricians, who may be less familiar with medical treatment regimens for ADHD and thus may exhibit greater concerns regarding ineffectiveness/suboptimal response of the treatment.

These limitations highlight some gaps in the existing literature and provide possible directions for future research. Studies using comparable definitions and follow-up periods for different subgroups of patients with ADHD are needed to fill the current knowledge gap on the actual rates of adherence to pharmacologic treatment for ADHD. In particular, the current review confirms that treatment patterns in adult ADHD are poorly understood and that further studies are still required to shed light on how disease management approaches in this population will be different from that in children and adolescents. Similarly, systematic comparisons across other subgroups based on medication class (stimulants versus nonstimulants) and formulations (LA versus SA) should also be considered to inform what treatment strategies should be adopted to maintain persistence and adherence for these subgroups. In addition, with the increasing use of adjunctive therapies in the treatment of ADHD, disease management can also benefit from more real-world evidence on the treatment patterns of adjunctive therapies. Large observational studies in which patients are closely followed could provide more reliable estimates of treatment persistence and adherence. Future research that comprehensively collects reasons for discontinuation of ADHD treatment – adjusted for differences in treatment settings, age groups, and medication type – is warranted and will help patients and clinicians choose, monitor, and improve future ADHD treatment regimens.

Conclusion

In this systematic literature review and analysis, persistence and adherence to pharmacologic treatments for ADHD were generally inadequate. The highest persistence was generally observed for patients taking LA stimulants (compared with all other formulations) although further comparative studies are needed. The most common reasons for discontinuation extracted from original studies included adverse effects of ADHD medication, treatment ineffectiveness/suboptimal response, and poor patient adherence to treatment. According to expert opinions, the main reasons for discontinuing ADHD medication were adverse effects of medication, dosing inconvenience, and social stigma associated with ADHD and psychiatric disorders in general. The findings suggest that although efficacy, social factors, convenience, and patient attitude may influence treatment adherence and discontinuation, tolerability remains the most important component to consider when deciding on a treatment regimen. Based on these findings, clinicians may be able to help improve treatment adherence and persistence in this chronic disease by educating caregivers and patients on treatment goals, administering LA medications, and continuing to closely follow-up with patients to verify if medication is still effective and well-tolerated and to ensure medication is switched when there are tolerability issues or lack of symptom control.

Table S1

A list of ADHD medications approved in North American and European countries

Stimulants/nonstimulants	Medication class	ADHD medications (Medication type, Formulation if available, Manufacturer)
Nonstimulants	Selective norepinephrine reuptake inhibitor	Strattera® (ATX; Eli Lilly and Company)
		Atomoxetine Teva (ATX; Teva)
	Alpha-2 adrenergic agonist	Intuniv® (GXR; Shire)
		Guanfacine/Guanfasiini immediate release (GIR)
		Kapvay® (clonidine hydrochloride, extended release; Concordia Pharmaceuticals)
		Clonidine immediate release (CIR)
Stimulants	Methylphenidate	Biphentin® (MPH; Perdue Pharma)
		Concerta® (MPH; Janssen Pharmaceuticals/ALZA Corporation)
		Daytrana® (MPH; Noven Therapeutics)
		Elmifiten® (dexmethylphenidate; Alfred E Tiefenbacher Gmbh & Co.)
		Equasym XL®/Equasym Retard®/Equasym Depot®/Quasym LP® (MPH; Shire)
		Focalin® (dexmethylphenidate; Novartis)
		Focalin XR® (dexmethylphenidate, extended release; Novartis)
		Metadate® (MPH; UCB Pharma)
		Metadate CD® (MPH, extended release capsules; UCB Pharma)
		Metadate ER® (MPH, extended release tablets; UCB Pharma)
		Medicebran® (MPH; Laboratorios Farmacéuticos Rovi)
		Medikid (MPH)
		Medikinet/Medikinet CR® (MPH; Medice)
		Medikinet® XL (MPH; Medice)
		Medikinet Retard® (MPH; Medice)
		Methylin® (MPH; Mallinckrodt/Shionogi)
		Methylin ER® (MPH, extended release; Mallinckrodt/Shionogi)
		Methylphenidat-1A pharma® (MPH; 1 A Pharma)
		Methylphenidat HEXAL® (MPH; Hexal)
		Methylphenidat-ratiopharm® (MPH; Ratiopharm)
		Methylpheni TAD® (MPH; TAD Pharma GmbH)
		Methylphenidat TB (MPH; Alfred E Tiefenbacher GmbH & Co.)
		Methylfenidaat HCl (MPH, hydrochloride)
		Methylfenidaat HCI AET (MPH, hydrochloride; Alfred E Tiefenbacher GmbH & Co.)
		Motiron® (MPH; Sandoz)
		Methylphenidate Rubio (MPH; Laboratorios Rubió)
		Omozin® (MPH; Laboratorios Rubió)
		Ritalin/Ritaline® (MPH; Novartis)
		Ritalin LA® (MPH, long acting; Novartis)
		Ritalin SR® (MPH, sustained release; Novartis)
		Rubifen® (MPH; Laboratorios Rubió)
		Tifinidat (MPH; Alfred E Tiefenbacher GmbH & Co.)
		Quillivant™ (MPH; Pfizer)
		Quillivant XR™ (MPH, extended release; Pfizer)
	Amphetamine	Adderall® (amphetamine/dextroamphetamine; Shire)
		Adderall XR® (AMPH/dextroamphetamine, extended release; Shire)
		Dexedrine® SR (dextroamphetamine, sustained release; Amedra Pharmaceuticals)
		Dexedrine® spansules® (dextroamphetamine; Amedra Pharmaceuticals)
		Dextroamphetamine ER (dextroamphetamine, extended release)
		Desoxyn® (methamphetamine hydrochloride; Recordati Rare Diseases, INC.)
		Dexedrine® (dextroamphetamine; Amedra Pharmaceuticals LLC)
		Dextrostat® (dextroamphetamine; Shire)
		Elvanse® (lisdexamfetamine; Shire)
		LiquADD® (dextroamphetamine; Auriga Laboratories)
		Metamina (dexamfetamin)
		Vyvanse® (lisdexamfetamine; Shire)

Notes: Intuniv® is approved in the US only; Biphentin® is approved in Canada only; Attentin® is approved in Germany only. Medikinet Retard® (not Medikinet XL®) and Equasym Retard® (not Equasym XL®) are approved in Germany. Equasym XL® is marketed as Metadate CD® in the US.

Abbreviations: ADHD, attention-deficit/hyperactivity disorder; ATX, atomoxetine; GXR, guanfacine extended release; GIR, guanfacine immediate release; CIR, clonidine immediate release; MPH, methylphenidate; AMPH, amphetamine.

Table S2

List of included original observational studies and bibliographic information

ID	Primary study citation	Reported discontinuation reasons
A1	McCarthy S, Wilton L, Murray M, Hodgkins P, Asherson P, Wong IC. Management of adult attention deficit hyperactivity disorder in UK primary care: a survey of general practitioners. Health Qual Life Outcomes. 2013;11:22.	Yes
A2	Erder MH, Signorovitch JE, Setyawan J, et al. Identifying patient subgroups who benefit most from a treatment: using administrative claims data to uncover treatment heterogeneity. J Med Econ. 2012;15(6):1078–1087.	No
A3	Barner JC, Khoza S, Oladapo A. ADHD medication use, adherence, persistence and cost among Texas Medicaid children. Curr Med Res Opin. 2011;27 Suppl 2:13–22.	No
A4	Kordon A, Stollhoff K, Niederkirchner K, Mattejat F, Rettig K, Schäuble B. Exploring the impact of once-daily OROS® methylphenidate (MPH) on symptoms and quality of life in children and adolescents with ADHD transitioning from immediate-release MPH. Postgrad Med. 2011;123(5):27–38.	Yes
A5	Mazzone L, Reale L, Mannino V, Cocuzza M, Vitiello B. Lower IQ is associated with decreased clinical response to atomoxetine in children and adolescents with attention-deficit hyperactivity disorder. CNS Drugs. 2011;25(6):503–509.	Yes
A6	Marcus SC, Durkin M. Stimulant adherence and academic performance in urban youth with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2011;50(5):480–489.	No
A7	Fernández-Jaén A, Fernández-Mayoralas DM, Pardos A, Calleja-Pérez B, Muñoz Jareño N. Clinical and cognitive response to extended-release methylphenidate (Medikinet) in attention deficit/hyperactivity disorder: efficacy evaluation. Adv Ther. 2009;26(12):1097–1110.	Yes
A8	Marcus SC, Wan GJ, Zhang HF, Olfson M. Injury among stimulant-treated youth with ADHD. J Atten Disord. 2008;12(1):64–69.	No
A9	Hervey-Jumper H, Douyon K, Franco KN. Deficits in diagnosis, treatment and continuity of care in African–American children and adolescents with ADHD. J Natl Med Assoc. 2006;98(2):233–238.	No
A10	Gimpel GA, Collett BR, Veeder MA, et al. Effects of stimulant medication on cognitive performance of children with ADHD. Clin Pediatr (Phila). 2005;44(5):405–411.	No
A11	Lage M, Hwang P. Effect of methylphenidate formulation for attention deficit hyperactivity disorder on patterns and outcomes of treatment. J Child Adolesc Psychopharmacol. 2004;14(4):575–581.	No
A12	Gormez V, Avery B, Mann H. Switching from immediate release to sustained release methylphenidate in the treatment of children and adolescents with attention deficit/hyperactivity disorder. Eur Rev Med Pharmacol Sci. 2013;17(17):2345–2349.	Yes
A13	Hautmann C, Rothenberger A, Döpfner M. An observational study of response heterogeneity in children with attention deficit hyperactivity disorder following treatment switch to modified-release methylphenidate. BMC Psychiatry. 2013;13:219.	Yes
A14	Sikirica V, et al. Immediate-release versus extended-release guanfacine for treatment of attention-deficit/hyperactivity disorder. Am J Pharm Benefits. 2013;5(4):e85–e94.	No
A15	Saloner B, Fullerton C, McGuire T. The impact of long-acting medications on attention-deficit/hyperactivity disorder treatment disparities. J Child Adolesc Psychopharmacol. 2013;23(6):401–409.	No
A16	Hodgkins P, Setyawan J, Mitra D, et al. Management of ADHD in children across Europe: patient demographics, physician characteristics and treatment patterns. Eur J Pediatr. 2013;172(7):895–906.	No
A17	Setyawan J, Hodgkins P, Guérin A, et al. Comparing treatment adherence of lisdexamfetamine and other medications for the treatment of attention deficit/hyperactivity disorder: a retrospective analysis. J Med Econ. 2013;16(7):962–975.	No
A18	Zetterqvist J, Asherson P, Halldner L, Långström N, Larsson H. Stimulant and non-stimulant attention deficit/hyperactivity disorder drug use: total population study of trends and discontinuation patterns 2006–2009. Acta Psychiatr Scand. 2013;128(1):70–77.	No
A19	Lachaine J, Beauchemin C, Sasane R, Hodgkins PS. Treatment patterns, adherence, and persistence in ADHD: a Canadian perspective. Postgrad Med. 2012;124(3):139–148.	No
A20	Braun S, Russo L, Zeidler J, Linder R, Hodgkins P. Descriptive comparison of drug treatment-persistent, -nonpersistent, and nondrug treatment patients with newly diagnosed attention deficit/hyperactivity disorder in Germany. Clin Ther. 2013;35(5):673–685.	No
A21	Pottegård A, Bjerregaard BK, Glintborg D, Kortegaard LS, Hallas J, Moreno SI. The use of medication against attention deficit/hyperactivity disorder in Denmark: a drug use study from a patient perspective. Eur J Clin Pharmacol. 2013;69(3):589–598.	No
A22	McCarthy S, Wilton L, Murray ML, Hodgkins P, Asherson P, Wong IC. Persistence of pharmacological treatment into adulthood, in UK primary care, for ADHD patients who started treatment in childhood or adolescence. BMC Psychiatry. 2012;12:219.	No
A23	van Stralen JP. The clinical impact of switching attention deficit hyperactivity disorder patients from OROS®-MPH to Novo-MPH ER-C®: A paediatric practice review. Paediatr Child Health. 2013;18(2):70–73.	No
A24	Lensing MB, Zeiner P, Sandvik L, Opjordsmoen S. Four-year outcome in psychopharmacologically treated adults with attention-deficit/hyperactivity disorder: a questionnaire survey. J Clin Psychiatry. 2013;74(1):e87–e93.	Yes
A25	Sikirica V, Pliszka SR, Betts KA, et al. Comparative treatment patterns, resource utilization, and costs in stimulant-treated children with ADHD who require subsequent pharmacotherapy with atypical antipsychotics versus non-antipsychotics. J Manag Care Pharm. 2012;18(9):676–689.	No
A26	Garbe E, Mikolajczyk RT, Banaschewski T, et al. Drug treatment patterns of attention-deficit/hyperactivity disorder in children and adolescents in Germany: results from a large population-based cohort study. J Child Adolesc Psychopharmacol. 2012;22(6):452–458.	No
A27	Ruggiero S, Rafaniello C, Bravaccio C, et al. Safety of attention-deficit/hyperactivity disorder medications in children: an intensive pharmacosurveillance monitoring study. J Child Adolesc Psychopharmacol. 2012;22(6):415–422.	Yes
A28	Torgersen T, Gjervan B, Nordahl HM, Rasmussen K. Predictive factors for more than 3 years’ duration of central stimulant treatment in adult attention-deficit/hyperactivity disorder: a retrospective, naturalistic study. J Clin Psychopharmacol. 2012;32(5):645–652.	No
A29	Ercan ES, Kose S, Kutlu A, Akyol O, Durak S, Aydin C. Treatment duration is associated with functioning and prognosis in children with attention deficit hyperactivity disorder. Bulletin of Clinical Psychopharmacology. 2012;22(2):148–160.	No
A30	Zoëga H, Rothman KJ, Huybrechts KF, et al. A population-based study of stimulant drug treatment of ADHD and academic progress in children. Pediatrics. 2012;130(1):e53–e62.	No
A31	Coletti DJ, Pappadopulos E, Katsiotas NJ, Berest A, Jensen PS, Kafantaris V. Parent perspectives on the decision to initiate medication treatment of attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2012;22(3):226–237.	No
A32	Goetz M, Yeh CB, Ondrejka I, et al. A 12-month prospective, observational study of treatment regimen and quality of life associated with ADHD in central and eastern Europe and eastern Asia. J Atten Disord. 2012;16(1):44–59.	Yes
A33	Georgiopoulos AM, Hua LL. The diagnosis and treatment of attention deficit-hyperactivity disorder in children and adolescents with cystic fibrosis: a retrospective study. Psychosomatics. 2011;52(2):160–166.	Yes
A34	Palli SR, Kamble PS, Chen H, Aparasu RR. Persistence of stimulants in children and adolescents with attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2012;22(2):139–148.	No
A35	Lawson KA, Johnsrud M, Hodgkins P, Sasané R, Crismon ML. Utilization patterns of stimulants in ADHD in the Medicaid population: a retrospective analysis of data from the Texas Medicaid program. Clin Ther. 2012;34(4):944–956.e4.	No
A36	Rothenberger A, Becker A, Breuer D, Döpfner M. An observational study of once-daily modified-release methylphenidate in ADHD: quality of life, satisfaction with treatment and adherence. Eur Child Adolesc Psychiatry. 2011;20 Suppl 2:S257–S265.	No
A37	Döpfner M, Görtz-Dorten A, Breuer D, Rothenberger A. An observational study of once-daily modified-release methylphenidate in ADHD: effectiveness on symptoms and impairment, and safety. Eur Child Adolesc Psychiatry. 2011;20 Suppl 2:S243–S255.	Yes
A38	Green T, Avda S, Dotan I, et al. Phenotypic psychiatric characterization of children with Williams syndrome and response of those with ADHD to methylphenidate treatment. Am J Med Genet B Neuropsychiatr Genet. 2012;159B(1):13–20.	Yes
A39	Powell SG, Thomsen PH, Frydenberg M, Rasmussen H. Long-term treatment of ADHD with stimulants: a large observational study of real-life patients. J Atten Disord. 2011;15(6):439–451.	Yes
A40	Hodgkins P, Sasané R, Christensen L, Harley C, Liu F. Treatment outcomes with methylphenidate formulations among patients with ADHD: retrospective claims analysis of a managed care population. Curr Med Res Opin. 2011;27 Suppl 2:53–62.	No
A41	Wolff C, Alfred A, Lindermüller A, et al. Effect of transitioning from extended-release methylphenidate onto osmotic, controlled-release methylphenidate in children/adolescents with ADHD: results of a 3-month non-interventional study. Curr Med Res Opin. 2011;27 Suppl 2:35–44.	Yes
A42	Chen CY, Yeh HH, Chen KH, Chang IS, Wu EC, Lin KM. Differential effects of predictors on methylphenidate initiation and discontinuation among young people with newly diagnosed attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2011;21(3):265–273.	No
A43	Didoni A, Sequi M, Panei P, Bonati M; Lombardy ADHD Registry Group. One-year prospective follow-up of pharmacological treatment in children with attention-deficit/hyperactivity disorder. Eur J Clin Pharmacol. 2011;67(10):1061–1067.	Yes
A44	Hodgkins P, Sasané R, Meijer WM. Pharmacologic treatment of attention-deficit/hyperactivity disorder in children: incidence, prevalence, and treatment patterns in the Netherlands. Clin Ther. 2011;33(2):188–203.	No
A45	Niederkirchner K, Slawik L, Wermelskirchen D, Rettig K, Schäuble B. Transitioning to OROS® methylphenidate from atomoxetine is effective in children and adolescents with ADHD. Expert Rev Neurother. 2011;11(4):499–508.	Yes
A46	Sitholey P, Agarwal V, Chamoli S. A preliminary study of factors affecting adherence to medication in clinic children with attention-deficit/hyperactivity disorder. Indian J Psychiatry. 2011;53(1):41–44.	Yes
A47	Torres A, Whitney J, Rao S, Tilley C, Lobel R, Gonzalez-Heydrich J. Tolerability of atomoxetine for treatment of pediatric attention-deficit/hyperactivity disorder in the context of epilepsy. Epilepsy Behav. 2011;20(1):95–102.	Yes
A48	van den Ban E, Souverein PC, Swaab H, van Engeland H, Egberts TC, Heerdink ER. Less discontinuation of ADHD drug use since the availability of long-acting ADHD medication in children, adolescents and adults under the age of 45 years in the Netherlands. Atten Defic Hyperact Disord. 2010;2(4):213–220.	No
A49	Scott NG, Ripperger-Suhler J, Rajab MH, Kjar D. Factors associated with atomoxetine efficacy for treatment of attention-deficit/hyperactivity disorder in children and adolescents. J Child Adolesc Psychopharmacol. 2010;20(3):197–203.	Yes
A50	Bejerot S, Rydén EM, Arlinde CM. Two-year outcome of treatment with central stimulant medication in adult attention-deficit/hyperactivity disorder: a prospective study. J Clin Psychiatry. 2010;71(12):1590–1597.	Yes
A51	Christensen L, Sasané R, Hodgkins P, Harley C, Tetali S. Pharmacological treatment patterns among patients with attention-deficit/hyperactivity disorder: retrospective claims-based analysis of a managed care population. Curr Med Res Opin. 2010;26(4):977–989.	No
A52	Atzori P, Usala T, Carucci S, Danjou F, Zuddas A. Predictive factors for persistent use and compliance of immediate-release methylphenidate: a 36-month naturalistic study. J Child Adolesc Psychopharmacol. 2009;19(6):673–681.	Yes
A53	Janols LO, Liliemark J, Klintberg K, von Knorring AL. Central stimulants in the treatment of attention-deficit hyperactivity disorder (ADHD) in children and adolescents. A naturalistic study of the prescription in Sweden, 1977–2007. Nord J Psychiatry. 2009;63(6):508–516.	Yes
A54	Winterstein AG, Gerhard T, Shuster J, Saidi A. Cardiac safety of methylphenidate versus amphetamine salts in the treatment of ADHD. Pediatrics. 2009;124(1):e75–e80.	No
A55	Banerjee S. Use of atomoxetine in children and adolescents with ADHD. Prog Neurol Psychiatry. 2009;13(2):18–20.	Yes
A56	Chou WJ, Chou MC, Tzang RF, et al. Better efficacy for the osmotic release oral system methylphenidate among poor adherents to immediate-release methylphenidate in the three ADHD subtypes. Psychiatry Clin Neurosci. 2009;63(2):167–175.	No
A57	Romano E, Thornhill S, Lacourse E. An 8-year follow-up study of profiles and predictors of methylphenidate use in a nationwide sample of boys. J Pediatr. 2009;155(5):721–727.	Yes
A58	Berger I, Dor T, Nevo Y, Goldzweig G. Attitudes toward attention-deficit hyperactivity disorder (ADHD) treatment: parents’ and children’s perspectives. J Child Neurol. 2008;23(9):1036–1042.	No
A59	Ramos-Quiroga JA, Bosch R, Castells X, et al. Effect of switching drug formulations from immediate-release to extended-release OROS methylphenidate: a chart review of Spanish adults with attention-deficit hyperactivity disorder. CNS Drugs. 2008;22(7):603–611.	No
A60	Winterstein AG, Gerhard T, Shuster J, et al. Utilization of pharmacologic treatment in youths with attention deficit/hyperactivity disorder in Medicaid database. Ann Pharmacother. 2008;42(1):24–31.	No
A61	Bokhari FAS, Heiland F, Levine P, Ray GT. Risk factors for discontinuing drug therapy among children with ADHD. Health Services and Outcomes Research Methodology. 2008;8(3):134–158.	No
A62	Kurscheidt JC, Peiler P, Behnken A, et al. Acute effects of methylphenidate on neuropsychological parameters in adults with ADHD: possible relevance for therapy. J Neural Transm. 2008;115(2):357–362.	Yes
A63	Darredeau C, Barrett SP, Jardin B, Pihl RO. Patterns and predictors of medication compliance, diversion, and misuse in adult prescribed methylphenidate users. Hum Psychopharmacol. 2007;22(8):529–536.	Yes
A64	Olfson M, Marcus SC, Zhang HF, Wan GJ. Continuity in methylphenidate treatment of adults with attention-deficit/hyperactivity disorder. J Manag Care Pharm. 2007;13(7):570–577.	No
A65	Moosa F, Lohawala A. ADHD – do guidelines translate into service? Child Adolesc Ment Health. 2007;12(2):73–75.	Yes
A66	Johnston JA, Ye W, Van Brunt DL, Pohl G, Sumner CR. Decreased use of clonidine following treatment with atomoxetine in children with ADHD. J Clin Psychopharmacol. 2006;26(4):389–395.	No
A67	Thompson AE, Nazir SA, Abbas MJ, Clarke J. Switching from immediate- to sustained-release psychostimulants in routine treatment of children with attention-deficit hyperactivity disorder. Psychiatric Bulletin. 2006;30:247–250.	Yes
A68	Charach A, Skyba A, Cook L, Antle BJ. Using stimulant medication for children with ADHD: what do parents say? A brief report. J Can Acad Child Adolesc Psychiatry. 2006;15(2):75–83.	Yes
A69	Kemner JE, Lage MJ. Impact of methylphenidate formulation on treatment patterns and hospitalizations: a retrospective analysis. Ann Gen Psychiatry. 2006;5:5.	No
A70	Concannon PE, Tang YP. Management of attention deficit hyperactivity disorder: a parental perspective. J Paediatr Child Health. 2005;41(12):625–630.	No
A71	Marcus SC, Wan GJ, Kemner JE, Olfson M. Continuity of methylphenidate treatment for attention-deficit/hyperactivity disorder. Arch Pediatr Adolesc Med. 2005;159(6):572–578.	No
A72	Monastra VJ. Overcoming the barriers to effective treatment for attention-deficit/hyperactivity disorder: a neuro-educational approach. Int J Psychophysiol. 2005;58(1):71–80.	Yes
A73	Sanchez RJ, Crismon ML, Barner JC, Bettinger T, Wilson JP. Assessment of adherence measures with different stimulants among children and adolescents. Pharmacotherapy. 2005;25(7):909–917.	No
A74	Romano E, Baillargeon RH, Fortier I, et al. Individual change in methylphenidate use in a national sample of children aged 2 to 11 years. Can J Psychiatry. 2005;50(3):144–152.	No
A75	Huskamp HA, Deverka PA, Epstein AM, et al. Impact of 3-tier formularies on drug treatment of attention-deficit/hyperactivity disorder in children. Arch Gen Psychiatry. 2005;62(4):435–441.	No
A76	Bussing R, Zima BT, Mason D, Hou W, Garvan CW, Forness S. Use and persistence of pharmacotherapy for elementary school students with attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2005;15(1):78–87.	Yes
A77	Perwien A, Hall J, Swensen A, Swindle R. Stimulant treatment patterns and compliance in children and adults with newly treated attention-deficit/hyperactivity disorder. J Manag Care Pharm. 2004;10(2):122–129.	No
A78	Miller AR, Lalonde CE, McGrail KM. Children’s persistence with methylphenidate therapy: a population-based study. Can J Psychiatry. 2004;49(11):761–768.	No
A79	Bauermeister JJ, Canino G, Bravo M, et al. Stimulant and psychosocial treatment of ADHD in Latino/Hispanic children. J Am Acad Child Adolesc Psychiatry. 2003;42(7):851–855.	Yes
A80	Thiruchelvam D, Charach A, Schachar RJ. Moderators and mediators of long-term adherence to stimulant treatment in children with ADHD. J Am Acad Child Adolesc Psychiatry. 2001;40(8):922–928.	Yes
A81	Grcevich S, Rowane WA, Marcellino B, Sullivan-Hurst S. Retrospective comparison of Adderall and methylphenidate in the treatment of attention deficit hyperactivity disorder. J Child Adolesc Psychopharmacol. 2001;11(1):35–41.	No
A82	Hazell PL, McDowell MJ, Walton JM. Management of children prescribed psychostimulant medication for attention deficit hyperactivity disorder in the Hunter region of NSW. Med J Aust. 1996;165(9):477–480.	No
A83	McCarthy S, Asherson P, Coghill D, et al. Attention-deficit hyperactivity disorder: treatment discontinuation in adolescents and young adults. Br J Psychiatry. 2009;194(3):273–277.	No
A84	Bowen J, Fenton T, Rappaport L. Stimulant medication and attention deficit-hyperactivity disorder. The child’s perspective. Am J Dis Child. 1991;145(3):291–295.	Yes
A85	Johnston C, Seipp C, Hommersen P, Hoza B, Fine S. Treatment choices and experiences in attention deficit and hyperactivity disorder: relations to parents’ beliefs and attributions. Child Care Health Dev. 2005;31(6):669–677.	Yes
A86	Dosreis S, Zito JM, Safer DJ, Soeken KL, Mitchell JW, Ellwood LC. Parental perceptions and satisfaction with stimulant medication for attention-deficit hyperactivity disorder. J Dev Behav Pediatr. 2003;24(3):155–162.	Yes
A87	Gau SS, Chen SJ, Chou WJ, et al. National survey of adherence, efficacy, and side effects of methylphenidate in children with attention-deficit/hyperactivity disorder in Taiwan. J Clin Psychiatry. 2008;69(1):131–140.	Yes
A88	dosReis S, Butz A, Lipkin PH, Anixt JS, Weiner CL, Chernoff R. Attitudes about stimulant medication for attention-deficit/hyperactivity disorder among African American families in an inner city community. J Behav Health Serv Res. 2006;33(4):423–430.	Yes
A89	Gau SS, Shen HY, Chou MC, Tang CS, Chiu YN, Gau CS. Determinants of adherence to methylphenidate and the impact of poor adherence on maternal and family measures. J Child Adolesc Psychopharmacol. 2006;16(3):286–297.	Yes
A90	Charach A, Gajaria A, Skyba A, Chen S. Documenting adherence to psychostimulants in children with ADHD. J Can Acad Child Adolesc Psychiatry. 2008;17(3):131–136.	Yes
A91	Ibrahim el SR. Rates of adherence to pharmacological treatment among children and adolescents with attention deficit hyperactivity disorder. Hum Psychopharmacol. 2002;17(5):225–231.	Yes

Table S3

List of included studies with expert opinions and bibliographic information

ID	Primary study citation
B1	Weiss M, Jain U, Garland J. Clinical suggestions for management of stimulant treatment in adolescents. Can J Psychiatry. 2000;45(8):717–723.
B2	Charach A, Fernandez R. Enhancing ADHD medication adherence: challenges and opportunities. Curr Psychiatry Rep. 2013;15(7):371.
B3	Rothenberger A, Rothenberger LG. Updates on treatment of attention-deficit/hyperactivity disorder: facts, comments, and ethical considerations. Curr Treat Options Neurol. 2012;14(6):594–607.
B4	Rothenberger A, Döpfner M. Editorial: Observational studies in ADHD: the effects of switching to modified-release methylphenidate preparations on clinical outcomes and adherence. Eur Child Adolesc Psychiatry. 2011;20 Suppl 2:S235–S242.
B5	Brinkman WB, Epstein JN. Treatment planning for children with attention-deficit/hyperactivity disorder: treatment utilization and family preferences. Patient Prefer Adherence. 2011;5:45–56.
B6	Graham J, Banaschewski T, Buitelaar J, et al; European Guidelines Group. European guidelines on managing adverse effects of medication for ADHD. Eur Child Adolesc Psychiatry. 2011;20(1):17–37.
B7	Chacko A, Newcorn JH, Feirsen N, Uderman JZ. Improving medication adherence in chronic pediatric health conditions: a focus on ADHD in youth. Curr Pharm Des. 2010;16(22):2416–2423.
B8	Rösler M, Casas M, Konofal E, Buitelaar J. Attention deficit hyperactivity disorder in adults. World J Biol Psychiatry. 2010;11(5):684–698.
B9	Van der Westhuuizen A. Evidence-based pharmacy practice (EBPP): attention deficit hyperactivity disorder (ADHD). SA Pharmaceutical Journal. 2010;77(8):10–14,16, 18–20.
B10	Buitelaar J, Medori R. Treating attention-deficit/hyperactivity disorder beyond symptom control alone in children and adolescents: a review of the potential benefits of long-acting stimulants. Eur Child Adolesc Psychiatry. 2010;19(4):325–340.
B11	Dopheide JA. The role of pharmacotherapy and managed care pharmacy interventions in the treatment of ADHD. Am J Manag Care. 2009;15(5 Suppl):S141–S150.
B12	Coury D. Dexmethylphenidate for attention deficit hyperactivity disorder. Expert Opin Pharmacother. 2009;10(16):2679–2685.
B13	Graham L. AHA releases recommendations on cardiovascular monitoring and the use of ADHD medications in children with heart disease. Am Fam Physician. 2009;79(10):905–910.
B14	Dopheide JA, Pliszka SR. Attention-deficit-hyperactivity disorder: an update. Pharmacotherapy. 2009;29(6):656–679.
B15	Barkley RA. Global issues related to the impact of untreated attention-deficit/hyperactivity disorder from childhood to young adulthood. Postgrad Med. 2008;120(3):48–59.
B16	Van Cleave J, Leslie LK. Approaching ADHD as a chronic condition: implications for long-term adherence. J Psychosoc Nurs Ment Health Serv. 2008;46(8):28–37.
B17	Charach A, Gajaria A. Improving psychostimulant adherence in children with ADHD. Expert Rev Neurother. 2008;8(10):1563–1571.
B18	Schlander M. Is NICE infallible? A qualitative study of its assessment of treatments for attention-deficit/hyperactivity disorder (ADHD). Curr Med Res Opin. 2008;24(2):515–535.
B19	Weisler RH. Review of long-acting stimulants in the treatment of attention deficit hyperactivity disorder. Expert Opin Pharmacother. 2007;8(6):745–758.
B20	Manos MJ, Tom-Revzon C, Bukstein OG, Crismon ML. Changes and challenges: managing ADHD in a fast-paced world. J Manag Care Pharm. 2007;13(9 Suppl B):S2–S13; quiz S14–S16.
B21	López FA. ADHD: new pharmacological treatments on the horizon. J Dev Behav Pediatr. 2006;27(5):410–416.
B22	Ashton H, Gallagher P, Moore B. The adult psychiatrist’s dilemma: psychostimulant use in attention deficit/hyperactivity disorder. J Psychopharmacol. 2006;20(5):602–610.
B23	Wolraich ML, Wibbelsman CJ, Brown TE, et al. Attention-deficit/hyperactivity disorder among adolescents: a review of the diagnosis, treatment, and clinical implications. Pediatrics. 2005;115(6):1734–1746.
B24	Dodson WW. Pharmacotherapy of adult ADHD. J Clin Psychol. 2005;61(5):589–606.
B25	Staufer WB, Greydanus DE. Attention-deficit/hyperactivity disorder psychopharmacology for college students. Pediatr Clin North Am. 2005;52(1):71–84, viii.
B26	Olfson M. New options in the pharmacological management of attention-deficit/hyperactivity disorder. Am J Manag Care. 2004;10(4 Suppl):S117–S124.
B27	Greydanus DE, Pratt HD, Sloane MA, Rappley MD. Attention-deficit/hyperactivity disorder in children and adolescents: interventions for a complex costly clinical conundrum. Pediatr Clin North Am. 2003;50(5):1049–1092, vi.
B28	Swanson J. Compliance with stimulants for attention-deficit/hyperactivity disorder: issues and approaches for improvement. CNS Drugs. 2003;17(2):117–131.
B29	Bussing R, Gary FA. Practice guidelines and parental ADHD treatment evaluations: friends or foes? Harv Rev Psychiatry. 2001;9(5):223–233.
B30	Smith BH, Waschbusch DA, Willoughby MT, Evans S. The efficacy, safety, and practicality of treatments for adolescents with attention-deficit/hyperactivity disorder (ADHD). Clin Child Fam Psychol Rev. 2000;3(4):243–267.
B31	Stine JJ. Psychosocial and psychodynamic issues affecting noncompliance with psychostimulant treatment. J Child Adolesc Psychopharmacol. 1994;4(2):75–86.
B32	Hodgkins P, Shaw M, Coghill D, Hechtman L. Amfetamine and methylphenidate medications for attention-deficit/hyperactivity disorder: complementary treatment options. Eur Child Adolesc Psychiatry. 2012;21(9):477–492.
B33	Jensen CE. Medication for children with attention-deficit hyperactivity disorder. Clin Social Work J. 2004;32(2):197–214.
B34	Garland EJ. Pharmacotherapy of adolescent attention deficit hyperactivity disorder: challenges, choices and caveats. J Psychopharmacol. 1998;12(4):385–395.
B35	Greenhill LL, Pliszka S, Dulcan MK, et al. Summary of the practice parameter for the use of stimulant medications in the treatment of children, adolescents, and adults. J Am Acad Child Adolesc Psychiatry. 2001;40(11):1352–1355.
B36	Pliszka S; AACAP Work Group on Quality Issues. Practice parameter for the assessment and treatment of children and adolescents with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2007;46(7):894–921.