| Literature DB >> 26062023 |
Iosief Abraha1, Fabiana Trotta1, Joseph M Rimland2, Alfonso Cruz-Jentoft3, Isabel Lozano-Montoya3, Roy L Soiza4, Valentina Pierini5, Paolo Dessì Fulgheri5, Fabrizia Lattanzio2, Denis O'Mahony6, Antonio Cherubini1.
Abstract
BACKGROUND: Non-pharmacological intervention (e.g. multidisciplinary interventions, music therapy, bright light therapy, educational interventions etc.) are alternative interventions that can be used in older subjects. There are plenty reviews of non-pharmacological interventions for the prevention and treatment of delirium in older patients and clinicians need a synthesized, methodologically sound document for their decision making. METHODS ANDEntities:
Mesh:
Year: 2015 PMID: 26062023 PMCID: PMC4465742 DOI: 10.1371/journal.pone.0123090
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 1Flow diagram of literature search and study selection.
Characteristics of Included Systematic Reviews/Meta-analyses.
| Systematic review | Aim | Search strategy date | Population | Intervention | Outcomes | Primary studies on non-pharmacological intervention included/total studies included in the review | Reviews also interested in pharmacological intervention |
|---|---|---|---|---|---|---|---|
|
| To summarize the evidence of earplugs and eye masks. | Unclear | Critically ill adults | Earplugs and eye masks | Sleep and delirium outcomes | 2/7 | No |
|
| To summarize the pathogenesis of postoperative delirium and to identify strategies for prevention and management. | March 2003 | Patients with hip fracture | Educational staff, multicomponent intervention, multidisciplinary team | Delirium prevention and treatment | 2/12 | Yes |
|
| To describe the usage, training, clinical and cost effectiveness of sitters in delirium | October 2011 | Heterogeneous population including patients at risk of delirium | Use of sitter | Unclear | 4/37 | No |
|
| To assess the effectiveness of interventions for preventing delirium | April 2013 | People (aged 65+ years) in permanent long-term care residence | Multi- or single-component interventions | Delirium prevention | 2/2 | Yes |
|
| To determine the effectiveness of interventions to prevent delirium. | May 1995 | Hospitalized patients | Educational staff, multicomponent intervention, Multidisciplinary team | Delirium prevention | 2/10 | Yes |
|
| To gather evidence about treatment prevention and outcome of delirium. | March 1998 | Not specified (any) | Educational staff, multicomponent intervention, Multidisciplinary team | Delirium prevention and treatment | 2/15 | Yes |
|
| To review evidence related to the effectiveness of systematic interventions in preventing or detecting and treating delirium. | March 1998 | Any | Educational staff, multicomponent intervention, multidisciplinary team | Delirium prevention and treatment | 2/17 | No |
|
| To outline current approaches to diagnosing and managing delirium in the elderly | 1998 | Unclear | Family support, multicomponent intervention | Delirium prevention and treatment | 1/10 | Yes |
|
| To assess prevalence, associated features, outcomes, and management of delirium superimposed on dementia. | February 2002 | Patients with dementia | Multicomponent intervention | Delirium prevention and treatment | 2/7 | Yes |
|
| To compare the effectiveness of acute geriatric unit care in the acute phase of illness or injury | Unclear (2012?) | Acutely ill or injured adults | Multicomponent intervention | Falls, pressure ulcers, delirium, functional decline, hospital stay, discharge destination, mortality, costs, hospital readmissions | 2/19 | No |
|
| To assess prevalence, etiology, prognostic factors, diagnosis and management of delirium | Unclear | Any | Multicomponent intervention | Delirium treatment and prevention | 1/unclear | Yes |
|
| To assess prevalence, diagnosis and treatment of delirium | November 2010 | Adult inpatients | Educational staff, multicomponent intervention, Multidisciplinary team | Delirium incidence. | 11/40 | Yes |
|
| To determine if ortho-geriatric collaboration models improve outcomes | July 2012 | Patients with hip fracture | Ortho-geriatric consultation, | In-hospital mortality, length of stay, long-term mortality | 2/18 | No |
|
| To assess the efficacy of interventions to prevent delirium and to explore which factors increase the effectiveness of these interventions | July 2009 | Patients at risk of delirium | Educational staff, multicomponent intervention, Multidisciplinary team | Delirium incidence | 4/16 | Yes |
|
| To assess the effective interventions for prevention and treatment of delirium | October 2007 | Patients aged 65 or older with delirium or at risk of developing delirium | Educational staff, multicomponent intervention | Delirium prevention and treatment | 6/11 | Yes |
|
| To provide an overview of epidemiology, causes, and non-pharmacological and pharmacological management of delirium | August 2012 | Any population | Pharmacological and non-pharmacological | Delirium prevention and treatment | 13/29 | Yes |
|
| To update evidence-based guidelines for the treatment of proximal femoral fractures | June 2008 | Patients with proximal femoral fractures. | Time to surgery, thromboprophylaxis, anaesthesia, analgesia, prophylactic antibiotics, surgical fixation of fractures, nutritional status, mobilization, rehabilitation and daily proactive geriatrics consultation | Surgical wound closure, management of postoperative delirium, osteoporosis treatment and hip protectors | 1/128 | Yes |
|
| To review the effect of an aging society on the utilization of critical care services and the physiology of aging as it applies to critical illness and prognosis and management issues in the intensive care unit | unclear | Older patients admitted in intensive care unit. | Daily proactive geriatrics consultation, bright light therapy, music therapy | Several outcomes of elderly patients admitted to intensive care unit including prevention of delirium | 2/5 | Yes |
|
| To determine the characteristics and efficacy of multicomponent intervention strategies for delirium | August 2003 | Hospitalized older people | Educational staff, multicomponent intervention | Incidence, duration and severity of delirium, change in cognitive functioning, functional rehabilitation, length of stay and mortality. | 7/7 | No |
|
| To review the evidence for clinical decisions that medical consultants make for patients with hip fracture and to develop recommendations for care | June 1997 | patients with hip fracture | Supportive reorientation and environmental manipulation | Prevention of delirium | 1/9 | No |
|
| To determine the efficacy of peri-operative interventions in decreasing the incidence of postoperative delirium. | January, March, August 2012 | Patients receiving non-cardiac surgery | Any | Incidence of delirium within seven days of surgery | 5/29 | Yes |
|
| To evaluate the effectiveness and safety of in-facility multi-component delirium prevention programs | September 2012 | Patients at high risk of developing delirium | Multicomponent programs | Incidence of delirium | 13/19 | No |
|
| To assess the effectiveness of interventions designed to prevent delirium | September 2006 | Hospitalized patients | Educational staff, multicomponent intervention | Incidence, duration and severity delirium. | 1/6 | Yes |
|
| To identify how music and singing may be used therapeutically by nurses in caring for older people. | Unclear | People 65 years and over with osteoarthritis, delirium, sleep difficulties, chronic obstructive pulmonary disease | Music and singing | pain in patients with osteoarthritis, post-operative delirium prevention, sleep difficulties. | 1/1 | No |
|
| To assess the etiology and risk factors for delirium and to review current strategies for prevention and treatment | unclear | unclear | Multicomponent intervention, multidisciplinary team | Incidence, duration and severity delirium, | 4/13 | Yes |
|
| To evaluate strategies for preventing post-operative delirium. | August 2012 | Adult patients receiving any surgical intervention. | Multiple types of intervention | Incidence, duration and severity delirium, | 5/37 | Yes |
Characteristics of Primary Studies.
Non-Pharmacological Interventions for Delirium Prevention in Surgical Setting.
| Author | Type of study | Population | Intervention | Outcome | Study period | Setting | Funding |
|---|---|---|---|---|---|---|---|
|
| Randomized trial | 199 patients with femoral neck fracture aged 70+ (mean age 82), 74% women | Staff education (focusing on the assessment, prevention and treatment of delirium and associated complication): application of comprehensive geriatric assessment, management and rehabilitation | Primary: number of days of post-operative delirium. Secondary: complications during hospitalization, length of stay, and in-hospital and one-year mortality. | May 2000 and December 2002 | A specialized geriatric ward or a conventional orthopedic ward | Government, not for-profit. |
|
| Randomized trial | 86 patients 65+ admitted emergently for surgical repair of hip fracture (mean age 79), 79% women, | Proactive geriatrics consultation | Primary: delirium incidence (DSI, (MDAS) (CAM) MMSE) Secondary outcomes: delirium severity (MDAS, CAM), cognitive status (MMSE), length of stay, nursing home discharge | not reported | Orthopedic dept. | Private non-profit |
|
| Controlled clinical trial | 171 people with hip fracture aged 65 and older; female 65% | inpatient geriatric consultation teams | Incidence and duration of delirium (CAM), severity of delirium (Delirium Index), and cognitive status (MMSE) | unclear | Two trauma wards | None |
|
| Before/after study | 263 patients with hip fracture, age ≥65 years; female 70%. | Multifactorial intervention (supplemental oxygen, hydration, nutrition, monitoring of vital physiological parameters, adequate pain relief, avoid delay in transfer logistics, daily delirium screening using OBS scale, avoid poly-pharmacy, and perioperative /anesthetic period protocol) | Delirium incidence (SPMSQ; OBS scale) | April 2003–April 2004 | Orthopedic ward | Government |
|
| Before/after study | 256 patients (mean age 71, female 46%) undergoing elective abdominal surgery (e.g. gastrectomy). | The intervention (modified Hospital Elder Life Program): daily hospital-based care protocol, which included 3 key protocols, i.e., early mobilization, nutritional assistance, and therapeutic (cognitive) activities 3 times daily. | Primary: functional and nutritional status, cognitive function. Secondary: depressive symptoms, cognitive function, and delirium (CAM) | August 2007–April 2009 | Gastrointestinal ward | Government, not for-profit. |
|
| Before/after study | 108 patients admitted for elective orthopedic surgery; age 65+; female 50% | Comprehensive geriatric assessment | Post-operative medical complications, delirium, pressure sores, pain control, delayed mobilization, and inappropriate catheter use. | 1. May–July 2003; 2. August 2003–February 2004 | Orthopedic ward | Private Not-for profit |
|
| Before/after study | 120 patients with a traumatic fracture of proximal femur, median age 81, 80% females. | Education of nursing staff, systematic cognitive screening, consultative services, use of a scheduled pain protocol | Delirium incidence(CAM); severity of delirium; cognitive and functional status (MMSE). | Unclear | Emergency room and 2 traumatological units | Private for profit/Government |
|
| Before/after study | 99 patients with hip fracture, average age 82 years, female 78% | Ten strategies protocol (oxygen delivery, nutrition and hydration, minimizing medications, regulation of bladder/bowel function, early mobilization, prevention and treatment of major peri- and post-operative complications. | Major outcomes: proportions of subjects with delirium (CAM), discharge destination and length of stay. | 15 August and 24 December 2001 | Surgical orthopedic setting | Not reported |
|
| Before/after study | 227 patients, mean age 79 years, female 82% | Preventing approaches related to: strange environment, altered sensory input, loss of control and independence, disruption in life pattern, immobility and pain, and disruption in elimination pattern. Ameliorative approaches related to: mild behaviors suggestive of confusion, sundowning, unsafe behavior, hallucinations or illusions, and fright. | Incidence of delirium or acute confusion identified using a score based on 4 types of behaviors. | unclear | Surgical orthopedic setting | Government, not for-profit. |
DSI, Delirium Symptom Interview; CAM, Confusion Assessment Method; MDAS, the Memorial Delirium Assessment Scale; MMS, Mini-Mental State Examination; OBS, Organic Brain Syndrome
Elements of the multicomponent non-pharmacological interventions across primary studies.
| Study | Staff education | Orientation protocol | Avoidance of sensory deprivation | Multi-disciplinary team | Sleep protocol | Early mobilization | Hydration | Nutrition | Drug list review | Oxygen delivery | Pain control | Elimination of unnecessary medications | Regulation of bowel/ bladder function | Prevention, early detection, and treatment of major postoperative complications | Environmental stimuli | treatment of agitated delirium | Delirium prevention, detection, treatment | Teamwork | Individual care planning | Secondary prevention of falls and fractures | Osteoporosis prophylaxis | Family education | Familiy support | therapetic activities protocol |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lundstrom 2007 | X | X | X | X | X | X | X | X | X | X | X | X | X | |||||||||||
| Marcantonio 2001 | X | X | X | X | X | X | X | X | X | X | ||||||||||||||
| Deschodt 2012 | X | X | X | X | X | X | X | X | X | |||||||||||||||
| Björkelund 2010 | X | X | X | X | X | X | X | |||||||||||||||||
| Milisen 2001 | X | X | X | X | X | |||||||||||||||||||
| Wong 2005 | X | X | X | X | X | X | X | X | X | X | ||||||||||||||
| Harari 2007 | X | X | X | X | X | X | ||||||||||||||||||
| Chen 2011 | X | X | X | |||||||||||||||||||||
| Williams 1985 | X | X | X | X | X | X | X | X | X | |||||||||||||||
| Martinez 2012 | X | X | X | X | ||||||||||||||||||||
| Inouye 1999 | X | X | X | X | X | X | X | X | ||||||||||||||||
| Vidan 2009 | X | X | X | X | X | X | X | X | ||||||||||||||||
| Yoo 2013 | X | X | X | X | X | X | X | X | X | |||||||||||||||
| Caplan 2007 | X | X | X | X | X | |||||||||||||||||||
| Skrobik 2010 | X | X | X | X | ||||||||||||||||||||
|
| X | X | ||||||||||||||||||||||
|
| X | X | X | X | X | X | X | X | ||||||||||||||||
|
| X | X | X | X | X | X | X | X | X | |||||||||||||||
|
| X | X | X | X |
RCT, randomized controlled trial; CCT, controlled clinical trial; BAS, before-after study;
(*) studies that evaluated non-pharmacological interventions to treat delirium
Fig 2Risk of Bias of Primary Studies of Multicomponent Non-Pharmacological Interventions for Prevention and Treatment of Delirium.
✔low risk of bias? unclear risk of bias X high risk of bias; RCT, Randomized Controlled Trial; CCT, Controlled Clinical Trial; BAS before-after studies (*) post-acute skilled nursing facilities.
GRADE quality of evidence summary table for the comparisons of multicomponent non-pharmacological interventions with usual care for delirium prevention or treatment.
| Quality assessment for comparison | No of patients | Effect | Quality | Importance | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| No of studies | Design | Risk of bias | Inconsistency | Indirectness | Imprecision | Other considerations | Non-pharmacological intervention | Usual care | Relative risk (95% CI) | Absolute | ||
|
| ||||||||||||
| Delirium incidence in surgical setting | ||||||||||||
| 2[ | RCT | Serious | No serious inconsistency | No serious indirectness | No serious imprecision | None | 76/164 (46.3%) | 105/161 (65.2%) | 0.71 (0.59 to 0.86) | 17 fewer per 100 (from 8 fewer to 24 fewer) | +++ Moderate | Critical |
| Delirium incidence in medical setting (Multicomponent intervention provided by family members) | ||||||||||||
| 1[ | RCT | Serious | No serious inconsistency | No serious indirectness | Serious | None | 8/144 (5.6%) | 19/143 (13.3%) | 0.42 (0.19 to 0.92) | 35 fewer per 100 (from 5 fewer to 48 fewer) | ++ Low | Critical |
| Delirium incidence in medical setting | ||||||||||||
| 1[ | RCT | Serious | No serious inconsistency | No serious indirectness | Serious | None | 6/182 (3.3%) | 4/212 (1.9%) | 1.75 (0.5 to 6.1) | 1 more per 100 (from 1 fewer to 10 more) | + Very low | Critical |
| Delirium incidence in medical setting | ||||||||||||
| 2[ | CCT | Serious | No serious inconsistency | No serious indirectness | No serious imprecision | None | 62/596 (10.4%) | 133/798 (16.7%) | 0.65 (0.49 to 0.86) | 21 fewer per 100 (from 12 fewer to 30 fewer) | +++ Moderate | Critical |
|
| ||||||||||||
| Delirium improvement | ||||||||||||
| 4[ | RCT | Serious | Serious | No serious indirectness | No serious imprecision | None | - | - | Not Pooled | - | + Very low | Critical |
| Functional status | ||||||||||||
| 4[ | RCT | Serious | Serious | No serious indirectness | No serious imprecision | None | - | - | Not pooled | - | + Very low | Critical |
(a) Allocation concealment not clear in one study (Lundstrom 2007); both studies exposed to performance bias.
(b) Unclear blinding of outcome assessor and large confidence interval.
(c) Allocation concealment inadequate; unclear blinding of outcome assessor; per-protocol analysis; and large confidence interval.
(d) Not randomized, controlled clinical trials.
(e) Two studies with unclear/inadequate allocation concealment; 3 studies did not report data on delirium improvement, inconsistency of results (1 study in favor of the experimental treatment and 1 with non-significant results).
(f) Two studies with unclear/inadequate allocation concealment; 2 of the 4 studies did not report data on functional status.
Fig 3Forest plot of risk ratios comparing multicomponent non-pharmacological interventions vs usual care for delirium prevention in older patients in surgical setting.
Characteristics of Primary Studies—Non-Pharmacological Interventions for Delirium Prevention in Medical Setting.
| Author | Type of study | Population | Intervention | Outcome | Study period | Setting | Funding |
|---|---|---|---|---|---|---|---|
|
| Randomized trial | 413 patients; mean age 81 years; 39% men | Acute Geriatric Ward (multidisciplinary team, multicomponent intervention, staff education, early rehabilitation, planning discharge) vs Medical Wards | Primary outcome: delirium incidence (CAM, daily assessment). Secondary outcomes: duration, severity and recurrence of delirium; mortality. | March 18 to December 8,1996 | Acute geriatrics ward and general medical wards | Government, private not for profit |
|
| Randomized trial | 287 hospitalized patients at intermediate or high risk of delirium (MMSE <24, prior hospitalization, alcoholism or metabolic imbalances on admission); mean age 78; 38% men | Family education, clock and calendar in the room, avoidance of sensory deprivation (glasses, denture and hearing aids), familiar objects in the room, reorientation of patient provided by family members, extended visitation (5 h daily). | Primary outcomes: incidence, severity and duration of delirium during hospitalization (CAM). Secondary outcomes: functional decline, length of stay, mortality, discharge location, need for new social support, number of prescribed drugs | 15 September 2009 to 30 May 2010 | Internal medicine ward of a Chilean Naval Hospital | Not reported |
|
| Controlled clinical trial | 852 subjects at intermediate or high risk of delirium, with at least: visual impairment, severe illness, cognitive impairment, high ratio of blood urea to creatinine); mean age 80; 39% men | Elder Life Program: a trained interdisciplinary team targeted the following risk factors: cognitive impairment, sleep deprivation, immobility, visual impairment, hearing impairment, and dehydration; daily monitoring of adherence. | Primary outcomes: delirium incidence (CAM, every two days) severity, duration, falls, length of stay, cognitive and functional status, cost effectiveness, residential care placement. | March 25, 1995 to March 18, 1998. | General-medicine units at a university-associated hospital | Government |
|
| Controlled clinical trial | 542 patients 70 years or older at intermediate or high risk of delirium (at least: visual impairment, acute disease, cognitive impairment, dehydration); mean age 83; 44% men | In the geriatric unit: staff education and specific actions in seven risk areas: orientation, sensory impairment, sleep, mobilization, hydration, nutrition, drug use; daily monitoring of adherence. | Primary outcomes: Incidence of delirium (intensive care delirium screening checklist, assessed 24 h), ICU length of stay, hospital length of stay, antipsychotic use, mortality. | January 15 to December 15, 2007 | Geriatric unit and internal medicine ward at University hospital in Madrid, Spain | Private non for profit |
|
| Controlled clinical trial | 283 older patients allocated to each group; 43% older than 80 years; male 41% | Interdisciplinary intervention by non-geriatrics specialist physicians vs usual care | Primary outcomes: delirium and transition to a nursing home. | Unclear | Medical setting | Private non for profit |
|
| Before/after study | 37 patients at intermediate/high risk of delirium, with at least: MMSE<24, sleep deprivation, any impairment of ADL, vision/hearing impairment, dehydration); mean age: 85; 21% men | The Recruitment of Volunteers to Improve Vitality in the Elderly program: re-orientation; cognitive stimulation; feeding and hydration assistance; vision and hearing protocols. | Primary outcome: delirium incidence (CAM, daily assessment). Secondary outcomes: duration, recurrence and severity of delirium; mortality. | March to August 2003 | Geriatric wards at a tertiary referral hospital, Australia. | Government |
|
| Before/after study | 1133 adult patients admitted >24 hours; mean age 63.3 years; 59% men | Teaching staff protocol–based ICU patient assessments targeting non-pharmacological and pharmacological management of pain, sedation and delirium | Primary outcomes: incidence, severity and duration of delirium (CAM, daily assessment +interview of family and nurses and review of medical records of the afternoon/night). Secondary outcomes: functional decline, length of stay, mortality, discharge location, number of prescribed drugs | Before: August 2003 to February 2004; After: April 2005 to November 2005 | A single tertiary care adult ICU (Canada) | Government |
CAM, Confusion Assessment Method; ICU, Intensive care unit
Fig 4Forest plot of risk ratios comparing multicomponent non-pharmacological interventions vs usual care for delirium prevention in older patients in medical setting.
Characteristics of Included Primary Studies—Non-Pharmacological Interventions for Delirium Treatment.
| Study | Type of study | Population | Intervention | Outcome | Study period | Setting | Funding |
|---|---|---|---|---|---|---|---|
|
| Randomized trial | 88 pts with delirium; mean age 85, male 58% | Consultation by geriatrician or psychiatrist and follow up by a liaison nurse. | Cognitive function (SPMSQ), behavior, mortality rate, length of stay, discharge | 8 weeks | Medical ward | Not reported |
|
| Randomized trial | 227 older patients with delirium admitted to a general medical service; mean age: 82; male 54%. | Consultation by a geriatric internist or psychiatrist and follow up by a liaison nurse. Nursing intervention protocol, Environment, Orientation, Familiarity, Communication, counteraction of immobilization | Primary outcomes: improvement of cognitive status. Secondary outcomes: severity of delirium; length of stay; functional status; death. | 8 weeks | Medical ward | Not reported |
|
| Randomized trial | 174 pts with delirium, age 83, male 25% | Comprehensive geriatric assessment and treatments, Avoiding conventional neuroleptics, Orientation, Physiotherapy, Geriatric interventions (nutrition, hip protection), Comprehensive discharge planning | Primary: mortality or permanent institution, secondary: length of stay, cognitive function, delirium intensity | From September 2001 to November 2002 | Medical ward | Not reported |
|
| Randomized trial | 125 pts with delirium, mean age 81, male 44%. | Multifactorial intervention program (Course in Geriatric Medicine Focusing on Delirium Training Concerning Caregiver-Patient Interaction, Reorganization of Nursing Care, Guidance for Nursing Staff) | Duration of delirium (diagnosis with DSM-IV), mortality, length of stay | 8 months | Medical ward | Not reported |
DSI, Delirium Symptom Interview; CAM, Confusion Assessment Method; MDAS, the Memorial Delirium Assessment Scale; MMS, Mini-Mental State Examination; SPMSQ, Short Portable Mental Status Questionnaire
Characteristics of Included Primary Studies—Single-Component Based Non-Pharmacological Intervention for Delirium Prevention.
| Study | Type of study | Population | Intervention | Outcome | Study period | Setting | Funding |
|---|---|---|---|---|---|---|---|
|
| Randomized trial | 22 patients undergoing esophageal cancer surgery, mean age 63 years, 100% men | Bright light therapy | Physical activity, incidence of post-operative arrhythmia and level of acute delirium (Japanese NEECHAM scale). | February 2006-October 2006 | Intensive care unit, post-operative care | Not reported |
|
| Randomized trial | 11 patients undergoing esophageal cancer surgery, mean age 60 years, 100% men | Bright light therapy | Postoperative adjustment of the circadian rhythm, delirium incidence (Japanese NEECHAM scale). | July- December 2003 | Intensive care unit, post-operative care | Not reported |
|
| Randomized trial | 136 patients in intensive care unit, mean age 59 years, 66% men | Sleep-wake rhythm (ear plugs) | Onset of delirium or confusion (NEECHAM scale), quality of sleep | November 2008-April 2009 | Intensive care unit | Not reported |
|
| Cluster randomized trial | 3203 residents living in nursing homes, median age 85, 28% men | Geriatric Risk Assessment MedGuide software used to identify resident-specific medications that may contribute to delirium and falls risk. | Incidence of potential delirium, falls, hospitalizations potentially due to adverse drug events, and mortality | 2003–2004 | Nursing homes | Government |
|
| Randomized trial | 66 patients undergoing elective hip or knee surgery, mean age 73 years, 100% men | Music therapy | Number of patients with more than one episode of delirium, ambulation readiness profile | 7 months | Surgical ward | Not reported |
|
| Randomized trial | 124 patients undergoing elective hip or knee surgery, mean age 77 years, 18% men | Music therapy | Incidence of delirium, level of patient satisfaction | Not reported | Surgical ward | Not reported |
|
| Randomized trial | 22 patients undergoing elective hip or knee surgery, mean age 75 years, 36% men | Music therapy | Acute confusion (NEECHAM scale), cognitive function post-surgery (MMSE) | Not reported | Surgical ward | Not reported |
|
| Controlled clinical trial | 250 patients, mean age 80 years, 40% men | Staff education | Point prevalence of delirium (modified delirium rating scale). Secondary outcome: recognition and diagnosis of delirium. | December 2001-August 2002 | Medical ward | Not reported |
|
| Cluster-randomized trial | 98 residents of 7 care homes, mean age 84, 46% men | Hydration management | Incidence of delirium (NEECHAM scale) | - | Nursing-home residence | Not for profit institution |
|
| Controlled before-after | 314 critically-ill patients | Reorientation protocol | Delirium incidence (CAM) | February-June 2008, July-December 2008 | Intensive care unit | None |
DSI, the Delirium Symptom Interview; CAM, Confusion Assessment Method; NEECHAM, Neelon and Champagne Confusion Scale; MDAS, Memorial Delirium Assessment Scale; MMS, Mini-Mental State Examination
Fig 5Risk of Bias of Primary Studies of Single Non-Pharmacological Interventions for Prevention of Delirium.
✔low risk of bias? unclear risk of bias X high risk of bias; RCT, Randomized Controlled Trial; CCT, Controlled Clinical Trial; BAS before-after studies; (*) Geriatric Risk Assessment MedGuide software.
GRADE quality of evidence summary table for the comparisons of single component non-pharmacological interventions with usual care for delirium prevention.
| Quality assessment for comparison | No of patients | Effect | Quality | Importance | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| No of studies | Design | Risk of bias | Inconsistency | Indirectness | Imprecision | Other considerations | Non-pharmacological intervention | Usual care | Relative risk(95% CI) | Absolute | ||
|
| ||||||||||||
|
| ||||||||||||
| 2[ | RCT | Serious | No serious inconsistency | Serious | Serious | None | 2/21(9.5%) | 7/20(35%) | 0.29 (0.07 to 1.25) | 25 fewer per 100 (from 33 fewer to 9 more) | + Very low | Critical |
|
| ||||||||||||
| 1[ | RCT | Serious | No serious inconsistency | No serious indirectness | Serious | None | 14/69(20.3%) | 13/67(19.4%) | 1.05 (0.53 to 2.06) | 1 more per 100 (from 9 fewer to 21 more) | ++ Low | Critical |
|
| ||||||||||||
| 1[ | Cluster RCT | Serious | No serious inconsistency | No serious indirectness | No serious indirectness | None | 169/1769(9.6%) | 264/1552(17%) | HR 0.42 (0.35 to 0.52) | 9 fewer per 100 (from 8 fewer to 11 fewer) | +++ Moderate | Critical |
|
| ||||||||||||
| 1[ | Cluster RCT | Serious | No serious inconsistency | No serious indirectness | Serious | None | 3/53(5.7%) | 3/45(6.7%) | 0.85 (0.18 to 4) | 1 fewer per 100 (from 5 fewer to 20 more) | + Very low | Critical |
|
| ||||||||||||
| 3[ | RCT | Serious | Serious | No serious indirectness | No serious imprecision | None | - | - | - | - | + Very low | Critical |
|
| ||||||||||||
| 1[ | CCT | Serious | No serious inconsistency | No serious indirectness | Serious | None | 12/122(9.8%) | 25/128(19.5%) | 0.5 (0.26 to 0.96) | 10 fewer per 100 (from 1 fewer to 14 fewer) | ++ Low | Critical |
|
| ||||||||||||
| 1[ | BA | Serious | No serious inconsistency | No serious indirectness | Serious | 32/144(22.2%) | 60/170(35.3%) | 0.63 (0.44 to 0.91) | 13 fewer per 100 (from 3 fewer to 20 fewer) | + Very low | Critical | |
(a) Allocation concealment not clear; blinding of outcome assessor; Japanese with esophageal cancer (indirectness); more than 20% exclusions; large confidence interval.
(b) Unclear number of included patients in final analysis; large confidence interval.
(c) Allocation concealment unclear.
(d) Inadequate randomization; outcome assessor not blinded; unclear final analysis; significant different at baseline (blood urea nitrogen and creatinine ratio).
(e) Inadequate/unclear allocation concealment; outcome assessor not blinded/unclear; results inadequately reported.
(f) High risk of selection bias (controlled clinical trial); outcome assessor not blinded; large confidence interval.
(g) High risk of selection bias (before-after study); outcome assessor not blinded; differences in baseline characteristics (diabetes, sepsis,…); large confidence interval