| Literature DB >> 30289912 |
Michelle A Kominiarek1, Linda C O'Dwyer2, Melissa A Simon3, Beth A Plunkett4.
Abstract
BACKGROUND: Providers need to be comfortable addressing obesity and gestational weight gain so they may give appropriate care; however, health care providers lack guidelines for the most effective educational strategies to assist in providing optimal care.Entities:
Mesh:
Year: 2018 PMID: 30289912 PMCID: PMC6173456 DOI: 10.1371/journal.pone.0205268
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 1Flowchart of study selection.
Description of studies included in the systematic review.
| Author/Year | Study Design/Year | Provider Characteristics | Patient Characteristics | Country/Setting | Inclusion/Exclusion for providers | Intervention | Provider Outcomes | Unit of analysis | Limitations |
|---|---|---|---|---|---|---|---|---|---|
| Lindberg 2014 [ | Retrospective cohort of pregnant women | Obstetricians, family physicians, or nurse midwives | 83–78% white | United States | No specific exclusion criteria for providers | (1) Pilot program for GWG counseling with “best practice alerts” using EMR smart sets | 2009 NAM consistent GWG counseling improved from 2.6% (n = 388 charts) to 51.0% (n = 345 charts), p<0.001 | Patient EMR | Total number of providers and their demographics not known |
| Lindhardt 2014 [ | Prospective cohort with pre vs. post- analytical design | 12 women with | Not applicable | Southern Denmark region | Able to be released from work duties to attend training | 3 day training course in MI for women with obesity | Overall MI scores increased in the “majority” but no change in empathy scores based on review of audiotaped consultations in 11/12 participants | HCP | Selection bias for HCP |
| Kinnunen 2008 [ | Non-randomized controlled trial of pregnant women | 23 PHN at six maternity and child health clinics | 77% participation rate | City of Tampere, Town of Hameenlinna, Finland | No specific exclusion criteria for providers | Patient counseling on physical activity, diet and preventing excessive GWG at sessions using “counseling cards” with 6 and 12 hours of training for control and intervention PHN, respectively | Mean satisfaction scores: 3.4 ± 1.2 study arrangements, | PHN for experience assessment | Only satisfaction and not specific knowledge change assessed |
| Daley 2015 [ | (1)Randomized controlled trial of pregnant women | 7 of 8 community midwives completed qualitative study | 36 low-risk women in usual care vs. 40 in intervention, 28 years old, 85–91% white ethnicity, 28–62% nulliparous, BMI 18–29.9kg/m2 at 1st appointment | United Kingdom | No specific exclusion criteria for providers | Attended 60–70 minute training course | (1) Quantitative: | (1) Patient EMR for quantitative | Relevance restricted to where weighing is not routine in pregnancy |
| Davis 2012 [ | Mixed-methods program evaluation of a service development initiative for overweight or obese women to limit GWG | Midwives responsible for offering service | BMI > 25 kg/m2 | South East Sydney and Central Coast of New South Wales, community settings | No specific exclusion criteria for providers | Training in nutrition, exercise, group facilitation skills, breastfeeding challenges, risks of obesity, and how to talk to women about their weight | Qualitative from 4 focus groups: | (1) Midwives | Length of training and number of midwives implementing service unknown |
| Basu 2014 [ | Prospective cohort with pre vs. post-analytic design | 32 of 43 registered midwives | Not available | Wales, UK | Community midwives employed within Health Board | 4 Training sessions over 3.5 hours on MI, nutrition, physical activity, weight management delivered by RD with group discussions and short lectures | Improved knowledge and confidence (p<0.005) per self-report | Midwives | Actual knowledge and change in practice not reported |
| Heslehurst 2015 [ | Simultaneous mixed methods study with (1) provider surveys and (2) case audits of a maternal obesity care pathway | 243 healthcare professionals (community based midwives, consultant obstetricians, consultant anesthetists, trainee obstetricians | Charts of 60 women with booking BMI > 40 kg/m2 | Multidisciplinary group in a large NHS Trust in Northeast England | No specific exclusion criteria for providers | No specific training sessions described | (1) Several communication barriers, wanted more training based on responses to surveys | (1) HCP | No provider level compliance with pathways or practice changes |
HCP Health Care Professional
PHN Public Health Nurse
RD registered dietician
NHS National Health Service
MI Motivational interviewing
GWG gestational weight gain
NAM National Academy of Medicine
EMR electronic medical record
Bias assessment with the Mixed Methods Appraisal Tool.
| Types of mixed methods | Methodological quality criteria | Lindberg 2014 [ | Lindhardt 2014 [ | Kinnunen 2008 [ | Daley 2015 [ | Davis 2012 [ | Basu 2014 [ | Heslehurst 2015 [ |
|---|---|---|---|---|---|---|---|---|
| Are there clear qualitative and quantitative research questions (or objectives), or a clear mixed methods question (or objective)? | ||||||||
| Do the collected data address the research question (objective)? | Yes | Yes | Yes | Yes | Yes | Yes | Yes | |
| 1.1. Are the sources of qualitative data (archives, documents, informants, observations) relevant to address the research question (objective)? | ||||||||
| 1.2. Is the process for analyzing qualitative data relevant to address the research question (objective)? | ||||||||
| 1.3. Is appropriate consideration given to how findings relate to the context, e.g., the setting, in which the data were collected? | ||||||||
| 1.4. Is appropriate consideration given to how findings relate to researchers’ influence, e.g., through their interactions with participants? | ||||||||
| 2.1. Is there a clear description of the randomization (or an appropriate sequence generation)? | ||||||||
| 2.2. Is there a clear description of the allocation concealment (or blinding when applicable)? | ||||||||
| 2.3. Are there complete outcome data (≥80%)? | ||||||||
| 2.4. Is there low withdrawal/drop-out (<20%)? | ||||||||
| 3.1. Are participants (organizations) recruited in a way that minimizes selection bias? | ||||||||
| 3.2. Are measurements appropriate (clear origin, or validity known, or standard instrument; and absence of contamination between groups when appropriate) regarding the exposure/intervention and outcomes? | ||||||||
| 3.3. In the groups being compared (exposed vs. non-exposed; with intervention vs. without; cases vs. controls), are the participants comparable, or do researchers take into account (control for) the difference between these groups? | ||||||||
| 3.4. Are there complete outcome data (80% or above), and, when applicable, an acceptable response rate (60% or above), or an acceptable follow-up rate for cohort studies (depending on the duration of follow-up)? | ||||||||
| 5.1. Is the mixed methods research design relevant to address the qualitative and quantitative research questions (or objectives), or the qualitative and quantitative aspects of the mixed methods question (or objective)? | ||||||||
| 5.2. Is the integration of qualitative and quantitative data (or results*) relevant to address the research question (objective)? | ||||||||
| 5.3. Is appropriate consideration given to the limitations associated with this integration, e.g., the divergence of qualitative and quantitative data (or results*) in a triangulation design? | ||||||||
RCT Randomized controlled trial