Barriers and facilitators to office-based opioid agonist therapy prescribing and effective interventions to increase provider prescribing: protocol for a systematic review
verfasst von:
Lara L. Nixon, Jazmin C. Marlinga, K. Alix Hayden, Kelly J. Mrklas
Opiate agonist therapy (OAT) prescribing rates by family physicians are low in the context of community-based, comprehensive primary care. Understanding the factors that support and/or inhibit OAT prescribing within primary care is needed. Our study objectives are to identify and synthesize documented barriers to, and facilitators of, primary care opioid agonist prescribing, and effective strategies to inform intervention planning and support increased primary care OAT prescribing.
Methods/design
We will systematically search EMBASE, CINAHL, PsycINFO, Cochrane Central Register of Controlled Trials, MEDLINE, and gray literature in three domains: primary care providers, opioid agonist therapy, and opioid abuse. We will retain and assess primary studies reporting documented participation, or self-reported willingness to participate, in OAT prescribing; and/or at least one determinant of OAT prescribing; and/or strategies to address determinants of OAT prescribing from the perspective of primary care providers in comprehensive, community-based practice settings. There will be no restrictions on study design or publication date. Studies limited to specialty clinics with specialist prescribers, lacking extractable data, or in languages other than English or French will be excluded. Two reviewers will perform abstract review and data extraction independently. We will assess the quality of included studies using the Joanna Briggs Institute Critical Appraisal Tool. We will use a framework method of analysis to deductively code barriers and facilitators and to characterize effective strategies to support prescribing using a combined, modified a priori framework comprising the Theoretical Domains Framework and the Consolidated Framework for Implementation Research.
Discussion
To date, no synthesis has been undertaken of the barriers and facilitators or effective interventions promoting OAT prescribing by primary care clinicians in community-based comprehensive care settings. Enacting change in physician behaviors, community-based programming, and health services is complex and best informed by using theoretical frameworks that allow the analysis of the available data to assist in designing and implementing interventions. In light of the current opioid crisis, increasing the capacity of primary care clinicians to provide OAT is an important strategy to curb morbidity and mortality from opioid use disorder.
Template for Intervention Description and Replication checklist and guide [73]
US FDA
United States Food and Drug Administration
Background
Of the pharmacotherapies available for opioid use disorder (OUD), two opiate-agonist agents, methadone and the combination therapy buprenorphine-naloxone, have been found to be effective in retaining patients in treatment and decreasing illicit opiate use [1, 2]. Both treatments are long-acting agonists that function at the level of the mu-opioid receptor to block the physical symptoms of opioid withdrawal and are designed to have minimal euphoric effects and block the euphoria associated with administering exogenous prescribed or illicit opioids [3]. Compared to abstinence alone in individuals with OUD, these agents reduce all-cause and overdose mortality and relapse to disordered patterns of opioid use and increase retention in addiction treatment programs [4‐6]. In pregnant patients with OUD, both methadone and buprenorphine-naloxone improved neonatal outcomes with decreased rates of prematurity, lower neonatal abstinence scores, and decreased length of hospital stay, with higher treatment retention rates and decreased relapse rates during pregnancy [7, 8]. With improvements in disease outcomes, patients with OUD also benefit from improved social outcomes, including decreased rates of incarceration and increased rates of employment and improved social functioning [9].
Despite these benefits, patients with OUD experience many barriers to accessing methadone and buprenorphine-naloxone. Stigma and lack of timely access to treatment have often been cited as deterrents to patients receiving care [10‐12]. Geographic differences in treatment availability add difficulty for patients outside of urban centers [13]. High-level barriers, such as financial coverage for therapies and regulatory restrictions, as well as institutional and provider-based attitudes, limit access to care [14]. Allied health team members similarly report challenges around providing opiate agonist therapy (OAT), with pharmacy services requiring additional supports [15] and nursing practices being affected by moral distress in the care of patients with addictions [16‐18]. Patients with OUD have expressed a preference for receiving OAT from their family physicians who can provide comprehensive care and relational continuity for physical and mental health issues [19]. While it is often asserted that community-based family physicians are well positioned to prescribe OAT, a number of patient- and practice-specific factors must be considered to incorporate addiction care into general practice [20].
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Initial data indicate that family physicians can successfully integrate medication-assisted treatment for OUD into comprehensive care [21, 22]. Despite this, methadone and buprenorphine-naloxone prescribing rates by family physicians remain low [23]. Studies have documented barriers to medication-assisted OUD treatment provision from a generalist perspective, often citing patient-, physician-, clinic-, and systems-based factors [24‐30]. However, in preliminary searching, we were unable to identify a synthesis describing factors that enable and/or hinder the use of medication-assisted OAT by family physicians.
Implementing clinical innovations is challenging and requires complex changes in clinical practice, better collaboration between disciplines, and/or changes in organizations [31]. Prescribing opioid agonists in the context of community-based, comprehensive primary care may require a change in all three of these (or additional) domains (e.g., regular and special patient monitoring, close communication with pharmacists, and development of on-call coverage by appropriately licensed and knowledgeable teams). Identifying potential barriers to change and strategies to promote change is enhanced by exploration informed by different theoretical perspectives [31]. Two frameworks integrating multiple theories relating to behavioral change are the Theoretical Domains Framework (TDF) [32‐34] and the Consolidated Framework for Implementation Research (CFIR) [35]. TDF is an evidence-based framework derived from 33 theories of behavior change and 128 constructs organized into 12 “theoretical domains” that focus on individual- and group-level determinants of change [33, 34]. CFIR consolidates 19 theories of implementation and consists of 5 domains (intervention characteristics, outer setting, inner setting, characteristics of individuals, and implementation process characteristics) complementary to TDF in their ability to systematically identify contextual, process, intervention, and individual characteristics of implementation.
This synthesis will use a modified combination of the TDF and CFIR frameworks to identify barriers to, facilitators of, and effective interventions for opioid agonist prescribing in comprehensive community-based care at multiple levels [36, 37]. The purpose for combining the frameworks is several-fold: first, TDF offers relative advantages in assessing individual- and group-level change factors compared to the CFIR; second, the CFIR offers relative advantages compared to the TDF in its ability to identify and describe in detail factors associated with context, interventions, and implementation processes; third, both frameworks are flexible and able to provide multi-level conceptualization; and fourth, the comprehensive theoretical perspective of the TDF offers researchers the opportunity to readily synthesize findings for optimized and rapid use with similarly structured intervention mapping techniques [38]. By combining the frameworks and modifying them slightly (e.g., subdomain merges to avoid overlapping codes in areas such as individual characteristics and environmental context/resources), we hope to provide the most comprehensive conceptual scope for coding, create important precursor knowledge for intervention design and mapping, and increase the usability of the evidence generated [36].
Although there is documented evidence for barriers, facilitators, and effective, provider-targeted interventions to increase opioid agonist prescribing in community-based comprehensive primary care, this body of evidence has not been synthesized in a form that is actionable using evidence-based, theory-driven intervention design and testing. The aim of this systematic review is to identify and synthesize available literature regarding barriers, facilitators, and effective strategies for primary care prescribing of OAT. The intent is to inform intervention planning and create ready-to-use evidence to encourage increased provider and policymaker use of this evidence-based addiction treatment practice.
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Methods
Research objectives
The specific objectives of this study are to:
1.
Locate the literature reporting barriers, facilitators, and effective strategies for primary care prescribing of OAT.
2.
Extract reported barriers, facilitators, and effective strategies for primary care OAT prescription and categorize these according to TDF/CFIR domains.
3.
Identify key themes within TDF/CFIR domains to inform the planning of future interventions to support primary care prescribing of OAT.
Study design
Protocol design, search strategy, synthesis, and reporting of findings from this systematic review will be guided by the Sampling Strategy-Type of Study-Approaches-Range of Years-Limits-Inclusion and Exclusions-Terms used-Electronic Sources (STARLITE) Search Reporting Standards [39], the Cochrane Collaboration Handbook of Systematic Reviews [40], The Centre of Reviews and Dissemination (CRD) guide [41], the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) Statement [42] and Protocols Extension (PRISMA-P) [43], and the Enhancing Transparency in Reporting the Synthesis of Qualitative Research (ENTREQ) reporting guidelines [44] (see Additional file 1). The synthesis will be guided by the Knowledge-to-Action (KTA) cycle [45‐47], an overarching meta-framework that identifies the multiple, dynamic, and interacting phases involved in knowledge creation and knowledge application in practice. Systematic study of barriers and facilitators to knowledge use is a critical part of the “Action” cycle, and a key precursor to intervention design and implementation. Systematic study of interventions to support the application of knowledge (in this case OAT prescribing) documents effective strategies and can inform the design, tailoring, and testing of interventions, as well as help to overcome identified barriers to knowledge use. These steps are core parts of engineering strategies that encourage the uptake and use of opioid agonist prescribing in primary care. Planned action theory underpins the KTA cycle, which is flexible and allows for the easy integration of other theory-based approaches to behavior change, including the TDF and CFIR.
Study eligibility criteria
Context
For the purposes of this study, we will define primary care as practice including comprehensive community-based continuous care focused on prevention and health promotion, as well as acute, chronic, and terminal illness management [48‐51]. Reference to using pharmacologic treatment for managing heroin and opiate-dependent patients using opioid-agonists dates back to the early 1970s; methadone was approved by the United States Food and Drug Administration (US FDA) in 1972 for this indication, and sublingual buprenorphine-naloxone was approved by the US FDA on October 8, 2002; as buprenorphine has been available for much longer in some European countries, we will not date-limit included studies [52‐56].
For the purposes of this systematic review, the term barrier will refer to any single- or multi-level factor negatively associated with, or that hinders the likelihood of, office-based primary care prescribing of opioid agonists. The term facilitator refers to any single- or multi-level factor positively associated with, or that increases the likelihood of, office-based primary care prescribing of opioid agonists [57]. Effective strategies to increase provider prescription of OAT are defined as any single- or multi-level intervention that reduces barriers or leverages facilitators and increases the likelihood of office-based primary care prescribing of opioid agonists (adapted from Mrklas et al. [58]).
Participants
We will include studies that involve primary care physicians or nurse practitioners (providers) in a full scope setting or comprehensive primary care (e.g., scope of practice not limited to addiction treatment). Further, we will include studies that report documented barriers to, facilitators of, and/or effective interventions in which providers participate in, or self-report willingness to participate in, any of the following: (1) OAT prescribing, and/or (2) at least one determinant of OAT prescribing, and/or (3) strategies to address determinants of OAT prescribing, from the perspective of primary care providers in comprehensive community-based practice settings.
We will exclude studies involving only specialty clinics or providers (e.g., addiction clinics or psychiatric clinics focused on addiction treatment), studies reporting secondary data (e.g., scoping or systematic review articles), studies that lack extractable data, and studies in any language other than French or English. Reviews will be excluded, but their bibliographies will be used to identify potential citations. No restrictions will be placed on publication date, study design, or geographic location.
Outcomes
The primary study outcomes will be documented barriers, facilitators, and effective strategies to increase primary care OAT prescribing from the perspective of primary care providers in comprehensive community-based practice settings. Documented determinants of opioid agonist prescribing may include multi-level factors, including those related to the individual prescriber, OAT and its implementation, and the practice and system setting. Some of the factors identified in the literature include the following: lack of comfort with managing patients with opioid dependence; concerns that patients will divert their opioid agonist; lack of experience, training, or education in using opioid agonists; provider fear of practice shifting to patients with opioid dependence; fear of staff or community resistance; burdensome licensing requirements to prescribe opioid agonists; inadequate community support services (e.g., addiction counselling); and inadequate reimbursement [59].
We will extract information about effective strategies in a structured, inductive, and iterative way, starting from outcomes previously reported in the literature (e.g., publication of opioid agonist prescribing best practice guidelines oriented to primary care prescribers [60]; increasing addiction training in undergraduate, graduate, and continuing medical education [59]; and clarifying regulatory conditions for prescribing opioid agonists) [24]. Given the known importance of contextual factors in practice patterns [28, 29], multiple study characteristics will be iteratively abstracted (e.g., setting, community size, practice type, and licensing requirements for OAT prescribing) (Table 1).
Table 1
Draft data extraction tool
Variable name
Description
Study characteristics
Author
Authors of publication
Year
Publication year
Country
Country of origin
Language
Language of publication
Funding source
Reported source of funding for the study
Population
Study population
Setting
Study setting
Study type
Study design
Community size
Rural urban or remote
Location of graduation
Location prescriber graduated from
Practice type
Private, group, solo, community health center
Licensing
Prescriber licensing to prescribe opioid agonists
Training
Training in addiction medicine or opioid agonist therapy
Training type
Type of training received in addiction medicine or opioid agonist therapy
Training type description
Description of training as reported by authors
Sample
Sample population
Study method
Study method used
Study participants
Number of study participants
Participant response rate
What proportion of participants responded
Gender
Reported gender of participants
Inclusion criteria
Reported inclusion criteria
Exclusion criteria
Reported exclusion criteria
Statistical analytic technique
Statistical technique(s) used in analysis
Documented Barriers and Facilitators
TDF domains
-Barriers or facilitators that reflect individual or group level influences on implementation will be coded to one of Michie et al 2005, TDF Domains (CFIR Domains II, III, and V will be used in lieu of TDF’s Environmental context and resources/Environmental constraints)
Knowledge
Skills
Social/professional role and identity
Beliefs about capabilities
Beliefs about consequences
Motivation and goals
Memory, attention, decision processes
Social influences
Emotion
Behavioral regulation
Nature of the behaviors
CFIR domains
-Barriers-facilitators that reflect context will be coded into one of Damschroder et al. 2009 CFIR Domains (and their respective subdomains), excluding Domain IV – Individual Characteristics, which will be replaced by TDF domains
I. Intervention characteristics (8)
II. Outer setting (4)
III. Inner setting (5)
V. Implementation process characteristics (4)
Outcomes
Self-reported willingness to participate in prescribing office-based OAT
Self-reported willingness to prescribe office-based OAT
Actual participation in office-based OAT prescribing
Reported participation in office-based OAT
Actual participation in at least one determinant of office-based OAT prescribing
Reported participation in at least one determinant of OAT prescribing
OAT determinants
Reported determinants
Documented strategies
(These strategies will be inductively analyzed in an iterative fashion, and coded as themes arise)
Reported strategies for enhancing provider prescription of OAT, or elements of OAT
Data sources and search strategy
The search strategy design was informed by, and will be executed with, the guidance of an academic librarian (KAH). Preliminary searching (Cochrane Database of Systematic Reviews, Campbell Collaboration, Joanna Briggs Institute EBP Database, PROSPERO, and MEDLINE) was unsuccessful in identifying an existing synthesis of the documented barriers and facilitators of, and effective interventions for, primary care provider OAT prescribing in the context of comprehensive community-based primary care.
Several key papers were used to identify appropriate Medical Subject Headings (MeSH terms) and keywords and develop the initial search strategy for feasibility testing in MEDLINE (OVID). As the search strategy prioritized sensitivity (i.e., comprehensiveness), the search incorporates three main concepts: primary care provider, opioid substitution treatment, and opioid addiction. The MEDLINE strategy was circulated for peer review (DL) using the PRESS Checklist [61‐63] and feedback integrated to create a final search strategy (Table 2). The MEDLINE search strategy will be adapted and translated for each database.
Table 2
Draft search strategy (MEDLINE)
#
Searches
1
exp Physicians, Primary Care/
2
exp General Practitioners/
3
exp Family Practice/
4
exp Physicians, Family/
5
exp Practice Patterns, Physicians’/
6
exp Nurse Practitioners/
7
exp Nurse Clinicians/
8
exp Primary Health Care/
9
exp Ambulatory Care/
10
exp Community Health Services/
11
exp Community Medicine/
12
exp Office Visits/
13
physician*.mp.
14
primary care physician*.mp.
15
family physician*.mp.
16
family doctor*.mp.
17
(general adj2 physician*).mp.
18
(general adj2 practitioner*).mp.
19
(family adj2 practitioner*).mp.
20
(primary care adj2 practitioner*).mp.
21
(nurse* adj2 clinician*).mp.
22
(nurse adj2 practitioner*).mp.
23
family practice*.mp.
24
family medicine.mp.
25
general practice*.mp.
26
outpatient practice*.mp.
27
primary care.mp.
28
primary care setting*.mp.
29
public sector healthcare.mp.
30
office-based.mp.
31
(private adj2 office*).mp.
32
(physician* adj2 office*).mp.
33
(office* adj2 visit*).mp.
34
(community adj3 care).mp.
35
(community adj3 healthcare).mp.
36
(community adj3 treatment).mp.
37
or/1-36
38
exp Opiate Substitution Treatment/
39
37 and 38
40
exp BUPRENORPHINE/
41
exp BUPRENORPHINE, NALOXONE DRUG COMBINATION/
42
exp Naloxone/
43
exp METHADONE/
44
(opioid adj2 treatment).mp.
45
(opioid adj2 therap*).mp.
46
(opioid adj2 substitution).mp.
47
(opioid adj2 replacement).mp.
48
(opioid adj2 maintenance).mp.
49
(opiate adj2 treatment).mp.
50
(opiate adj2 therap*).mp.
51
(opiate adj2 substitution).mp.
52
(opiate adj2 replacement).mp.
53
methadone.mp.
54
(methadone adj2 treatment).mp.
55
(methadone adj2 therap*).mp.
56
(methadone adj2 substitution).mp.
57
(methadone adj2 replacement).mp.
58
Buprenorphine.mp.
59
(buprenorphine adj2 treatment).mp.
60
(buprenorphine adj2 therap*).mp.
61
(buprenorphine adj2 substitution).mp.
62
(buprenorphine adj2 replacement).mp.
63
naloxone.mp.
64
(naloxone adj2 treatment).mp.
65
(naloxone adj2 therap*).mp.
66
(naloxone adj2 substitution).mp.
67
(naloxone adj2 replacement).mp.
68
(buprenorphine naloxone adj2 treatment).mp.
69
(buprenorphine naloxone adj2 therap*).mp.
70
(buprenorphine naloxone adj2 substitution).mp.
71
(buprenorphine naloxone adj2 replacement).mp.
72
(medication assisted adj2 treatment).mp.
73
(medication assisted adj2 therap*).mp.
74
(maintenance adj2 treatment).mp.
75
(maintenance adj2 therap*).mp.
76
(substitution adj2 therap*).mp.
77
opioid agonist*.mp.
78
or/40-77
79
exp Opioid-Related Disorders/
80
exp Heroin Dependence/
81
exp Morphine Dependence/
82
exp Opium Dependence/
83
“opioid use”.mp.
84
“opioid use disorder*”.mp.
85
Opioid related disorder*.mp.
86
(opioid adj2 disorder*).mp.
87
(opioid adj2 addict*).mp.
88
(opioid adj2 abuse).mp.
89
(opioid adj2 dependen*).mp.
90
or/79-89
91
37 and 78 and 90
92
39 or 91
93
limit 92 to (english or french)
Electronic databases
We will search MEDLINE Epub Ahead of Print, In-Process & Other Non-Indexed Citations, Ovid MEDLINE(R) Daily and Ovid MEDLINE(R), EMBASE, PsycINFO, CINAHL Plus with Full Text, and Cochrane Central Register of Controlled Trials.
Gray literature and search strategy
We will also include gray literature. As noted by several researchers, systematically searching for gray literature is a challenging process [64‐66]. Using recommendations by Godin et al. [66], we have developed a preliminary list of gray literature sources identified to date, and the detailed gray literature plan will emerge from these and included peer-reviewed studies as they are identified. We will search theses/dissertation databases and repositories, gray literature databases, associations/societies, and community and government agency reports, as well as conference websites (Table 3).
Table 3
Preliminary gray literature resources
Resource type
Name
Description
URL
Dissertations
Proquest Dissertations and Theses Global
Global listing of dissertations and theses. Note, as open access archiving increases, fewer dissertations/theses are submitted to this resources
Subscription via University of Calgary
British Library Ethos (e-theses online service)
Includes open access dissertations/theses from the UK
Independent and non-partisan research organization that objectively evaluates the clinical and economic value of prescription drugs, medical tests, and other health care and health care delivery innovations
Our search will be supplemented by hand reviewing bibliographies of included articles and articles gathered from the authors’ personal files. The research team will also contact existing stakeholder groups (Canadian Research Initiative in Substance Misuse [CRISM] and the Canadian Society of Addiction Medicine [CSAM]) with expertise in OAT to identify relevant existing or emerging literature on this topic.
Study selection
We will download search findings into Endnote, systematically de-duplicated, and create a merged library. The library will be exported into a draft MS Excel screening tool for title-abstract (level 1 [L1]) and full-text (level 2 [L2]) screening. The MS Excel screening tool will be piloted using 1–2 articles and finalized prior to using it. Two investigators (LLN, JCM) will calibrate screening by independently reviewing a 5% random sample of citations. Inter-rater agreement (kappa) [40] will be calculated and disagreements discussed to consensus for both level 1 and level 2 screening. If the kappa is < 0.60, study eligibility criteria will be revisited to focus on the screening criteria, and subsequent rounds of independent duplicate calibration will be undertaken until the desired kappa is achieved between investigators. Feedback and edits made to the screening tool during calibration will be discussed to consensus and the tool finalized.
Title and abstract [level 1 (L1)] screening
Once calibration is confirmed, the same two investigators (LLN, JCM) will review the title and abstract of all citations the search generates using the predetermined inclusion and exclusion criteria. The same two co-investigators (LLN, JCM) will calibrate screening of full-text articles independently and in duplicate. Studies meeting L1 inclusion-exclusion criteria will be submitted to full-text review (L2).
Full-text review [level 2 (L2) screening] and data extraction
We will retrieve full-text versions of all studies meeting the L1 inclusion-exclusion criteria for an in-depth review to confirm inclusion or record reasons for exclusion. In the manner described above, we will calibrate screening on a random sample (5%) of full-text articles in a similar fashion to level one, independently and in duplicate, by the same two co-investigators (LLN, JCM). Calibration will proceed until the concordance (kappa) between abstractors is k ≥ 0.60.
Methodological quality and risk of bias
Two researchers (LLN, JCM) will assess, independently and in duplicate, the quality of included studies [70] using the Joanna Briggs Institute (JBI) Critical Appraisal Checklist for Qualitative Research, [71] which focuses on congruity within studies and is highly coherent. Risk of bias and validity of results in studies reporting quantitative data, will be assessed using Joanna Briggs Institute (JBI) Critical Appraisal Tools, to be determined by specific study design [72]. Investigators will choose 1–2 full-text studies and pilot the methodological quality assessment process to calibrate prior to conducting quality assessments for all included studies. Investigators will discuss discrepancies to resolution or refer to a third investigator (KJM) for a final decision. If the team determines the study is significantly flawed, the research team will discuss extreme scores and studies excluded to avoid inappropriate statistical and/or conceptual influence.
Data extraction and analysis
We will use the Framework Analytic Method [74] as the primary method of data analysis to combine deductive and inductive qualitative and quantitative analysis (led by LLN, JCM, with KJM supporting). Ritchie and Spencer [74] designed this analytic method for use in applied settings and as a way to explore and/or inform social and public policy and programming. The framework approach also aligns well with systematic review methods and process, allowing the data to be identified, assessed, reduced, and summarized. Its advantage is that it provides a level analytic field within with which the team can consider evidence from multiple sources and theoretical origins (qualitative, quantitative, deductive, inductive). This approach helps guide the current research and enables the team to gather and consider findings and their implications within the proposed study in greater detail. This approach is useful in multi-disciplinary teams where familiarity with qualitative methodologies may be discrepant yet led by experienced qualitative researchers.
As detailed in the “Background” section above, we will use an a priori identified framework, a modified combination of the TDF and CFIR frameworks. Each framework has published template code books with definitions of their respective domains and subdomains [33, 35]. During L2 screening and full-text review, LLN and JCM will become familiar with the data, identify and extract data of interest relating to primary care prescribers’ perceptions of determinants of OAT prescribing, and study demographics as outlined in Table 1. We will tabulate extracted data into an Excel spreadsheet and indicate for each data element whether it is a direct participant quote or analyzed data (e.g., results of thematic analysis or statistical analysis). Calibrating data extraction between the two researchers will be conducted as in level 1 screening, with subsequent rounds of calibration if kappa is < 0.60.
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Two researchers (LLN, JCM) will conduct a pilot coding exercise to practice applying the a priori TDF-CFIR framework codes to extracted data. The researchers will identify the extracted data as barriers or facilitators and categorically code each, as appropriate, into the framework [32, 33, 35] (see Table 1) using pre-determined code definitions and a coding structure into a qualitative analytic software program (NVivo [67]). For example, fear of patients diverting their OAT (giving or selling it to others) is an identified barrier for some primary care clinicians considering prescribing; this would be coded in the TDF domain “Beliefs about consequences.” LLN and JCM will independently code three randomly selected studies for pilot coding, and discrepancies will be resolved through consensus-finding or reviewed with a third researcher (KJM).
After the initial pilot coding exercise, the same two researchers (LLN, JCM) will code (“index”) all of the extracted data into the modified combined TDF-CFIR framework domains and subdomains. Code definitions will be strictly applied, and double codes will be applied only when necessary. Any barriers, facilitators, or strategies arising that do not align with the a priori framework will be cataloged and analyzed inductively to generate appropriate codes; these will be captured thematically using a team-agreed category name and definition.
After initial coding, the data extracted from the remaining studies and associated extracted data will be split between the coders, as has been done in other framework analysis studies [68]. After coding five different studies, both researchers (LLN, JCM) will independently code the same sixth study and meet to ensure coding consistency and discuss discrepancies. This will continue until data extracted from all included studies are coded. This approach will promote consistent application of the codes, testing, and possible refining of the code definitions to reflect the extracted data context and help develop a potential subset of domains/subdomains that are most relevant to the studies included. Studies with multiple reports will be cataloged and examined. If they overlap, their data will be extracted but combined. Once full-text review has been completed, a dated library of retained articles will be generated in Endnote and the search, study tools, library, and link to the published study protocol will be accessible on the Open Science Framework [69, 70].
Once deductive and inductive coding (indexing) has been completed, investigators will review all coded data within domains and subdomains to identify themes and possible relations among them (e.g., hierarchical or overlapping concepts). This will involve looking within and across domains, as well as within and across included studies; in keeping with framework analysis, this sorting and synthesizing process will benefit from using matrices generated by NVivo. This will allow three researchers (LN, JCM, KJM) as a group to view all coded data and their domains at once and by consensus; the team will inductively identify and describe patterns of similar views in the coded data relating to barriers and facilitators to primary care OAT prescribing.
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We will also review each domain and associated data to determine quantitatively and qualitatively those likely to have the greatest influence on primary care prescribing of OAT. The former will involve frequency counts of the number of data elements coded in a particular domain, subdomain, or inductively generated category, as well as the number of studies from which extracted data was coded to a particular domain/category. We will also look for evidence of the importance of each coded perceived barrier, facilitator, or strategy based on statements by study participants (primary data) or findings reported by the study authors. We will generate “heat maps” with NVivo’s data density tool which uses a warm-to-cool color spectrum to represent frequency counts of the coded data. This gives a sense of where the “conversation” sits with regard to the coding framework, providing a visual representation of the synthesis of the findings.
We will examine the extracted strategies as a group to determine whether they can be combined. Finally, where it is feasible, the team will attempt to map identified effective strategies backwards onto precursor barrier-facilitator categories using the Theoretical Domains Framework [75], COM-B, and Behaviour Change Wheel [38, 75] to help enhance readiness of the data for subsequent use in modifying the intervention and/or study design.
Based on preliminary searching, we anticipate both quantitative and qualitative studies describing barriers, facilitators, and intervention strategies will emerge in the literature; however, due to heterogeneity and outcomes measures, we do not anticipate being able to conduct a meta-analysis. Should multiple studies with similar characteristics (context, outcomes measures) arise in the review, the team will explore the possibility of meta-analysis.
We will report study capture and flow using a PRISMA diagram (Fig. 1) [42]. Study characteristics will be presented in tabular format using descriptive statistics (frequencies and categories [n/%]). Barriers and facilitators will be reported similarly and using a heat map to quantify both the frequency and type of codes arising across included studies. We will provide coded data in the final systematic review report to facilitate its uptake and use by theorists and other researchers in the design of intervention strategies aimed at enhancing opioid agonist prescribing in primary care.
Fig. 1
Draft flowchart for selection of studies
×
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We will group interventions by type and summarize them narratively, if a sufficient number of eligible studies exist. Extracted strategies will be presented in tabular format, according to themes, as appropriate, and if meta-analysis is possible, appropriate statistics and forest plots will be used to report findings. We will make every effort to describe intervention strategies using key elements of interventions outlined by the TIDieR checklist; however, we anticipate missing data in this area given the documented lack of detail in most intervention reports [76]. If it is possible to map intervention strategies back to precursors, we will collate this information and present it in tabular format in the final report. We will report methodological quality in tables, according to tool results, and include the findings in an appendix in the final manuscript and note selective reporting within studies. All amendments to the protocol will be itemized as part of the study audit trail and reported on in the final manuscript.
Discussion
Through this review, we will systematically identify and synthesize the evidence base related to barriers and facilitators to OAT prescribing perceived by primary care providers. By deductively coding the evidence using a modified combination of the TDF and CFIR frameworks, as well as applying inductive methods to identify unanticipated factors, the results of this review will provide a broad conceptual understanding of the determinants of implementing OAT prescribing that could help inform the evaluation of current interventions or the rapid development of new, evidence-based and theory-driven innovations promoting primary care prescribing to improve access to OAT in the current opioid public health crisis in North America.
A potential limitation of this study is that we are relying on data reported and interpreted by others. There is an associated potential risk of “reporting bias” with primary authors presenting selected data to support their project aims and excluding data relevant to this systematic review. In spite of these potential limitations, we propose that the enhanced analytic effort of the available primary literature proposed in this review recognizes both the need to comprehensively document and evaluate the literature pertaining to barriers, facilitators, and effective interventions for OAT prescribing in primary care settings and the need to consider how context may influence the same.
In closing, the intent of this systematic review is to generate findings and facilitate the design of high-quality, theory-driven, evidence-based intervention strategies to encourage primary care providers to prescribe opioid agonists. It is hoped the study results will have immediate and sustained relevance to individual practitioners, as well as educators, system planners, and policymakers.
Acknowledgements
Kind thanks to: Diane Lorenzetti (Medical Librarian, Health Sciences Library, and Adjunct Assistant Professor, Department of Community Health Sciences, Cumming School of Medicine at the University of Calgary) for providing a comprehensive PRESS review of the study search strategy and Bradley Lewis (MD CCFP-EM, Department of Family Medicine University of Alberta) and Roni Shanoada (BSc Honors-Medical Biophysics, Western University) who both assisted with initial conceptualization and early literature searches while a family medicine resident and summer research student, respectively, at the University of Calgary, supervised by LLN.
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Competing interests
The authors declare that they have no competing interests.
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Barriers and facilitators to office-based opioid agonist therapy prescribing and effective interventions to increase provider prescribing: protocol for a systematic review
verfasst von
Lara L. Nixon Jazmin C. Marlinga K. Alix Hayden Kelly J. Mrklas
