| Literature DB >> 23640785 |
Gabriela L M Ghisi1, Peter Polyzotis, Paul Oh, Maureen Pakosh, Sherry L Grace.
Abstract
Physicians play an important role in CR referral and enrollment. Despite established benefits and recommendations, cardiac rehabilitation (CR) enrollment rates are pervasively low. The reasons cardiac patients are missing from CR programs are multifactorial and include provider factors. A number of studies have now investigated physician factors associated with referral to CR programs and patient enrollment. The objective of this study was to qualitatively and systematically review this literature. A literature search of MEDLINE, PsycINFO, CINAHL, Embase, and EBM was conducted for published articles from database inception to October 2011. Overall, 17 articles were included following a process of independent review of each article by 2 authors. Seven (41.2%) were graded as good quality according to Downs and Black criteria. There were no randomized controlled trials. Results showed that medical specialty (ie, cardiac specialists more likely to refer; n = 8 studies) and other physician-reported reasons (eg, physician report of their reasons for CR referral and physician sex) were related to referral. Physician factors related to patient enrollment in CR were physician endorsement, medical specialty, being referred, and physician attitudes toward CR. Physician factors are consistently related to CR referral and enrollment. The role of physician endorsements in promoting patient enrollment should be optimized and exploited.Entities:
Mesh:
Year: 2013 PMID: 23640785 PMCID: PMC3736151 DOI: 10.1002/clc.22126
Source DB: PubMed Journal: Clin Cardiol ISSN: 0160-9289 Impact factor: 2.882
Search Strategy
| Concept | Search Terms–MEDLINE | Search Terms–Embase |
|---|---|---|
| Cardiac conditions | Coronary disease | Coronary artery disease |
| Heart disease | Heart disease | |
| Cardiovascular disease | Cardiovascular disease | |
| Coronary artery disease | Heart infarction | |
| Myocardial infarction | Myocardial infarction | |
| Cardiac rehabilitation | ||
| Practitioner focus | Attitudes to health personnel | Doctor patient relation |
| Physician's practice patterns | Medical specialist | |
| Physician–patient relations | Physician | |
| Professional competence | Cardiovascular surgeon | |
| Physician | Cardiologist | |
| Physician's role | Advanced practice nurse | |
| Cardiovascular surgeon | ||
| Cardiologist | ||
| Nurse practitioners | ||
| Rehabilitation /referral | Referral and consultation | Physician attitude |
| Access/adherence /enrollment | Prejudice | Clinical practice |
| Patient acceptance of healthcare | Health personnel attitude | |
| Patient compliance | Patient referral | |
| Ambulatory care | Patient attitude | |
| Attitude to health | Patient selection | |
| Health services accessibility | Ambulatory care | |
| Healthcare disparities | Attitude to health | |
| Outpatients | Healthcare disparity | |
| Inpatients | Outpatient | |
| Patient dropouts | Outpatient department | |
| Treatment refusal | Cardiac patient | |
| Patient participation | Rehabilitation patient | |
| Refusal to participate | Heart rehabilitation | |
| Patient selection | Patient dropout | |
| Physician or provider perception | Cardiac rehabilitation | |
| Patient care management | Physician or provider perception | |
| Health behavior | Health behavior | |
| Cardiac inpatient or outpatient | Cardiac inpatient or outpatient | |
| Gatekeeping | Cardiac referral or access or enrollment | |
| Eligibility determinants | Cardiac rehabilitation patient | |
| Cardiac referral or access or enrollment | Rehabilitation center | |
| Rehabilitation | Rehabilitation center | |
| Cardiac rehabilitation patient | Cardiac rehabilitation program | |
| Rehabilitation centers | Cardiology clinic | |
| Rehabilitation center | Coronary care unit | |
| Cardiac rehabilitation program | Cardiac care | |
| Cardiology clinic | Patient compliance | |
| Cardiac care facilities | Program access | |
| Cardiac care | Program adherence | |
| Patient compliance | Program utilization | |
| Program access | Program enrollment | |
| Program adherence | Patient attendance | |
| Program utilization | Health behavior | |
| Program enrollment | ||
| Patient attendance | ||
| Health behavior |
Modified Version of the Downs and Black Checklist
| No. | Question | Yes | No | Unclear |
|---|---|---|---|---|
| Reporting (7) | ||||
| 1 | Is the hypothesis/aim/objective of the study clearly described? | □ | □ | □ |
| 2 | Are the main outcomes to be measured clearly described in the Introduction or Methods section? | □ | □ | □ |
| If the main outcomes are first mentioned in the Results section, the question should be answered no. | ||||
| 3 | Are the characteristics of the patients included in the study clearly described? | □ | □ | □ |
| In cohort studies and trials, inclusion and/or exclusion criteria should be given. In case–control studies, a case definition and the source for controls should be given. | ||||
| 4 | Are the interventions of interest clearly described? | □ | □ | □ |
| Treatments and placebo (where relevant) that are to be compared should be clearly described. | ||||
| 6 | Are the main findings of the study clearly described? | □ | □ | □ |
| Simple outcome data (including denominators and numerators) should be reported for all major findings so that the reader can check the major analyses and conclusions. (This question does not cover statistical tests that are considered below.) | ||||
| 9 | Have the characteristics of patients lost on follow‐up been described? | □ | □ | □ |
| This should be answered yes where there were no losses to follow‐up or where losses to follow‐up were so small that findings would be unaffected by their inclusion. This should be answered no where a study does not report the number of patients lost to follow‐up. | ||||
| 10 | Have actual probability values been reported (eg, for the main outcomes except where the probability value is less than 0.001? | □ | □ | □ |
| For example, 0.035 rather than <0.05) | ||||
| External validity (3) | ||||
| 11 | Were the subjects asked to participate in the study representative of the entire population from which they were recruited? | □ | □ | □ |
| The study must identify the source population for patients and describe how the patients were selected. Patients would be representative if they comprised the entire source population, an unselected sample of consecutive patients, or a random sample. Random sampling is only feasible where a list of all members of the relevant population exists. Where a study does not report the proportion of the source population from which the patients are derived, the question should be answered as unable to determine. | ||||
| 12 | Were those subjects who were prepared to participate representative of the entire population from which they were recruited? | □ | □ | □ |
| The proportion of those asked who agreed should be stated. Validation that the sample was representative would include demonstrating that the distribution of the main confounding factors was the same in the study sample and the source population. | ||||
| 13 | Were the staff, places, and facilities where the patients were treated, representative of the treatment the majority of patients receive? | □ | □ | □ |
| For the question to be answered yes, the study should demonstrate that the intervention was representative of that in use in the source population. The question should be answered no if, for example, the intervention was undertaken in a specialist center unrepresentative of the hospitals most of the source population would attend. | ||||
| Internal validity–bias (4) | ||||
| 17 | In trials and cohort studies, do the analyses adjust for different lengths of follow‐up of patients, or in case–control studies, is the time period between the intervention and outcome the same for cases and controls? | □ | □ | □ |
| Where follow‐up was the same for all study patients the answer should be yes. If different lengths of follow‐up were adjusted for by, for example, survival analysis, the answer should be yes. Studies where differences in follow‐up are ignored should be answered no. | ||||
| 18 | Were the statistical tests used to assess the main outcomes appropriate? | □ | □ | □ |
| The statistical techniques used must be appropriate to the data. For example, nonparametric methods should be used for small sample sizes. Where little statistical analysis has been undertaken but where there is no evidence of bias, the question should be answered yes. If the distribution of the data (normal or not) is not described, it must be assumed that the estimates used were appropriate and the question should be answered yes. | ||||
| 19 | Was compliance with the intervention/s reliable? | □ | □ | □ |
| Where there was noncompliance with the allocated treatment or where there was contamination of 1 group, the question should be answered no. For studies where the effect of any misclassification was likely to bias any association to the null, the question should be answered yes. | ||||
| 20 | Were the main outcome measures used accurate (valid and reliable)? | □ | □ | □ |
| For studies where the outcome measures are clearly described, the question should be answered yes. For studies that refer to other work or that demonstrates the outcome measures are accurate, the question should be answered as yes. | ||||
| Internal validity–confounding (selection bias) (4) | ||||
| 21 | Were the patients in different intervention groups (trials and cohort studies) or were the cases and controls (case–control studies) recruited from the same population? | □ | □ | □ |
| For example, patients for all comparison groups should be selected from the same hospital. The question should be answered unable to determine for cohort and case–control studies where there is no information concerning the source of patients included in the study. | ||||
| 22 | Were study subjects in different intervention groups (trials and cohort studies) or were the cases and controls (case–control studies) recruited over the same period of time? | □ | □ | □ |
| For a study that does not specify the time period over which patients were recruited, the question should be answered as unable to determine. | ||||
| 25 | Was there adequate adjustment for confounding in the analyses from which the main findings were drawn? | □ | □ | □ |
| This question should be answered no for trials if: the main conclusions of the study were based on analyses of treatment rather than intention to treat, the distribution of known confounders in the different treatment groups was not described, or the distribution of known confounders differed between the treatment groups but was not taken into account in the analyses. In nonrandomized studies, if the effect of the main confounders was not investigated or confounding was demonstrated but no adjustment was made in the final analyses, the question should be answered as no. | ||||
| 26 | Were losses of patients to follow‐up taken into account? | □ | □ | □ |
| If the number of patients lost to follow‐up is not reported, the question should be answered as unable to determine. If the proportion lost to follow‐up was too small to affect the main findings, the question should be answered yes. | ||||
Figure 1Flow diagram of study selection process.
Characteristics of the Studies Included in This Review (N = 17)
| Study Author (Year), Country | Study Design | Subjects | Description of Sample and Size | Methods | Quality Assessment Classification (Points) |
|---|---|---|---|---|---|
| Ades et al. (1992), USA | Cross‐sectional | Patients | Cardiac inpatients eligible for CR, n = 226 | Guided interview: to collect demographic, medical, and psychosocial data. Telephone interview (prior to discharge or shortly thereafter): to describe the strength of their primary physician's recommendation regarding CR participation (graded from 1 to 5). | Fair (11) |
| Ayanian et al. (2002), USA | Retrospective cohort | Patients | Inpatients with a diagnosis of AMI, n = 35 520 | Patients identified in 7 states during 1994 and 1995. From Medicare claims, it was identified ambulatory visits to cardiologists, internists, and family practitioners. | Good (15) |
| Barber et al. (2001), USA | Cross‐sectional | Patients | Cardiac inpatients eligible for CR, n = 347 | Phase I patients: follow‐up by mail survey +3 months after discharge mailed questionnaire. Phase II patients: follow‐up by phone +6 weeks after discharge phone interview. | Good (16) |
| Bittner et al. (1999), USA | Prospective cohort | Patients | Cardiac inpatients after discharge and eligible for CR, n = 995 | Patients eligible for CR were identified from hospital discharge dataset. Referral rates to the CR program among patients hospitalized for CHD were computed over an 18‐month period. | Fair (10) |
| Dunlay et al. (2009), USA | Prospective cohort | Patients | Cardiac inpatients post‐MI after discharge and eligible to CR, n = 179 | Subjects completed a 46‐item questionnaire before hospital discharge (to measure health motivation, person's judgment of their own capacities as related to controlling their heart disease, and self‐assessment of health status, importance of CR to the patient, motivating factors, education, living situation, transportation availability, insurance, and fears and concerns about rehabilitation. | Good (15) |
| Grace et al. (2004), Canada | Cross‐sectional | Physicians | Primary care physicians, cardiologists, and cardiovascular surgeons, n = 179 | Survey included sociodemographic characteristics, a hypothetical case scenario, physicians were asked whether they would refer the patient, and a 26‐item questionnaire asking questions about patients characteristics influenced the physician's referral practices and physician's attitude about CR. | Good (14) |
| Grace et al. (2008), Canada | Prospective cohort | Patients Physicians | Cardiologists and outpatients; cardiologists, n = 97 and outpatients, n = 1268 | Cardiologists completed a survey regarding CR attitudes. Outpatients were surveyed prospectively to assess factors affecting CR enrollment. Patients were mailed a follow‐up survey 9‐months later to self‐report CR enrollment. The enrollment was checked by the CR site. | Good (18) |
| Grace, Grewal, Stewart (2008), Canada | Cross‐sectional | Physicians | Primary care physicians and cardiac specialists (cardiologists or cardiovascular surgeons); n = 104 primary care physicians and n = 81 cardiac specialists | Questionnaire application (mailed), which included sociodemographic items, and 26 investigator‐developed items scored on a 5‐point Likert scale about factors affecting physician's referral. | Fair (12) |
| Jones et al. (2003), Canada | Cross‐sectional, qualitative | Patients | Outpatients eligible to CR, enrollers and nonenrollers, n = 20 enrollers and n = 9 nonenrollers | A 16‐item questionnaire was used to measure the importance of variables that have been found to be associated with participation in CR. A semistructured interview guide was also developed to promote discussion of perceptions and experiences with CR. | Poor (6) |
| King et al. (2001), Canada | Prospective cohort | Patients | Cardiac inpatients ready for discharge after an AMI or CABG, n = 304 | Two weeks and 6 months after discharge, respondents were given a list of factors commonly thought to influence attendance at CR. | Fair (9) |
| Mak et al. (2005), China | Prospective cohort | Patients | Cardiac patients recruited for a phase I CR program (not proceeding to phase II), n = 41 | Evaluation of factors related to phase II: baseline assessment, comprehensive program and documentation of barriers. | Fair (7) |
| Missik (2001), USA | Cross‐sectional | Patients | Women enrolled and nonenrolled in CR after a cardiac event, n = 370 | A self‐reported instrument (eg, to collect data about physician referral to CR, health insurance coverage) and medical records reviews were used to collect data. | Fair (12) |
| Pell et al. (1996), Scotland | Retrospective cohort | Patients | Inpatients with a discharge diagnosis of MI, n = 881 | Scottish morbidity record data were used to identify all patients discharged from Glasgow hospitals from June 1994 to November 1994 with MI. | Fair (11) |
| Scott et al. (2005), Australia | Retrospective cohort | Patients | Patients who died or were discharged after troponin‐positive ACS, n = 2156 | The proportion of highly eligible patients in total and in each category who received specific clinical interventions during admission or at discharge were determined at the level of individual patients using intervention‐specific eligibility criteria derived from evidence‐based clinical practice guidelines. | |
| Stiller and Holt (2004), USA | Cross‐sectional | Patients | Outpatients with at least 1 cardiac diagnosis and eligible for phase II CR, n = 203 | Participants were approached before their discharge from the hospital. Three‐weeks after their discharge, patients were mailed a questionnaire. Patients were also contacted by phone. | Fair (9) |
| Suter et al. (1992), USA | Cross‐sectional | Physicians | Cardiologists, cardiovascular surgeons, internists, and family practitioners, n = 32 | Contact letter (physicians randomly selected). Those who responded receive a questionnaire and should return it within 2 weeks. Thirty‐two questionnaires returned. | Poor (4) |
| Yates et al. (2003), USA | Cross‐sectional | Patients | Cardiac inpatients hospitalized over a 1‐year period at a regional (rural) medical center, n = 222 | Mail surveys. | Good (13) |
Abbreviations: ACS, acute coronary syndrome; AMI, acute myocardial infarction; CABG, coronary artery bypass grafting; CR, cardiac rehabilitation; MI, myocardial infarction.
Hypothetical.
Started.
Completed.
Summary of Findings of the Studies Included in this Review (N = 17)
| Study Author (Year), Country | CR Outcome | Physician Factor | Results |
|---|---|---|---|
| Ades et al. (1992), USA | Enrollment | Strength of the primary physician's recommendation | Low physician recommendation to CR: participation was 1.8%; high physician recommendation to CR: participation was 66% ( |
| Ayanian et al. (2002), USA | Referral | Appointment with a cardiologist | Patients who saw a cardiologist were more likely to be referred that those who did not to report having received CR ( |
| Barber et al. (2001), USA | Referral, enrollment | Appointment at discharge with a cardiologist/cardiac surgeon | Appointment with a cardiac specialist compared to family physician at hospital discharge: referral to CR (OR = 2.33, |
| Bittner et al. (1999), USA | Referral | Appointment at discharge with a cardiologist/cardiac surgeon | Trend toward higher referral rates among cardiologists compared with cardiovascular surgeons, internists, and other medical specialties ( |
| Dunlay et al. (2009), USA | Referral, enrollment | In‐hospital care by a cardiologist, referral | Factors related to enrollment: in‐hospital care by a cardiologist ( |
| Grace et al. (2004), Canada | Referral | Physicians' perceptions of referral practices, medical specialty | Factors related to referral: geographic access, uncertainty regarding which provider was responsible for referral, perceptions of patient motivation, multifactorial nature of CR, patient characteristics. Family physicians were less likely to refer than cardiologists and cardiac surgeons ( |
| Grace et al. (2008), Canada | Enrollment | Recommendation of CR, intentions to refer, positive perceptions of CR | Physician factors related to CR enrollment: recommendation of CR utilization was significant ( |
| Grace, Grewal, Stewart (2008), Canada | Referral | Medical specialty, physicians' perceptions of CR | Primary care physicians were more likely to endorse lack of familiarity with CR site locations ( |
| Jones et al. (2003), Canada | Enrollment | Physician recommendation | Physician recommendation was significant factor for patients when deciding to enroll or not ( |
| King et al. (2001), Canada | Enrollment | Physician recommendation | A factor for patients who decided to enroll (68% of patients were influenced by physicians). |
| Mak et al. (2005), China | Enrollment | Physician recommendation, referral | CR enrollment was associated with being referred by a physician (7% of patients identified lack of referral as a barrier to CR enrollment). |
| Missik (2001), USA | Enrollment | Physician referral | Women's participation in CR was related to physician referral ( |
| Pell et al. (1996), Scotland | Referral, enrollment | Appointment with a cardiac specialist | Referral: more likely to be referred to CR than if seen by general physician (OR = 1.59, |
| Scott et al. (2005), Australia | Referral | Cardiologist involvement | Cardiologist involvement (transfer or nontransfer to cardiology unit) was not related to CR referral ( |
| Stiller and Holt (2004), USA | Referral | Physician sex | The only variable related to referral was physician sex ( |
| Suter, Bona, Suter (1992), USA | Referral | Perceptions of CR | Majority of respondents indicated that patients who have survived a MI or have undergone CABG are most likely to benefit from outpatient CR. Reasons for nonreferral: unlikelihood of medical insurance coverage, perceived lack of patient motivation, perceptions of unqualified CR staff, practical reasons (distance), and safety concerns. |
| Yates et al. (2003), USA | Enrollment | Physician recommendation, referral | Patients were more likely to participate if their physician explained its benefits (OR = 6.54) and if they were told about it during hospitalization (OR = 4.12, |
Abbreviations: ACS, acute coronary syndrome; AMI, acute myocardial infarction; CABG, coronary artery bypass grafting; CR, cardiac rehabilitation; OR, odds ratio.