Health status as a risk factor in cardiovascular disease: A systematic review of current evidence

Health status as a risk factor in cardiovascular disease: A systematic review of current evidence

Paula M.C. Mommersteeg PhDa, E-mail The Corresponding Author, Johan Denollet PhDa, John A. Spertus MD, MPHb and Susanne S. Pedersen PhDa, Corresponding Author Contact Information, E-mail The Corresponding Author, E-mail The Corresponding Author

aCenter of Research on Psychology in Somatic Diseases (CoRPS), Tilburg University, Tilburg, The Netherlands

bMid-America Heart Institute and University of Missouri–Kansas City, Kansas City, Missouri


Received 25 July 2008;
accepted 26 September 2008.
Available online 19 December 2008.

Background

Patient-perceived health status is receiving increased recognition as a patient-centered outcome in chronic heart failure (CHF) and coronary artery disease (CAD), but poor health status is also associated with adverse prognosis. In this systematic review, we examined current evidence on the influence of health status on prognosis in CHF and CAD.

Methods

We conducted a search of PubMed using a set of a priori–defined search terms, the Web of Science for newly cited articles, and the reference lists of eligible articles, resulting in 34 articles.

Results

Poor physical health status was a significant predictor for adverse health outcomes in patients with CHF and CAD. In CHF, poor physical health status seemed to be a stronger predictor of hospitalization than mortality. Little evidence was found that poor mental health status is associated with adverse prognosis in CHF and CAD. A disease-specific measure was a better predictor in CHF, but not in CAD. The majority of studies adjusted for an objective measure of disease severity. Neither the index event nor time to follow-up appeared to influence the predictive value of health status.

Conclusions

Poor physical health status is associated with adverse CAD and CHF prognosis. Heterogeneity across studies makes definitive conclusions difficult as to which components of health status may be detrimental to patients' health, and how health status as a potential risk factor should be assessed, monitored, and intervened upon in clinical practice.

Article Outline

Methods
Description of studies
Sample sizes and populations
Time of baseline assessment
Health status questionnaires
End points
Follow-up length
Confounders
Reporting the results
Results
Impact of health status on clinical outcomes
Physical health status in CHF
Physical health status in CAD
Mental health status in CHF
Mental health status in CAD
Discussion
References

Health status is receiving increased recognition as an important patient-centered outcome in patients with cardiovascular disease (CVD).1 In patients with established disease, health status refers to “the range of manifestation of disease in a given patient including symptoms, functional limitation, and quality of life, in which quality of life is the discrepancy between actual and desired function.”2 Self-rated health, encompassing health status and quality of life, has been associated with both incident fatal and nonfatal heart disease in population-based studies3 and with hospital readmissions and mortality in patients with CVD.[4], [5], [6], [7] and [8]

Patients' evaluation of their health status does not necessarily concur with that of physicians,[9] and [10] with physicians often failing to identify functional disabilities reported by patients.9 Patient-reported health status also seems to be a risk factor for mortality in patients with CVD of equal or greater magnitude than traditional biomedical risk factors.8 Taken together, this suggests that knowledge of health status, as perceived by the patient, may both provide a unique window into patients' clinical status and be prognostically important, such that it can enhance secondary prevention interventions as a relatively low-cost assessment with which to identify high-risk patients.

In a 2002 editorial, Rumsfeld2 suggested that health status should be added to the amalgam of clinical factors used for risk stratification in clinical practice. Six years later, there is little evidence that health status measurements have become part of standard assessment, even though its routine measurement has been established as a performance measure of high-quality care by the American College of Cardiology, the American Heart Association, the American Medical Association,11 and the National Quality Forum (http://www.qualityforum.org/projects/ongoing/ambulatory). One of the critical barriers to the adoption of health status assessments in clinical care could be ambivalence about its utility in risk stratification. To better clarify the potential role of routine health status assessment, the objective of this systematic review was to evaluate the evidence on the influence of health status on prognosis in CVD patients and describe the implications for clinical practice and future research.

Methods

PubMed was searched in the period between January 1980 and August 2007, using the following search terms: Quality of life, health status, health status indicators, functioning, coronary artery disease, CAD, heart failure, cardiovascular disease, CVD, CABG, percutaneous coronary intervention, PTCA, myocardial revascularization, coronary artery bypass, patient readmission, hospitalization, mortality, survival analysis, and prognosis. The search was limited to articles published in peer-reviewed English medical journals in adults (>18 years). Studies were included in the review if they focused on patients with established coronary artery disease (CAD) or chronic heart failure (CHF), used a standardized measurement of quality of life or health status, or asked patients to rate their health using a purpose-designed question, and analyzed the association between health status and (all-cause) mortality, hospital readmission, or a combination of mortality and readmission. Studies using a mixed sample of patients with CAD or CHF with other disease entities (eg, stroke, diabetes, or heart transplantation) focusing on hospital length of stay as the only outcome were excluded.

Figure 1 provides an overview of the search and selection of articles. The title and abstract of the 1,561 articles were reviewed by one author (P.M.C.M.), whereas the 52 articles meeting the inclusion criteria were reviewed by the first and last author (P.M.C.M. and S.S.P.). An additional search on Web of Science for newly cited articles based on the shortlist (forward citation, November 2007) led to 4 additional articles.[12], [13], [14] and [15] A hand search of the reference list of these 31 articles identified 3 additional articles,[16], [17] and [18] with the review being based on 34 articles. Although the initial objective of this study was to perform a meta-analysis, this was not possible given the heterogeneity between studies.



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Figure 1. Flowchart of the selection of studies.


Description of studies

The 34 identified articles (Table I) were all prospective cohort studies that used self-report measures of health status at baseline, or within a few days (72 hours) to weeks after the index event (ie, hospitalization for CHF, myocardial infarction [MI], percutaneous coronary intervention [PCI], or coronary artery bypass graft surgery [CABG]). In some instances, CHF outpatients were also included. Two studies used retrospective information on health status.[13] and [19]

Table I.

Study descriptives and confounders

Reference
Ref. no.
n
Population
Quality of life
Outcome measurelow asterisk
Follow-up length
Confounders







DemographicDisease severityComorbidity







Age/SexSmokingHypertensionDisease severity§HypercholesterolaemiaPrevious hospitalizationRenal functioning#DiabetesComorbidity††Medication use‡‡
Alla et al, 2002[38]108CHFHRQoLM, H18 mA/S

DSHypercholesterolaemiaPHRF
CMM
Bosworth et al, 1999[24]2885CAD, CABG, PCISR-health, SF36, DASIM3.5 yA/SSmokingHyDS

RFDiabetesCM
Bouvy et al, 2003[16]152CHFMLHFQM18 mA/S
HyDS
PHRFDiabetesCMM
Chocron et al, 2000[17]209CABGNHPM3 yA/S

DS
PHRFDiabetesCM
Curtis et al, 2002[25]1778CABGSF36M1 mA/S
HyDSHypercholesterolaemiaPHRFDiabetesCM
Deaton et al, 1998[26]93CABGHSQ12H3 mA/SSmokingHyDS
PH
Diabetes

Dixon et al, 2001[31]945MI, CHF, IHDMacNewM/H12 mA/SSmokingHy

PH

CM
Faller et al, 2007[12]231CHFSF36, KCCQM2.7 yA/S
HyDSHypercholesterolaemia
RFDiabetes
M
Formiga et al, 2006[13]88CHFADLM/H12 mA/SSmokingHyDSHypercholesterolaemiaPHRFDiabetes

Havranek et al, 2001[40]545CHFSR-healthM/H2.8 mA/S

DS




M
Heidenreich et al, 2006[34]505CHFKCCQM/H12 mA/S
HyDS
PHRFDiabetesCMM
Herlitz et al, 1998[27]1290CABGNHPM5 yA/SSmokingHyDS
PHRFDiabetesCM
Ho et al, 2005[14]3160CABG, valve replacementSF36M6 mA/SSmokingHyDS
PHRFDiabetesCM
Hülsmann et al, 2002[15]96CHFMLHFQM/H12 mA/S

DS




M
Koch et al, 2007[4]6305CABGDASIM8.6 yA/SSmokingHyDS
PHRFDiabetesCM
Konstam et al, 1996[35]5025CHFHRQoLM, H3.0 yA/S
HyDS
PH
DiabetesCM
Kosiborod et al, 2007[5]1358MI, CHFKCCQM, M/H14 mA/S
HyDSHypercholesterolaemiaPHRFDiabetesCMM
Lenzen et al, 2007[28]3786CAD, MI, CABG, PCIEQ-5DM12 mA/SSmokingHyDSHypercholesterolaemiaPH
Diabetes
M
Lim et al, 1998[32]375MIMacNewM/H18 mA/SSmokingHyDS
PH


M
Mayer et al, 2003[19]123CABGSF36M18 mA/S
Hy


RFDiabetesCM
Mejhert et al, 2004, 2006[20] and [21]208CHFNHPM3.1 yA/S
HyDS
PHRFDiabetesCMM
Mozaffarian et al, 2003[33]8908CADSAQM24 mA/SSmokingHyDS
PHRFDiabetesCM
Murberg et al, 1999[36]119CHFHRQoLM24 mA/S
HyDS
PH


M
Pedersen et al, 2007[6]667PCIMacNewM/H<6>A/SSmoking
DS
PH
DiabetesCMM
Piotrowicz et al, 2007[23]1058MISF12M, H and M/H3.0 yA/SSmokingHyDS


Diabetes
M
Rodriguez-Artalejo et al, 2005[7]394CHFSF36, MLHFQM, H6.6 m, 6.2 mA/S

DS
PHRFDiabetesCMM
Rumsfeld et al, 1999[29]2480CABGSF36M6 mA/SSmokingHyDS
PHRFDiabetesCMM
Schwarz et al, 2003[39]156CHFFSM, H3 mA/S
HyDS
PHRFDiabetesCM
Soto et al, 2004[22]1516MIKCCQM, M/H12 mA/SSmokingHyDSHypercholesterolaemiaPHRFDiabetesCMM
Spertus et al, 2002[8]4484CADSAQM, H12 mA/SSmokingHyDS
PHRFDiabetesCM
Stull et al, 2001[18]3884CHFHRQoL, PsyQoLH3.1 yA/S
HyDS
PHRFDiabetesCM
Subramanian et al, 2007[37]459CHFSF36, CHQ, KCCQM5 yA/S
HyDSHypercholesterolaemiaPHRFDiabetesCMM
Westin et al, 2005[30]349MI, CABG, PCIHRQoLM10 yA/SSmokingHy
Hypercholesterolaemia



M

ADL, Activity of daily living; CHQ, McMaster Chronic Heart Failure Questionnaire; DASI, Duke Activity Scale Index; EQ-5D, EuroQoL; FS, functional status; HSQ12, health status questionnaire 12; HRQoL, health-related quality of life; IHD, ischemic heart disease; KCCQ, Kansas City Cardiomyopathy questionnaire; MacNew, MacNew heart disease quality of life instrument; MLHFQ, Minnesota living with heart failure; NHP, Nottingham Health Profile; PsyQoL, Psychosocial quality of life; SAQ, Seattle Angina Questionnaire; SF-12/36, Short Form Health Survey 12/36 items; SR-health, Self-rated health.

low asteriskM, Mortality; H, hospitalization; M/H, mortality or hospitalization.

Hy, Hypertension or systolic blood pressure, diastolic blood pressure.

§DS, Disease severity; left ventricular ejection fraction, multivessel disease, Killip Class, NYHA class, or angina severity.

PH, Previous hospitalization or event.

#RF, Renal functioning; creatinine.

††C, Comorbidity other, eg, COPD, PI, or Charlson comorbidity index.

‡‡M, Medication use.


Sample sizes and populations

The median number of patients included in the studies was 545 (mean ± standard deviation 1,628 ± 2,119), with a range from 88 to 8,908. The sample sizes are depicted in Figure 2.



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Figure 2. Frequency curve of the sample sizes for the included studies (n = 33) (study no. 20/21 is included once).


To detect potential differences between types of cardiovascular disease (CVD), we stratified studies by CAD and CHF (Table II and Table III). In total, 47% (n = 16) of the studies focused on patients with CAD. Although 1 study excluded patients with MI or angina complaints,[20] and [21] three studies combined CHF with MI,[5], [22] and [23] which are listed under CHF. The index event was CABG in 33% (n = 11) of the studies,[4], [14],

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