| Literature DB >> 31890321 |
Giorgione G Cabral1, Ana C Dantas de Souza2, Isabelle R Barbosa3, Javier Jerez-Roig4, Dyego L B Souza2,4.
Abstract
OBJECTIVE: This study investigates the impact of multimorbidity on work through a literature review of longitudinal studies.Entities:
Keywords: Morbidity; Multimorbidity; Review; Work; Workers
Year: 2019 PMID: 31890321 PMCID: PMC6933240 DOI: 10.1016/j.shaw.2019.08.004
Source DB: PubMed Journal: Saf Health Work ISSN: 2093-7911
Fig. 1Flowchart for study selection in the review. PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses. Natal, 2018. (Adapted from PRISMA).
Bias analysis for the included studies, according to the Newcastle-Ottawa quality assessment scale
| Study | Selection | Comparability | Outcome/Exposure | Total score | |||||
|---|---|---|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4 | 1 | 1 | 2 | 3 | ||
| Ubalde-Lopez et al., 2017 | 0 | 1 | 0 | 0 | 2 | 0 | 1 | 0 | |
| Ubalde-Lopez et al., 2017 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | |
| Sundstrup et al., 2017 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | |
| Ervasti et al., 2015 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | |
| Ervasti et al., 2014 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | |
| Fouad et al., 2017 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | |
| Kivimäki et al., 2007 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | |
Selection: 1, Representativeness of the exposed cohort; 2, Selection of the nonexposed cohort; 3, Ascertainment of exposure; 4, Demonstration that outcome of interest was not present at the start of the study. Comparability: 1, Comparability of cohorts on the basis of the design or analysis. Outcome: 1, Assessment of outcome; 2, Follow-up long enough for outcomes to occur; 3, Adequacy of follow-up of cohorts.
This study was assessed through the items for case–control studies.
Data collected from the studies included in the review
| Study | Country | Design | Sample size, percentage (%) of women, age range, and mean [years old] | Chronic diseases included | Outcomes evaluated | Main results, measures of association, and confidence interval (CI) |
|---|---|---|---|---|---|---|
| Ubalde-Lopez et al., 2017 | The Netherlands | Cohort, prospective study (one year follow-up) | n = 156, 58.6%, 18-63 (42) | Injuries, musculoskeletal, mental, cardiovascular, respiratory, neurological, digestive, urogenital, skin, endocrine/metabolism, blood and congenital diseases and tumors | Work functioning scores using the Work Role Functioning Questionnaire (WRFQ), by latent class growth analysis (LCGA). LCGA identifies differentiated subpopulations (latent classes), each with its own specific longitudinal trend. | Multimorbidity did not predict membership in any trajectory. The increasing score trajectory levels of work functioning were lower among those with high baseline multimorbidity score. |
| Ubalde-Lopez et al., 2017 | Spain | Cohort, prospective study (two years follow-up) | n = 372 370 (for sickness absence incidence), 27%, NS | Musculoskeletal disorders (MSDs), mental health disorders (MHDs), and cardiovascular diseases (CVDs) | Incidence and duration of sickness absence | Among men with multimorbidity, overall sickness absence (SA) incidence was 11%, 60% higher [relative risk (RR) = 1.60; 95% CI: 1.57–1.68] than among men without multimorbidity (7%). This was similar in women (RR = 1.54; 95% CI: 1.36–1.74). No significant associations between multimorbidity and duration of SA episodes, regardless of the presence or absence of prior SA episodes, except for women with MHD who had no prior SA episodes and high sex-specific multidimensional multimorbidity score (HR = 3.43; 95% CI: 1.00–11.76) |
| Sundstrup et al., 2017 | Denmark | Cohort, prospective study (two years follow-up) | n = 10 427, 54.3%, NS (43.5) | Depression, asthma, diabetes, cardiovascular disease, cancer, impaired hearing, eczema, back disorders, or other conditions | Risk of long-term sickness absence (LTSA), it was defined as the registry of ≥ six consecutive weeks | There was an association between the number of chronic diseases and risk of LTSA. This association was stronger among employees with poor work ability (either physical or mental). Compared with employees with no diseases and good physical work ability, the risk estimate for LTSA was 1.95 (95% CI: 1.50–2.52) for employees with ≥3 chronic diseases and good physical work ability, whereas it was 3.60 (95% CI: 2.50–5.19) for those with ≥ three chronic diseases and poor physical work ability. |
| Ervasti et al., 2015 | Finland | Cohort, retrospective study (seven-year follow-up) | n = 9908, NS, 18-65 (NS) | Other psychiatric disorders, cardiovascular disease, hypertension, diabetes, asthma, and cancer | Return to work after a depression-related absence episode exceeding nine days | A present or recent other condition was associated with a 19% to 52% increased risk of slower return to work. After adjustments for sex, age, occupational position, and employment contract, cancer (HR = 0.66, 95% CI = 0.47–0.92), diabetes (HR = 0.73, 95% CI = 0.62–0.86), hypertension (HR = 0.76, 95% CI = 0.67–0.85), cardiovascular disease (HR = 0.78, 95% CI = 0.62–0.99), other psychiatric disorders (HR = 0.78, 95% CI = 0.74–0.83), musculoskeletal disorders (HR = 0.82, 95% CI = 0.77–0.87), and asthma (HR = 0.84, 95% CI = 0.75–0.94). Two or more other chronic conditions in addition to depression were associated with delayed return to work when compared with absences with depression only (HR = 0.76, 95% CI = 0.72–0.81). |
| Ervasti et al., 2014 | Finland | Cohort, retrospective study (seven-year follow-up) | n = 9946, 84.3%, 18-65 (45.7) | Other psychiatric disorders, cardiovascular disease, hypertension, diabetes and musculoskeletal disorders | The occurrence of a recurrent disability episode due to a depressive disorder (new disability episode due to depressive disorder after the end of the preceding disability episode; no new disability episodes due to depression, disability pension with other diagnosis, old-age pension, death, or end of follow-up. | The risk of a recurrent disability episode due to other psychiatric disorder (HR = 1.82, 95% CI: 1.68–1.97), cardiovascular disease (HR = 1.39, 95% CI: 1.04–1.87), hypertension (HR = 1.44, 95% CI: 1.17–1.78), diabetes (HR = 1.43, 95% CI: 1.11–1.85), and musculoskeletal disorders (HR = 1.17, 95% CI: 1.06–1.28); the model was adjusted for sex, age, socioeconomic status, and employment contract. |
| Fouad et al., 2017 | Egypt | Case–control study | n = 516, NS, ≤60 (NS) | Cardiovascular diseases, respiratory diseases, liver and digestive disorders, genitourinary and kidney disorders, musculoskeletal disorders, neurological (CNS and peripheral), diabetes mellitus, mental disorders, and others | Work productivity was measured in three domains: absenteeism, presenteeism, and critical incidents in the past four weeks. | Absenteeism RR 7.41 (95% CI: 5.47–10.05), presenteeism RR 3.77 (95% CI: 3.12–4.56), and excess negative incidents RR 30.10 (95% CI: 3.96–229.06). |
| Kivimäki et al., 2007 | Finland | Cohort, prospective study (one-year follow-up) | n = 33 148,80.2%, 17–65 (NS) | Diabetes, cardiovascular diseases (hypertension and established macrovascular disease: angina, myocardial infarction, and stroke or transient ischemic attack), and noncardiovascular comorbidity (asthma, bronchitis, prolapsed intervertebral disc, osteoarthritis, rheumatoid arthritis, peptic ulcer, fibromyalgia, migraine, depression, other psychiatric disorder) | Sickness absence episodes (>three days) | Among employees with diabetes, the presence of three or more noncardiovascular comorbid chronic conditions was associated with a HR = 2.68 (95% CI: 1.97–3.65) times increased risk of sickness absence after controlling for age, sex, and the number of risk factors and cardiovascular diseases. Among nondiabetic employees, the presence of three or more cardiovascular chronic conditions was associated with a 2.14-fold (95% CI: 1.51–3.03) increased risk of sickness absence, and the presence of three or more noncardiovascular chronic conditions was associated with a 2.73-fold (95% CI: 2.59–2.89) increased risk of sickness absence. |
NS: not stated.