Multimorbidity of chronic non-communicable diseases in low- and middle-income countries: A scoping review.

BACKGROUND: Multimorbidity is rising in low- and middle-income countries (LMICs). However, the evidence on its epidemiology from LMICs settings is limited and the available literature has not been synthesized as yet.
OBJECTIVES: To review the available evidence on the epidemiology of multimorbidity in LMICs.
METHODS: PubMed, Scopus, PsycINFO and Grey literature databases were searched. We followed the PRISMA-ScR reporting guideline.
RESULTS: Of 33, 110 articles retrieved, 76 studies were eligible for the epidemiology of multimorbidity. Of these 76 studies, 66 (86.8%) were individual country studies. Fifty-two (78.8%) of which were confined to only six middle-income countries: Brazil, China, South Africa, India, Mexico and Iran. The majority (n = 68, 89.5%) of the studies were crosssectional in nature. The sample size varied from 103 to 242, 952. The largest proportion (n = 33, 43.4%) of the studies enrolled adults. Marked variations existed in defining and measuring multimorbidity. The prevalence of multimorbidity in LMICs ranged from 3.2% to 90.5%. CONCLUSION AND RECOMMENDATIONS: Studies on the epidemiology of multimorbidity in LMICs are limited and the available ones are concentrated in few countries. Despite variations in measurement and definition, studies consistently reported high prevalence of multimorbidity. Further research is urgently required to better understand the epidemiology of multimorbidity and define the best possible interventions to improve outcomes of patients with multimorbidity in LMICs.

Introduction

Multimorbidity often refers to the presence of two or more or three or more chronic conditions in a given individual.[1,2] Multimorbidity is a growing issue and posing a major challenge to health care systems around the world.[3] Global prevalence estimates ranged from 12.9% (in the general population) to 95.1% (among people 65 years and older).[4] A large difference in the prevalence of multimorbidity was observed across studies conducted both in primary care (3.5% to 98.5%) and in the general population (13.1% to 71.8%).[5] Evidence shows a rising trend in the prevalence of multimorbidity in the low- and middle-income countries (LMICs).[3]

Demographic changes such as population aging is contributing for the development of multimorbidity of chronic conditions.[3] Multimorbidity is also socially patterned, where a higher prevalence is observed among socioeconomically deprived populations than their wealthier counterparts in high income countries (HICs).[6,7] Similarly, women are more likely than men to have higher odds of multimorbidity.[4,8] Individual lifestyle factors including obesity,[9] physical inactivity,[10,11] harmful use of alcohol,[12] and psychosocial factors, such as negative life events and believing in external locus of control are also factors associated with multimorbidity.[13,14]

Living with multimorbidity is associated with disability, lower quality of life, premature mortality, greater use of health care service resources and unplanned hospital admissions.[1,15] Management of multimorbidity is much more complicated and demanding for the health system, patients and their families compared to those patients living with a single chronic condition.[16,17] Furthermore, the rapid emergence of infections such as COVID-19 are fueling the complexity and posing a huge burden to the health system and worsening outcomes of patients with preexisting chronic diseases and multimorbidity.[18,19]

The impact of multimorbidity might even further increase in LMICs where health systems are overwhelmed by the burden of communicable diseases (such as HIV, TB and Malaria) and maternal, neonatal and nutritional health problems.[2] On the other hand, health systems in LMICs are largely configured with conventional one-size fits all chronic disease care, rather than designing a model of care for every possible combination of chronic conditions.[6] As a result, patients receive fragmented, inefficient and ineffective care, which could lead to conflicting medical advice and preventable hospitalizations and mortality.[20]

The development of health delivery models that adequately respond to this complex situation in LMICs requires clarity on the epidemiology within the context. However, there is paucity of evidence on the magnitude, distribution and patterns of multimorbidity. The objectives of this study were to review the available evidence on the epidemiology of multimorbidity and to identify gaps in evidence in LMICs.

Methods

Design

We followed the methods suggested by Arksey and O’Malley for conducting scoping reviews[21] and adhered to the Preferred Reporting Items for Systematic Review and Meta-Analyses Extension for Scoping Reviews (PRISMA-ScR) checklist and reporting guideline[22] (Supplemental file-4). Our detailed review protocol has been published elsewhere.[23] In summary, we followed the following steps: (1) identifying the research question; (2) identifying relevant studies; (3) selecting studies; (4) charting the data; (5) collating, summarizing and reporting the results.

Data bases and search strategy

PubMed (MEDLINE), Scopus, PsycINFO and Cochrane databases were searched to identify articles. For grey literature, we searched WorldCat, Open Grey, Global Index Medicus and Latin American & Caribbean Health Sciences Literature (LILACS) databases. The search terms used for epidemiology of multimorbidity included ‘comorbidity’ OR ‘co-morbidity’ OR ‘multimorbidity’ OR ‘multiple chronic conditions’ AND ‘chronic disease’ OR ‘noncommunicable diseases’ OR ‘non-communicable diseases’ AND ‘low-and middle-income countries.’ We used the World Bank Country and Lending Groups list of LMICs for 2019–2020 (https://blogs.worldbank.org/opendata/new-country-classifications-income-level-2019-2020) and the detailed search strategy is shown in Supplemental file-1.

In addition, we reviewed the reference lists of all the included studies and identified relevant studies in the final synthesis. Search results were downloaded into an EndNote library and citation manager for easy review and removal of duplicates. To enhance accuracy and completeness of our search, we employed elements of the Peer Review of Electronic Search Strategies (PRESS EBC Elements).[24] There was no restriction on publication date and both published and unpublished papers were considered. Our search ended on August 5th, 2019.

Inclusion/exclusion criteria

We included studies if they made any statement about the epidemiology of multimorbidity in LMICs. The search was limited to papers written in English. Exclusion criteria included studies from HICs, study protocols, commentaries, editorials and case reports. The full search strategy is shown in the supplemental file submitted with this manuscript (Supplemental file 1) and also published elsewhere.[23]

Study selection

A two-stage screening process was employed to select relevant studies from those identified in our search. First, two authors (FAE and BA) removed duplicates and screened titles of the studies to select articles relevant for abstract review together. In stage two, we reviewed abstracts independently to identify studies relevant for full-text review. We assessed inter-rater reliability (using Cohen’s Kappa) of screened abstracts between the two reviewers. The two investigators (FAE and BA) independently reviewed the full-text of articles to determine their eligibility based on the inclusion criteria. When there was disagreement on inclusion of a specific article for full-text review, the article was reviewed a second time by both reviewers together and a consensus decision reached.

A spread sheet was used to extract pertinent information from the included articles. The information captured from each relevant article included primary author, year of publication, country/ies of origin, aim of the study, study design, study setting, population age group, sample size, number and types of disease conditions used to define multimorbidity, data sources, method of data collection, intervention detail (if any), outcome assessed (if any), key results and overall limitation of the study. The spreadsheet is attached as a supplemental file (Supplemental file-2).

Analysis

We described studies in terms of their geographic location, methodologies employed to define and measure multimorbidity, findings and limitations. We synthesized evidence based on the following themes: (1) epidemiology of multimorbidity, (2) methodological approaches on studying epidemiology of multimorbidity and (3) knowledge gaps in the LMIC context. The breadth of current literature within the epidemiology of multimorbidity in LMICs was mapped and the methodologies underpinning multimorbidity research were summarized.

Results

Characteristics of included studies

The searches yielded a total of 33,110 articles. Of these 11,240 records were duplicates and removed. Upon screening the titles, 20,676 records were further removed and 1,215 articles were retained for abstract reading. Following an abstract review by both authors independently, 327 articles (all published) were found to be eligible by both or either of the reviewers for a full-text review. The two reviewers agreed on the inclusion of 310 of the 327 articles included for the full text review (Cohen’s kappa 0.87). Having reviewed the full-texts of studies independently, we further excluded 259 articles. Two full-text articles by Chang and colleagues[25,26] were re-reviewed together because reviewers did not initially agree on keeping both studies for the final inclusion. We resolved the disagreement through discussion and decided to include both articles for data charting. We reviewed the reference list of all the included 68 articles and identified eight more studies relevant for inclusion giving a total of 76 studies included for studying the epidemiology of multimorbidity. Reasons for exclusion of the remaining articles included focus on a single noncommunicable disease (NCD), comorbidity studies (studies that assessed the presence of a specific additional morbidity in people with a chronic NCD), articles written in languages other than English, and studies in HICs based on the recent classification (Figure 1).

Figure 1.

Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) flowchart of the literature search.

Among the included publications, the first paper was published in 2010.[27] Most of the studies (n = 46, 60.5%) had a primary purpose of reporting the prevalence and patterns of multimorbidity. Of the total 76 studies, 52 (68.4%) were conducted in only six middle-income countries: Brazil,[27-42] China,[43-54] South Africa,[25,26,55-64] India,[65-72] Mexico[73,74] and Iran.[75,76] Studies based on multicountry data (n = 11) were based on data obtained from the World Health Organization’s (WHO’s) Study on Global Ageing and Adult Health (SAGE) and World Health Surveys.[77-80] Other individual studies were conducted in Indonesia,[81] Serbia,[82] Bangladesh,[83] Malaysia,[84] Vietnam,[85] Argentina[86] and Armenia.[87] Six more individual studies were conducted in Sub-Saharan Africa (SSA) including Ghana,[88] Nigeria,[89] Burkina Faso,[90] Zimbabwe,[91] Ethiopia[92] and Malawi[93] (Supplemental file-2 and 3).

The majority (n = 66, 86.8%) of the studies were cross-sectional and the remaining 10 studies[31,44,50,56,75,76,84,87,89,94] were cohorts by design. Most (n = 47, 61.8%) of the studies were population based and 22 (29%) were facility based, while the remaining seven (9%) were community based studies. The sample size of the included studies varied from 103 to 242,952 and included both males and females (Supplemental file-3). The S-3 contains the description of 76 studies included for studying epidemiology of multimorbidity in LMICs.

Regarding data sources, a significant number of studies were conducted based on data primarily collected for other studies, such as the WHO’s SAGE data,[25,26,55,67,68,95,96] World Health Survey data[77-80,97] or national health survey data[31,35,49,52,54,56,57,62,70,82,83,98] or other types of data such as electronic medical records.[50,58,59,73,75,76,82] Four pairs of studies used common data to answer different objectives: Chang et al.[25,26], Pati et al.[69,72], Alimohammadian et al.[75,76] and Stubbs et al.[78,79] Only 29 (38%) studies used data primarily collected for multimorbidity studies (Table 1).

Table 1.

Age group, number of conditions considered and data sources used to define and measure multimorbidity in LMICs.

Age group in years	Authors	Number of conditions considered	Authors
All ages	[47,58]	3–6	[28,33,43,55,56,58–62,68,77,85,93]	Data sources used	Authors
≥13	[64]	8–12	[25–27,30–32,36,38,41,44,57,63,67, 71,73–76,78–80,83,86,91,95–99]	Data primary collected for multimorbidity studies	[28,30,32–34,36–40,42,43,45,47, 48,51,59–61,63,65,66,71,72,74, 90,92,93,100]
≥15	[34,54,56,62]	13–20	[29,35,37,40,42,45,48,49,51–53,64–66,72,81,82,84,86,88,90,94]
				Survey data from electronic records World health survey data	[77–80,97]
≥18	[27,30,31,33,37,39,41, 43,53,60,61,63, 65–69,71,72,77–80, 86,88,91–93,96–100]	21–40	[34,39,46,47,50,54,89,92,100]	Global aging and adult health (SAGE survey) data	[25,26,55,67,68,95,96,99]
18–64	[42]			Other national data sources	[27,29,35,41,44,46,49,52,53,56,  57,62,70,75,76,81–84,86,94,98]
≥20	[38,44,82]			Medical records	[31,50,58,60,64,73,88,89,91]
24–69	[35]
≥40	[25,26,55,59,81,87]
40–75	[75,76]
≥45	[49,50]
≥50	[95]
≥60	[28,29,32,40,46,48,51, 52,57,70,73,74,83–85,90]
60–79	[36]
≥65	[89,94]
≥80	[45]

Definition and measurement of multimorbidity

While most studies (n = 56, 73.7%) defined multimorbidity as the presence of two or more chronic conditions, some studies[30,34,38-40,50,57,101] used the presence of three or more chronic conditions as their definition. All studies used simple counting of the number of chronic conditions from a list of individual diseases with the list varying substantially from one study to another. Researchers listed a minimum of three[33,93] and a maximum of 40[50] chronic conditions to determine presence of multimorbidity. The largest proportion of the studies (n = 28, 39%) used from 8–12 chronic conditions to determine multimorbidity (Table-1). However, no study used weighted multimorbidity indices such as the Charlson index which is useful in predicting outcomes that have immediate importance to patients, including disease severity and mortality[102] (Supplemental file-3).

Studies used different approaches to diagnose chronic conditions in their study participants. Self-report was the main method (n = 33, 43.4%), followed by a combination of self-report and physical or mental assessment (n = 25, 32.9%), review of medical or electronic records[31,46,50,58,60,64,73,85,89,91] and direct physical assessment alone[63,85,90,99] (Supplemental file-3).

Among diseases and conditions considered for the definition of multimorbidity, Diabetes mellitus (DM) was the most frequently listed condition (in 68 studies, 94.4%). Hypertension was listed in 60 (83.3%) studies, followed by COPD (40 studies), arthritis (39 studies), heart diseases and stroke (38 studies each), cancer and depression (33 studies each), asthma (30 studies) and angina (27 studies) (Table 2). The full list of conditions considered is indicated in Supplemental file-2.

Table 2.

The top 25 list of conditions considered for measuring multimorbidity in LMICs.

Disease type/condition	Number of studies listing the condition (n = 72)	Percentage
Diabetes mellitus	68	94.4
Hypertension	60	83.3
Chronic obstructive pulmonary disease (COPD)	40	55.6
Arthritis	39	54.2
Heart diseases (heart failure and myocardial infarction)	38	52.8
Stroke	38	52.8
Cancer	33	45.8
Depression	33	45.8
Asthma	30	41.7
Angina	27	37.5
Chronic kidney disease	22	30.6
High cholesterol/dyslipidemia	20	27.8
Chronic liver disease	18	25.0
Visual impairment	18	25.0
TB	17	23.6
Hearing problem	12	16.7
Osteoporosis	8	11.1
HIV	8	11.1
Rheumatism	7	9.7
Anemia	5	6.9
Chronic back pain	5	6.9
Obesity	5	6.9
Endotulism	5	6.9
Psychosis	4	5.6
Anxiety	2	2.8

Patterns of multimorbidity

The leading four domains of multimorbidity identified were cardio-metabolic (hypertension, heart attack, angina, heart failure, stroke, diabetes, hyperlipidemia and obesity), respiratory (asthma and COPD), mental (depression, anxiety) and musculoskeletal (arthritis, rheumatism and osteoporosis) (Supplemental file-2). Regarding the patterns of disease combinations (clusters of conditions), the most prevalent conditions were co-occurring with each other (dyads). For example, hypertension was mostly clustered with diabetes, heart disease, COPD, depression, arthritis, stroke or hypercholesterolemia.[37-40,52,53,59,81,93,99,100] Similarly, diabetes was commonly clustered with hypertension, angina, obesity, depression, COPD, asthma or arthritis.[37-40,52,53,56,59,81,93,99,100] A combination of three or more of these and other conditions were also reported.[26,30,31,37,38,49,60,63,71]

Prevalence of multimorbidity

The prevalence of multimorbidity ranged from 3.2% (93) to 90.5%.[52] The prevalence rates varied depending on population age and the number of conditions considered. For example, the study by Price and colleagues in Malawi[93] enrolled participants from the general population and only considered three disease conditions, whereas, the study by Wang and colleagues in China[52] was conducted among elderly (≥60 years) and included a list of 16 different disease conditions. Prevalence of multimorbidity seemed to have a pattern of increasing prevalence with increasing age. It ranged from 3.2% (93) to 67.8%[37] among adults aged 18 or older, 19.4%[76] to 80%[59] among people aged 40 and older, and 27.3%[74] to 90.5% in participants aged 60 and older.[52] The prevalence in the general population was also found to be higher in females (25%–52.2%) (54, 75) than males (13.4%–38.6%).[75,85]

Correlates of multimorbidity

All studies that analyzed correlates of multimorbidity (n = 43, 56.6%) identified advanced age to be strongly associated with multimorbidity. Forty-one (95.3%) of these 43 studies found female sex to be a risk factor for multimorbidity. In a few studies,[63,100] however, males were found to be more affected than females. Similarly, the association between socioeconomic status and multimorbidity was not consistent. For example, while being wealthy was a risk factor in some studies,[25,39,62,66,68,70,72,81,92,93] being poor was a risk factor in others.[34,38,40,49,53,54,78] In a few studies, higher levels of education were associated with increased risk of multimorbidity.[39,63,72]

Discussion

This scoping review summarizes the evidence on the epidemiology of multimorbidity in LMICs. We also described knowledge gaps in the epidemiology and measurement of multimorbidity, as well as areas of focus for future research, policy and practice in LMICs.

Evidence on the epidemiology of multimorbidity in LMICs is limited although the region bears 80% of the global burden of NCDs.[103] This finding is consistent with a recent review by Xu and colleagues (3) that reported only 5% of multimorbidity research studies originated in LMICs. The imbalance in the research output was also characterized by the wide interval in year of publication of the first paper on multimorbidity between HICs in 1976[104] and LMICs in 2010.[27]

Moreover, not only were LMICs less represented in multimorbidity research, but also most of (n = 52, 68.4%) the available studies in LMICs were confined to only six middle-income countries (Brazil, China, South Africa, India, Mexico and Iran). This skewed distribution of multimorbidity studies demonstrates that there is a lack of focus on studying the phenomenon in other LMICs where it is likely to be more prevalent.[26]

Marked variation exists among studies with respect to the methodologies employed to define and measure multimorbidity. Studies were heterogeneous in terms of age of the participants involved, the type and number of chronic conditions considered and sources of data used to define multimorbidity. Use of different methodologies resulted in differences in the prevalence estimates and difficulty in comparing and pooling the results. The two most important factors playing a role in varying prevalence estimates in this review were age of the population enrolled and the number of conditions considered for defining multimorbidity. Consistent with studies in HICs,[4,105] a constant increase in multimorbidity prevalence was observed in studies which involved participants aged 60 years or more[26,38,39,46,49,74,84] and among studies including 12 or more conditions on their list.[38,39,72] Evidence in HICs has shown that a list of 12–20 conditions is an appropriate threshold to estimate multimorbidity prevalence in a stable way.[5] The majority of studies (n = 51, 70.9%) included in this review used 8–20 health conditions to define multimorbidity.

The debate on the types of chronic conditions to consider and whether risk factors, such hypercholesteremia, high blood pressure and obesity, and symptoms such as pain and anemia, should be included in the list for identifying multimorbidity has not been settled globally.[5] The type and list of conditions considered in this review were not consistent across the studies reviewed either. However, recent recommendations have highlighted the inclusion of chronic conditions posing a significant burden to the given population. Inclusion of chronic infections such as HIV in the list to define multimorbidity has also been emphasized.[106,107]

As shown above, the prevalence in LMICs varies from 3.2% to 90.5% which is comparable to the findings from HICs (3.5%–100%).[11] In the face of a struggle against communicable, maternal, neonatal and nutritional health problems, the emergence of multimorbidity in low and middle income countries portends a rise in a quadruple burden of disease for the health care systems.[108-110]

Consistent with other studies,[11,111] the most prevalent conditions identified across the studies reviewed include diabetes, hypertension, COPD, arthritis, heart disease, stroke, cancer and depression. Most of these diseases shaped the patterns of multimorbidity. The nature of the clusters of conditions were mostly concordant; that is, diseases having common risk factors or that follow common pathological pathways co-existed. For example, hypertension was clustered with other cardiometabolic conditions such as diabetes, hypercholesterolemia, heart diseases and stroke. Similarly, diabetes was commonly clustered with hypertension, angina, obesity and heart diseases. Clusters are important predictors of several health and functional outcomes and understanding their nature is helpful for prevention and management of multimorbidity.[112]

It is globally known that additional life-years constitute an additional opportunity for acquiring other chronic conditions.[4] Studies show that with increasing age, numerous underlying physiological changes occur. These include gradual accumulation of a wide variety of molecular and cellular damage that leads to a risk of chronic diseases with an increased chance of experiencing more than one chronic condition at the same time.[113] However, the rise in the prevalence of multimorbidity starts around the age of 40,[6] and the absolute number of individuals with multimorbidity is often higher in those under 65 years with a flattening of the odds of multimorbidity after 70 years of age.[7]

Most studies in our review have shown that there was higher prevalence of multimorbidity among females than males. The higher likelihood of multimorbidity in women is congruent with findings in HICs.[114] This may due to the fact that females have a longer chance of survival,[115] have higher consultation rates leading to higher rates of diagnosis[116] or there is a difference in the prevalence of the underlying conditions included in multimorbidity definitions.[4]

The effect of socioeconomic status on multimorbidity was inconclusive in our review. While studies in India,[72] South Africa[26,63] and Malawi[93] reported that multimorbidity is higher among wealthy individuals, studies in Iran,[75,76] China[49] and Brazil[38] reported multimorbidity to be higher among people living with low socioeconomic status (SES). Low health care-seeking behavior and probability of underdiagnoses might have contributed to hide the real picture of multimorbidity in the rapidly emerging and urbanizing population of India and African countries.[72] However, in HIC studies, multimorbidity is more common and occurring at an earlier age in areas of high socioeconomic deprivation than their wealthier counterparts.[7,117,118]

Multimorbidity impacts both patients and the health care systems in many ways.[6,7,119,120] The effect on individuals include death at younger age,[121-123] impairments of physical and social functioning,[7,124] poor quality of life,[125-127] mental health problems,[7,78] high cost of care[128] and higher rates of adverse effects of treatment and complex interventions.[129] In LMICs, however, there is a limited body of evidence on the impacts of multimorbidity on patient-centered outcomes, such as health related quality of life (HRQoL) and functionality.[6,130]

The evidence base on the most effective ways to treat patients living with several medical conditions is sparse in LMICs.[106] Therefore, it is likely that patients with multimorbidity face accumulating and overwhelming complexity resulting from the sum of uncoordinated responses to each of their problems.[131-133] Adding to this, the current emergence of COVID-19 is demanding a change in the way patients with chronic conditions and multimorbidity are managed and followed.[18,19] Furthermore, the risk of dying due to COVID-19 is high among people living with chronic conditions and multimorbidity.[134]

Implication for research, policy and practice

The knowledge base on the epidemiology of multimorbidity is not yet substantial and not evenly distributed among LMICs. The current literature is highly heterogeneous in methodology and has a range of limitations. Most studies were cross-sectional surveys and were based on data obtained primarily collected for other studies.[135] Longitudinal studies are required to better estimate the risk, understand the onset of multimorbidity and explain the causative pathways.[136] Estimating multimorbidity among patients visiting primary health care services is also possible.[5] However, the epidemiological denominator in the health care setting may not necessarily represent the underlining characteristics of the general population.[137] Although providing a precise list of conditions suitable for the LMICs context is beyond the scope of this review, considering a list of 8 to 12 chronic conditions that are highly prevalent and burdensome to the given society would help comparing and pooling prevalence estimates.

Employing standardized tools and a blend of methods including self-report, direct physical assessment, and complementing these data sources with medical records and prescription data, can help to capture the real picture of existing conditions.[138] Integrating biomarker data into other measures of multiple chronic condition may have also notable advantages particularly for individuals with undiagnosed conditions.[130] A simple count of chronic conditions is not sufficient,[4,5,139] but employing validated weighted scales would help understand the overall burden and patterns of clustering of chronic conditions.[5] Moreover, determining HRQoL, functionality and lived experiences of people with multiple chronic conditions is instrumental to design effective interventions in LMICs.[106,140]

It is imperative to define the best possible model of health care for people with multimorbidity in LMICs.[107] Multimorbidity should drive a shift in the way health policies are developed and guide the health care system in tackling this challenge.[20,141] In this sense, it is clear that priority should be directed to reorient and strengthen the primary care services.[142] The provision of patient-centered care in which all health care providers work together with patients to ensure coordination, consistency and continuity of care over time is essential.[143,144] The development of clinical practice guidelines should fuel a reform in the academic curriculum and continuing training programs to accommodate the new scenario in health professions’ education.

Strengths and limitations of this review

This is the first scoping review conducted in LMICs and provides a comprehensive insight into the nature and distribution of multimorbidity studies in LMICs. We have clearly identified the existing knowledge gap in terms of the epidemiology and management approaches of multimorbidity in LMICs. However, only including publications written in English may represent a segment of the research conducted in LMICs. Nevertheless, a particular effort was made to employ a comprehensive search strategy and navigate through a wide set of databases and identify all relevant studies in LMICs.

Conclusion and recommendations

Studies on the epidemiology of multimorbidity in LMICs are limited, while published studies are concentrated in only a few countries. The lag in studying multimorbidity in LMICs may have also contributed to the delay in designing effective interventions for those living with multimorbidity. Further research is urgently required to better understand the epidemiology of multimorbidity in LMICs. Furthermore, understanding models of multimorbidity care is an important next step in research in the context of growing prevalence of multimorbidity and its complex relationship with chronic infectious diseases, and the fact that the conventional health care is inadequate to meet the needs of patients with multiple chronic conditions warrants urgent research interventions.

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