Self-reported disability in relation to mortality in rural Malawi: a longitudinal study of over 16 000 adults

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Study Justification:
The study aimed to investigate the association between self-reported disability and mortality in adults in rural Malawi. This research is important because understanding the impact of disability on mortality can help inform interventions and policies to improve access to healthcare and other services for individuals with disabilities.
Highlights:
– The study included over 16,000 adults aged 18 and over residing in the Karonga Health and Demographic Surveillance Site (HDSS) in rural Malawi.
– Participants were asked about difficulty in six functional domains and classified as having disabilities if they reported ‘a lot of difficulty’ or ‘can’t do at all’ in any domain.
– The study found that adults reporting disability had a significantly higher all-cause mortality rate compared to those without disabilities.
– The mortality rate from non-communicable diseases (NCDs) was also higher among people with disabilities.
– The findings suggest that self-reported disability can predict mortality at all adult ages in rural Malawi.
Recommendations for Lay Reader:
Based on the study findings, it is recommended to:
1. Improve access to healthcare and other services for individuals with disabilities in rural Malawi.
2. Develop interventions targeted at reducing mortality from non-communicable diseases among people with disabilities.
3. Increase awareness and understanding of disability-related issues among healthcare providers and the general population.
4. Advocate for policies and programs that promote inclusivity and equal opportunities for individuals with disabilities.
Recommendations for Policy Maker:
In light of the study findings, policy makers are encouraged to:
1. Allocate resources to improve healthcare infrastructure and services in rural areas, with a focus on accessibility for individuals with disabilities.
2. Develop and implement policies that promote the inclusion of people with disabilities in all aspects of society, including education, employment, and social services.
3. Support research and data collection on disability prevalence, healthcare utilization, and outcomes to inform evidence-based policies and interventions.
4. Collaborate with community organizations and disability advocacy groups to ensure the voices and needs of individuals with disabilities are represented in policy-making processes.
Key Role Players:
1. Ministry of Health: Responsible for implementing policies and programs related to healthcare access and disability services.
2. Community Organizations: Involved in advocating for the rights and needs of individuals with disabilities and providing support services.
3. Disability Advocacy Groups: Play a crucial role in raising awareness, promoting inclusivity, and influencing policy decisions.
4. Healthcare Providers: Responsible for delivering quality healthcare services to individuals with disabilities and implementing inclusive practices.
Cost Items for Planning Recommendations:
1. Infrastructure Development: Budget for improving healthcare facilities and making them accessible for individuals with disabilities.
2. Training and Capacity Building: Allocate funds for training healthcare providers on disability-inclusive care and services.
3. Awareness Campaigns: Budget for public awareness campaigns to reduce stigma and increase understanding of disability-related issues.
4. Research and Data Collection: Allocate resources for conducting further research on disability prevalence, healthcare utilization, and outcomes.
5. Program Implementation: Budget for implementing interventions and programs aimed at improving access to healthcare and other services for individuals with disabilities.
Please note that the cost items provided are general categories and not actual cost estimates. The specific costs will depend on the context and scope of the interventions and programs implemented.

The strength of evidence for this abstract is 8 out of 10.
The evidence in the abstract is strong, but there are some areas for improvement. The study design is longitudinal, which allows for a stronger analysis of the relationship between self-reported disability and mortality. The sample size is large, with over 16,000 participants, increasing the generalizability of the findings. The study also adjusts for confounders and explores the relationship between disability and mortality in the context of other health conditions. However, the abstract could be improved by providing more specific information on the methods used, such as the statistical analysis and the specific disability domains assessed. Additionally, it would be helpful to include the main findings and their implications for future interventions.

OBJECTIVES: We investigated whether self-reported disability was associated with mortality in adults in rural Malawi. SETTING: Karonga Health and Demographic Surveillance Site (HDSS), Northern Malawi. PARTICIPANTS: All adults aged 18 and over residing in the HDSS were eligible to participate. During annual censuses in 2014 and 2015, participants were asked if they experienced difficulty in any of six functional domains and were classified as having disabilities if they reported ‘a lot of difficulty’ or ‘can’t do at all’ in any domain. Mortality data were collected until 31 December 2017. 16 748 participants (10 153 women and 6595 men) were followed up for a median of 29 months. PRIMARY AND SECONDARY OUTCOME MEASURES: We used Poisson regression to examine the relationship between disability and all-cause mortality adjusting for confounders. We assessed whether this relationship altered in the context of obesity, hypertension, diabetes or HIV. We also evaluated whether mortality from non-communicable diseases (NCD) was higher among people who had reported disability, as determined by verbal autopsy. RESULTS: At baseline, 7.6% reported a disability and the overall adult mortality rate was 9.1/1000 person-years. Adults reporting disability had an all-cause mortality rate 2.70 times higher than those without, and mortality rate from NCDs 2.33 times higher than those without. CONCLUSIONS: Self-reported disability predicts mortality at all adult ages in rural Malawi. Interventions to improve access to healthcare and other services are needed.

The Karonga Health and Demographic Surveillance Site (HDSS) in Northern Malawi comprises a population of around 40 000 individuals, which is largely representative of the rural Malawian population in terms of age and sex structure.11 12 Census information is collected on the population annually, along with continuous reporting of births, deaths and migration by community key informants. Verbal autopsy is done after every death using a semistructured interview of a family member using an adaptation of a WHO instrument.13 Two clinically trained reviewers independently assign cause of death based on this interview. In case of disagreement, a third reviewer arbitrates. Since 2014, the WG Short Set questions on disability have been added to the annual census questionnaire, alongside the existing questions on demographic, health and social indicators. The disability questions were only asked if the participant was physically seen by the fieldworker, although they could be answered through a proxy, after obtaining written consent or assent. Therefore, no disability data were collected from anyone away from home on the day of the census. The questions, translated into the local language of Chitumbuka, are: In this analysis, we used data on adults aged 18 and over from the first two consecutive census rounds to include the disability questions. The first was in 2014–2015 (round 1), the second in 2015–2016 (round 2). Baseline disability status was taken from the round 1 census data where possible. For participants with no disability data from round 1, data from round 2 were used. Anyone who moved into the HDSS between rounds 1 and 2, or turned 18 between rounds 1 and 2, and answered disability questions at round 2 was also included. Other sociodemographic information was taken from the same interview as the disability data. Follow-up was undertaken until 31 December 2017. Data on body mass index (BMI), hypertension and diabetes were gathered from a survey of all adults performed within the HDSS population in 2013–2015 on prevalence of major NCDs and their risk factors.14 In this screening, height and weight were measured twice, and the mean was used to calculate BMI. Participants were asked if they had previously been diagnosed with hypertension or diabetes, and whether they were taking any regular medication. Resting blood pressure was measured three times with 5 min in between, and a mean of the second and third measures was used. Blood was taken for plasma glucose measurement after at least 8 hours of fasting. These data were collected a mean of 1.2 years prior to the disability data (maximum 3.5 years). Data on HIV status were collated from numerous sources including an HIV serosurvey in 2011 and the 2013–2015 NCD survey. Data on new HIV diagnoses were also collected from consenting participants at government clinics within the HDSS. Participants were categorised as HIV positive if they had ever reported a diagnosis of HIV or had a positive antibody test. They were categorised as negative for 4 years after a negative HIV test, after which time their status was categorised as missing in case of a new infection in the interim. Age was grouped into categories of 18–34, 35–44, 45–54, 55–64, 65–69, 70–74, 75–79 and 80+ years; narrower age bands were chosen at higher ages as self-reported disability is strongly associated with older age. Education level was defined as no education, primary (including partially completed), secondary (including partially completed) and tertiary. Occupation was categorised into not working (including unemployed, unable to work and retired), manual work, farming or fishing and non-manual work (including professional work). Participants were defined as in a union if they were married or cohabiting, and not if single, divorced or widowed. Categories of BMI were <18.5 kg/m² (underweight), 18.5–24.9 kg/m² (healthy weight), 25–29.9 kg/m² (overweight) and 30+ kg/m² (obese). Hypertension was defined as systolic blood pressure ≥140 mm Hg, diastolic blood pressure of ≥90 mm Hg or use of antihypertensive medications. Diabetes was defined as fasting blood sugar ≥7.0 mmol/L or a self-reported diagnosis of diabetes. Disability was defined as answering ‘a lot of difficulty’ or ‘can’t do at all’ in any domain. Cause of death among adults was broadly categorised into communicable disease, NCDs, maternal death, external (including injury and poisoning) and unspecifiable/other. Prevalence of self-reported disability was calculated with 95% CIs by sociodemographic and health characteristics. Poisson regression analysis was used to calculate adult mortality rate ratios (RR), comparing people reporting ‘some difficulty’ and ‘a lot of difficulty or can’t do at all’ with ‘no difficulty’ in each disability domain. For these analyses, individuals contributed exposure time during their residence in the HDSS from the date the disability survey was completed, until the earliest of 31 December 2017, death or outmigration. Returning and repeat migrants only contributed person-years while resident in the HDSS. Age and sex were included a priori in the adjusted model, and baseline occupation, education level and union status were sequentially added to the model to check for confounding. Any variable that altered the RR more than 10% was kept in the adjusted model. Each of obesity, hypertension, diabetes and HIV status at baseline was also added to the models to check for confounding or effect modification. Cause-specific mortality was also calculated. We performed complete case analysis, so that any participants with missing data for any of the variables in the model were excluded. Sensitivity analyses, including an ‘unknown’ category for BMI, hypertension, diabetes and HIV were also performed. All significance tests were likelihood ratio tests. Malawi Epidemiology and Intervention Research Unit works closely with the community in which this research was conducted. Regular meetings with senior community members take place to ensure that study objectives align with the priorities of the community, and that the methodology and procedures are appropriate and acceptable. Research findings are disseminated similarly.

Based on the provided information, it seems that the study focuses on the association between self-reported disability and mortality in rural Malawi. The study highlights the need for interventions to improve access to healthcare and other services. While the specific innovations for improving access to maternal health are not explicitly mentioned in the given text, here are some potential recommendations that could be considered:

1. Mobile health clinics: Implementing mobile health clinics that can travel to remote areas, providing maternal health services and check-ups to women who may have limited access to healthcare facilities.

2. Telemedicine: Utilizing telemedicine technology to connect healthcare providers with pregnant women in remote areas, allowing them to receive prenatal care and consultations without the need for physical travel.

3. Community health workers: Training and deploying community health workers who can provide education, support, and basic maternal health services to women in rural areas, bridging the gap between communities and healthcare facilities.

4. Transportation support: Establishing transportation support systems, such as ambulances or transportation vouchers, to ensure that pregnant women can easily access healthcare facilities for prenatal care, delivery, and postnatal care.

5. Health education programs: Implementing comprehensive health education programs that focus on maternal health, including prenatal care, nutrition, hygiene, and birth preparedness, to empower women with knowledge and promote healthy practices.

6. Maternal health incentives: Introducing incentives, such as financial assistance or rewards, to encourage pregnant women in rural areas to seek regular prenatal care and deliver in healthcare facilities.

7. Collaborations with local organizations: Partnering with local organizations, community leaders, and traditional birth attendants to raise awareness about the importance of maternal health and promote the utilization of healthcare services.

It is important to note that these recommendations are general and may need to be tailored to the specific context and needs of rural Malawi. Further research and consultation with local stakeholders would be necessary to determine the most effective and feasible innovations for improving access to maternal health in this setting.
AI Innovations Description
The recommendation to improve access to maternal health based on the study findings is to implement interventions that focus on improving access to healthcare and other services for individuals with disabilities in rural Malawi. This is because the study found that self-reported disability was associated with higher mortality rates in adults in rural Malawi, including mortality from non-communicable diseases (NCDs).

To address this issue, it is important to develop innovative solutions that specifically target the needs of individuals with disabilities in accessing maternal health services. Some potential recommendations for innovation include:

1. Accessibility improvements: Enhance the physical accessibility of healthcare facilities by providing ramps, handrails, and other assistive devices to ensure that individuals with disabilities can easily access maternal health services.

2. Sensitization and training: Conduct sensitization programs and training sessions for healthcare providers to raise awareness about the needs and rights of individuals with disabilities. This can help healthcare providers better understand and address the specific challenges faced by this population in accessing maternal health services.

3. Assistive technologies: Explore the use of assistive technologies, such as mobile health applications or telemedicine, to improve access to maternal health services for individuals with disabilities. These technologies can provide remote consultations, appointment reminders, and educational resources, making healthcare more accessible and convenient.

4. Community-based support: Establish community-based support networks or peer support groups for individuals with disabilities, including pregnant women, to provide emotional support, share experiences, and exchange information on accessing maternal health services. These networks can also serve as advocacy platforms to raise awareness about the needs of individuals with disabilities in accessing healthcare.

5. Policy and advocacy: Advocate for the development and implementation of policies that prioritize the inclusion of individuals with disabilities in maternal health programs. This can involve working with government agencies, non-governmental organizations, and other stakeholders to ensure that maternal health services are accessible and inclusive for all.

By implementing these recommendations, it is possible to develop innovative solutions that can improve access to maternal health for individuals with disabilities in rural Malawi, ultimately reducing maternal mortality rates and improving overall maternal health outcomes.
AI Innovations Methodology
Based on the provided information, it seems that you are looking for innovations to improve access to maternal health in rural Malawi. Here are a few potential recommendations:

1. Mobile Clinics: Implementing mobile clinics that can travel to remote areas and provide maternal health services, including prenatal care, delivery assistance, and postnatal care. These clinics can reach women who have limited access to healthcare facilities.

2. Telemedicine: Utilizing telemedicine technology to connect pregnant women in rural areas with healthcare professionals. This allows for remote consultations, monitoring, and guidance throughout pregnancy, reducing the need for travel and improving access to specialized care.

3. Community Health Workers: Training and deploying community health workers who can provide basic maternal health services, education, and support to pregnant women in their communities. These workers can also serve as a link between the community and healthcare facilities.

4. Health Education Programs: Implementing comprehensive health education programs that focus on maternal health, including prenatal care, nutrition, hygiene, and family planning. These programs can empower women with knowledge and skills to make informed decisions about their health.

To simulate the impact of these recommendations on improving access to maternal health, a methodology could include the following steps:

1. Define the target population: Identify the specific population group (e.g., pregnant women in rural areas of Malawi) that will be the focus of the simulation.

2. Collect baseline data: Gather relevant data on the current state of maternal health access in the target population, including factors such as distance to healthcare facilities, availability of services, and utilization rates.

3. Define indicators: Determine key indicators that will be used to measure the impact of the recommendations, such as the number of women receiving prenatal care, the rate of skilled attendance at birth, or the reduction in maternal mortality.

4. Develop a simulation model: Create a mathematical or computational model that simulates the impact of the recommendations on the defined indicators. This model should take into account factors such as population size, geographical distribution, healthcare infrastructure, and the effectiveness of the proposed interventions.

5. Input data and run simulations: Input the baseline data into the simulation model and run multiple simulations to estimate the potential impact of the recommendations. This can help identify the most effective interventions and their expected outcomes.

6. Analyze results: Analyze the simulation results to assess the potential impact of the recommendations on improving access to maternal health. This can include evaluating changes in the defined indicators and comparing different scenarios or combinations of interventions.

7. Refine and validate the model: Continuously refine and validate the simulation model based on real-world data and feedback from experts and stakeholders. This ensures that the model accurately represents the target population and provides reliable predictions.

By following this methodology, policymakers and healthcare providers can gain insights into the potential impact of different innovations and make informed decisions on how to improve access to maternal health in rural Malawi.

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