Addressing NCD Co-Morbidities: Shared Opportunities for Action. fotolia

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Addressing NCD Co-Morbidities: Shared Opportunities for Action fotolia

Introduction Noncommunicable diseases (NCDs) are now widely recognised as a major challenge to health and sustainable human development in the 21 st century. NCDs are the leading cause of death and disability worldwide, responsible for 68% of global mortality 1. This figure projected to reach 74% by 2030 1, exacting a heavy and growing toll on the health and economic security of all countries. Increasingly, it is low- and middle-income countries (LMICs) and the poorest and most vulnerable populations which are hardest hit by these largely preventable diseases. The primary focus of the global NCD response has been on the four major diseases namely cardiovascular disease (CVD), cancer, diabetes, and chronic respiratory diseases and four risk factors tobacco use, unhealthy diet, physical inactivity, and harmful use of alcohol identified by the World Health Organization (WHO) and the UN as those responsible for the greatest burden. There is, however, a range of diseases and conditions - including mental and neurological disorders, autoimmune disorders such as psoriasis, bone and joint conditions such as osteoporosis and arthritis, and renal, oral, eye and ear diseases that are linked to the four most prominent NCDs. Driven by similar risk factors, together with demographic changes including rapid urbanisation and ageing populations, these diseases are closely interconnected. Often, two or more NCDs manifest in the same individual, referred to as NCD co-morbidities. NCD co-morbidities can occur because diseases share the same risk factors, with tobacco use being a risk for cancer, CVD and dementia 2 ; or because some diseases predispose individuals to developing others, as in the case of diabetes, which is a risk factor for CVD, stroke, osteoporosis 3, kidney failure and depression 4. As a result, these conditions can benefit from a comprehensive and integrated response. Health systems also increasingly have to manage patients living with infectious diseases such as HIV/AIDS and tuberculosis (TB) alongside NCDs. This issue is particularly acute in LMICs facing a double burden of disease. With effective antiretroviral treatment, people living with HIV are living longer and develop NCDs associated with ageing. Furthermore, some antiretroviral drugs may also increase risk to people living with HIV of developing certain NCDs, for example through insulin resistance 5, leading to increased risk of diabetes and CVD; while HIV infection itself increases the risk of CVD 6, and some cancers 7. Diabetes is a known risk factor for active TB and reactivation of latent TB 8. It has also been observed that vulnerable populations affected by NCDs are more likely to develop seasonal influenza 9. The Compounded Challenge of NCD Co-Morbidities NCD co-morbidities impose years of disability and compounded financial burden on those affected, their families, health systems, and national economies. While the prevalence of co-morbidities varies, it increases substantially with age in all countries, with higher rates in urban than rural areas 10, and disproportionately affecting those who are poorest. Social-economic inequalities are exacerbated for people living with co-morbidities, with the most drastic implications for those living in developing countries enduring a double burden of NCDs and chronic infectious diseases. NCD co-morbidities are associated with greater healthcare utilisation and financial burden including, in most cases, higher out-of- pocket expenditures - often more than double for NCD co-morbidities than for a single NCD 10, Globally, health systems are ill-equipped to respond to the challenges posed by NCD co-morbidities. In the first instance, health systems have evolved to address acute issues, rather than to provide the continuous care required for chronic conditions, including NCDs. Furthermore, many health systems are configured to treat singular diseases in a siloed, vertical approach, which is inappropriate and ineffective for people living with NCD co-morbidities. Given the complexities involved in clinical management decisions, developing clinical practice guidelines on managing co-morbidities for primary care practitioners is vital.

Interconnected Diseases, Common Solutions Since the UN Political Declaration on NCDs in 2011, governments have adopted a series of bold political commitments to guide the response and an ambitious global goal of achieving a 25% reduction in premature NCD mortality by 2025. However, progress to date has been insufficient and uneven. Of 174 countries featured in the 2015 WHO Progress Monitor on NCDs, only 29% have guidelines for the management of major NCDs, which is an essential first step towards provision of effective care. Even once this is achieved, there is an urgent need to move away from single-disease approaches, and to reorient health systems to integrate care packages across multiple chronic conditions, through a holistic person centred approach. Stronger health systems underpinned by primary health care (PHC) are crucial to effectively manage NCDs. PHC is often the first gateway to health services for people with NCDs and plays a central coordinating role in the prevention, diagnosis and long-term management of chronic diseases. In order to address NCD co-morbidities, concerted efforts are needed not only for treatment of chronic diseases but also to reduce population risk factors for NCDs. This can be achieved through intersectoral health promotion and other primary and secondary prevention. This must be done throughout the lifecourse, including through integration with the reproductive maternal newborn child and adolescent health (RMNCAH) agenda, since many opportunities for NCD prevention exist in early life. The impact of investing in reduction of exposure to common risk factors to relieve the burden of NCD co-morbidities is significant - up to 80% of heart disease, stroke, and type 2 diabetes, and over a third of the most common cancers could be prevented by eliminating exposure to their shared risk factors 11. In countries bearing a double burden of infectious diseases and NCDs, there is an especially strong case to integrate care enabling people living with NCDs, HIV and TB to access the care they need. Health services need to be reorganised to address populations needs holistically and effectively, and to make best use of resources, especially in settings where these are most limited. In some countries, evidence shows that offering comprehensive care to patients suffering from both stroke and HIV in the same place is feasible and can achieve success, with retention of patients in care in HIV, diabetes and hypertension in Cambodia remaining at 70-90% after three years 12. Within the broader context of universal health coverage (UHC), investment for health and adequate health insurance for all should be at the core of policies to promote better access to health services across populations and reduce out-of-pocket expenditures.

Osteoporosis, NCD Co-Morbidities, and Fracture Risk istock Like many other NCDs, risk factors for osteoporosis include tobacco use, alcohol use, unhealthy diet (specifically a lack of calcium or vitamin D), and age. Certain medications, including those used to treat some cancers, can also increase risk of developing osteoporosis 13. Cancer is a major risk factor for bone loss and fractures. This is due both to direct effects of cancer cells on the skeleton and of cancer therapies on bone cells 14. People living with type 1 diabetes have lower bone mineral density (BMD) and higher risk of fractures. Evidence is accumulating that patients with complications of type 2 are also at increased risk of certain types of osteoporotic fractures. Globally, one third of women and one fifth of men over the age of 50 will suffer an osteoporotic fracture 15, 16, 17. There are more than 8.9 million fractures annually. A fracture occurs every three seconds 18. In women, osteoporosis accounts for more days in hospital than other diseases including breast cancer, myocardial infarction, and diabetes 19. Approximately half of all people who have had one osteoporotic fracture will have another, with the risk of additional fractures increasing with each new broken bone 20. A prior fracture is associated with an 86% increased risk of any fracture 21,22. Despite the global threat posed by fragility fractures, and the availability of safe and cost-effective therapies that could reduce the number of fractures, gaps in care are preventing millions of at-risk individuals from being diagnosed and treated worldwide. The world s population is ageing, which means that the burden of fractures will increase dramatically, placing severe strains on the capacity and finances of healthcare systems worldwide. Highly effective osteoporosis treatments substantially reduce fracture risk, but are often not routinely offered to fragility fracture sufferers. In some countries, up to 80% of fracture patients are not diagnosed or treated for osteoporosis 23. A practical and effective solution to tackling the increasing burden of fractures is the implementation of Fracture Liaison Services (FLS) and Orthogeriatric Service models of care. These services, which identify and manage the patients at highest risk of future fracture, have been successfully developed and are increasingly included in clinical guidelines. However, their implementation must be expanded globally.

IOF s Capture the Fracture (CtF) is a global programme to facilitate the implementation of coordinated, multi-disciplinary models of care for secondary fracture prevention. IOF CAPTURE the FRACTURE The IOF Capture the Fracture focuses on the following three areas: Setting standards Facilitating change Creating awareness A Best Practice Framework (BPF), currently available in nine major languages, serving as an international benchmark for FLS by defining essential and aspirational elements of FLS service delivery. The BPF serves as the measurement tool for IOF to award Capture the Fracture Best Practice Recognition in celebration of successful FLS worldwide. There are currently over 180 FLS in the IOF network, and over 300 members following the CtF programme, in particular. Mentorship programmes have been set up to facilitate the transfer of knowledge and skills by connecting experienced FLS champions with any institutions willing to establish a new FLS Implementation guides and toolkits available on the CtF website www. capturethefracture.org with a comprehensive suite of resources to support healthcare professionals and administrators to establish a new FLS or improve an existing FLS. An on-going series of webinars provides an opportunity to learn from experts across the globe who have established highperforming FLS, and contributed to development of guidelines and policy on secondary fracture prevention, providing potential FLS with country specific advice in local languages. Dissemination of articles about the CtF programme and BPF within relevant scientific publications Presence at national international conferences as part of on-going awareness and advocacy efforts.

ncdalliance.org iofbonehealth.org REFERENCES 1 World Health Organization. Projections of mortality and causes of death, 2015 and 2030. Online database WHO Regions accessed 28 October 2016: http://www. who.int/healthinfo/global_burden_disease/projections/en/ 2 Alzheimer s Disease International. World Alzheimer Report 2014, Dementia and Risk Reduction: An analysis of protective and modifiable factors. 2014. 3 Brown SA & Sharpless JL. Osteoporosis: An Under-appreciated Complication of Diabetes. Clinical Diabetes 2004; 22(1): 10-20. 4 Mezuk B et al. Depression and type 2 diabetes over the lifespan: a meta-analysis. Diabetes Care 2008; 31(12):2383-90 5 Hruz PW. Molecular mechanisms for insulin resistance in treated HIV-infection. Best Pract Res Clin Endocrinol Metab. 2011; 25(3): 459 468. 6 Triant VA. Cardiovascular Disease and HIV Infection. Current HIV/AIDS Reports 2013; 10(3), 199 206. 7 Silverberg MJ et al. Cumulative incidence of cancer among persons with HIV in North America: a cohort study. Annals of Internal Medicine 2015; 163, 215 8 Ai J-W et al. Updates on the risk factors for latent tuberculosis reactivation and their managements. Emerg Microbes Infect. 2016; 5(2): e10. 9 Palache A et al. The Link between Seasonal Influenza and NCDs: Strategies for Improving Vaccination Coverage. Health, 2014; 6, 2724-2735 10 Lee JT et al. Impact of Noncommunicable Disease Multimorbidity on Healthcare Utilisation and Out-Of-Pocket Expenditures in Middle-Income Countries: Cross Sectional Analysis. PLoS ONE 2015; 10(7): e0127199. 11 World Health Organization. Preventing NCDs: A Vital Investment, WHO Global Report 2008. 12 UNAIDS (2011). Chronic care of HIV and noncommunicable diseases: How to leverage the HIV experience. 2011. 13 Jehle P. (2003). Steroid-induced osteoporosis: how can it be avoided? Nephrol. Dial. Transplant. 18 (5): 861-864. doi: 10.1093/ndt/gfg067 14 Drake, M. T. (2013). Osteoporosis and Cancer: Current Osteoporosis Reports, 11(3), 163 170. 15 Melton LJ, 3rd, et al. (1998) Bone density and fracture risk in men. J Bone Miner Res 13:1915. 16 Melton LJ, 3rd, et al. (1992) Perspective. How many women have osteoporosis? J Bone Miner Res 7:1005. 17 Kanis JA, et al. (2000) Long-term risk of osteoporotic fracture in Malmo. Osteoporos Int 11:669. 18 Johnell O & Kanis JA (2006) An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporos Int 17:1726 19 Kanis JA, et al. (1997) Guidelines for diagnosis and management of osteoporosis. The European Foundation for Osteoporosis and Bone Disease. Osteoporos Int 7:390. 20 Lindsay R, et al. (2001) Risk of new vertebral fracture in the year following a fracture. JAMA 285:320. 21 Kanis JA, et al. (2004) A meta-analysis of previous fracture and subsequent fracture risk. Bone 35:375 22 Roux C, et al. (2007) Mild prevalent and incident vertebral fractures are risk factors for new fractures. Osteoporos Int 18:1617. 23 Nguyen TV, et al. (2004) Osteoporosis: underrated, underdiagnosed and undertreated. Med J Aust 180:S18.