|REPORT FROM THE FIELD
|Year : 2013 | Volume
| Issue : 2 | Page : 113-117
Monitoring medicines use to support national medicines policy development and implementation in the Asia Pacific region
Elizabeth E Roughead1, Karma Lhazeen2, Engko Socialine3, Salmah Bahri4, Byong Joo Park5, Kathleen Holloway6
1 Quality Use of Medicines and Pharmacy Research Centre, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, Australia
2 Department of Medical Services, Chief Programme Officer in Essential Medicine and Technology Division, Ministry of Health, Bhutan
3 Directorate General of Pharmaceutical Services and Medical Devices, Ministry of Health, Indonesia
4 Director of Pharmacy Practice and Development, Ministry of Health, Malaysia
5 Department of Preventative Medicine, Seoul National University College of Medicine, Seoul, Korea and Korea Institute of Drug Safety and Risk Management, Seoul, Republic of Korea; Regional Adviser in Essential Medicines, World Health Organization Regional Office for South-East Asia, New Delhi, India
6 Regional Adviser in Essential Medicines, World Health Organization Regional Office for South-East Asia, New Delhi, India
|Date of Web Publication||12-Dec-2013|
Elizabeth E Roughead
Quality Use of Medicines and Pharmacy Research Centre, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, 5001, Australia
Critical to the successful implementation of a national medicines strategy is evaluation of the policy and ongoing monitoring of medicine use. Methods for monitoring medicines use within countries vary depending on the country and its stage of medicines policy development and implementation. In this paper, we provide four case studies on monitoring medicines use to support national medicines policy development and implementation. Cases come from Bhutan, Indonesia, Malaysia and the Republic of Korea.
Keywords: Bhutan, case studies, Indonesia, Malaysia, national medicines strategy, rational medicines use, Republic of Korea
|How to cite this article:|
Roughead EE, Lhazeen K, Socialine E, Bahri S, Park BJ, Holloway K. Monitoring medicines use to support national medicines policy development and implementation in the Asia Pacific region. WHO South-East Asia J Public Health 2013;2:113-7
|How to cite this URL:|
Roughead EE, Lhazeen K, Socialine E, Bahri S, Park BJ, Holloway K. Monitoring medicines use to support national medicines policy development and implementation in the Asia Pacific region. WHO South-East Asia J Public Health [serial online] 2013 [cited 2020 Oct 1];2:113-7. Available from: http://www.who-seajph.org/text.asp?2013/2/2/113/122946
| Introduction|| |
Access to essential medicines is a serious challenge for many countries in the Asia Pacific region. For this reason, the World Health Organization (WHO) has been working with countries to develop national medicines policies.  These policies aim to: (i) support access to high-quality, safe and effective medicines; and (ii) support the rational (or quality use) of those medicines. Throughout the region, countries are in various states of implementation of their strategies, with some countries in the early stages, while other countries have well-developed, fully functional policies.  In May 2012, the Asia Pacific Conference on National Medicines Policies was held in Sydney, Australia.  Delegates from countries throughout the region shared their knowledge, skills and experiences in implementing their national medicines policies. One subject discussed was how countries are monitoring medicine utilization. Knowledge of the impact of the medicines policy, particularly on access to and use of medicines, is critical to support further development and implementation.
In this paper, we describe four different approaches to evaluation of medicines policy implemented by four countries in the region with differing circumstances. The case studies come from Bhutan, a small lower-middle-income country, Indonesia, a large lower-middle-income country, Malaysia, an upper-middle-income country and the Republic of Korea, a high-income country. The countries represent different health systems at different stages in their policy development. Not surprisingly, their methods for monitoring medicine use also vary, ranging from paper-based systems in regional health centres to sophisticated electronic data sets capturing complete populations and held centrally. The lessons learnt from these countries individually and collectively may assist other countries in monitoring medicines use.
Bhutan is a small country of 730 000 people with a gross national income per person of $5730 (2011 data; purchasing power parity in international dollars [PPP dollars]).  Health expenditure per person is $236.2 (PPP dollars) and life expectancy at birth is 67 years.  Bhutan first established an essential drugs policy in 1986, which included a national essential drugs list. By 1987, the national drug policy was in place. The first standard treatment guideline was implemented in 1989 and a national formulary was in place by 1994. Supporting legislation was passed in 2005 and the revised national drug policy developed in 2007.
To support implementation of the policy, the Bhutan Government established the Essential Medicines and Technology Division in 2008. The division is responsible for providing systematic, evidenced-based information to the Ministry of Health to support decision-making for new technologies; the assessment of use of medical supplies at all levels of health facilities; and the promotion of rational prescribing, good storage and dispensing practices. To evaluate progress, the division uses a subset of the World Health Indicators for monitoring medicines policy.  Drug utilization reports that assess drug consumption and prescribing patterns are collected every 6 months and a monthly prescription survey to assess rational use of medicines is also done. 1 Reports are currently collected from almost half the hospitals and approximately a quarter of the health facilities in Bhutan.
Evaluation has shown that almost all medicines prescribed are from the essential drugs list and prescribing by generic name increased to more than 85% in 2012. Approximately 90% of prescriptions also record a diagnosis. Just over 40% of prescriptions include at least one antibiotic, while 4% include injectable drugs and 5% include steroids. Monitoring involves only whether drugs belong to the national essential medicines list and the number of medicines per prescription; more detailed aspects of the use of medicines-e.g., whether they are correctly indicated, given in the correct dose or underutilized - are not monitored. Since the government provides all medicines and the private sector is almost nonexistent outside border towns and the capital city, nonessential medicine use is very low. The same indicators are used for primary care centres and district hospitals. Monitoring in the few referral hospitals in Bhutan is not reported.
Some of the challenges with implementation include provision of staff time and training to analyse the reports and motivation of health facilities to complete the reports, particularly when district staff are not able to analyse their own data and when feedback of results is delayed because of human resource constraints. The continuous collection of surveys over time is enabling documentation of improvements in medicine use and early identification of emerging problems.
Indonesia is a large lower-middle-income country, with a population of 231 million people and a gross national income per person of $4810 (2012 data; PPP dollars).  Health expenditure per person is $126.9 (PPP dollars) and life expectancy at birth is 69 years.  The geographical distribution of people across the 13 000 islands that make up the country creates some challenges in medicine management. Indonesia established its national medicines policy in 1983. After sustained implementation and, in particular, a decentralization policy that delegated the authority of health services to local government, the national medicines policy was revised in 2006. In implementing the revised policy, the Ministry of Health paid serious attention to activities supporting rational use of medicine as one of the three main objectives of the national medicines policy.
Good progress has been made implementing the rational use of medicines programme, particularly at the primary health-care level, including implementation of educational, regulatory and managerial strategies as well as monitoring medicine use at health centres throughout the country. The monitoring activities involve collection of data by use of the WHO Indicators for National Drug Policies.  Data are collected within a sampling frame, which involves two primary health-care facilities within each of two district health offices from each province across the country.
There are 33 provinces throughout the country. Data are collected daily by the health centres, using paper-based forms and including 25 cases for each indicator. These data are sent monthly to the district or municipal health office, where the data are compiled and reports sent every 3 months to the provincial health office. These data are further aggregated and sent every 6 months to the Ministry of Health. The final aggregation at the Ministry of Health enables an annual report of the national performance indicators to be produced. This method of data collection enables aggregation of results and yearly indicators to be assessed as well as variation in medicine use by province to be assessed.
Results from 27 provinces showed that antimicrobial use reduced between 2010 and 2011 for nonpneumonia upper respiratory tract infections (from 60.02% to 41.36%) and nonspecific diarrhoea (from 62.33% to 36.88%). Longer-term trends will need to be established to draw conclusions about whether this fall in use is sustained. Average number of medicine items per prescription - an indicator of polypharmacy - reduced slightly from 3.59 to 3.47 but the percentage of patients receiving an injection for myalgia was unchanged (3.72% in 2010 and 3.96% in 2011). Barriers to monitoring use include human resource constraints in primary health-care units to collect data.
Malaysia is an upper-middle-income country of 29 million people with an estimated gross national income of $15 720 per person (2011 data; PPP dollars).  Health expenditure per person is $558.6 (PPP dollars) and life expectancy at birth is 74 years.  Malaysia's national medicines policy was first established in 2006.  The policy includes core components of the quality, safety and efficacy of medicines, drug availability, drug affordability and quality use of medicines. It also includes supportive components of human resource development, research and development, technical cooperation and management.
Malaysia monitors medicine use with a combination of data sources, including the National Pharmacy Services Statistics, National Medicines Use Survey (NMUS) and the National Medicines Price Survey.  The National Pharmacy Service Statistics aims to collect data on pharmacy services throughout Malaysia. Monitoring occurs quarterly and is useful for policy-makers to improve pharmacy services. The NMUS is supported by the Ministry of Health and aims to provide information on the use of medicines over time at the institutional, local, regional and national level. The data are used to estimate utilization, provide an overall pattern of prescribing, and enable an assessment of quality. Quality is assessed by comparisons of use with known patient demographics and the known prevalence of clinical conditions. The data are also used to estimate expenditure on pharmaceuticals, to describe price variation and to monitor and evaluate the effect of interventions to improve medicine use. The data used in the NMUS include procurement data from public (hospitals and clinics) and private (hospitals) health institutions, prescription data from private general practitioners, as well as medicines dispensing data from retail pharmacies. Data are not available from import or production data, domestic sales data or household consumption. Thus, the data are limited to prescription-only or pharmacy medicines and a few over-the-counter medicines (such as acetylsalicylic acid) but do not include traditional medicines and dietary supplements. Private medical specialists are also not included, thus prescriptions of highly specialized medicines for particular conditions may be underestimated.
Medicines are coded in the data set according to the WHO Anatomical and Therapeutic Chemical Classification  with the defined daily dose (DDD)  consistent with the WHO definition and based on the main indication in adults. Limitations include that prescription does not necessarily indicate consumption and no household consumption data are collected. Data are published annually.  Data are used to monitor total consumption and identify differences in use in the public or private sector. [Table 1] shows the 10 therapeutic categories of most-used medicines in 2007. As shown in [Table 2], at the level of individual drugs, the top two medicines were metformin and glibenclamide for diabetes, followed by beta-blockers and calcium channel blockers. Antiinflammatory and antirheumatic products were more commonly used in the private sector. Four years of data are now available (2004-2007) and changing trends in use can be monitored by comparing survey results over time. The use of the DDD measure also enables comparisons to be made with countries that collect data in a similar manner, such as Australia. 
A medicine pricing survey is also undertaken to examine costs per prescription and medicines prices for new listed medicines. Data are collected at facility level and are based on a basket of selected essential medicines and take into account both procurement price and availability and price to the patient.  Publications resulting include the private sector medicines retail price list and the recommended price list for national essential drugs list.  Studies of the use of medicines by Malaysian consumers are now under way, with the first national study undertaken in 2008. Findings showed that 56% of consumers still did not understand the proper use of their medicines, 51% were unaware of their trade name and 56% were not aware of common side-effects.  However, 61% realized traditional medicines can have side-effects.  Based on these findings, further innovative strategies on effective educational intervention targeting consumers were implemented in order to empower consumers with pertinent information on medicines use. An electronic pharmacy system is now in development and may assist further development of the data collection in the future. Constraints include funding and human resources, both in availability and skilled personnel.
Republic of Korea
The Republic of Korea is a high-income country of 50 million people, and an estimated gross national income of $29 860 per person (2012 data; PPP dollars).  Health expenditure per person is $2180.7 (PPP dollars) and life expectancy at birth is 81 years.  The Republic of Korea does not have a formal national medicines policy but has established a system of national health insurance. In 1999, the National Health Act was passed and the National Health Insurance Corporation established in 2000. This provides health coverage for all citizens and includes pharmaceutical insurance. To support the national insurance scheme, a national e-health platform was implemented, which provides the major data source for monitoring medicine use; the major components are the Health Insurance Review and Assessment Service (HIRA) database and the Hospital Electronic Medical Record database. The HIRA database incorporates claims that are paper based, diskettes, compact disks or electronically delivered data files from medical care institutions. The data set covers the whole population and includes prescribing and dispensing information, as well as information on physicians, residents, medical care institutions, medical services and medical supply. The database has been validated by comparison with medical records.  The dataset has been used for retrospective drug utilization. Examples include use of thiazolidinediones in people with diabetes with and without heart failure and patterns of switching in health care. ,
Drug utilization review was established in the Republic of Korea in 2004, when the Ministry of Health established the Drug Utilization Review Committee and announced the first contraindicated medicines list. In 2005, responsibility for drug utilization review was transferred to the Korea Food and Drug Administration, which developed a drug-drug interaction list and an age-contraindicated drugs list. By 2010, a nationwide concurrent drug utilization review system for both physicians and pharmacists had been established, enabling checks for interactions and contraindications in real time. The aim of the drug utilization review programme is to develop "structured, ongoing initiatives that interpret patterns of drug use in relation to predetermined criteria, and attempt to prevent or minimize inappropriate prescription.  The target of the programme has included contraindicated medicines due to interactions, medicines to be avoided in the elderly or in children and medicines to be avoided in pregnancy. Prior to national roll-out, the programme was trialled in a single medical institution, then trialled between institutions, in both a city and provincial area, to ensure feasibility, acceptability and effectiveness. The database also enables advanced pharmacoepidemiological studies to be undertaken including those identifying adverse drug events and outcomes research. Examples of studies already undertaken include the risk of death when using cisapride concurrently with contraindicated medicines. 
| Discussion|| |
While the four countries have very different systems for monitoring medicines use, monitoring medicines use was considered a facilitator of medicines policy development and rational medicines use in all countries. Enablers of success included data collection that was relevant to the needs of the individual and society in each particular country and ownership of the data by decision-makers.
One of the constraints observed in all countries, regardless of sophistication of monitoring, was the lack of trained workforce and incentives for data collection. In all countries, collection and management of data requires a diverse skill base and capacity building is required, particularly for validating, analysing and interpreting data, as well as report presentation. Lack of awareness of and support by key decision-makers was identified as a barrier and was reflected in limited budgets for data collection and for training the workforce.
To facilitate medicines monitoring, efficient and effective methodologies , should be employed, together with clearly and concisely reported data, timely and frequent reporting and defined roles and responsibilities of all participants. Feedback to stakeholders to facilitate quality use of medicines enables further data collection. Countries or institutions should start with simple but efficient systems and build on small successes and appropriate technology should be used to enhance monitoring. Successful monitoring of medicines use requires local, regional and national level ownership, as well as understanding and use of the data at all levels.
| Acknowledgment|| |
The authors gratefully acknowledge the contribution of Dr Nani Sukasediati for her contribution in reviewing this manuscript.
| Notes|| |
1 Examples of data-collection forms are available from the authors
| References|| |
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[Table 1], [Table 2]
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