Literature DB >> 32130252

Availability, cost and affordability of essential cardiovascular disease medicines in the south west region of Cameroon: Preliminary findings from the Cameroon science for disease study.

Anastase Dzudie1,2,3,4, Epie Njume2,5, Martin Abanda2, Leopold Aminde2,6, Ba Hamadou3, Bonaventure Dzekem2, Marcel Azabji3, Marie Solange Doualla1,3, Marcelin Ngowe1, Andre P Kengne2,7.   

Abstract

BACKGROUND: More than 80% of premature deaths due to cardiovascular disease (CVD) occur in low- and middle-income countries. However, access to, and affordability of medications remain a challenge in these countries.
OBJECTIVE: To assess the availability, cost and affordability of essential cardiovascular medicines in the South West region of Cameroon.
METHODS: In an audit of 63 medicine outlets, twenty-six essential medicines were surveyed using the World Health Organisation (WHO) /Health Action International methodology. Availability, costs and the ratio of the median price to the international reference price were evaluated in public, confessional, private facility medicine outlets, and community pharmacies. Affordability was assessed by calculating the number of days' wages it will cost the lowest-paid unskilled government worker to purchase a month worth of chronic treatment.
FINDINGS: Availability ranged from 25.3% (public facility outlets) to 49.2% (community pharmacies) for all medicines. This was higher in urban and semi-urban compared to rural outlets. Cost of medicines was highest in community pharmacies and lowest in public facility outlets. Aspirin, digoxin, furosemide, hydrochlorothiazide and nifedipine were affordable (cost a day's wage or less). Medicines for heart failure and dyslipidaemia (beta blockers, angiotensin converting enzyme inhibitors and statins) required 2-5 days and 6-13 days wages respectively for one month of chronic treatment.
CONCLUSION: Overall availability of CVD essential medicines was lower than WHO recommendations, and medicines were largely unaffordable. While primary prevention is pivotal, improving availability and affordability of medicines especially for public facilities would provide additional benefit in curbing the CVD burden.

Entities:  

Year:  2020        PMID: 32130252      PMCID: PMC7055918          DOI: 10.1371/journal.pone.0229307

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Globally, cardiovascular disease (CVD) is the leading cause of death with 80% of these deaths occurring in low- and middle-income countries (LMIC) [1-4],. In SSA countries as reported elsewhere, the rise in this burden of CVD is influenced by population growth, ageing, increasing urbanisation and lifestyle changes [2, 5, 6]. The cost of CVD on individuals and households, healthcare systems and countries is prohibitive, especially in SSA. This cost is both direct (hospitalisation, rehabilitation services, physician visits, drugs) and indirect: cost associated with morbidity and mortality (losses of productivity due to premature death and short- or long-term disability) [7]. It has been shown that the combined impact of diabetes and CVDs may undermine the future development and prosperity of this region [8-11]. In 2012, the world health organization (WHO) formulated the 25 × 25 Goal which aims at achieving a 25% reduction in the number of premature deaths (occurring before 70 years of age) due to non-communicable disease (NCD) by 2025 [12]. This was followed by a Global Action Plan (GAP) that includes, amongst others, a target of 80% availability and affordability of essential medicines (EMs) for treatment and secondary prevention of CVDs and other NCDs, and at least 50% of eligible people to receive drug therapy and counselling (including glycaemic control) to prevent heart attacks and strokes [13, 14]. An availability of medicines for cardiovascular diseases ranging from 9.1% to 50%, and 36.4 to 59.1% in rural and urban settings respectively was reported in the West region of Cameroon in 2012 [15]. There is ample evidence on the use of pharmacological treatment for secondary prevention of cardiovascular events [12, 16, 17], thus affordable access to EM is urgently warranted in efforts to reduce the burden of CVD [18]. It has been estimated that up to 80% of the burden of NCDs in many countries can be reduced with the use of appropriate medicines [14]. In spite of this proven benefit of EM, their availability in many low- and middle-income countries is sub-optimal. The Prospective Urban Rural Epidemiology (PURE) study showed that the use of proven medicines (antiplatelet, β blockers, angiotensin-converting enzyme inhibitors or angiotensin receptor blockers and statins) in patients with coronary heart disease or stroke is low, particularly in low-income countries, where 80% took no medicines [19]. This implies that there is a huge gap between standard clinical practice (based on high-quality evidence) and the current practice in those settings. To bridge this gap, it is vital to understand the potentially modifiable health system barriers at each level of care, in order to inform appropriate solutions. The aim of this study was thus to assess the availability and affordability of essential CVD medicines, how these vary across various medicine outlets and finally compare the availability and affordability pattern with medications for selected endemic infectious diseases in Cameroon.

Materials and methods

Ethics approval and consent to participate

Ethical approval was obtained from the Institutional Ethics Committee for Research on Human Health of the University of Douala (ref: IEC-UD/506/02/2016/T). Administrative approval was obtained the South West Regional Delegation of Public Health. Administrative approval was also obtained from the District Medical Officers where possible, otherwise consent was obtained directly from the head of selected medicine outlets. The purpose of the study was explained to the head of each participating medicine outlet and to any other informant. Participants were not under any obligation to be part of the study and could withdraw from the study at any point without repercussions. A signed informed consent was obtained from the head of the medicine outlet, and verbal consent was from other staff of the participating medicine outlet.

Setting

The study was conducted in the South West Region (SWR), one of ten regions in Cameroon with a population of over 1,384,286 persons as of January 2015 and population density of 32.96 persons/square kilometre [20]. The SWR has six administrative divisions each of which is further divided into subdivisions. The Health System in Cameroon comprises three levels-the Central level develops health policies and strategies, and coordinates, regulates their implementation; the Intermediate level provides technical support to; the Peripheral (or operational) level which host the Health Districts and related services, implementing policies designed at the Central level There are eighteen health districts (HD) in which public, private and confessional (religious or faith-based) health facilities provide healthcare services. The public health facilities get their medicine supply from the regional drug programme (SWR Fund for Health Promotion) and sell following national guidelines, while private and confessional health facilities obtain theirs from the regional drug programme and from private suppliers. Access to medicines from both public and private facilities is at a cost.

Selection of medicine outlets

A regional survey was conducted in all 4 sectors (public, private and confessional facility outlets, and private community pharmacies) in 6 survey areas (administrative divisions) and medicine outlets were selected using cluster and simple random sampling techniques, informed by the WHO/HAI methodology [21]. In each survey area, the main public health facility outlet was included and four other public facility outlets closest to the main public facility outlet randomly selected. Five private and five confessional outlets closest to the main public facility were also randomly selected. All community pharmacies within one kilometre of the main public facility medicine outlet were selected. Inclusion of the private community pharmacies was on the assumption that they offered the greatest possibility of getting medicines not found at the health facility outlets. Of 108 medicine outlets selected, 63 medicine outlets were surveyed; 24 outlets of public facilities, 18 outlets of private facilities, 11 outlets of confessional facilities and 10 private community pharmacies. Excluded from the study were health facilities without a pharmacy, non-consenting health facilities and private community pharmacies and medicine outlets requiring more than day’s travel from the main public health facility. Some facility outlets which were initially selected were not eventually surveyed because during data collection, it was realised that they were remote settlements which could not be reached within a day, from the main public health facility and thus were excluded.

Selection of medicines

Twenty-six EM were selected from the 19th WHO model core list [22]. These included: amiloride, amlodipine, aspirin, atenolol, atorvastatin, bisoprolol, captopril, clopidogrel, digoxin, enalapril, epinephrine, furosemide, glyceryl trinitrate, hydralazine, hydrochlorothiazide, isosorbide dinitrate, long acting penicillin, methyl dopa, nifedipine, propanolol, simvastatin, spironolactone and verapamil. Evidence, including their cost-effectiveness supports the use of these medicines in reducing morbidity and mortality and thus widely recommended for secondary prevention [20, 23]. The selection of these medicines was also guided by the list of medicines selected by a WHO team and other investigators in previous studies [15, 18, 24]. For the purpose of comparing between the availability of non-communicable and communicable diseases medicines, medicines for HIV/AIDS and tuberculosis; tenofovir, lamivudine, emtricitabine, efavirenz, zidovudine, nevirapine, abacavir, ritonavir-boosted lopinavir and ritonavir-boosted atazanavir were also surveyed in public and some confessional facilities since these are solely distributed at those facilities.

Data collection

Information on availability and cost was obtained using an interviewer-administered data collection tool adapted from the medicine price data collection form in the World Health Organisation/Health Action International (WHO/HAI) Manual [25]. For each medicine outlet, availability was ascertained by seeing a given essential medicine on the day of the survey. Information collected for each medicine included the availability of the cheapest brand of any medicine dosage, cost per tablet and cost per pack or vial paid by the consumers. A pilot study based on a convenient sample was conducted to test the data collection tool for any limitations and appropriate adjustments made prior to conducting the main study.

Data analysis

Data were analysed using SPSS® statistical software v.20 for Windows® (IBM, Chicago, USA). Availability was assessed by estimating the percentage of outlets in which any dose was found overall, by sector, and by setting (urban, semi-urban or rural). Availability was categorised as very low (< 30%), low (30–49%), fairly high (50–80%) and high (> 80%) [15]. For cost of medicines, the unit price (price per tablet or vial) was used to determine the price of each medicine. The median price (MP) of each medicine was also calculated in CFA/francs, and converted to US dollars using the exchange rate on the first day of data collection (1 US dollar = 602.46 francs CFA, February 2016). Median values were used as a better representation of the mid-point values as price is often skewed. The International Reference Price (IRP) was obtained from the 2014 edition of the International Drug Price Indicator Guide published by the Management Sciences for Health (MSH) [25]. The MSH International Drug Price Indicator Guide prices represent median prices of medicines supplied to LMIC by different suppliers and are recommended as the most useful standard for comparison [15]. Buyer Median Price (BMP) was used when Supplier Median Price (SMP) was unavailable. The median price ratio (MPR) was calculated for each medicine presentation. This ratio compares how much greater or less the local MP is than the IRP [15, 25]. The MPR is an assessment of the purchasing efficiency of the system. A MPR of 1.5 or less was considered reasonable for all medicine forms [15]. To assess variability of prices across sectors, only medicines available in more than one sector and in more than one outlet in that sector were selected. Affordability was estimated using local MP, defined daily dose and average monthly wage of the lowest paid unskilled government worker, according to the WHO/HAI standard manual [15, 26, 27], which was 36,270 francs CFA, at the time of the survey [28]. The number of days’ wages required to pay for one month course of treatment was also calculated. A month’s course of chronic treatment requiring 1 day’s wages or less was considered affordable [26, 27].

Availability of data and material

Data cannot be made publicly available as the consent form did not include provisions for data sharing. Facility-level data can be made available to interested researchers with the approval of the Cameroon National Ethics Committee. The contacts of the Cameroon National Ethics Committee are available at https://healthresearchweb.org/en/cameroon/ethics_2120

Results

Distribution of outlets

The general characteristics of the health facilities with medicine outlets included in this study are presented in Table 1. Twenty-four (38.1%) public facility outlets, 18 (28.6%) private facility outlets, 11 (17.5%) confessional facility outlets and 10 (15.9%) private community outlets were surveyed. The catchment population of the surveyed facilities ranged from 1444 to 109000 individual, while the number of staff member per facility ranged from 4 to 225.
Table 1

Average population and personnel profile.

MinimumMaximumMedian
Average population served by the Health Facility in which outlet is located144410900013269.50
Number of Health workers in the Health Facility213714.00
Number of Nurses in the Health Facility16910.00
Number of Doctors (GPs) in the Health Facility0131.00
Number of Specialist in the Health Facility080
Number of Internists or Cardiologists020
Total number of Staff in the Health Facility422522.00

Availability of medicines

For all medicines, the mean availability was 33% overall, 49.2% in private community, 44.0% in confessional facility outlets, 26.1% in private and 25.3% public facility outlets. Long acting penicillin had a high availability at 92.1%, and >80% in all sectors and categories; while glyceryl trinitrate and isosorbide dinitrate were completely absent. Hydrochlorothiazide was more than 70% available in all sectors and categories. Spironolactone and verapamil were only found in confessional and private community outlets. Atorvastatin, amiloride, bisoprolol, clopidogrel and simvastatin were only found in private community outlets. Neither aspirin 100mg nor 81mg was found in public facility outlets. The percentage availability within outlets is shown in Table 2. Anti-retroviral and anti-tuberculosis medicines were 100% available at all designated treatment centres.
Table 2

Availability of all medicines across surveyed medicine outlets and by urbanicity.

MedicinePercentage Availability
Public facility outlet; % (n)Confessional facility outlet; % (n)Private facility outlet; % (n)Private community outlet; % (n)Urban; % (n)Semi- urban; % (n)Rural; % (n)
Medicines for IHD/Stroke
Aspirin41.7 (10)81.8 (9)61.1 (11)100.0 (10)82.4 (14)64.0 (16)47.6 (10)
Atorvastatin0.0 (0)0.0 (0)0.0 (0)20.0 (2)5.9 (1)4.0 (1)0.0 (0)
Clopidogrel0.0 (0)0.0 (0)0.0 (0)30.0 (3)11 .8 (2)4.0 (1)0.0 (0)
Glyceryl trinitrate0.0 (0)0.0 (0)0.0 (0)0.0 (0)0.0 (0)0.0 (0)0.0 (0)
Isosorbide dinitrate0.0 (0)0.0 (0)0.0 (0)0.0 (0)0.0 (0)0.0 (0)0.0 (0)
Simvastatin0.0 (0)0.0 (0)0.0 (0)50.0 (5)17.6 (3)8.0 (2)0.0 (0)
Medicines for heart failure
Digoxin4.2 (1)72.7 (8)16.7 (3)30.0 (3)35.3 (6)25.0 (6)14.3 (3)
Furosemide70.8 (17)81.8 (9)77.8 (14)100.0 (10)88.2 (15)80.0 (20)71.4 (15)
Spironolactone0.0 (0)27.3 (3)0.0 (0)70.0 (7)23.5 (4)20 .0 (5)4.8 (1)
Medicines for Cardiac arrest
Epinephrine16.7 (4)90.9 (10)44.4 (8)0.0 (0)17.6 (3)40.0 (10)42.9 (9)
Medicines for diabetes
Glibenclamide79.2 (19)100.0 (11)56.6 (10)100.0 (10)82.4 (14)84.0 (21)71.4 (15)
Insulin79.2 (19)81.8 (9)50.0 (9)100.0 (10)91.4 (16)72.0 (18)61.9 (13)
Metformin83.3 (20)90.9 (10)77.8 (14)100.0 (10)88.2 (15)92.0 (23)76.2 (16)
Medicines for hypertension and other cardiac diseases
Amiloride0.0 (0)0.0 (0)0.0 (0)40.0 (4)23 (4)0.0 (0)0.0 (0)
Amlodipine16.7 (4)36.4 (4)5.6 (1)90.0 (9)47.1 (8)32.0 (8)9.5 (2)
Atenolol0.0 (0)9.1 (1)5.6 (1)40.0 (4)17.6 (3)12.0 (3)0.0 (0)
Bisoprolol0.0 (0)0.0 (0)0.0 (0)40.0 (4)11.8 (2)8.0 (2)0.0 (0)
Captopril0.0 (0)81.8 (9)5.6 (1)50.0 (5)29 .4 (5)28.0(7)14.3 (3)
Enalapril0.0 (0)0.0 (0)5.6 (1)50.0 (5)23.5 (4)8.0 (2)0.0 (0)
Hydrochlorothiazide79.2 (19)90.9 (10)72.2 (13)100.0 (0)88.2 (15)84.0 (21)76.2 (16)
Long-acting penicillin95.8 (23)90.0 (10)83.3 (15)100.0 (10)100 (17)92.0 (23)85.7 (18)
Hydralazine0.0 (0)18.2 (2)0.0 (0)0.0 (0)0.0 (0)4.0 (1)4.8 (1)
Methyl dopa41.7 (10)63.6 (7)16.7 (3)50.0 (5)35.3 (6)32.0 (8)52.4 (11)
Nifedipine70.8 (17)63.6 (7)66.7 (12)0.0 (0)29.4 (5)68.0 (17)66.7 (14)
Propranolol12.5 (3)54.5 (6)11.1 (2)0.0 (0)11.8 (2)20.0 (5)19.0 (4)
Verapamil0.0 (0)9.1 (1)0.0 (0)20.0 (2)5.9 (1)8.0 (2)0.0 (0)
Medicines for communicable diseases
Anti-retrovirals100 (8)100 (4)NANA100 (3)100 (6)100 (4)
Anti-TB medicines100 (13)100 (4)NANA100 (3)100 (7)100 (3)

Median prices, median price ratio and affordability of medicines

Among the surveyed medicines, only hydralazine (1.07), methyl-dopa (0.55) had reasonable MPR (MPR ≤1.5). Digoxin 0.25mg, furosemide 40mg, hydrochlorothiazide 25mg and nifedipine 20mg were affordable (cost a day’s wage or less, of the lowest paid unskilled government worker, for 30 days of chronic treatment). Angiotensin converting enzyme inhibitors and beta blockers required 2 to 5 days’ wages, while statins required 6 to 13 days’ wages. Table 3 shows the cost and affordability of cardiovascular medicines. Medicines for HIV/AIDS and tuberculosis are distributed free of charge.
Table 3

Median price, median price ratio and affordability of cardiovascular medicines.

Medicine doseDefined daily doseMedian PriceIRP/USDMedian Price RatioCost of 30 days’ treatmentNumber of days wages for 30 days treatment
CFAFUSDCFAFUSD
Aspirin 100mg100mg43.330.07190.002035.9513002.161.08
Amlodipine 5mg5mg116.830.19390.02527.6935055.822.90
Atenolol 50mg75mg107.000.17760.010317.2448157.993.98
Atorvastatin 20mg20mg279.330.46360.05528.40838013.916.93
Bisoprolol 5mg10mg116.670.19370.06602.93700011.625.79
Captopril 25mg50mg50.000.08300.01395.9730004.982.48
Clopidogrel 75mg75mg530.000.87970.077511.351590026.3913.15
Digoxin 0.25mg0.25mg30.000.04980.01214.169001.490.74
Enalapril 10mg10mg210.000.34860.005959.08630010.465.21
Epinephrine 1mg0.5mg500.000.82990.33392.49750012.456.20
Furosemide 40mg40mg20.000.03320.00674.956001.004.95
Hydralazine 20mg100mg3000.004.97964.67171.07450000746.94372.22
Hydrochlorothiazide 25mg25mg39.000.06470.004315.0511701.940.97
Methyl dopa 500mg1000mg40.000.06640.12000.5524003.981.99
Nifedipine 20mg30mg27.500.04560.02501.8212382.051.02
Propranolol 40mg160mg30.000.04980.00756.6436005.982.98
Simvastatin 20mg30mg360.710.59870.053111.271623226.9413.43
Spironolactone 25mg75mg120.000.19920.04324.611080017.938.93
Verapamil 240mg240330.000.54780.08796.23990016.438.19

IRP: International reference price

IRP: International reference price

Variability in cost and affordability of medicines

The cost of medicines was highest in private community outlets, relatively similar between confessional and private facility outlets and lowest in public facility outlets. The variability in prices and affordability across sectors for some selected medicines is shown in Tables 4 and 5.
Table 4

Median prices across sectors for some selected medicines.

MedicinesMedian Prices (CFAF) per Sector
Public facility outletConfessional facility outletPrivate facility outletPrivate community outlet
Aspirin 100mgNA12.510.045.5
Captopril 25mgNA50.0NA94.3
DigoxinNA30.050.091.7
Epinephrine 1mg/ml80.0500.0500.0NA
Furosemide 40mg5.025.027.576.6
Hydrochlorothiazide 50mg5.050.025.0NA
Methyl dopa 250mg25.050.040.0133.3
Nifedipine 20mg20.030.037.5NA
SpironolactoneNA50.0NA120.0
Table 5

Affordability of some selected medicines across sectors.

MedicineDefined daily dosePublic facility outletConfessional facility outletPrivate facility outletPrivate community outlet
Cost of 30 days treatment (CFAF)Number of day’s wages for 30 daysCost of 30 days treatment (CFAF)Number of day’s wages for 30 daysCost of 30 days treatment (CFAF)Number of day’s wages for 30 daysCost of 30 days treatment (CFAF)Number of day’s wages for 30 days
Furosemide 40mg40mg1500.17500.68250.722981.9
Hydrochlorothiazide 50mg25mg750.067500.63750.311701
Methyl dopa 250mg1000mg30002.560005480041599613.2
Nifedipine 20mg30mg9000.713501.11687.51.4NANA

Discussion

In this survey exploring the availability and affordability of essential CVD medicines, we found mean availability of 33%, ranging between 25.3% in public facility outlets and 49.2% in private community pharmacies, in the South West Region of Cameroon. This was in sharp contrast with 100% availability and HIV and anti-tuberculosis medicines at approved treatment facilities. Medicines cost highest in private community pharmacies, were similar between confessional and private facility outlets and lowest in public facility outlets. Digoxin 0.25mg, furosemide 40mg, hydrochlorothiazide 25mg and nifedipine 20mg were the only four affordable out of the 26 surveyed medicines. Overall, the availability of hydrochlorothiazide in all outlets was 82.5%, consistent with 85.1% in Brazil, 100% in Sri Lanka but much higher than 5.9% in Bangladesh in 2007 [27], and the 43.7% reported in Haiti in 2013 [29]. Hydrochlorothiazide 50mg availability across all sites was higher than the 40% previously reported in the West region of Cameroon [15]. However, Atenolol 50mg availability in our study was consistent with previous report from the West region of Cameroon, but much lower than 66% in Sri Lanka in 2014 [24] and 44.5% in Haiti. Availability of furosemide (79.4%) and propranolol (17.5%) were lower than 100% and 20% reported in the West region of Cameroon. Furosemide availability in our study was higher than 56.2% in Haiti but lower than 95% reported but lower than in Sri Lanka. Simvastatin’ availability was close to previous report in the West region of Cameroon, but higher than 2.3% in Haiti but considerably lower than 49% in Sri Lanka. The availability of oral antidiabetics- glibenclamide and metformin was higher in the rural areas than what was reported in the West region of Cameroon. Only the 500mg formulation of aspirin was available in public facilities probably because the low dose formulation is not found Cameroon’s National Essential Medicine List. Availability of medicines in urban and semi-urban outlets was considerably higher than in rural outlets, probably because rural outlets preferably stock medicines for communicable diseases [14] which are symptomatic at onset and readily diagnosed as opposed to cardiovascular diseases and diabetes which are asymptomatic until complications set in, at which point patients migrate to urban centres for further care. This variability in the availability of EM in outlets in different settings may be accounted for, at least in part, by the concentration of private medicine outlets (private facilities and community pharmacies) in the urban and semi-urban settings. The low availability in public sector outlets and rural outlets compared to other sectors may be due to insufficient spending to procure sufficient medicines for patients’ needs. It may also be as a result of low demand, perhaps suggesting that the medicines which were not available are not being prescribed by health professionals. Further, it may portray a poor distribution system to more remote medicine outlets. The cost (price) of medicines was highest in private community outlets, relatively similar between confessional and private facility outlets, but slightly higher in the latter. The lowest prices were found in public facility outlets. Median prices were several folds higher than the IRP, especially in the non-public sectors. This may be due to the procurement system being inefficient, absence of price control or higher mark-ups in the private outlets to cover running cost and make profit. Aspirin in the private sector (private health facilities and private community pharmacies) cost more than 35 times the IRP (MPR = 35.96) and hydrochlorothiazide more than 15 times the IRP (MPR = 15.06). This is higher than in Nepal and Sri Lanka where the MPRs for aspirin of 12 and 10 respectively were reported. The MPR of hydrochlorothiazide was reported to be 11 in Sri Lanka [18]. Only digoxin, furosemide, hydrochlorothiazide and nifedipine were affordable (cost a day’s wage or less for a course of one month treatment). The rest of the medicines were largely unaffordable with beta blockers and angiotensin converting enzyme inhibitors requiring more than 2 days’ wages for a month-long treatment. Considering that some patients may be taking multidrug regimens, the relative unaffordability of single medicines surmises that multidrug regimens will be even more unaffordable We found that treating a patient with ischaemic heart disease with a combination of BB (atenolol), ACEI (captopril), a statin (simvastatin) and aspirin cost 19.8 days’ wages for a month of chronic treatment, which is greater than in Sri Lanka (1.5 days’ wages), Nepal and Pakistan (5 days’ wages) and Malawi (18.4 days’ wages) [15, 27], but lower than 41.3 days’ wages reported in the West region of Cameroon [27]. In the public sector where cost was relatively lower, the availability of medicines was low. As such, patients either turn to confessional and private sectors where medicines are more available albeit the comparatively higher cost, or forgo treatment altogether [13]. The unaffordability of medicines has been blamed largely on poverty, lack of effective insurance systems and out-of-pocket payments [14, 15, 29]. The concept of insurance systems is relatively new in Cameroon [6]. A study reported that only 4.4% of Cameroonian informal sector workers had health insurance [9]. As such, chronic treatment stretches household resources to the limit, often competing with other basic household needs. These notwithstanding, the availability of medicines for communicable diseases; anti-TB and anti-retroviral medicines was 100% in all designated treatment centres irrespective of sector or urban-rural location. This most likely implies that very little attention is directed towards CVD compared to HIV/AIDS, tuberculosis and other communicable diseases. Indeed, a National Multi-sectoral Action Plan on NCDs is yet to be made available publicly. This is rather unfortunate because, even though communicable diseases are undeniably more prevalent, the prevalence of CVD is steadily rising due to the worsening risk profiles, which are projected to almost double by 2030 if current trends persist [27]. The findings in this study suggest that management of CVD and its risk factors remains a major public health challenge as treatment is observed cost several days’ wages of the lowest-paid unskilled government worker. Furthermore, medicines are largely purchased by out-of-pocket payments due to the absence of universal health coverage and few health insurance schemes. Studies show that many people fall into the “medical poverty trap” every year due to CVD-related expenditures [30]. Going by these findings, it is therefore evident that we are a long way from achieving the WHO global targets for the control of NCD, especially global target 9. Since the distribution of medicines for communicable diseases is guided by national policy, it is therefore imperative that medicines for CVD fall under similar policies. It is important to appraise the situation of CVD, in terms of availability of diagnostic equipment, evidence-based management on a nation-wide scale, and design policies which aim at addressing the shortcomings, with the ultimate goal of attaining the WHO global targets but even more importantly, providing low-cost medicines on a wide scale to be used for primary and secondary prevention of cardiovascular events. Also, given that the WHO is currently focusing on improvement in access to affordable EM, it is important to have reliable mechanisms which can monitor trends in the supply system availability over time because relying on ad hoc systems may lead to information gaps and wastage of limited resources [14]. This is the first region-wide survey on this scale in Cameroon using methods adapted from the WHO/HAI methodology which has been validated in previous studies. This survey has provided a situational analysis of cardiovascular diseases in the South West region, in terms of the availability and affordability of essential medicines. While it may be impractical to extrapolate findings in this study to the entire country, the findings however, provide a glimpse at what may obtain in the other nine regions. Our study has a number of limitations: availability was based on the presence of a particular medicine in the medicine outlet at the time of the survey. It is possible that outlets may have just run out of medicines at the time of the survey and this may not be true a reflection of their availability. Secondly, drug stores and roadside medicine vendors, which probably play an important role in the distribution of medicines, were not included in the survey. However, patients are usually advised to purchase their medicines from hospitals and private community pharmacies, to avoid use of substandard products. The method of sampling which followed the WHO/HAI standard manual may also have an effect on the results.

Conclusion

Overall, the mean availability of essential medicines for CVD was 33%, much lower than the 80% recommended by the WHO Global Action Plan for Prevention of NCD. Additionally, the available medicines were largely unaffordable. While recognizing the key impact of primary prevention, there is an urgent need for the health system to scale up availability and affordability of medicines for treatment and secondary prevention of cardiovascular disease. Lessons from prior population level efforts in HIV and TB treatment and prevention are likely to offer guidance for setting implementation agendas in the sphere of CVD.

Finalised data collection tool.

(DOCX) Click here for additional data file. 27 Nov 2019 PONE-D-19-21246 Availability, Cost and Affordability of Essential Cardiovascular Disease Medicines in the South West Region of Cameroon: Preliminary Findings from the Cameroon Science for Disease study PLOS ONE Dear Dr. Njume, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. ============================== This is a well written Manuscript. Address the minor comments raised by the reviewers and return for re-consideration. ============================== We would appreciate receiving your revised manuscript by 15th December 2019. When you are ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). This letter should be uploaded as separate file and labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. 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The PLOS ONE style templates can be found at http://www.journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and http://www.journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf 2. Please provide a copy of the finalised data collection tool used in the study, in both the original language and English, as Supporting Information. 3. Please ensure that your references are numbered in the order they appear in the text. For example, in the Introduction section the reference numbers appear to go from 18 straight to 22. 4. Please cite and discuss the following related work in the body of the manuscript (introduction and discussion): https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0111812 5.  We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions. In your revised cover letter, please address the following prompts: a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent. b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories. We will update your Data Availability statement on your behalf to reflect the information you provide. [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: Yes ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: 1. Selection of essential drugs list needs to be revisited. Essentialness of isosorbide mono nitrate and methyldopa is controversial 2. The drug list (127) does not mention about anti-diabetic drugs in the table 2 3. Definition of affordability needs to be defined at the beginning and the cutoff taken may need revision as it is too low Reviewer #2: Comments are available on attachment ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: Yes: Chamila Mettananda Reviewer #2: No [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files to be viewed.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org. Please note that Supporting Information files do not need this step. Submitted filename: PLOS comments.docx Click here for additional data file. 13 Jan 2020 Availability, Cost and Affordability of Essential Cardiovascular Disease Medicines in the South West Region of Cameroon: Preliminary Findings from the Cameroon Science for Disease study Dear Editor, Season’s greetings. Below is a point-by-point response to each of the points raised by the you, and the reviewer(s): Introduction; Line 47. CVD is the leading cause of death globally. …… Line 49/50. Recent projections show that suggest that deaths from CVDs will continue to rise, surpassing all other causes by 2030. I thought these two lines from the start are contradictory. Because if the first says CVD is the leading cause of death globally, and then the next says it will surpass all other causes by 2030, then it needs to be clarified. Response Thank you for this pertinent comment. The lines have been clarified to read: Line 47/48/50: Globally, cardiovascular disease (CVD) is the leading cause of death with 80% of these deaths occurring in low- and middle-income countries (LMIC). Methodology Line 99. I think it would be important to throw in some line that explains what a health district (HD) and how it is structured, because this concept is used in other countries but it actually mean varied things. OR even probably explain aliitle elaborately how the Cameroon health system is structured and the medicine distribution and supply chain. Do people access medicines from public and private facilities at a cost? Response The Health System in Cameroon is explained, and the question on access to medicines from public and private facilities answered: Lines 102-105/110: The Health System in Cameroon comprises three levels-the Central level develops health policies and strategies, and coordinates, regulates their implementation; the Intermediate level provides technical support to; the Peripheral (or operational) level which host the Health Districts and related services, implementing policies designed at the Central level Access to medicines from both public and private facilities is at a cost Line 108/109. What was the justification for choosing the main public hospital, AND then four others closest to it? I think a justification line needs to be added in there, because I note that in line 112/113, the community Pharmacies closest are included and their inclusion was justified. But I am wondering what that also implies for introducing clustering biases an effects in the data. Response The process of selection of medicine outlets is in line with the WHO/HAI standard methodology (page 27). Community pharmacies were not mentioned in the WHO/HAI manual hence their inclusion was justified. This is in the manuscript; (line 114/115) Line 118, implies to me that the sampling and selection of outlets especially community pharmacies, was based more on convenient sampling probably to reduce study costs. But I am wondering whether this could have had recognizable effects on the data an ultimately the understanding and interpretation of results? Response We thank the reviewer for this comment. We agree with the reviewer that our sampling procedure could have effected of the on the results. We have acknowledged this as a limitation in the discussion (limitation section). Line 171/174. I thought this section touches on ethics and data confidentiality issues and therefore could have fitted well in the section of ethics at the start of the methodology section. But again this depends on how PLOS wants a paper structured. Response This section is not strictly related to ethical and data confidentiality of the study methodology but rather, a response to PLOS requirement of make data publicly available in all cases, with few exceptions. Results Line 176/181. I thought the write-up in this section was sufficient and in any case could be expanded, making the Table 1, irrelevant because its information has already been explained. I find it not adding any value to this. Response The table was added instead of expanding on the write-up for clarity It provides additional information on the cadre of personnel at the facilities hosting outlets, which can be an indication of the services rendered, and thus the kinds of medications to be found at these outlets. Line 195 onwards. I find that the write-ups are virtually a repetition of the table 2. It is always recommended that once you use a table, you could only explain the key issues in the table that the readers should take note of. But you cannot repeat an entire table by writing. Response Sections of text which were virtually repetitive from 211 following. Line 236. I should have made this comment in methodology. The study considered the wage of a lowest paid unskilled government worker. Can they include the justification for using this reference category? Is it that the lowest paid government workers are the ones who have a higher burden of disease in this CVD or NCD area? Or is it that once the lowest paid Government worker can afford this treatment then everyone else above them is expected to afford? How does a lowest paid government worker compare with a peasant individual without any gainful work or in agriculture? Would it have been useful to compare with incomes of those in agriculture or no gainful work at all? I think some clarification for selection of the reference case may be convincingly necessary. Response We agree with the reviewer that other references could have been used. However, we preferred to use an internationally recommended reference. The lowest paid unskilled government worker is used as the reference in the WHO/HAI standard manual. We have added this in the corresponding section (line 173/174). Line 280. I found Table 4, not necessary. In the first place I don’t know what the figures are, and whether they are dollar values or something else or percentages. I would recommend that Table 5 communicates better the idea of cost and affordability. This is because cost, moving forward is quoted in dosage (30 days of required dosage). So I would think Table 4 is generally irrelevant. Response Table 4 compares the median prices in CFA (seen at the top of the table) for a daily dose of across medicine outlets. General **These drugs seem to have been taken as a package. However, I was wondering for CVD for example, whether an entire drug package should be available to treat a CVD case OR there is this one or two essential drug that if not available, then a patient is in problems. Could you have identified that “essential” of “essentials” and assessed their availability? Response The medicines were selected from the “WHO Model List of Essential Medicines. 19th List. 2015” cited (24) in the Methodology section. CVDs typically require more than one medicine and as the condition, worsens or progress, or other complications set in, even more medicines may need to be added. Between lines 321/324, we reported and compared affordability of a multidrug regimen for the treatment of ischaemic heart disease. *****I would have expected some result on the possible reasons or factors associated with the variation in MPs across the sectors, and this would tie in well with an earlier comment I made of …describing the structure of the health system and probably the supply chain so we can know where the costs and therefore higher markups are likely to be associated. Response The Health System in Cameroon has been described in a response to made above. Possible factors responsible for variation in MPs are found on lines 318/319 ***We could have also benefitted from knowing whether geographical considerations have an influence on costs of drugs, that’s looking at urban and rural, those within vicinities of big public facilities compared to those a little further away from them. How do their medicine prices compare? I know you did this comparison only on ‘availability’. Response Availability of medicines was lowest in public sectors which generally had the lowest MPs (for medicines which were available) and were more likely to be located in rural settings. Further, the prices in these public outlets were the same, irrespective of the geographical location. Private facility and community outlets which had highest level of availability and MPs are mostly based in the semi-urban and urban settings (lines 312). We could not assess if geographical locations influenced the affordability because the medicines were not available to begin with. Discussion **Why was aspirin missing in virtually public facilities? Does it have something to do with essential medicines list? Or change in prescriptive policy? I thought I would find this argument in the discussion. Response Thank you. Line 307/308 addresses this remark. “Only the 500mg formulation of aspirin was available in public facilities probably because the low dose formulation is not found Cameroon’s National Essential Medicine List”. Line 309/315. I would have thought some small amount of qualitative would have explained these facts you are imputing on doctors not prescribing certain drugs. I think a KI interview would have added value. Response Unfortunately, this was not assessed. We acknowledge the pertinence and will be exploring this as a follow-up of this study Line 352. I think the issue of a reference wage case, needs to be explained, otherwise it may end-up in this section of limitations. But it should be elaborated in the earlier sections. Response We used an internationally recommended reference, the lowest paid unskilled government worker which is recommended in the WHO/HAI standard manual. We have explained this in the corresponding section (line 173/174).. **** I thought results would have also been contextualized alittle more. Availability was very low in public facilities. How does this relate with the broader context of the Cameroon economy, public expenditure on health, per capital health expenditure, or generally the health financing structure of Cameroon, or the generic problems that are often reported of medicine distribution and supply chain challenges, pilferage (medicine thefts from public facilities ending into private), the big numbers that report in public facilities and hence depleting the available stocks, medicine waste, etc. These issues are not unique, and so I am surprised that they seem not to feature prominently in the discussion. Response This context is provided in lines 314/316 A brief context of the Health System and Drug Procurement and distribution is presented in lines 102/110 in the methodology section. ***I did ask a question, whether medicines in public facilities were also paid for. And this comment could be because you never explained to us the structure of Cameroon health system. I know many public health systems are free, and so I could not understand what cost mean for a public system that may be free being costed. Response I have indicated in the methodology section that medicines are paid for in public facilities., line 110 ***Some comments about if there exists a policy reform now on NCDs in Cameroon may be good to understand whether NCD agenda has now been put on the priority list of issues. Some health systems are still focused on CDs and even their EMS has not changed to reflect the new NCD realities. Could this have an impact on the low stocks we have witnessed in the public and the confessional sectors? Response A National Multi-sectoral Action Plan on NCDs was elaborated by a working group (I represented my organisation) towards the end of 2018 but the final document has never been made available publicly. Indeed, more focus rests on CDs clearly reflected in the 100% availability and cost-free medications for HIV/AIDS and TB. This has been added to the discussion section (340/341). Submitted filename: Response to Reviewers.docx Click here for additional data file. 4 Feb 2020 Availability, Cost and Affordability of Essential Cardiovascular Disease Medicines in the South West Region of Cameroon: Preliminary Findings from the Cameroon Science for Disease study PONE-D-19-21246R1 Dear Dr. Mesumbe, We are pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it complies with all outstanding technical requirements. Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication. Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at https://www.editorialmanager.com/pone/, click the "Update My Information" link at the top of the page, and update your user information. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. With kind regards, Geofrey Musinguzi, MPH, PhD Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: 25 Feb 2020 PONE-D-19-21246R1 Availability, Cost and Affordability of Essential Cardiovascular Disease Medicines in the South West Region of Cameroon: Preliminary Findings from the Cameroon Science for Disease study. Dear Dr. Njume: I am pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. For any other questions or concerns, please email plosone@plos.org. Thank you for submitting your work to PLOS ONE. With kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Geofrey Musinguzi Academic Editor PLOS ONE
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