Keywords
Pharmacy, Contraception, Family Planning, Senegal
Pharmacy, Contraception, Family Planning, Senegal
Limited access to family planning services has been linked to the high rates of unmet need for contraception found in many African countries1. Over the years, many countries have attempted to fill gaps in health services by capitalizing on private sector facilities, including privately run clinics, social franchising, and pharmacies2. Research has shown drug shops and pharmacies to be a major source for contraceptives, particularly oral contraceptive pills (OCPs), emergency contraception, and condoms, especially for hard to reach women such as those who are younger or unmarried3–5. Historically, low-income clients have been priced out of private facility services, but several programs are working to decrease financial barriers, including by increasing access to insurance and implementing savings products and voucher systems6.
Hand in hand with increasing access through the private sector is task-sharing, in which lower level cadres of health providers are trained to provide certain health services that previously were the sole purview of a higher cadre7. Task sharing is a mechanism used in many countries to increase access to a variety of health services, including family planning. For example, community health workers in the public sector, and pharmacy and drug shop staff in the private sector, have all been trained in various countries to provide OCPs and injectable contraception—the two most popular forms of contraception in sub-Saharan Africa—without the need for a prescription written by a higher-level clinician, even when it is the first time the woman is using the method8.
In urban settings in particular, task-sharing of OCPs and injectables through pharmacies offers distinct benefits for improving access to family planning services. In contrast to health facilities, which are often limited in numbers, pharmacies tend to be plentiful in urban and peri-urban areas. Thanks to the range of possible reasons for visiting pharmacies, the purpose of the visit can be disguised, providing a layer of confidentiality to women. In addition, research has shown that direct pharmacy access to OCPs poses little risk to women; appropriately trained pharmacy staff are able to counsel for and provide the pill9,10, and further research has shown that women can even self-screen for eligibility of OCPs with relative accuracy by self-administering a checklist11,12. Sale and provision of injectable contraceptives in pharmacies and drug shops is also common in the developing world, thanks to social marketing13,14. Moreover, when compared with the alternative of pregnancy, the risks of complications in pregnancy and immediately post-partum exceed the risks associated with hormonal contraception15. Lastly, new packaging of injectable contraception designed to allow women to self-inject could eliminate the need for administration by a skilled professional for many, further increasing the impact pharmacies could have in improving access to contraception16.
This research focuses on Senegal, where pharmacists are currently forbidden from dispensing OCPs and injectable contraception without a prescription, and are not allowed to write prescriptions themselves. Women in Senegal are officially obliged to visit a health facility to initiate either of these methods of family planning. However, the Senegalese National Family Planning Action Plan for 2012–201517 acknowledged the barriers imposed by a prescription requirement as a limitation to the regulatory framework of family planning and the expansion of family planning in Senegal. The removal of prescription barriers was also noted in Senegal’s 2012 Program and Service Delivery commitment to Family Planning 2020 (FP 2020), and the updated National Strategic Framework for Family Planning 2016–202018, calls for finalizing and validating the laws and regulations governing the pharmaceutical sector.
As an estimated 44% of Senegal’s 14 million people live in an urban setting, and 38% of the total population living on less than $1.90 per day, urban poverty is a concern19,20. Given a total fertility rate of 5.0, a contraceptive prevalence rate (CPR) of 20.3%, and an unmet need for family planning at 25.6% overall, rising to nearly 30% for the lowest wealth quintile, increasing family planning access amongst the poorest women could help Senegal to reach its commitment to FP 2020 with a CPR of 45% by 202021. Senegal sees the need and is clearly interested in updating their national policies regarding accessing family planning through pharmacies, and this research aims to provide evidence as they work to make final decisions.
This article reports on research initiated by FHI 360 under the Bill & Melinda Gates Foundation-funded Urban Reproductive Health Initiative (UHRI), led by IntraHealth International in Senegal, to assess the potential for expanding access to family planning through pharmacies. Specific objectives were to assess the quality of the services currently provided through pharmacies, and to examine pharmacy staff and client interest in pharmacy-based family planning services. This research aimed to provide evidence for a potential policy change that would help Senegal reach its family planning goals by expanding access through pharmacies.
This was a cross-sectional, descriptive study employing a pharmacy audit, a survey with pharmacy staff, and a survey with pharmacy clients.
We obtained a list of all pharmacies (551) in the URHI project area stratified by district. Eight of the project districts were in Dakar and two were urban districts outside of Dakar. The study primary outcome was the proportion of pharmacies that provide counseling for family planning methods as measured through self-reported pharmacy audits. We assumed that 65% of the pharmacies in our target districts would have received training on family planning counseling through one of two earlier projects funded for pharmacy training (the Health Services Improvement project, or RPS in French, and the Senegal Maternal, Newborn, and Child Health/Family Planning/ Malaria project). Thus, we determined that a sample size of 225 pharmacies would be needed to achieve a 95% confidence interval with five percent precision for the proportion of interest including a finite population correction. To be conservative we planned on sampling 250 pharmacies to allow for 10% refusal. A proportional stratified sample of pharmacies was selected,, with allocation proportional to number per district.
Pharmacy audit: Eligibility criteria for pharmacies included location within UHRI districts and willingness of the owner of the pharmacy to participate in the study. We attempted to speak with the most knowledgeable person present, or the one who had worked there the longest, but collective input was also allowed.
Pharmacy staff: In each selected pharmacy, we attempted to interview one pharmacist, one assistant pharmacist, and one counter staff or trainee. When more than one was present for a given position, the one whose first name came first alphabetically was selected. If none of the three were not present the day of the interviews, that position was not included.
Clients: Eligible clients were women (aged 18–49, plus married women aged 15–17) exiting the selected pharmacies over a two-day period for each pharmacy. Initially, we conducted exit interviews with all women of reproductive age (as assessed by the survey takers) regardless of current family planning use in the first 50 pharmacies. Subsequently, after the first 50 we made the decision to cap the number of non-users of family planning interviewed at five per pharmacy to ensure data collectors had enough time to find and interview users of family planning. We interviewed all current users of family planning who consented, regardless of whether they sourced their method through the pharmacy or elsewhere.
Prior to initiating the study in any pharmacy, the research staff reached out to pharmacy owners and explained the purpose of the research, emphasizing confidentiality and that there was no threat of penalty from the regulatory division of the Ministry of Health and Social Action, the Direction de la Pharmacie et du Médicament (DPM), for any findings or responses and that responses would not be linked to particular pharmacies. Trained female data collectors conducted pharmacy audits, interviews with pharmacy staff, and client interviews between March and June 2015. Interviews with pharmacy staff, including for the audit, were conducted inside, whereas clients were intercepted and interviewed outside of the pharmacy so that pharmacy staff would not overhear their responses. Data collectors were required to have the equivalent of a technical degree (Brevet de Fin d'Etudes Moyennes) and to have previously participated in at least three household surveys, but they did not have clinical training.
Written informed consent was obtained from all participants prior to conducting each type of interview in French, Wolof, or other local languages. No compensation was provided. The study was approved by Senegal’s national ethics committee (Comité National d'Ethique pour la Recherche en Santé; approval number, SEN14/25) and FHI 360’s Protection of Human Subjects Committee (approval number, 564606-1).
Table 1 outlines the information gathered through each of the three questionnaires (questionnaires are available on Harvard Dataverse22). Data from each survey were analyzed descriptively using SPSS version 17.0. We constructed two separate composite indicators of pharmacy staff knowledge of OCPs and injectable contraception based on responses to the survey with pharmacy staff. Points were awarded as shown in tables (see Results section). Staff were considered highly knowledgeable of OCPs if they received five or more out of eight possible points on questions related to OCPs, and three or more out of five points on questions related to injectables.
In total, we performed audits at 225 pharmacies, and interviewed 486 pharmacy personnel and 3,569 pharmacy clients. Due to a pharmacy refusal rate of 7% (18) and an additional 7% of pharmacies found to be closed exceeding the anticipated non-response rate, 25 replacement pharmacies were randomly selected within the same stratum according to the non-response rate for that stratum. All replacement pharmacies were open and consented to participate. Of the 486 pharmacy personnel interviewed, 182 were pharmacists, 94 were assistant pharmacists, 206 were counter staff, and 4 were interns. In total 56% of pharmacy staff respondents were men.
Of the total 3,569 clients interviewed, 398 (11%) were current family planning users who procured their method through a pharmacy, 1,761 (49%) were current users of family planning who procured their method elsewhere, and 1,410 (40%) were non-users of family planning. The average age of our respondents was 30.6 years. Our respondents were most commonly married (76%), living with their partner (83%) and had a previous pregnancy (79%). In total, 53% had one to two children, and the most common education level was primary (29%) (see Table 2).
Overall, 54% (95% CI: 48%-61%) of pharmacies reported offering counseling on at least one method of family planning method. On the day of the audit, 99% of pharmacies had at least one brand of OCP in stock; the most common was Securil (approximately 0.70 USD), stocked by 98%. Between 73 and 79% also reported they stocked at least one of the next three most commonly mentioned brands. In addition, over 99% of pharmacies indicated they had emergency contraception in stock on the day of the audit, and just under 99% said they had condoms, while 83% of pharmacies said they had the injectable contraceptive Depo Provera.
Nearly three-quarters (72%) of pharmacies said they had a private space available to offer counseling in the pharmacy; however, 76% did not have any counseling materials available to assist pharmacy staff in counseling. Although available in only 10% of pharmacies, the most common materials were manuals and guides, with items such as flipcharts and counseling cards, available in fewer than 5% of pharmacies. Almost all pharmacies reported that OCPs (94%) and injectables (96%) required a prescription for purchase (see Table 3).
In total, 49% of pharmacists and 47% of assistant pharmacists reported receiving training on family planning during their professional studies. A third of pharmacists and 12% of assistants reported being trained after their professional studies (the questions were not asked of counter staff); of these, 53% and 50%, respectively, had received training on counseling for family planning. Among those with any training on family planning counseling, all had received training on counseling for use of OCPs and 82% on injectables. Nearly 90% of all pharmacists and assistant pharmacists, including those who had received training on family planning previously, expressed a desire for training on counseling for family planning, and 86% in how to offer methods.
Table 4 outlines a series of questions asked to determine pharmacy staff knowledge of counseling issues related to OCPs. Scores ranged from 0–7 out of a possible 8 with an average of 1.6. Three staff (all pharmacists) (0.6%) met the criteria of five or more points to be considered highly knowledgeable about OCPs. Ten percent (10%) scored three points or more out of the eight possible points, and 44% scored two points or more. The average number of points earned on the OCP knowledge questions was slightly higher for those who reported receiving training of family planning during their professional studies (2.06) than those who did not report having received training (1.72).
Questions and responses | % (n) | |
---|---|---|
In general, at what time during the menstrual cycle do you recommend that the client begin using oral contraceptives? | ||
Anytime as long as the client is reasonably sure she is not pregnant. | 3 (13) | 1 point |
At the beginning of her cycle | 78 (381) | |
All other responses (anytime during her menstrual cycle, don’t know/no response) | 19 (92) | |
In general, after finishing a 21-day pack of pills, how many days should the client wait before starting the next pack of pills? | ||
7 days/one week | 66 (322) | 1 point |
Other (Most common responses under “other: included “it depends,” and “start immediately.”) | 16 (77) | |
All other numerical responses | 18 (87) | |
In general, after finishing a 28-day pack of pills, how many days should the client wait before starting the next pack of pills? | ||
No wait/start immediately. | 62 (302) | 1 point |
Other (The most common response under “other: was “I don’t know.”) | 15 (73) | |
All other numerical responses | 23 (111) | |
In general, how many weeks after giving birth should a breastfeeding woman wait before starting combined oral contraceptives? | ||
24 weeks/6 months | 7 (32) | 0.5 point |
I don’t know | 40 (192) | |
All other numerical responses | 54 (262) | |
In general, how many weeks after giving birth should a breastfeeding woman wait before starting progestin-only oral contraceptives? | ||
Six weeks or earlier | 18 (86) | 0.5 point |
I don’t know | 49 (237) | |
All other numerical responses | 33 (163) | |
What are the most common side effects of oral contraceptives?a | ||
Five or more correct side effects | 5 (25) | 1 point |
Four side effects listed | 12 (57) | |
Three side effects listed | 24 (118) | |
Two side effects listed | 31 (151) | |
One side effect listed | 20 (99) | |
Zero side effects listed | 7 (36) | |
Which drugs or type of drugs reduce the effectiveness of oral contraceptive pills?b | ||
Two or more correct drugs listed | 6 (29) | 1 point |
One correct drug listed | 15 (74) | |
Zero correct drugs listed | 79 (383) | |
What are the reasons not to use oral contraceptive pills?c | ||
Five or more correct reasons listed | 3 (12) | 1 point |
Four correct reasons listed | 4 (17) | |
Three correct reasons listed | 13 (61) | |
Two correct reasons listed | 21 (104) | |
One correct reason listed | 26 (126) | |
Zero correct reasons listed | 34 (166) | |
In what situations should you recommend a back-up method for oral contraceptives?d | ||
Two or more correct situations listed | 5 (23) | 1 point |
One situation listed | 45 (219) | |
Zero situations listed | 50 (244) |
OCP, oral contraceptive pill
a Correct responses include for headache, nausea, vomiting, vertigo, breast tenderness, spotting/breakthrough bleeding, weight gain.
b Correct responses include seizure medicine, antiretroviral (ART), tuberculosis medicine
c Correct responses include if client is pregnant, history of heart/circulation problems, breast cancer, severe liver disease, heavy smoker over 35 years old, breastfeeding first six months post-partum for combined OCPs, breastfeeding in first six weeks post-partum for Progestin-only OCPs, severe/complicated diabetes.
d Correct responses include if client forgets 3 or more pills, if she vomited soon after taking pill, if she starts the pill after the first 5 days of her menstrual cycle, if she forgets to take Progestin-only pill by more than 3 hours
The majority (78%) of respondents’ knowledge adhered to the outdated protocol that a woman should initiate OCPs on the first day of her period, rather than current recommended practice, which allows women to start at any time during her cycle as long as she is reasonably sure she is not pregnant. While 59% of pharmacists and assistant pharmacists were able to name one or two common side effects, few (5.2%) were able to name five or more. While only 7% of respondents knew that a breastfeeding woman should wait twenty-four weeks/six months before initiating combined oral contraceptives, 18% knew that she could initiate progesterone-only pills either right away (current guidance), or after six weeks (previous guidance).
Table 5 outlines the series of questions asked to determine pharmacy staff knowledge of counseling issues related to injectable contraception. Scores ranged from 0–4 out of a possible 4 with an average of 0.9. Six staff (four pharmacists, one assistant pharmacist, and one counter staff) (1.2%), met the criteria of three or more points to be considered highly knowledgeable about injectables; 16% scored two or more points. As with OCPs, the average score was slightly higher for staff who reported having received training on family planning while in school. Those who reported receiving training averaged 1.1 points, versus 0.99 for those not reporting having received training.
Questions and responses | % (n) | |
---|---|---|
In general, at what time during the menstrual cycle do you recommend that the client begin using Depo Provera? | ||
Anytime as long as the client is reasonably sure she is not pregnant. | 5 (25) | 1 point |
No response/I don’t know | 48 (235) | |
All other responses (anytime during her menstrual cycle, don’t know/no response) | 46 (224) | |
For how long is Depo Provera effective? | ||
Three months/13 weeks | 73 (305) | 1 point |
No response/I don’t know | 19 (93) | |
All other numerical responses | 18 (86) | |
When should a woman return for a re-injection of Depo? | ||
From 2 weeks before up to 4 weeks after | 1 (4) | 1 point |
Up to 2 weeks before | 1.4 (7) | 0.5 point |
Up to 4 weeks after | 1 (4) | 0.5 point |
On the exact date | 64 (313) | |
All other responses | 32 (153) | |
What are common side effects of Depo Provera?a | ||
Four or more correct side effects listed | 10 (48) | 1 point |
Three correct side effects listed | 21 (101) | |
Two correct side effects listed | 28% (137) | |
One correct side effect listed | 20 (99) | |
Zero correct side effects listed | 20 (99) | |
What are the reasons not to use Depo Provera?b | ||
Four or more correct reasons listed | 4 (19) | 1 point |
Three correct reasons listed | 7 (35) | |
Two correct reasons listed | 20 (98) | |
One correct reason listed | 25 (119) | |
Zero correct reasons listed | 44 (214) |
a Correct responses include prolonged/heavy/irregular bleeding, amenorrhea, headaches, mood changes, weight gain, dizziness, abdominal pain/boating, reduced sex drive.
b Correct responses include if client is pregnant, breast cancer, very high blood pressure, severe liver disease, unexplained vaginal bleeding, breastfeeding in first 6 weeks postpartum, thrombosis/blood clots, rheumatic lupus disease.
While nearly three-quarters (73%) of staff knew the duration of effectiveness to be three months per injection, few understood that women have a window from two weeks before to four weeks after her previous injection was set to expire to receive her reinjection. Whereas 21% of respondents could name three side effects associated with injectables, only 10% could name four. A total of 20% of respondents could name two reasons not to use injectables, but only 4% could name four or more reasons.
In total 21% of the entire sample (3,567) had ever used the pharmacy to get a contraceptive. Of clients currently using a modern family planning method, 31% used OCPs, 30% used injectables, 20% used implants and 10% used IUDs. A total of 70% of users obtained their methods through a public health facility, 19% from a pharmacy and 10% from another source. Current users who procured their method through a pharmacy received OCP (69%), condoms (21%), emergency contraception (5%) and injectables (3%).
Among the 390 current users who obtained a method from a pharmacy, 54 (14%) reported that they or their partner had received counseling at the pharmacy the last time they procured their method. Table 6 provides further information about that experience, including privacy and details of the counseling received. When asked, 52% of clients who had ever procured family planning through a pharmacy reported receiving a method without a prescription (390 of 741); 50% reported having bought OCPs and 2% injectables.
Among non-users of family planning, and current users who did not obtain their method through a pharmacy (n=3,074), 47% said they would be interested in procuring a method through a pharmacy. Of those who were not interested in procuring through a pharmacy (n=1,008), 34% cited that they were dissatisfied with the quality of services through the pharmacy, and 12% noted high costs for their lack of interest.
Of the non-users of family planning who indicated having an interest in family planning, and current users procuring through a source other than a pharmacy (n=1,495), half or more would not be willing to pay for their method in the pharmacy (Figure 1). A total of 62% would, however, be willing to pay for counseling from pharmacy staff. The mean amount they would be willing to pay for counseling was 1679 CFA (approximately 3 USD) with a median and mode of 1000 CFA (approximately 2 USD).
Findings from both the pharmacy audit and the client survey show that most pharmacies in the UHRI project area provide method-specific counseling, and that they largely adhere to the law requiring a prescription to purchase OCPs and injectables. Both OCPs and injectables were in good supply, and the vast majority of pharmacies had a private space where counseling could be performed. We found that pharmacies were not only an important point of supply for family planning methods, but also that there was latent demand. There was a relatively high level of interest among women, including new or re-starting users, to supply through pharmacies.
Our findings also identified several possible ways to more fully leverage the potential of pharmacies to serve the family planning needs of women in urban settings and translate opportunities into gains in modern contraceptive prevalence. First, the proportion of pharmacies offering counseling was less than initially assumed based on information on prior programs offering training to pharmacies, and few pharmacies had access to counseling materials such as posters, flip charts, or brochures. Second, the limited family planning training provided to pharmacists and assistant pharmacists was reflected in some knowledge gaps, particularly with regards to up to date and detailed information. More detailed training on family planning counseling as part of the pharmacy licensure training program as well as opportunities for pharmacists and assistant pharmacists to refresh their skills through more broadly offered training could help address these challenges, especially given the fact that providers in this study expressed interest in more training on methods and counseling. An implemented training program should also consider issues of quality control, and how to ensure that quality standards are being met in practice.
Price, however, appears to be an important consideration for women and could be a challenge given the for-profit nature of pharmacy-based service provision. The majority of women interviewed were unwilling to pay for their method, though most were willing to pay for counseling obtained through the pharmacy, which reflects the typical payment structure of public health facilities, where women pay a small fee for methods and a separate fee for a family planning consultation. Programmatic components that aim to decrease financial barriers to family planning methods and other health services obtained through the private sector should be considered in Senegal to expand the potential of pharmacies to reach women of all income levels and contribute to gains in contraceptive prevalence, including increasing access to insurance and implementing savings products and voucher systems. With a goal of reaching the urban poor, price sensitivities should be addressed in a way that keeps sales of family planning products profitable for pharmacy owners while still affordable for women. Insurance, vouchers, and other approaches to reduce financial barriers should be considered for implementation in Senegal, to ensure financial accessibility through private service delivery points.
Our study had several limitations. Because the sampling of pharmacy clients was capped for non-users of family planning, we oversampled current users of family planning who obtain services in the pharmacy setting. We limited interviews of non-users because we wanted to ensure survey takers had enough time available to gather information from users of family planning. Other design options such as directly asking pharmacy staff about their practices or conducting a mystery client study were considered at the design stage, but met with opposition from ethics committees. Nevertheless, we attempted to address this shortcoming by triangulating pharmacy staff responses of knowledge of prescription requirements with client acknowledgement of having previously purchased a method without a prescription, creating a proxy for sales without a prescription. Social desirability bias may have led to an inflated proportion of staff who reported requiring prescriptions.
Given high rates of success with task-sharing in other environments, the availability of contraceptive commodities and private counseling space within most urban-Senegalese pharmacies, and client interest in receiving family planning directly through pharmacies, Senegal’s urban pharmacies are well-positioned to meet the country’s increasing desire for modern contraception. Prescription requirements, however, may impose barriers to women seeking services. For this reason, and because many medical experts consider such requirements unnecessary, Senegal should consider lifting these prescription requirements to fully realize the potential to lower unmet need and raise CPR in urban settings, particularly in light of successful experiences in other countries.
With proper training, including the use of job aids, pharmacy staff could provide effective counseling, screening, and provision of OCPs and injectables, thus eliminating the current burdens of time and travel that accompany the prescription requirement for women seeking contraception in urban areas of Senegal.
Replication data from this study are available on Harvard Dataverse: https://doi.org/10.7910/DVN/UQ3NWN22
Data are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).
This work is supported by the Bill and Melinda Gates Foundation [OPP1005927]. This funds the Urban Reproductive Health Initiative, of which this research is part of and was initiated by FHI 360 and led by IntraHealth International in Senegal.
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Health policy and planning, health policy and regulatory analysis, health advocacy, health financing, private health sector, public-private dialogue, private sector assessments, health markets
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | |||
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