Abstract
Background:
Monthly intramuscular injections of benzathine penicillin G (BPG) remain the cornerstone of secondary prophylaxis for acute rheumatic fever and rheumatic heart disease (RHD). The barriers to successful delivery of BPG may be patient- or service-delivery-dependent.
Objective:
The aim of the present study was to explore the perceived acceptability and implementation challenges of BPG treatment for RHD, from the perspective of healthcare providers (HCPs).
Methodology:
A descriptive qualitative study using semi-structured interview guides was conducted in four public hospitals in Ethiopia. Physicians and nurses who had at least 1 year of experience in delivering RHD secondary prophylaxis were recruited. The interviews were audio recorded, transcribed verbatim, and translated into English for analysis using framework method thematic analysis. Identified behavioral factors were mapped onto a theoretical framework of acceptability (TFA), and the Capability, Opportunity, Motivation-Behavior (COM-B) model.
Result:
Twenty-two interviews were conducted with HCPs (mean age 39 years, 55% nurses). Insights into BPG use and acceptability were categorized into four major themes related to: (1) individual factors (e.g., fear of anaphylactic reaction), (2) health system barriers (e.g., BPG shortage), (3) patient/caregiver perceptions (e.g., reliance on injectables, over expectation of treatment outcomes), and (4) product (e.g., injection pain, needle blockage).
Conclusions:
HCPs identified facilitators and barriers which highlight the complexities associated with BPG as secondary prophylaxis for RHD in Ethiopia. Based on these data, we suggest RHD control programs should (1) provide cross-disciplinary training and education programs to support safe and context-appropriate delivery of BPG (2) improve resourcing of health facilities to facilitate safe drug delivery, (3) establish a comprehensive system for auditing severe adverse reactions post-BPG injection to generate robust pharmacovigilance data, and consider alternative approaches to BPG delivery including access to improved formulations (e.g., BPG suspension formulations in pre-filled syringes).
Highlights:
– Key barriers included (a) resistance from healthcare providers to administer benzathine penicillin G (BPG) due to their concerns about injection-related severe adverse events, and potential repercussions should an event occur, (b) poor community and healthcare provider awareness of the disease and its treatment, (c) lack of resources to manage adverse events, and (d) injection pain.
– Key enablers included (a) perceived superior treatment benefits of BPG and (b) co-administration of lidocaine/analgesics to reduce injection pain.
– Recommendations to address identified challenges include (a) improved training/education on RHD diagnosis, disease progression, and treatment, (b) improved access to supportive resources, (c) active adverse reaction monitoring and reporting, and (d) encouraging the provision/access of globally subsidized BPG suspension formulations in pre-filled syringes.
Keywords: Rheumatic heart disease, Benzathine Penicillin G, COM-B model, Theoretical framework of acceptability
Introduction
Acute rheumatic fever (ARF) is an illness following an autoimmune response to Streptococcus pyogenes (Group A Streptococcus) infection of the upper respiratory tract, skin or mucosa (1). If untreated, ARF can affect the heart valves leading to rheumatic heart disease (RHD) (2). This preventable complication remains a major public health problem. In 2019, the global incidence and prevalence of RHD were estimated at 2.8 million and 40.5 million respectively, resulting in >300,000 deaths and 10.7 million disability-adjusted life-years (3). Despite declines in global mortality- and disability-adjusted life-years trends worldwide, the burden of RHD remains concerningly high in low- and middle-income countries within Oceania, South Asia, and sub-Saharan Africa, and in underprivileged populations within developed nations; e.g., Aboriginal and immigrant populations within Australia (4,5,6).
Benzathine penicillin G (BPG) remains the recommended secondary prophylaxis to prevent recurrent Group A Streptococcal infections by the World Health Organization (WHO) and is the cornerstone of ARF/RHD control programs (7). While BPG prophylaxis is highly effective and affordable, suboptimal delivery of BPG (7) is a common challenge in many endemic nations, including Ethiopia (8,9,10), resulting in increased morbidity and progressive heart damage (11).
The burden of rheumatic heart disease is high in Ethiopia, with a prevalence of approximately 3% (12). When diagnosed, most patients already have established severe valvular damage (13). The national treatment guideline recommends monthly intramuscular BPG injections for secondary prophylaxis of ARF/RHD (14). However, only two-thirds of RHD patients receive optimal BPG secondary prophylaxis, defined as receiving at least 80% of planned injections (8,15).
In most low- and middle-income countries, the only injectable BPG formulation available is a powdered preparation. Compared with more expensive suspensions in pre-filled syringes available in other settings (e.g. Bicillin®), powdered BPG preparations have reported quality concerns which may contribute to needle blockage and pharmacokinetic variability (16,17). Moreover, studies from Ethiopia (18), Uganda (19), and Sudan (20) have demonstrated low knowledge and skills of service providers relevant to ARF/RHD as barriers to successful control programs (21,22).
Anecdotal evidence suggests that suboptimal adherence to BPG injections may be due to fear of needle blockages and severe adverse events, which are sometimes fatal (23,24). Although the actual risk of anaphylaxis due to penicillin is low, occurring in 1 in 100,000 individuals (25), a survey by the World Heart Federation found that among 39 clinicians prescribing BPG, 20% reported a patient dying from anaphylaxis, while 26% were aware of a fatal anaphylactic reaction to BPG (24). As a result, healthcare providers (HCPs) may prescribe oral antimicrobials such as amoxicillin or phenoxymethylpenicillin, which are less effective alternative therapies for ARF/RHD (16,26,27,28,29).
Despite emerging evidence supporting subcutaneous delivery (30,31,32), RHD secondary prophylaxis currently requires painful monthly intramuscular injections over prolonged periods, leading to poor treatment uptake (9,33,34,35). Addressing the low uptake of secondary prophylaxis for ARF/RHD has been identified as a public health priority (26,36). Health sector-level barriers to BPG delivery are incompletely understood, with limited published research on the perspectives of HCPs and other stakeholders who play a decisive role in the delivery of BPG (21,26,33). The aim of this study was, therefore, to gain insight into the drivers of BPG acceptability for secondary prophylaxis of ARF/RHD in Ethiopia, from the perspective of HCPs.
Methods
A descriptive qualitative study design was implemented to explore the perspectives of HCPs on patient experience, treatment acceptability, and implementation challenges of BPG secondary prophylaxis for ARF/RHD. The Consolidated Criteria for Reporting Qualitative Research (COREQ) (37) was used to design, conduct and report study findings (Supplementary Table 1).
Ethical Approval
Ethical approval was obtained from the University of Gondar Institutional Review Board (VP/RTT/05/756/2022) and Curtin University Human Research Ethics Committee (HRE2022–0221).
Site selection
To identify varying practices of secondary prophylactic care across Ethiopia, four public hospitals were selected for recruitment of participants: Gondar (University of Gondar Hospital; Amhara Region), Debre Tabor (Debre Tabor Comprehensive Specialized Hospital; Amhara Region), Dire Dawa (Dil-Chora Referral Hospital, Dire Dawa City Administration), and Arba Minch (Arba Minch Comprehensive Specialized Hospital; South Region). The selected hospitals are the only secondary or tertiary care hospitals in their catchment area. As the Ethiopian health sector development plan has implemented a three-tiered health-delivery system, general hospitals provide secondary-level services to 1–1.5 million people, and specialized referral hospitals provide tertiary services to 3.5–5 million people (38).
Participants
HCPs (physicians and nurses) with at least 1 year of experience in delivering RHD secondary prophylactic care services and willing to participate in the study and provide informed consent, were recruited using purposive sampling methods. This enabled the recruitment of a diverse range of participants (age and duration of experience). The sample size was determined using the principles of thematic saturation (39). While data saturation was agreed to have been achieved after 18 interviews, due to altered treatment practice at one research site (Gondar), a further four participants were interviewed to ensure thematic consistency.
Data collection
Semi-structured interview topic guides were developed, being informed by previous reports (40) and pilot observations of perceived gaps at one of the study sites (Gondar). Topic guides were piloted with two senior service providers (one nurse and one physician) to ensure questions were clear and comprehensive. Minor changes were made to the order and structure of the questionnaire. Semi-structured questionnaires (Supplementary text file) were prepared in both local (Amharic) and English languages, with participants able to select their language of choice.
At each study site, key staff involved in the delivery of ARF/RHD secondary prophylaxis were contacted with support letters from the University of Gondar to participate in the study and to identify other potential staff to be invited to participate. After introducing the study objectives written, informed consent was obtained prior to the interview and participants were guaranteed confidentiality to encourage full and free reflection of their views. In-depth interviews were conducted in person by a trained investigator (EMB, PhD student, Male, no prior relationship with participants) at each respective health institution, between April and June 2022. Each interview spanned 15 to 45 min and was audio-recorded.
Data analysis
Audio-recorded interviews were transcribed verbatim, translated by Google Translate, and edited by an investigator fluent in Amharic and English (EMB). To ensure accuracy and reliability, a randomly selected subset of transcripts and translations were crosschecked against the audio records using back-translation (to local language) by an independent reviewer.
Using qualitative description analysis, transcribed responses were evaluated (EMB) to identify patterns, themes, commonalities, and differences, and to develop codes for study variables using QSR NVivo [Release 1.7.1 (1534), QSR International, Massachusetts, USA]. Similar codes were categorized into coherent and defined domains. To finalize the analysis of the shared perspectives between subjects, themes of responses were generated inductively using the framework method thematic analysis (41). The emerging sub-themes of perceived barriers and facilitators for the BPG secondary prophylaxis implementation services were then mapped onto the Capability, Opportunity and Motivational-Behavior (COM-B) (42) (Supplementary Table 2) and Theoretical Framework of Acceptability (TFA) (43) (Supplementary Table 3) models, and potential solutions mapped onto the Behavioral Change Wheel (BCW) model (42) (Supplementary Table 4). The integration of the TFA, which assesses service/intervention acceptability (43), and the COM-B model, which identifies factors influencing behavior (42), offers a practical approach to pinpoint key areas for successful practice changes and insights into strategies to overcome challenges to evidence-based change. To ensure consistency of analysis, six (~25%) transcripts were randomly selected and reviewed by a second investigator (BRM) for theme selection and coding. All discrepancies were reviewed (EMB and BRM), and theme tags were refined and redistributed to reach a consensus. The sociodemographic data of participants were described by frequencies, percentages, or means ± SD, as appropriate.
Results
A total of 22 participants were recruited into the study across all research sites: Arba Minch (n = 4), Debre Tabor (n = 6), Dire Dawa (n = 4), and Gondar (n = 8). Of these, 10 participants (45%) were female and 12 (55%) were employed as nurses. On average, nurses and physicians had 7.5 years (range: 1–23 years) and 6.75 years (range: 4–13 years) of experience treating patients with ARF/RHD, respectively (Table 1).
Table 1.
Sociodemographic data of participants.
| |||||
---|---|---|---|---|---|
SITE | |||||
| |||||
TOTAL | ARBA MINCH | DEBRE TABOR | DIRE DAWA | GONDAR | |
| |||||
Participants (n) | 22 | 4 | 6 | 4 | 8 |
| |||||
Age (years) | 39 ± 10 | 36 ± 1 | 38 ± 10 | 36 ± 9 | 42 ± 13 |
| |||||
Gender [n (%)] | |||||
| |||||
Male | 12 (55%) | 2 | 3 | 1 | 6 |
| |||||
Female | 10 (45%) | 2 | 3 | 3 | 2 |
| |||||
Profession [n (%)] | |||||
| |||||
Nurse | 12 (55%) | 2 | 4 | 3 | 3 |
| |||||
Physician | 10 (45%) | 2 | 2 | 1 | 5 |
| |||||
Experience (years)† | 7.2 ± 4.8 | 7.0 ± 4.8 | 4.8 ± 5.7 | 8.2 ± 5.3 | 8.6 ± 3.9 |
|
Data are presented as mean ± SD or number (%).
†Participant experience (in years) in delivering services for ARF/RHD patients; particularly involvement in assessment and follow up, prescribing antibiotics and injecting BPG for secondary prophylaxis.
Four main themes were identified, with factors influencing the use of BPG for secondary prophylaxis of ARF/RHD characterized as (1) individual factors, (2) health-system related, (3) patient related, or (4) product related. Of the four main themes, 17 subthemes were identified (12 were recognized as barriers and 5 were identified as facilitators) and mapped on TFA and COM-B models (Supplementary Table 5). A summary table of key enablers and barriers of BPG secondary prophylaxis is also provided (Supplementary Table 6).
Individual factors
All HCPs identified that a significant barrier to the successful delivery of BPG was the fear of a serious adverse event after intramuscular administration. Whilst the majority agreed that BPG was an effective treatment and superior to oral therapy, the availability and willingness of HCPs to prescribe/administer BPG was strongly influenced by concerns about potential adverse reactions. These concerns were further compounded by fears for the HCPs’ own safety, stemming from prior fatalities attributed to BPG administration and anecdotal reports of attempts at retribution by patients’ families against HCPs. This fear was particularly evident in nurses, who are tasked with injecting the medication. Several nurses reported they believed there was a strong correlation between the anticipated incidence of severe adverse events and the health status of the participant on the day of presentation for injection. If the patient was severely unwell, there was a perceived higher risk, compared to patients with mild to moderate disease who presented in reasonable health. Moreover, only a few participants had direct experience with patient deaths following BPG injection, and they noted that all the patients who died after receiving the injection had a history of BPG exposure.
As experts, we think that if they are seriously ill, they will go into shock due to injection… but we think it will make a difference for those who have mild to moderate RHD.
(Nurse, Debre Tabor)
… Next to his death, his family said to us we will beat and kill health professionals outside in the city. When they said so, everyone stopped delivering the medication
(Nurse, Gondar)
She comes to us every 2 months and had been on BPG before… She was in critical condition… We administered BPG to her, and then she immediately went into shock… She died while on oxygen.
(Nurse, Debre Tabor)
A strong sentiment was that the ‘…risk of anaphylactic shock scares me’. Ultimately, the fear of severe adverse events occurring post-injection led to a lack of willingness to ‘voluntarily administer the injection’, only doing so because, without the medication, ‘patients suffer’. Whilst this theme was reported across all research sites, in Gondar the fear of anaphylaxis led to few nurses being prepared to deliver BPG, hence less effective oral alternatives were prescribed by doctors at this site. However, most of the nurses did not deny that better treatment outcomes were achieved from BPG administration, compared to oral therapies.
There was also evidence of a level of disconnect between nurses and physicians with respect to liability if severe/fatal adverse events occurred. Nurses indicated that the lack of clinical oversight provided by doctors at the time of injection contributed to their fear. One nurse stated,
Doctors are not involved other than prescribing. The pressure is on us, and I don’t think doctors understand our worries. There is no doctor you can consult within the injection room. If sudden death happens, it will be considered due to us, nothing else.
(Nurse, Debre Tabor)
Nurses also perceived that they were the only HCPs at risk (not the prescribing physicians) and would be held responsible if an adverse event occurred after injection. To reduce the burden of responsibility, nurses at several research sites reported they obtained written consent from families/patients prior to BPG as a means of trying to avoid/minimize liability for possible adverse outcomes. At some hospitals (Debre Tabor and Arba Minch), nurses had to be assigned to administer BPG to ensure ongoing service provision.
Physicians highlighted that a significant challenge to the efficient delivery of BPG was the reluctance of hospital nurses to administer intramuscular BPG.
There is a fear with the nurses, there is a situation where they say that they will not give injections, but they bother us, but in the end, we get along with them.
(Physician, Dire Dawa)
Physicians also reported that nurses were potentially the most significant barrier to the efficient delivery of BPG, as they are often reluctant to administer the injection. This reluctance was identified as being primarily due to previous experiences with severe adverse events, as well as information they have received about such incidents, threats, and the complexities surrounding the overall context. The low level of patient/community awareness, along with the challenges related to processes and structures (e.g., emergency management of anaphylaxis), has further reinforced the nurses’ reticence in administering BPG.
Nurses often refuse to inject. It (BPG) is not given in our hospital because they refuse totally. The reason they refuse is because they have experienced death when giving the medicine…because of this, it is heard that they are not giving the medicine and it is spreading to other places, so the information is now becoming a general problem.
(Physician, Gondar)
Whilst all physicians emphasized the importance of BPG for secondary prophylaxis, and their willingness to prescribe treatment, they acknowledged that the potential danger of anaphylaxis during injection of BPG in patients with advanced RHD was an important consideration.
Regardless of their fears related to drug administration, all physicians and most nurses highlighted the importance of BPG and their perception of clinical improvement in patients who received therapy.
From the perspective of physicians, there is still better acceptance and confidence on the efficacy of BPG
(Physician, Gondar)
Moreover, most HCPs perceived that the patients had better treatment adherence with BPG than the alternative oral treatments, with the additional benefit of reduced pill burden.
We currently only use amoxicillin. The problem with it is the pill burden. Adherence is an issue.
(Physician, Gondar)
From what I have read, the efficacy (of amoxicillin) I have seen in the past is equal… adherence is the key. For BPG side effect is the problem whereas for amoxicillin adherence is the problem.
(Physician, Debre Tabor)
Health System Realted
A common shared sentiment was that ARF/RHD was a significant health burden in Ethiopia and a leading cause of morbidity and mortality in children. Despite this, health services and disease prioritization did not match that of other diseases.
As a pediatrician, I would say attention has to be given to the treatment (BPG) like TB and HIV. It is sad to see the children suffer… RHD is a neglected disease.
(Physician, Arba Minch).
Whilst comprehensive treatment guidelines (14) are readily available in Ethiopia, training and logistics to support and guide BPG administration, and to manage severe adverse reactions, were not readily available at the time of this study. This lack of training and support contrasts with other priority conditions, such as tuberculosis, HIV, and malaria, which may receive more attention due to stakeholder priorities and for which detailed training programs are available to support diagnostic and therapeutic interventions.
Broad health education was highlighted as a significant influencing factor in how the community, and even HCPs, perceived ARF or RHD.
The community does not understand the sequalae very well. They don’t understand that RHD/heart disease is related to bacteria and the tonsils. So, this needs attention. There is a problem of not understanding the importance of prophylaxis and the disease, even physicians are not close enough to BPG and the prophylaxis
(Physician, Dire Dawa)
As a result, it was noted that patients often presented with late disease with established complications, and there was a lack of commitment toward treatment compliance. Moreover, several participants noted a suboptimal commitment by some HCPs to immediately commence patients on prophylaxis, adequately monitor treatment compliance, or assess their monthly response to treatment. It was perceived that a lack of understanding of disease pathogenesis and treatment characteristics significantly contributed to the observed behavior of both patients and HCPs.
A further cause for concern was the lack of preparedness and resources that were provided by health centers to support the administration of BPG and respond to associated side effects. Several nurses highlighted that hospitals/injection rooms did not provide adequate supplies of resuscitation kits, adrenaline, medical support, and equipment for monitoring participant health and vital signs.
The biggest drawback was that when we gave BPG, resuscitation material was not ready. We just take a consent and then inject. We didn’t secure IV early. Adrenaline, mask and other things may not be available. If the patient was shocked, it was not possible to give help on the spot. Although I was not present, the patient expired when they rushed to bring them to ICU.
(Nurse, Arba Minch)
This reported lack of supportive services exacerbated the fear of injecting BPG, particularly in patients who were in end-stage disease or presenting unwell. The availability of BPG was also identified as a limitation. Patients were directed to purchase the drug in private pharmacies when a stable supply was not available in the treating hospital.
… it was not available for 3 months in the hospital. They brought the medicine from private sources and elsewhere to be injected. There were those who did not get BPG and took amoxicillin alternatively.
(Nurse, Arba Minch)
Participants also reported that many cases of RHD were in rural areas where health services are not well supported. As a result, patients had to travel great distances, under financial constraints, to attend follow-up appointments in the referral hospital and may not be assessed satisfactorily or in a timely manner. As patients face financial hardship, both for travel and costs of attending hospital/waiting for treatment, this burden was thought to contribute to suboptimal treatment compliance and efficacy, which could be resolved through effective training and additional resources provided in non-referral centers.
Patients come by appointment, but they come from faraway places, and they are harassed. And it would be good if they were treated locally… When a specialist doctor is needed it is better to come every 2 to 3 months, otherwise they can be treated in their local area… Those who come from far away and spend a lot of money, but only receive medicine and get injected, they are rarely examined during follow-up. If so, they can do some follow-up at their nearest medical facility. For patients, monthly attendance has a significant impact on adherence.
(Nurse, Dire Dawa)
Co-administration of anesthetic or analgesic agents (lidocaine or diclofenac) also aided compliance during treatment, resulting in less frequent adverse events.
We do not inject BPG alone. We are giving it with antipain (diclofenac) because the patients go into pain shock easily when we inject them without antipain… if we add antipain, it is not dangerous.
(Nurse, Debre Tabor)
Patients/Caregivers Related
It was reported that due to poor health-seeking behavior and limited access to healthcare, many patients were diagnosed with RHD once the disease was well established.
They come after the patient shows congestive or other non-congestive heart failure symptoms. Therefore, the chances of early detection are slim. At the end they come with severe acute malnutrition and compensated heart failure because they are not seen.
(Physician, Gondar)
Several HCPs noted that early detection of ARF and prompt corrective treatment could be negated by patients seeking traditional medicines/practices for sore throat in childhood, whereby the patients may undergo uvulectomy at the hands of a traditional healer. The use of unproven traditional treatments (e.g., uvulectomy) and the resulting delay in seeking hospital care increase the potential for disease complications and the missed opportunities for early prevention further driving patient behavior and contributing to poor treatment compliance. Moreover, several participants noted that the over-expectation of prophylaxis among RHD patients (such as expecting it to be curative) and hesitancy to attend monthly follow-ups due to pain, time constraints, and financial concerns all contribute to poor adherence. Feelings of despair after years of follow-up further exacerbate challenges.
They take BPG more often and they think they will be saved. When there is no change, there is a state of despair and asking what the medicine will do. … as a result, they lose adherence for the follow up.
(Physician, Arba Minch)
However, strong facilitators for successful treatment were seen as the patient’s/caregivers’ willingness to accept treatment advice provided by HCPs, and their preference for a monthly injection rather than more frequent oral regimen alternatives.
Patients love something that can be injected rather than something that needs to be swallowed
(Nurse, Gondar)
Product related
Both BPG formulation and route of administration were reported to pose significant challenges. The perceived risk of anaphylaxis and/or pain-related cardiac events, thought responsible for the reported cases of death during administration, were also reported to be a significant barrier. However, the pain of injection was linked to the method of administration (deep intramuscular injection) alongside formulation concerns (product brands) resulting in needle blockage. Additionally, factors contributing to needle blockage included delays after reconstitution (due to sedimentation), patient positioning, and administering without local anesthetics or analgesics.
If you try to inject BPG with delay… it will immediately form a crystal and blocks the needle
(Nurse, Debre Tabor)
If you delay, it will dry out in the syringe… the water and the medicine will separate easily, the medicine sediments. If the patient is uncomfortable and then delays you, it will be difficult to push.
(Nurse, Arba Minch)
We give it with diclofenac, first it helps to reduce pain and second to further dilute BPG after reconstitution as BPG has crystal forming characteristics.
(Nurse, Debre Tabor)
… as I told you, about 6 children died. When we inject BPG, we add about 0.3 cc of lidocaine and inject it mostly on the thigh muscle. A 14-year-old boy died immediately without giving time for resuscitation when one of our friends administered it to him
Nurse, Gondar
Good nutrition and hydration prior to injection were also reported to prevent or at least minimize adverse events, which was often recommended by nurses to their patients whenever they attended for BPG injection.
Discussion
Our study is the first to investigate the acceptability and challenges of BPG secondary prophylaxis for ARF/RHD from the perspective of HCPs in multiple centers in Ethiopia, and it is one of few studies worldwide (21,22,40,44). Several factors affecting ARF/RHD secondary prophylaxis have been identified and mapped to the TFA construct, COM-B, and BCW models to elucidate the requirements for behavioral change interventions (42).
Fear of sudden severe adverse reactions, or retribution in the event of fatal reactions, were identified as barriers to consistent and successful BPG implementation. To overcome fear-related barriers, two contrasting scenarios emerged across treatment centers. In centers where BPG delivery continued, many HCPs implemented informal written consent procedures to be signed by family members prior to each BPG injection. Whilst this somewhat alleviated fear of retribution, HCPs perceived that this practice contributed to poor treatment adherence due to increased patient hesitancy to commit to BPG treatment. In contrast, at the University of Gondar Hospital, BPG administration was ceased and replaced by oral amoxicillin, due to the refusal of nursing staff to administer BPG injections. However, decreased treatment adherence, likely due to patient preference for injectables over oral regimens (45,46), was also a perceived outcome. Interestingly, despite a fear of treatment-induced anaphylaxis, providers overwhelmingly perceived BPG as the superior prophylactic treatment for ARF/RHD, which aligns with previous reports (47,48,49). This suggests that the decision not to implement BPG administration in some settings was in part driven by fear of severe adverse events, rather than a lack of confidence in the effectiveness of BPG.
In 2015, Ethiopia hosted the Social Cluster of the African Union Commission to develop a ‘roadmap’ of key actions that needed to be taken by African governments to eliminate ARF and RHD. Seven key priority areas were adopted within this strategy, including decentralizing technical expertise and technology for diagnosing and managing ARF and RHD, initiating national multi-sector RHD programs within noncommunicable disease control programs of affected countries, and ensuring adequate supply of high-quality BPG (23). Despite this, participants in the current study perceived ARF/RHD to be a neglected or low-priority health problem in Ethiopia, likely attributed to an apparent lack of national ARF/RHD control strategy (45) and health system challenges (50). In alignment with the proposed African Union Commission roadmap and RHD control goals established by the WHO (51) and World Heart Federation (7), the organization and strengthening of existing healthcare systems (51,52), defining and adaptation of best clinical practices (5,40,53), and promotion of early detection and treatment are all potential strategies for stronger RHD management programs in high burden developing countries (51). Thus, training HCPs on the burden of RHD, its management, and the risks of BPG injection pain and anaphylaxis, while emphasizing best practices for BPG administration, appears to be essential for improving BPG delivery. Additionally, implementing patient and community awareness programs could enhance the effectiveness of these services, ultimately reducing the burden of RHD and improving health outcomes.
Our study identified that health-seeking behavior of RHD patients, as per the HCPs’ perspective, is poor. It is known that the majority of the Ethiopian population live in rural areas and have low rates of literacy (54) which may contribute to limited access to healthcare services and suboptimal health outcomes (55). By contrast, the use of traditional medicine among the community is significant, with estimates that approximately 80% of the population uses complementary and alternative therapies (56).
As reported in previous studies, the possible risk of severe adverse reaction (57,58,59), pain and needle block are prominent product-related barriers of BPG secondary prophylaxis for ARF or RHD (16,17,33). In this study, HCPs noted that contributing factors for needle blockage and injection pain included delays in administration (after reconstitution, due to sedimentation), patient position (side-lying position), delivering without local anesthetics/analgesics and product brands, as also reported previously (25,53).
Although only a few participants had direct experience with patient deaths following BPG injection, an important observation in our study was that HCPs reported all known BPG administration-related deaths occurred in patients with long histories of receiving BPG as RHD secondary prophylaxis. This suggests that stimulated physiologic cascades (i.e., vasovagal reactions) due to anxiety, poor health, and/or injection pain (24,27,53,60), rather than penicillin anaphylaxis, is the principal driver of fatal outcomes. This finding is consistent with previous reports that fatalities associated with BPG were in patients with severe cardiac compromise (24). Consistent with this concept, the reported prevalence of severe adverse events in patients receiving BPG for syphilis treatment is very low (60,61,62). By comparison, a grey-literature retrospective study of RHD patients in Ethiopia reported a 21% prevalence of BPG-related adverse reactions, the majority of which were limited to injection site swelling, with no fatalities observed (63). These reports underscore the importance of systematic monitoring and reporting of severe adverse reactions following BPG injections. Such practices are essential for generating conclusive pharmacovigilance data, which can inform risk-benefit assessments and evidence-based therapeutic decisions. Auditing treatment outcomes, particularly the incidence and management of severe adverse events associated with BPG, would benefit from the active involvement of HCPs and regulatory bodies to strengthen and fully operationalize adverse reaction monitoring and reporting systems in Ethiopia (64,65) and globally as the safety of BPG intramuscular injection becomes an increasing concern (24,53).
Product-related barriers could be addressed by using alternatives to powdered BPG, such as BPG suspension formulations in pre-filled syringes (e.g., Bicillin®). Furthermore, recent reports of subcutaneous delivery of BPG, which are perceived to be ‘less painful and longer-lasting’, may offer a potential solution to the product-related challenges and improve treatment adherence, due to less frequent administration schedules (30,31,32). However, as BPG suspension formulations are more expensive than powdered BPG and require cold-chain storage, deploying BPG suspension in pre-filled syringes to low-income settings would require financial and logistic support from global sponsors and agencies.
Despite the barriers to BPG use for ARF or RHD secondary prophylaxis that were identified in our study sites, important facilitators were reported by participants. For example, HCPs recognized the superior treatment efficacy of BPG for ARF/RHD and improved adherence, compared to alternative oral regimens (45,47,48,49). HCP-initiated techniques to improve treatment delivery were also recognized including the addition of local anesthetics/analgesics for pain relief and prevention of needle blockage, ensuring the patient was placed in a supine position during, and for a period after, BPG injection, and deferring BPG administration in unwell patients (49,53,62). Patient-related facilitators were also identified in this study, including good counseling and a preference for monthly (or less frequent) injections to improve compliance and treatment outcomes (46).
This qualitative study had limitations. For feasibility, study recruitment was limited to hospitals within major urban areas (servicing large catchment areas), with participants approached based on their experience treating RHD. As such, the reported perceptions may not reflect the acceptability, barriers, and facilitators of ARF or RHD secondary prophylaxis of all HCPs across Ethiopia, or in other clinical settings. Another limitation of this study was that it was based on self-reported feedback, which is susceptible to recall bias and may lack a clear distinction, between firsthand experiences and anecdotal accounts. Furthermore, as a single investigator was responsible for data collection, translation, and preliminary analysis, some interpretation/analysis bias may have occurred. However, to mitigate the potential bias, we followed the widely used COREQ checklist (37), an independent review of the translation, the involvement of a second investigator in the extraction and analysis of collected data, and contributions from all investigators in the interpretation and reporting of our results.
Conclusion
Our study revealed that although BPG is the mainstay of ARF and RHD therapy in Ethiopia, several barriers impact successful service delivery and patient outcomes. Despite a low incidence of BPG injection-related severe adverse events, anecdotal ‘historical evidence’ appeared to drive HCP anxiety with respect to BPG administration and impending successful BPG implementation. We suggest that improved resourcing of RHD services would be highly beneficial, including comprehensive education of HCPs on RHD prevention, management, and risk mitigation as well as training in BPG administration and management of critical incidents (e.g., anaphylaxis), and the provision of essential resuscitation equipment. Enhancing patient and community education to improve awareness of RHD and perceptions of therapy-related adverse outcomes also could address the current barriers and shift the paradigm of poor BPG acceptability. Finally, in addition to considering improved BPG formulations, pharmacovigilance research on risks of severe adverse reactions to BPG and identifying associated risk factors, would provide valuable evidence to support RHD secondary prophylaxis and inform the management of potential adverse reactions.
Additional Files
The additional files for this article can be found as follows:
COREQ 32-item checklist.
Interview topic guide.
COM-B model definition.
TFA constructs definition.
BCW definition.
Themes mapped on TFA and COM-B.
Key enablers and barriers to BPG secondary prophylaxis.
Acknowledgements
The authors are thankful to the healthcare providers who volunteered their time to be part of this study and cooperated in the data collection procedures. Eshetie Melese Birru is a recipient of the Curtin University International Postgraduate Research Scholarship.
Competing Interests
The authors have no competing interests to declare.
Author Contributions
Conceptualization: EMB, KTB, and BRM; Methodology: EMB, KTB, and BRM; Data curation, and data analysis: EMB and BRM; Validation: EMB, BRM, and KTB; Study Investigation: EMB, KTB, and BRM; Project Resources: EMB; Funding acquisition: Not applicable; Writing of Original Draft: EMB and BRM; Writing-review and editing: EMB, KTB, BRM, LM, and SE; Visualization: EMB, KTB, BRM, LM, and SE; Supervision: KTB and BRM. Design, operational aspects: EMB, KTB, and BRM.
References
- 1.Cunningham MW. Post-streptococcal autoimmune sequelae: Rheumatic fever and beyond. In Ferretti JJ, Stevens DL, Fischetti VA (Eds.) Streptococcus pyogenes: Basic biology to clinical manifestations [Internet]. Oklahoma City (OK): University of Oklahoma Health Sciences Center; 2016. Available from: https://www.ncbi.nlm.nih.gov/books/NBK333434/2016. [PubMed] [Google Scholar]
- 2.Cunningham MW. Streptococcus and rheumatic fever. Current Opinion in Rheumatology. 2012; 24(4):408–416. DOI: 10.1097/BOR.0b013e32835461d3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Ou Z, Yu D, Liang Y, et al. Global burden of rheumatic heart disease: Trends from 1990 to 2019. Arthritis Research & Therapy. 2022; 24(1):138. DOI: 10.1186/s13075-022-02829-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.de Dassel JL, Ralph AP, Carapetis JR. Controlling acute rheumatic fever and rheumatic heart disease in developing countries: Are we getting closer? Current Opinion in Pediatrics. 2015; 27(1):116–123. DOI: 10.1097/MOP.0000000000000164 [DOI] [PubMed] [Google Scholar]
- 5.Kerrigan V, Kelly A, Lee AM, et al. A community-based program to reduce acute rheumatic fever and rheumatic heart disease in northern Australia. BMC Health Services Research. 2021; 21:1–15. DOI: 10.1186/s12913-021-07159-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Roberts KV, Maguire GP, Brown A, et al. Rheumatic heart disease in Indigenous children in northern Australia: Differences in prevalence and the challenges of screening. Medical Journal of Australia. 2015; 203(5):221.e1–7. DOI: 10.5694/mja15.00139 [DOI] [PubMed] [Google Scholar]
- 7.Remenyi B, Carapetis J, Wyber R, Taubert K, Mayosi BM. Position statement of the World Heart Federation on the prevention and control of rheumatic heart disease. Nature Reviews Cardiology. 2013; 10(5):284–292. DOI: 10.1038/nrcardio.2013.34 [DOI] [PubMed] [Google Scholar]
- 8.Adem A, Dukessa Gemechu T, Jarso H, Reta W. Rheumatic heart disease patients’ adherence to secondary prophylaxis and associated factors at hospitals in Jimma zone, Southwest Ethiopia: A multicenter study. Patient Preference and Adherence. 2020:2399–2406. DOI: 10.2147/PPA.S281413 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Kevat PM, Reeves BM, Ruben AR Gunnarsso R. Adherence to secondary prophylaxis for acute rheumatic fever and rheumatic heart disease: A systematic review. Current Cardiology Reviews. 2017; 13(2):155–166. DOI: 10.2174/1573403X13666170116120828 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Rémond M, Severin K, Hodder Y, et al. Variability in disease burden and management of rheumatic fever and rheumatic heart disease in two regions of tropical Australia. Internal Medicine Journal. 2013; 43(4):386–393. DOI: 10.1111/j.1445-5994.2012.02838.x [DOI] [PubMed] [Google Scholar]
- 11.Rémond MG, Coyle ME, Mills JE, Maguire GP. Approaches to improving adherence to secondary prophylaxis for rheumatic fever and rheumatic heart disease: A literature review with a global perspective. Cardiology in Review. 2016; 24(2):94–98. DOI: 10.1097/CRD.0000000000000065 [DOI] [PubMed] [Google Scholar]
- 12.Berhanu H, Mekonnen Y, Workicho A, et al. The prevalence of rheumatic heart disease in Ethiopia: A systematic review and meta-analysis. Tropical Diseases, Travel Medicine and Vaccines. 2023; 9(1):16. DOI: 10.1186/s40794-023-00192-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Tadele H, Mekonnen W, Tefera E. Rheumatic mitral stenosis in children: More accelerated course in sub-Saharan patients. BMC Cardiovascular Disorders. 2013; 13:1–6. DOI: 10.1186/1471-2261-13-95 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Ministry of Health Ethiopia. Standard treatment guidelines for general hospitals, 4th edition. Addis Ababa; 2021. [Accessed on 20 July 2024]. Available from: https://doctorsonlinee.com/wp-content/uploads/2022/04/STG-Final-4th-edtion-2021-3.pdf. [Google Scholar]
- 15.Mekonen KK, Yismaw MB, Abiye AA, Tadesse TA. Adherence to Benzathine Penicillin G secondary prophylaxis and its determinants in patients with rheumatic heart disease at a cardiac center of an Ethiopian Tertiary Care Teaching Hospital. Patient Preference and Adherence. 2020:343–352. DOI: 10.2147/PPA.S238423 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Wyber R, Taubert K, Marko S, Kaplan EL. Benzathine penicillin G for the management of RHD: Concerns about quality and access, and opportunities for intervention and improvement. Global Heart. 2013; 8(3):227–234. DOI: 10.1016/j.gheart.2013.08.011 [DOI] [PubMed] [Google Scholar]
- 17.Hand RM, Senarathna SG, Page-Sharp M, et al. Quality of benzathine penicillin G: A multinational cross-sectional study. Pharmacology Research & Perspectives. 2020; 8(6):e00668. DOI: 10.1002/prp2.668 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Techane T, Legesse B, Ayalew Y, Hailu A. Rheumatic heart disease knowledge and associated factors among nurses working in cardiac centers at public and private hospitals of Addis Ababa: Cross sectional study. BMC Nursing. 2022; 21(1):130. DOI: 10.1186/s12912-022-00910-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Ochora M, Kyasimire L, Lutasingwa D, et al. Primary healthcare workers’ awareness of acute rheumatic fever & rheumatic heart disease: A study in public health facilities in southwestern Uganda. Pediatric Health, Medicine and Therapeutics. 2024:223–229. DOI: 10.2147/PHMT.S461168 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Osman GM, Abdelrahman SM, Ali SK. Evaluation of physicians’ knowledge about prevention of rheumatic fever and rheumatic heart disease before and after a teaching session. Sudan Journal of Paediatrics. 2015; 15(2):37–42. Available from: https://pubmed.ncbi.nlm.nih.gov/27493434/. [PMC free article] [PubMed] [Google Scholar]
- 21.Nalubwama H, Pulle J, Atala J, et al. A qualitative study of patients’ experiences, enablers and barriers of rheumatic heart disease care in Uganda. Global Heart. 2023; 18(1):6. DOI: 10.5334/gh.1181 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Edwards JG, Barry M, Essam D, et al. Health system and patient-level factors serving as facilitators and barriers to rheumatic heart disease care in Sudan. Global Health Research and Policy. 2021; 6(1):35. DOI: 10.1186/s41256-021-00222-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Watkins D, Zuhlke L, Engel M, et al. Seven key actions to eradicate rheumatic heart disease in Africa: The Addis Ababa communiqué: Cardiovascular topics. Cardiovascular Journal of Africa. 2016; 27(3):184–187. DOI: 10.5830/CVJA-2015-090 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Marantelli S, Hand R, Carapetis J, Beaton A, Wyber R. Severe adverse events following benzathine penicillin G injection for rheumatic heart disease prophylaxis: Cardiac compromise more likely than anaphylaxis. Heart Asia. 2019; 11(2):e011191. DOI: 10.1136/heartasia-2019-011191 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Wyber R, Johnson T, Marantelli S, Carapetis J. RHD Action. Global Status of BPG report. The benzathine penicillin G report; 2016. Available from: https://rhdaction.org/sites/default/files/RHD%20Action_Global%20Status%20of%20BPG%20Report_Online%20Version.pdf. Accessed on 10 Nov 2024. [Google Scholar]
- 26.Ali S, Long A, Nikiema JB, Madeira G, Wyber R. Availability and administration of benzathine penicillin G for the prevention of rheumatic fever in Africa: Report of the Working Group on Penicillin, Pan-African Society of Cardiology Task Force on Rheumatic Heart Disease. Cardiovascular Journal of Africa. 2019; 30(6):369–372. DOI: 10.5830/CVJA-2019-042 [DOI] [Google Scholar]
- 27.Berkovitch M, Ashkenazi-Hoffnung L, Youngster I, et al. Fatal and near-fatal non-allergic reactions in patients with underlying cardiac disease receiving benzathine penicillin G in Israel and Switzerland. Frontiers in Pharmacology. 2017; 8:843. DOI: 10.3389/fphar.2017.00843 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Lue H-C, Chen C-L, Wei H. Some problems in long-term prevention of streptococcal infection among children with rheumatic heart disease in Taiwan. Japanese Heart Journal. 1976; 17(5):550–559. DOI: 10.1536/ihj.17.550 [DOI] [PubMed] [Google Scholar]
- 29.Manyemba J, Mayosi BM. Intramuscular penicillin is more effective than oral penicillin in secondary prevention of rheumatic fever-a systematic review. South African Medical Journal. 2003; 93(3):212–218. Available from: https://www.proquest.com/scholarly-journals/intramuscular-penicillin-is-more-effective-than/docview/73336241/se-2. [PubMed] [Google Scholar]
- 30.Kado J, Salman S, Hla TK, et al. Subcutaneous infusion of high-dose benzathine penicillin G is safe, tolerable, and suitable for less-frequent dosing for rheumatic heart disease secondary prophylaxis: A phase 1 open-label population pharmacokinetic study. Journal of Antimicrobial Chemotherapy. 2023; 67(12):e0096223. DOI: 10.1128/aac.00962-23 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Kado JH, Salman S, Henderson R, et al. Subcutaneous administration of benzathine benzylpenicillin G has favourable pharmacokinetic characteristics for the prevention of rheumatic heart disease compared with intramuscular injection: A randomized, crossover, population pharmacokinetic study in healthy adult volunteers. Journal of Antimicrobial Chemotherapy. 2020; 75(10):2951–2959. DOI: 10.1093/jac/dkaa282 [DOI] [PubMed] [Google Scholar]
- 32.Cooper J, Enkel SL, Moodley D, et al. “Hurts less, lasts longer”; a qualitative study on experiences of young people receiving high-dose subcutaneous injections of benzathine penicillin G to prevent rheumatic heart disease in New Zealand. PLoS One. 2024; 19(5):e0302493. DOI: 10.1371/journal.pone.0302493 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Gasse B, Baroux N, Rouchon B, et al. Determinants of poor adherence to secondary antibiotic prophylaxis for rheumatic fever recurrence on Lifou, New Caledonia: A retrospective cohort study. BMC Public Health. 2013; 13:1–9. DOI: 10.1186/1471-2458-13-131 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Russell K, Nicholson R, Naidu R. Reducing the pain of intramuscular benzathine penicillin injections in the rheumatic fever population of Counties Manukau District Health Board. Journal of Paediatrics and Child Health. 2014; 50(2):112–117. DOI: 10.1111/jpc.12400 [DOI] [PubMed] [Google Scholar]
- 35.Derya E-Y, Ukke K, Taner Y, Izzet AY. Applying manual pressure before benzathine penicillin injection for rheumatic fever prophylaxis reduces pain in children. Pain Management Nursing. 2015; 16(3):328–335. DOI: 10.1016/j.pmn.2014.08.013 [DOI] [PubMed] [Google Scholar]
- 36.Rémond M, Wheaton G, Walsh W, Prior D, Maguire G. Acute rheumatic fever and rheumatic heart disease—priorities in prevention, diagnosis and management. A report of the CSANZ Indigenous Cardiovascular Health Conference, Alice Springs 2011. Heart, Lung and Circulation. 2012; 21(10):632–638. DOI: 10.1016/j.hlc.2012.05.006 [DOI] [PubMed] [Google Scholar]
- 37.Tong A, Sainsbury P, Craig J. Consolidated criteria for reporting qualitative research (COREQ): A 32-item checklist for interviews and focus groups. International Journal for Quality Health Care. 2007; 19(6):349–357. DOI: 10.1093/intqhc/mzm042 [DOI] [PubMed] [Google Scholar]
- 38.Health Sector Development Program IV 2010/11–2014/15. [Internet]. Federal democratic republic of Ethiopia ministry of health. 2010. Available from: https://www.healthynewbornnetwork.org/hnn-content/uploads/HSDP-IV-Final-Draft.
- 39.Francis JJ, Johnston M, Robertson C, et al. What is an adequate sample size? Operationalising data saturation for theory-based interview studies. Psychology & Health. 2010; 25(10):1229–1245. DOI: 10.1080/08870440903194015 [DOI] [PubMed] [Google Scholar]
- 40.Chamberlain-Salaun J, Mills J, Kevat PM, Rémond MG, Maguire GP. Sharing success–understanding barriers and enablers to secondary prophylaxis delivery for rheumatic fever and rheumatic heart disease. BMC Cardiovascular Disorders. 2016; 16:1–10. DOI: 10.1186/s12872-016-0344-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Gale NK, Heath G, Cameron E, Rashid S, Redwood S. Using the framework method for the analysis of qualitative data in multi-disciplinary health research. BMC Medical Research Methodology. 2013; 13:1–8. DOI: 10.1186/1471-2288-13-117 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Michie S, Van Stralen MM, West R. The behaviour change wheel: A new method for characterising and designing behaviour change interventions. Implementation Science. 2011; 6:1–12. DOI: 10.1186/1748-5908-6-42 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Sekhon M, Cartwright M, Francis JJ. Acceptability of healthcare interventions: An overview of reviews and development of a theoretical framework. BMC Health Services Research. 2017; 17:1–13. DOI: 10.1186/s12913-017-2031-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Barker H, Oetzel JG, Scott N, et al. Enablers and barriers to secondary prophylaxis for rheumatic fever among Māori aged 14–21 in New Zealand: A framework method study. International Journal for Equity in Health. 2017; 16:1–10. DOI: 10.1186/s12939-017-0700-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Belay W, Dessie A, Ahmed H, et al. Secondary prevention of rheumatic heart disease in Ethiopia: A multicenter study. BMC Cardiovascular Disorders. 2022; 22(1):26. DOI: 10.1186/s12872-022-02473-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Ilievski J, Mirams O, Trowman R, Barr RK, Manning L. Patient preferences for prophylactic regimens requiring regular injections in children and adolescents: A systematic review and thematic analysis. BMJ Paediatrics Open. 2024; 8(1). DOI: 10.1136/bmjpo-2023-002450 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.WHO Expert Consultation. Rheumatic fever and rheumatic heart disease: Report of a WHO Expert Consultation, Geneva, 29 October —1 November 2001. WHO Technical Report Series; 923. Geneva: World Health Organization; 2004. [Accessed on September 20, 2024]. Available from: https://iris.who.int/handle/10665/42898. [Google Scholar]
- 48.Gerber MA, Baltimore RS, Eaton CB, et al. Prevention of rheumatic fever and diagnosis and treatment of acute Streptococcal pharyngitis: A scientific statement from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee of the Council on Cardiovascular Disease in the Young, the Interdisciplinary Council on Functional Genomics and Translational Biology, and the Interdisciplinary Council on Quality of Care and Outcomes Research: Endorsed by the American Academy of Pediatrics. Circulation. 2009; 119(11):1541–1551. DOI: 10.1161/CIRCULATIONAHA.109.191959 [DOI] [PubMed] [Google Scholar]
- 49.Ralph AP, Noonan S, Wade V, Currie BJ. The 2020 Australian guideline for prevention, diagnosis and management of acute rheumatic fever and rheumatic heart disease. Medical Journal of Australia. 2021; 214(5):220–227. DOI: 10.5694/mja2.50851 [DOI] [PubMed] [Google Scholar]
- 50.Travis P, Bennett S, Haines A, et al. Overcoming health-systems constraints to achieve the millennium development goals. Lancet. 2004; 364(9437):900–906. DOI: 10.1016/S0140-6736(04)16987-0 [DOI] [PubMed] [Google Scholar]
- 51.World Health Organization. 71st World Health Assembly adopts resolution calling for greater action on rheumatic heart disease. 2019. [Accessed July 2019]. Available from: https://www.who.int/ncds/management/rheumatic-heart-disease-resolution/en.
- 52.Noubiap JJ, Agbor VN, Bigna JJ, et al. Prevalence and progression of rheumatic heart disease: A global systematic review and meta-analysis of population-based echocardiographic studies. Scientific Report. 2019; 9(1):1–14. DOI: 10.1038/s41598-019-53540-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Sanyahumbi A, Ali S, Benjamin IJ, et al. Penicillin reactions in patients with severe rheumatic heart disease: A presidential advisory from the American Heart Association. Journal of American Heart Association. 2022; 11(5):e024517. DOI: 10.1161/JAHA.121.024517 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Wolf M, Gottwald S, Galyean T, Morris R, (Eds.) Global literacy and socially excluded peoples. Proceedings from the Socially Excluded Peoples Meeting, Pontifical Academy of Social Sciences; 2013. [Accessed on July 2024]. Available from: https://www.pas.va/content/dam/casinapioiv/pas/pdf-volumi/scripta-varia/sv123/sv123-wolf.pdf.
- 55.Berkman ND, Sheridan SL, Donahue KE, Halpern DJ, Crotty K. Low health literacy and health outcomes: An updated systematic review. Annals of Internal Medicine. 2011; 155(2):97–107. DOI: 10.7326/0003-4819-155-2-201107190-00005 [DOI] [PubMed] [Google Scholar]
- 56.Kassaye KD, Amberbir A, Getachew B, Mussema Y. A historical overview of traditional medicine practices and policy in Ethiopia. EJHD. 2006; 20(2):127–134. DOI: 10.4314/ejhd.v20i2.10023 [DOI] [Google Scholar]
- 57.Taubert K, Marko SB. Access to essential medicines: Illuminating disparities in the global supply of benzathine penicillin G in the context of rheumatic fever/rheumatic heart disease prevention. Journal of American College of Cardiology. 2013; 61(10S):E2004. DOI: 10.1016/S0735-1097(13)62004-5 [DOI] [Google Scholar]
- 58.International Rheumatic Fever Study Group. Allergic reactions to long-term benzathine penicillin prophylaxis for rheumatic fever. Lancet. 1991; 337(8753):1308–1310. DOI: 10.1016/0140-6736(91)92979-C [DOI] [PubMed] [Google Scholar]
- 59.WHO Drug Information. Benzathine penicillin: Fatal mega-unit injections. WHO Drug Information. 200;14(4), 230. Retrieved from: https://www.proquest.com/scholarly-journals/benzathine-penicillin-fatal-mega-unit-injections/docview/215681759/se-2. [Google Scholar]
- 60.Galvao TF, Silva MT, Serruya SJ, et al. Safety of benzathine penicillin for preventing congenital syphilis: A systematic review. PLoS One. 2013;8(2):e56463. DOI: 10.1371/journal.pone.0056463 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Liu M, Fan Y, Chen J, et al. Efficacy and safety of treatments for different stages of syphilis: A systematic review and network meta-analysis of randomized controlled trials and observational studies. Microbiology Spectrum Journal. 2022;10(6):e0297722. DOI: 10.1128/spectrum.02977-22 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Morsy M, Mohamed MA, Abosedira MM, et al. Lidocaine as a dilutant for benzathine penicillin G reduces injection pain in patients with rheumatic fever: A prospective, randomized, double-blinded crossover study. Australian Journal of Basic Applied Sciences. 2012; 6:236–240. DOI: 10.1097/00006454-199810000-00008 [DOI] [Google Scholar]
- 63.Hanna Mekonnen. Prevalence of benzathine penicillin adverse reaction in patients with rheumatic heart disease taking monthly benzathine penicillin. Addis Ababa University, Addis Ababa, Ethiopia; 2021. [Accessed on 16 December 2024]. Available from: https://etd.aau.edu.et/server/api/core/bitstreams/95e075f3-fb43-439d-b456-311e890d0bad/content#:~:text=Allergic%20reaction%20following%20BPG%20administration,actively%20treated%20for%20cardiac%20failure. [Google Scholar]
- 64.FMHACA. Guideline for Adverse Drug Events Monitoring (Pharmacovigilance), Food, Medicine and Health Care Administration and Control Authority of Ethiopia, 3rd edition; 2014. [Accessed on 16 December 2024]. Available from: https://www.medbox.org/document/guideline-foradverse-drug-events-monitoring-pharmacovigilance-ethiopi.
- 65.Hailu AD, Mohammed SA. Adverse drug reaction reporting in Ethiopia: Systematic review. BioMed Research International. 2020; 2020(1):8569314. DOI: 10.1155/2020/8569314 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
COREQ 32-item checklist.
Interview topic guide.
COM-B model definition.
TFA constructs definition.
BCW definition.
Themes mapped on TFA and COM-B.
Key enablers and barriers to BPG secondary prophylaxis.