The Challenges and Knowledge Gaps in Malaria Therapy: A Stakeholder Approach to Improving Oral Quinine Use in the Treatment of Childhood Malaria in Ghana.
Malaria is a serious and potentially fatal disease caused by the parasite, Plasmodium. There are four species of this parasite which cause the disease in humans, namely, P. falciparum, P. vivax, P. malariae, and P. ovale. These parasites are transmitted basically through the bites of female Anopheles mosquitoes [1, 2]. Malaria caused by P. falciparum is the deadliest form and the most predominant in Africa. The P. vivax is less dangerous but more widespread . Symptoms of malaria are generally nonspecific and commonly consist of fever, malaise, weakness, gastrointestinal complaints (nausea, vomiting, and diarrhoea), neurological complaints (dizziness, confusion, and coma), and myalgia . Others include headache, chills and/or cough, back and joint pains, delirium, convulsions, and anaemia .
Malaria continues to be a major public health concern in many countries of the world despite the efforts and progress made in reducing malaria cases and deaths. An estimated number of 214 million cases of malaria were recorded across the world in 2015 and this resulted in 438,000 malaria deaths, 90% of which occurred in Africa . The disease burden is highest in poor, rural areas and deprived populations, contributing annually to an estimated 1.3% reduction in economic growth in high-burden countries , and reduces school attendance, impairs cognitive development in children, and lowers productivity .
Malaria can be effectively prevented and treated using tools that exist today . A multipronged approach using insecticide treated nets (ITNs), indoor residual spraying (IRS), intermittent preventive treatment (IPT) of pregnant women and children, and prompt diagnosis and treatment using ACTs and other antimalarial agents such as quinine has been proven to prevent death and significantly reduce illness . The way forward then is to improve education and sensitization of the populace, establishment of effective collaborations and the provision of the right tools, and improving access. Being largely a disease of poverty, malaria and its effects would be greatly reduced by improvement in the living conditions of the people. Others will include the adaptation of new approaches to the handling and treatment of malaria. The engagement and use of community health officers from both healthcare and social services sectors could help develop malaria plans and policies capable of providing preventive, promotional, and medical care to individuals and communities.
With children being the most vulnerable group among malaria patients, this study sought to identify the challenges and knowledge gabs associated with these interventions that would need to be addressed in order to improve and enhance malaria treatment outcomes, especially with the use of quinine in children.
2. Materials and Methods
2.1. Study Design. This was a cross-sectional study. The primary study method was the use of a well- structured questionnaire. It was carefully designed such that respondents had options to choose responses ranging from strongly agree, agree, neutral, and disagree to strongly disagree.
2.2. Study Site. This study was undertaken at a government children's hospital chosen because of its role in the healthcare delivery in the country. The hospital is located within the Ashiedu Keteke Sub- Metro area of the Greater Accra region. It is situated very close to the central business district of Ghana's capital, Accra, and very close to the popular Makola market, which facilitates easy access.
2.3. Study Population. Participants in the study were healthcare personnel, parents, guardians, and caregivers. These were selected as the target population because of their relationship with the child and their roles in paediatric healthcare delivery. A total of 748 participants were involved.
2.4. Sampling. Participants were purposively selected and included both men and women who were at least twenty years old at the time of sampling.
2.5. Ethical Considerations. Ethical approval for the study was obtained from the Committee on Human Research, Publication and Ethics, Kwame Nkrumah University Science and Technology, and Komfo Anokye Teaching Hospital (Ref: CHRPE/AP/017/17). Participants in the study were provided with the participant information leaflet and signed the consent forms prior to their participation. Those who could not read had it explained to them in their local dialect and their consent was thereafter given before they participated. The rationale of the study and all the issues concerning human ethics were carefully explained in the introduction to the online forms.
2.6. Data Collection Procedure. Data collection was made by a well-structured and self-administered questionnaire to obtain quantitative primary data. The study was conducted by the use of both hard copy and online questionnaire. The online questionnaire for quantitative data collection was via Internet based Google forms for the distribution of questionnaires and data collection through participant emails and web link invitations. Reminder emails were sent to the respondents during the data collection period to enhance respondent participation. In the case of participants with poor Internet connectivity and power cuts, respondents were given hard copies of the questionnaire with explanation of information contained in the leaflet to obtain due consent and followed up promptly for the collection of the filled-in questionnaire. Prior to the administration of the survey questionnaires, the duration, competency, and suitability of the questionnaires were pretested and returned a Cronbach's alpha reliability statistic of 0.904, an indication that the questionnaires were competent [11, 12].
The entire questionnaire was composed of two major parts. Part I took the biodata of the respondents. Part II on the other hand was subsectioned into various categories and captured data on the respondents' knowledge on malaria, preventive measures and treatment seeking attitude, paediatric drug formulations, antimalarial drug use options, quinine antimalarial therapy, and novel quinine formulations for children. The questionnaire (Part II) was designed in the form of Likert rating scale, from (1) strongly agree, (2) agree, (3) neutral, and (4) disagree to (5) strongly disagree. Participants indicated their level of agreement with the statements in each section by ticking the appropriate option.
2.7. Statistical Processing of Data. The SPSS version 20 was used to test for the internal consistency of the questionnaires to solicit the intended responses from the participants in the pretest. Data from 20 respondents obtained using Google forms (spreadsheets) were entered into the SPSS, and the Cronbach's alpha reliability statistic was determined.
The online forms were filled and returned, while responses from the hard copy questionnaires were filled manually into the Google forms. For the continuous data processing of the items in Part I, percentages were generated from the responses in the summary of the Google forms spreadsheet for the univariate analysis. Quantitative data for Part II was processed and automatically formatted into aggregated data charts for univariate analysis.
3. Results and Discussion
3.1. Biodata Distribution of the Study Participants. A total of 748 successfully completed questionnaires were obtained and comprised of 59% female and 41% male respondents. Majority of the respondents (53%) had attained tertiary education and 35% had secondary education, with the other 12% having left school at the primary level or other forms of basic education. Majority of the respondents (73%) were parents, guardians, or caregivers, while the other 27% were clinicians, nurses, and pharmacists. About 21% of the respondents were unemployed, but a greater proportion (79%) were either employed or self-employed (Table 1).
3.2. Causes and Modes of Malaria Transmission. The study revealed that most of the respondents had a high level of understanding of the causes of malaria and its mode of transmission. Majority of the respondents associated malaria with the Plasmodium parasite (68%) and its spread through the bites of the infected female Anopheles mosquitoes (75%) (Figure 1). The extent of knowledge of the true causes of malaria from this study is similar to some earlier findings in Nigeria , Zimbabwe , Cameroon , and India , which all indicated an improvement over some related studies previously undertaken in Ghana and elsewhere. In those earlier findings, malaria was largely associated with some misconceptions such as drinking of dirty water, eating of oily foods, standing in the sun among others [17, 18].
Generally, the participants agreed that malaria cases become more widespread during the rainy season (75%) and identified children and pregnant women as the most vulnerable population (65%) for malarial attacks. Fortunately, the respondents (82%) indicated that malaria is not an evil disease as they dispelled the influence of witchcraft as a cause of malaria. The high knowledge level observed can be attributed to the educational levels of the participants in this study as some other findings also related education to one's awareness of malaria [19, 20].
Essentially, knowledge of the real causes and modes of transmission of malaria would be beneficial in the quest for malaria prevention.
3.3. Awareness of the Signs and Symptoms of Malaria. Majority of the respondents rightfully identified the signs and symptoms of malaria to include fever (75%), headache and dizziness (74%), general weakness (73%), nausea and vomiting (62%), loss of appetite (68%), and the resultant anaemia (63%) (Figure 2). These findings are similar to reports from some related works undertaken earlier on the subject [21, 22]. Knowledge of the right signs and symptoms would principally influence an individual's ability to take prompt and proper action at the onset of malaria, thereby triggering an appreciable treatment seeking attitude. The WHO and UK malaria treatment guidelines recommend early diagnosis and treatment as very essential in fighting malaria [23, 24].
Substantial understanding of the signs and symptoms of malaria can be crucial for home management of malaria and, hence, reduce severity and mortality. Therefore, even though there was considerable level of awareness of the clinical signs and symptoms of malaria, health authorities would need to intensify educational programmes among the populace aimed at maximum or near maximum malaria management and control.
3.4. Knowledge of the Methods of Malaria Prevention. Malaria is deadly, yet it is an entirely preventable and treatable disease . Methodologies range from the interference of breeding grounds and larva control to putting into practice of personal and household protective measures . Generally, the knowledge about malaria prevention methods was high among the participants (Figure 3). While 97% agreed on the use of ITNs, 92% indicated IRS as means of preventing malaria. ITNs and IRS as well as environmental cleanliness have been used as malaria control mechanisms over the years .
Our study has also identified the use of mosquito repellents and netted windows and doors, while the wearing of protective clothes against mosquito bites was also emphasised, similar to several other study findings [26, 27]. Refreshingly, these measures are relatively cheaper than the use of IRS and ITNs  and can be implemented at ordinary household levels. The results established clearly that there is a relationship between the knowledge of the causes of malaria and its prevention. It also seems clear that the education and interventions by the National Malaria Control Programme is yielding the desired impact, and if intensified, the anticipated malaria cases will subside . Therefore, children under 5 years and pregnant women in malaria endemic communities should continue to be targets in the malaria control programmes such as free or subsidized ITNs distribution and effective treatment via maternal and child health clinics.
3.5. Malaria Disease Management. The incidence of malaria was high in the study population, especially childhood malaria as 84% of respondents had children who had experienced malaria in the past. Further, 93% agreed that malaria is a serious and life-threatening disease which can kill if not treated promptly. The high level of knowledge of the deadly nature of malaria is encouraging, because proper measures would be taken to prevent or manage it should their family members get infected. Unfortunately, however, despite the fact that majority of the respondents had high level of knowledge on apt malaria prevention methods, their children (84%) still had episodes of malaria infection at one point or the other.
It therefore appears that the challenges to malaria prevention are still enormous and complicated. Lack of adequate protective clothing, the hot and humid Tropical African weather which does not support or encourage thorough body covering and use of ITNs, abundance of the mosquito vector in the subregion coupled with changes in their feeding times and habits, lack of effective IRSs, or the mere inability to implement the knowledge on malaria prevention exacerbates these challenges. Mboera et al. , in a similar study observed that in spite of high levels of knowledge of malaria in Tanzania, its morbidity was still high, and they suggested that misguided application of antimalarial drugs and delayed health seeking attitude as well as reliance on clinical findings in the absence of laboratory confirmation were accountable.
Treatment seeking attitude was good although pockets of participants agreed on undertaking home treatment with either previously bought drugs or herbal products. Essentially, majority of the respondents sought formal healthcare services from hospitals, clinics, or the community health workers , although some other studies  contradict this in favour of home treatment of some kind.
Interestingly, the study showed that 77% of the participants would seek treatment within 24 hours once symptoms showed up, which is in line with the targets of the Abuja Summit on Malaria which among other things envisaged that at least 60% of those having malaria should seek treatment within 24 hours of the onset of symptoms .
Nevertheless, some of the participants identified long distances to health facilities, high transportation, consultation and treatment costs, unfriendly attitude of some healthcare workers, unnecessary delays at the health facilities, and busy work schedules as some of the reasons for not seeking formal healthcare (Table 2).
Some form of continuing health education is still necessary to help these parents understand the need to take their children to healthcare centres for treatment in spite of these difficulties and challenges. Maybe the introduction of some basic incentives for prompt healthcare seeking attitudes, especially with children and pregnant women, could greatly enhance this. Also, since malaria is still a major killer in Africa, there is the need to restructure the health systems to facilitate the use of community health officers (CHOs) to take malaria control to the populace rather than wait and expect them to use the health facilities, in view of the high level of poverty and low literacy in these communities. The use of CHO services has been widely demonstrated to be very effective and have resulted in the elimination of most childhood killer diseases in many communities, improving family planning services and lifestyles of, especially, mothers and children .
Meanwhile some health workers in the various centres would need a rethink in attitude towards patients and guardians who seek healthcare services from them. This may require further training and continuous professional development, where some of these findings are conveyed to these practitioners.
3.6. Desirable Attributes of Paediatric Drug Formulations. The use of off-label and unlicensed medicines in children is widespread, yet the effects of these medicines on children have not been properly studied. Healthcare professionals, parents, or caregivers are often confronted with the necessity to manipulate an adult medicine for children which has the potential for high levels of dosage errors, instability, poor bioavailability, and unintended side-effects. Children under five years have been the target for antimalarial drug therapies over the years. The availability and suitability of antimalarial drug formulations for the child are essential if the fight against paediatric malaria is to be won.
Suitable formulations for children make it easier for parents and caregivers to administer antimalarial agents effectively, resulting in better therapeutic outcomes [34, 35]. Paediatric formulation ought to satisfy the needs: convenient and reliable administration, acceptability and palatability, minimum dosing frequency, end-user needs of patients of diverse ages, and the preferences of patients including caregivers in different parts of the world [36, 37].
Age-appropriate dosage forms are necessary to ensure compliance and effective therapeutic outcomes . Liquid formulations hitherto had been the formulation of choice for paediatric use but issues of compliance and safety have been expressed. Liquid formulations can easily undergo microbial contamination if proper storage conditions are not followed. Most antimalarial agents also have unpleasant taste and bitter tasting drugs are usually poorly tolerated by children. A significant proportion (85%) of the study participants were aware of some paediatric antimalarial drug formulations in circulation and showed preference for formulations which are palatable, easily acceptable, and in an attractive packaging (Figure 4).
Palatability and dysphagia persist as the two paramount challenges to paediatric drug product development, because neither is trivial and therefore continues to be major obstacles to the development of 'child-friendly' dosage forms .
3.7. Antimalarial Drug Knowledge. The study uncovered that some antimalarial drugs were more common among the participants than others (Table 3). Quinine came topmost (92%) followed by chloroquine (90%) as the antimalarial agents most of the respondents were familiar with. This may be because of the unique bitter taste of the duo as many people are more likely to remember bad taste. The availability of quinine tonic on the market may have an influence. In addition, quinine has been in use for treating malaria for over two centuries now and so the awareness of it among the respondents is fairly understandable. Unfortunately, chloroquine, though well known, has fallen into disuse and is no longer recommended due to drug resistance resulting from dosing errors, inappropriate use, or misuse and abuse.
The knowledge of the respondents on the ACTs was appreciable, but artesunate-amodiaquine (92%) and artemether-lumefantrine (87%) were the most common among the respondents (Table 3). Lonart (92%), Coartem (87%), Lumether (78%), and Malar-2 (67%) were, respectively, the leading marketed brands of ACTs, in respect of the knowledge of the respondents. The Governments' recent policy on the use of ACTs and the education and advertising that have gone on with it could have played a major role in this outcome. The challenges here are the lack of proper understanding of the term ACT and the proliferation of numerous brands with varying efficacy and effectiveness. In addition, treatment failures with these unreliable brands have emphasised the use of quinine.
3.8. Knowledge of Quinine Antimalarial Therapy. Quinine has been an age-old drug used for the treatment of malaria. Although, the WHO does not recommend it as a first line antimalarial drug for uncomplicated malaria, quinine is still used in the treatment of severe malaria and in cases where the ACTs fail to give the required therapeutic outcome. It was known among majority of the study participants that quinine is used for treating both complicated and uncomplicated malaria (Table 4), as supported by the UK malaria treatment guidelines .
Quinine, a cinchona alkaloid, has been an important antimalarial agent for a long time and continues to be effective against chloroquine-resistant P. falciparum malaria . In settings where multidrug resistant strains prevail, a 7-day regimen of quinine plus tetracycline or doxycycline or clindamycin gives cure rates of over 90% for patients with P. falciparum malaria . Quinine use in children is chiefly in the form of syrups which are sweetened because of its bitter taste. There are no other paediatric formulations of quinine, and when treating children, care should be taken to ensure correct doses are administered and retained because of its bitter taste and the fear of vomiting.
The unpalatability of quinine syrups as well as the crushed tablets may lead to the use of subtherapeutic dosages, noncompliance, and potential development of parasitic resistance. The study has revealed that the participants were familiar with the difficulties regarding quinine use in children, such as the bitter taste, and agreed that the bitterness of quinine is affecting their children's acceptance of the drug. As such the oral administration of large of volumes of quinine syrup may be difficult to achieve in children. Hence, 89% of the respondents agreed that they would be happy if the bitterness of quinine can be masked. This poses a challenge and places a burden of trust and responsibility on academia and industry players to act decisively and quickly. The WHO initiative "Make Medicine Child Size", aimed at increasing awareness and access to child specific medicines , and the European Paediatric Formulation initiative  both seek to promote the preparation of effective and safe children medications by facilitating the sharing of expertise between key stakeholders in the health industry. These are aimed at identifying and dealing with common challenges in developing formulations for paediatric populations. Ideally, formulations meant for children should possess minimal frequency of dosing, insignificant impact on lifestyle, minimum safe excipients, and wide range of applicability and should as well be easy to produce, stable, elegant, cost-effective, and commercially available [44, 45].
3.9. Choice of Novel Oral Paediatric Quinine Formulations. As a solution to some of the challenges enumerated with respect to quinine use in children, the study sought to determine the formulation of choice of quinine for paediatric use. It became clear that majority of the participants (91%) generally favoured oral thin film/strip formulation and some 92% of the respondents agreed that they would appreciate a formulation that guarantees a good mouth feel (Figure 5).
Fast dissolving oral thin films have become the cutting-edge form of oral solid dosage forms in view of more flexibility and comfort . They are more easily tolerated by patients and caregivers with respect to their ease-of-delivery, accurate dosing, and portability [47-49]. It enhances the dissolution and efficacy of drugs in a matter of seconds in the oral cavity once it gets into contact with saliva and therefore requires no water or mastication for administration [50, 51].
The predetermined form of oral dissolving thin films (ODTFs) offers an accurate and easily swallowed dose without water that allows for portable and convenient "give and go" administration by a caregiver or parent . It facilitates quick absorption and instant bioavailability of drugs due to high blood flow and permeability within the oral cavity.
Fast dissolving thin films are particularly useful in patients of such groups as paediatric, geriatric, emetic, and the bedridden [53, 54]. Oral thin films have the fundamental benefit of accuracy of dosing as compared to liquids, and there is no fear of choking as in the case of tablets and capsules. The novelty of the oral thin film is that it dissolves rapidly in the mouth invariably within 10-15 seconds .
Therefore, quinine in ODTFs with a good 'mouth feel' will provide the key to an efficient and effective use of quinine in childhood malaria.
The study demonstrated the availability of substantial knowledge of various aspects of malaria as well as its devastating burden, especially in children. Yet, the significant knowledge did not yield much in reduction of malaria episodes. The study has thus emphasised the need to ensure that tools such as insecticides treated nets and efficacious antimalarial agents are made available and utilised effectively in the fight against malaria. The availability of appropriate formulations of paediatric antimalarial agents such as quinine and its right usage would be key in any future malaria control strategies. The formulation of choice for quinine in the light of this study is the fast dissolving oral thin film which comes along with it efficient taste masking opportunities as well as guaranteeing a good mouth feel. Additionally, to control malaria some level of education is needed. Populations that demonstrate incorrect knowledge of malaria and its therapy may be illiterate or possess a low level of formal education. Therefore, there is a need for continued education since malaria control has so many facets and education is key to its success. Malaria control should be handled in a systematic, multisectoral, and coordinated manner to be effective.
Abbreviations ACTs: Artemisinin-based combination therapies IRS: Indoor residual spraying IPT: Intermittent preventive treatment ODTFs: Oral dissolving thin films WHO: World Health Organization.
The data used to support the findings of this study are available from the corresponding author upon request.
Ethical approval for the study was obtained from the Committee on Human Research, Publication and Ethics, Kwame Nkrumah University Science and Technology, and Komfo Anokye Teaching Hospital (Ref: CHRPE/aP/017/17). The rationale of the study and all the issues concerning human ethics were also carefully explained for participants in the introduction to the online forms.
Participants in the study were provided with the participant information leaflet and signed the consent forms prior to their participation. Those who could not read had it explained to them in their local dialect and their consent was thereafter given before they participated.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
Marcel Tunkumgnen Bayor and Joshua Boateng conceived the study. Marcel Tunkumgnen Bayor, Isaac Ayensu, Stephen Yao Gbedema, and Bartholomew Yir-Erong designed the study. Marcel Tunkumgnen Bayor coordinated the study. Bartholomew Yir-Erong performed the study and analysed the data. Bartholomew Yir-Erong and Marcel Tunkumgnen Bayor drafted the manuscript. All the authors contributed content to the draft manuscript. All authors also revised, read, and approved the final manuscript.
Bartholomew Yir-Erong obtained a study grant from the Ghana Education Trust Fund (GETFUND). The study team is very grateful to the management of the Princess MarieLouis Children Hospital for granting them the opportunity to use their facility. A huge appreciation also goes to the study participants for being a part of this effort.
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Bartholomew Yir-Erong (iD), (1) Marcel Tunkumgnen Bayor (iD), (1) Isaac Ayensu (iD), (2) Stephen Yao Gbedema, (1) and Joshua Boateng (iD) (1,3)
(1) Department of Pharmaceutics, Kwame Nkrumah University of Science & Technology, Kumasi, Ghana
(2) Department of Pharmaceutical Chemistry, Kwame Nkrumah University of Science & Technology, Kumasi, Ghana
(3) Department of Pharmaceutical, Chemical and Environmental Sciences, University of Greenwich, Medway Campus, KentME4 4TB, UK
Correspondence should be addressed to Marcel Tunkumgnen Bayor; firstname.lastname@example.org
Received 21 June 2018; Accepted 30 October 2018; Published 14 November 2018
Academic Editor: Gaetano Lamberti
Caption: Figure 1: Awareness of the causes of malaria.
Caption: Figure 4: Desirable attributes of paediatric drug formulations.
Table 1: Sociodemographic distribution of the study participants. Characteristic Frequency (n) Percentage (%) Age range in years 20-30 267 35.69 1 o 256 34.23 41-50 123 18.05 51-60 64 9.22 61--70 17 2.27 70 + 3 0.54 Gender Male 303 40.51 Female 455 59.49 Marital status Single 289 38.64 Married 459 61.36 Education level Primary 74 9.89 Secondary 265 35.43 Tertiary 393 52.54 Other 16 2.14 Employment status Unemployed 159 21.26 Self-employed 279 37.30 Employed 310 41.44 Role in care giving Healthcare professional 199 26.60 Parent/guardian/caregiver 549 73.40 Table 2: Malaria treatment interventions and healthcare seeking attitude. Treatment interventions & healthcare seeking attitude Strongly agree (%) Agree (%) Malaria affected my child in the past 54.4 29.3 Malaria is deadly if not treated 79.4 14 Treatment seeking attitude I do home treatment 24.5 23.4 Use herbal drugs in home treatment 17.9 21 Drugs bought previously 17.5 24.2 Begin treatment within 24 hrs 55.6 21.1 Begin treatment after three days 6 7.8 Child will get better after sometime so I just wait 4.4 6.6 Outcome of home treatment Home treatment successful 15.8 21.7 Home treatment made illness worse 8 21.4 Home treatment failed 16.6 17.9 Reasons for seeking healthcare I expect blood test to be done at the hospital 53.5 31.7 I expect prompt action at the health facility 67.6 20.6 Source(s) of healthcare outside the home I seek healthcare at hospital/clinic 56.1 25.8 Healthcare from community health worker 16.8 31 Traditional/spiritual leaders for divination & treatment 2.1 4.8 Religious leaders for prayers 6.3 4.5 Hospital if home treatment fails 13.4 19.9 Reasons for not seeking healthcare Unnecessary delays at hospitals 25.9 24.7 Unfriendly attitude of health some workers 24.1 25.3 Long distances to health centres 13 17.5 High cost of transportation, consultation and treatment 26.3 23.7 Busy work schedules 10.4 13.2 I buy drugs from pharmacy 20.5 30.6 Treatment interventions & healthcare seeking attitude Neutral (%) Disagree (%) Malaria affected my child in the past 8.7 3.1 Malaria is deadly if not treated 3.9 1.3 Treatment seeking attitude I do home treatment 26.9 13.6 Use herbal drugs in home treatment 29.1 14.8 Drugs bought previously 26.2 15.9 Begin treatment within 24 hrs 13.6 5.2 Begin treatment after three days 22.1 26.7 Child will get better after sometime so I just wait 21.8 19.3 Outcome of home treatment Home treatment successful 44.5 9.8 Home treatment made illness worse 49.2 14 Home treatment failed 44.3 11.6 Reasons for seeking healthcare I expect blood test to be done at the hospital 8.7 3.5 I expect prompt action at the health facility 6.4 3.2 Source(s) of healthcare outside the home I seek healthcare at hospital/clinic 11.1 3.1 Healthcare from community health worker 25.8 12 Traditional/spiritual leaders for divination & treatment 11.6 18.7 Religious leaders for prayers 12.3 16.7 Hospital if home treatment fails 23.4 17 Reasons for not seeking healthcare Unnecessary delays at hospitals 26.9 10.4 Unfriendly attitude of health some workers 27.7 11.9 Long distances to health centres 37.6 18 High cost of transportation, consultation and treatment 21.5 14.2 Busy work schedules 34.1 22.6 I buy drugs from pharmacy 27.3 9.9 Treatment interventions & healthcare seeking attitude Strongly disagree (%) Malaria affected my child in the past 4.5 Malaria is deadly if not treated 1.3 Treatment seeking attitude I do home treatment 11.6 Use herbal drugs in home treatment 17.1 Drugs bought previously 16.2 Begin treatment within 24 hrs 4.4 Begin treatment after three days 37.4 Child will get better after sometime so I just wait 48 Outcome of home treatment Home treatment successful 8.3 Home treatment made illness worse 7.4 Home treatment failed 9.6 Reasons for seeking healthcare I expect blood test to be done at the hospital 2.7 I expect prompt action at the health facility 2.1 Source(s) of healthcare outside the home I seek healthcare at hospital/clinic 3.9 Healthcare from community health worker 14.3 Traditional/spiritual leaders for divination & treatment 62.7 Religious leaders for prayers 60.2 Hospital if home treatment fails 26.3 Reasons for not seeking healthcare Unnecessary delays at hospitals 12 Unfriendly attitude of health some workers 11.1 Long distances to health centres 13.9 High cost of transportation, consultation and treatment 14.3 Busy work schedules 19.7 I buy drugs from pharmacy 11.8 Table 3: Knowledge on the availability of some antimalarial drugs. Antimalarial drug Strongly agree (%) Agree (%) Chloroquine 57.5 32.8 Quinine 66 25.8 Amodiaquine 59.6 30.5 Halofantrine 17 16.7 Primaquine 12.7 16.3 Mefloquine 11.6 17.6 Artesunate 57.1 22.5 Dihydroartemisinin 18.9 23.8 Piperaquine 12.4 24.6 Sulfadoxine & Pyrimethamine 19.5 20.9 ACTs Artesunate + amodiaquine 69.5 22.5 Artemether + lumefantrine 61 25.5 Dihydroartemisinin + piperaquine 21.1 25.3 Artesunate + Mefloquine 10.8 21.4 Artesunate + Sulfadoxine & Pyrimethamine 12.2 22.2 Marketed Brands of ACTs Lonart 63.8 28.5 Coartem 57.8 29.4 Lumether 50.9 27.5 Malar- 43.3 23.7 P-Alaxin 35.3 24.9 Danmether 31 20.5 Gen-M 34.5 15.6 Antimalarial drug Neutral (%) Disagree (%) Chloroquine 5.5 1.5 Quinine 5.2 1.3 Amodiaquine 6.3 1.7 Halofantrine 41.6 13.8 Primaquine 44.1 14.6 Mefloquine 43.9 2.7 Artesunate 12.6 3.1 Dihydroartemisinin 34.4 13.2 Piperaquine 36.8 14.3 Sulfadoxine & Pyrimethamine 34.6 12.7 ACTs Artesunate + amodiaquine 4.3 1.3 Artemether + lumefantrine 8.2 2.4 Dihydroartemisinin + piperaquine 33.2 11.9 Artesunate + Mefloquine 40.1 16.8 Artesunate + Sulfadoxine & Pyrimethamine 39.3 15.6 Marketed Brands of ACTs Lonart 4.5 1.1 Coartem 7 2.5 Lumether 14.3 3.3 Malar- 19.7 7 P-Alaxin 24.5 8 Danmether 31 9 Gen-M 25.4 9.8 Antimalarial drug Strongly disagree (%) Chloroquine 2.8 Quinine 1.6 Amodiaquine 1.9 Halofantrine 11 Primaquine 12.3 Mefloquine 12.4 Artesunate 4.8 Dihydroartemisinin 9.8 Piperaquine 11.9 Sulfadoxine & Pyrimethamine 12.3 ACTs Artesunate + amodiaquine 2.4 Artemether + lumefantrine 2.9 Dihydroartemisinin + piperaquine 8.6 Artesunate + Mefloquine 10.8 Artesunate + Sulfadoxine & Pyrimethamine 10.8 Marketed Brands of ACTs Lonart 2.1 Coartem 3.3 Lumether 3.9 Malar- 6.4 P-Alaxin 7.4 Danmether 8.6 Gen-M 14.7 Table 4: Knowledge on quinine antimalarial therapy. Knowledge on quinine Strongly Agree (%) Neutral (%) antimalarial therapy agree (%) I've given quinine to a child 38.4 27.3 16 for malaria before Quinine treats both complicated 35.4 41.4 14.2 and uncomplicated malaria Quinine has a bitter taste 70.5 17.9 7.4 Quinine's bitterness is 59.1 25.7 10.6 affecting my child's acceptance I will be happy if the 71.9 16.6 7.1 bitterness can be masked Tinnitus, headache, nausea, etc. 23.3 26.2 37 appear after taking quinine Oral administration of large 58.8 24.7 10.3 volumes of quinine syrup may be difficult to achieve Knowledge on quinine Disagree (%) Strongly antimalarial therapy disagree (%) I've given quinine to a child 7.4 11 for malaria before Quinine treats both complicated 3.3 5.6 and uncomplicated malaria Quinine has a bitter taste 1.6 2.7 Quinine's bitterness is 1.2 3.5 affecting my child's acceptance I will be happy if the 1.6 2.8 bitterness can be masked Tinnitus, headache, nausea, etc. 4.9 8.6 appear after taking quinine Oral administration of large 2.5 3.6 volumes of quinine syrup may be difficult to achieve Figure 2: Knowledge of the signs and symptoms of malaria. Strongly Agree Neutral Disagree Strongly agree disagree Fever, Chills 74.9 21.9 2.4 0.4 0.4 shivering Dizziness, 73.3 22.7 3.2 0.3 0.5 headache & sweating Joints and 72.6 22.3 4.3 0.4 0.4 general body weakness Nausea, 61.4 23.9 10.8 2 1.9 vomiting & diarrhoea Cough 39.4 23.5 23.7 8.6 4.8 Loss of 67.1 25.3 6.4 0.7 0.5 appetite Anaemia 63.1 21.3 10 3.2 2.4 Note: Table made from bar graph. Figure 3: Awareness of the methods of prevention of malaria. Strongly Agreed Neutrals Disagree Strongly agreed disagreed Sleeping under 81.7 16.3 1.4 0.3 0.3 ITNs Indoor 67.1 25.7 5.1 1.3 0.7 residual spraying(IRS) Netted windows 64.9 23.6 6.6 3 2 & doors Mosquito 65.7 27 5.1 1.7 0.4 repellents & sprays Protective 58.3 21.3 7.7 7.9 4.9 Clothes Environmental 79.1 16.1 2.7 1.4 0.6 cleanliness Note: Table made from bar graph. Figure 5: Novel paediatric quinine formulations. Strongly Agree Neutral Disagree Strongly disagree disagree Fast 76.7 14.4 6.7 0.7 1.4 dissolving strips Orodispersible 26.9 3.3 28.9 4.6 6.7 tablets Xerogels 20.7 24.3 37.3 9.1 8.6 Chewable tablets 23 29.9 30 8.4 8.7 for older children good mouth feel 80.4 11.6 6.1 0.9 1 Note: Table made from bar graph.
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|Title Annotation:||Research Article|
|Author:||Yir-Erong, Bartholomew; Bayor, Marcel Tunkumgnen; Ayensu, Isaac; Gbedema, Stephen Yao; Boateng, Josh|
|Publication:||Journal of Pharmaceutics|
|Date:||Jan 1, 2018|
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