- Open Access
Health worker adherence to malaria treatment guidelines at outpatient health facilities in southern Malawi following implementation of universal access to diagnostic testing
© The Author(s) 2017
- Received: 1 November 2016
- Accepted: 12 January 2017
- Published: 23 January 2017
Appropriate diagnosis and treatment are essential for reducing malaria mortality. A cross-sectional outpatient health facility (HF) survey was conducted in southern Malawi from January to March 2015 to determine appropriate malaria testing and treatment practices four years after implementation of a policy requiring diagnostic confirmation before treatment.
Enrolled patients were interviewed, examined and had their health booklet reviewed. Health workers (HWs) were asked about training, supervision and access to the 2013 national malaria treatment guidelines. HFs were assessed for malaria diagnostic and treatment capacity. Weighted descriptive analyses and logistic regression of patient, HW and HF characteristics related to testing and treatment were performed.
An evaluation of 105 HFs, and interviews of 150 HWs and 2342 patients was completed. Of 1427 suspect uncomplicated malaria patients seen at HFs with testing available, 1072 (75.7%) were tested, and 547 (53.2%) tested positive. Testing was more likely if patients spontaneously reported fever (odds ratio (OR) 2.6; 95% confidence interval (CI) 1.7–4.0), headache (OR 1.5; 95% CI 1.1–2.1) or vomiting (OR 2.0; 95% CI 1.0–4.0) to HWs and less likely if they reported skin problems (OR 0.4; 95% CI 0.2–0.6). Altogether, 511 (92.7%) confirmed cases and 98 (60.3%) of 178 presumed uncomplicated malaria patients (at HFs without testing) were appropriately treated, while 500 (96.6%) of 525 patients with negative tests did not receive anti-malarials. Only eight (5.7%) suspect severe malaria patients received appropriate pre-referral treatment. Appropriate treatment was more likely for presumed uncomplicated malaria patients (at HFs without testing) with elevated temperature (OR 1.5/1 °C increase; 95% CI 1.1–1.9), who reported fever to HWs (OR 5.7; 95% CI 1.9–17.6), were seen by HWs with additional supervision visits in the previous 6 months (OR 1.2/additional visit; 95% CI 1.0–1.4), or were seen by older HWs (OR 1.1/year of age; 95% CI 1.0–1.1).
Correct testing and treatment practices were reasonably good for uncomplicated malaria when testing was available. Pre-referral treatment for suspect severe malaria was unacceptably rare. Encouraging HWs to elicit and appropriately respond to patient symptoms may improve practices.
- Case management
- Health worker
Approximately 214 million malaria cases and 438,000 malaria deaths occurred worldwide in 2015 . Use of artemisinin-based combination therapy (ACT) for uncomplicated malaria and parenteral quinine or artemisinins for severe malaria is highly effective in preventing malaria deaths when prompt diagnosis and timely treatment is initiated . Since 2010, to better target anti-malarial treatment and more appropriately manage non-malarial fevers, the World Health Organization (WHO) has recommended diagnostic testing of all suspect malaria patients before initiating treatment . Nearly all malaria-endemic countries have updated their malaria case-management policies to reflect these recommendations and most have made rapid diagnostic tests (RDTs) for malaria widely available at health facilities (HFs). However, gaps in health worker (HW) practices based on current recommendations have been reported in a variety of settings. A recent systematic review and meta-analysis of 14 studies, 11 of which were conducted after 2010, reported that administration of appropriate malaria treatment based on RDT results ranged from 39.7% in Zambia to 99.9% in Zanzibar .
The entire population of Malawi (18 million people) is at risk for malaria . An estimated six million cases of malaria occur annually, accounting for 29% of outpatient visits across all ages and 40% of all hospitalizations among children under five years of age. Presumptive treatment of malaria among febrile patients was the norm until 2011, when the Malawi National Malaria Control Programme (NMCP) adopted the WHO recommendation to diagnostically confirm malaria cases before initiating treatment . To support this initiative, the Malawi Ministry of Health (MoH) made RDTs widely available in HFs across the country later that year. Prompt and effective case management of malaria patients is one of the key malaria control efforts in Malawi , but previous studies have indicated shortcomings in correct treatment. Prior to the widespread availability of RDTs in Malawi, a 2011 national HF survey reported that only 67% of patients with uncomplicated malaria received a prescription for the first-line ACT, artemether-lumefantrine (AL) . In addition, 31% of patients without malaria received AL , and 22% of patients with a negative microscopy test at the HF were prescribed AL .
To promote HWs’ knowledge and adherence to national malaria treatment guidelines, the NMCP has utilized a multipronged approach, including provision of in-service and refresher training, distribution of printed copies of the guidelines and periodic supportive supervision. In 2014 and 2015, HWs in Malawi received refresher training on malaria case management based on the latest malaria treatment guidelines released in July 2013. In addition to recommending testing of suspect uncomplicated malaria patients before administration of ACT, the guidelines emphasized immediate administration of rectal (primarily at community level) or parenteral artesunate or parenteral quinine as pre-referral, life-saving treatment for severe malaria at outpatient HFs .
The objective of this survey was to assess the quality of malaria case management at outpatient HFs, based on HW adherence to Malawi’s latest national malaria treatment guidelines, almost 4 years after roll-out of RDTs and several months after malaria case-management refresher training.
In addition, an evaluation of HF, HW and patient-level attributes and their associations with appropriate testing and treatment of suspect uncomplicated malaria patients was performed to identify opportunities to improve case-management quality.
Study design and data collection
This cross-sectional study was conducted in southern Malawi, a region with malaria prevalence estimates among children under 5 years old of 30%  and among 5 to 21 years olds of 60% . The survey collected baseline data for a cluster-randomized, controlled trial to evaluate the effectiveness of mobile phone text-message reminders to HWs to improve the case management of fever, pneumonia and diarrhoea. Seven of 13 districts in the region were selected if their HWs had received malaria case-management refresher training in 2014. The seven districts were: Chikwawa, Nsanje, Thyolo, Blantyre, Chiradzulu, Mulanje, and Phalombe. The majority (89%) of HFs in Malawi are operated by either the MoH or Christian Health Association of Malawi (CHAM) , and all such HFs follow the national malaria treatment guidelines. MoH facilities provide free services, while CHAM facilities require a small co-pay. The survey was performed to provide baseline data for a cluster-randomized controlled trial of text message reminders to HWs to assess their impact on HW adherence to national malaria treatment guidelines.
Only health centres and district, community or rural hospitals operated by the MoH or CHAM with a functional outpatient department (OPD), and road accessibility were included. The targeted sample size was 105 facilities based on sample sizes needed for the larger text message trial. From 22 January to 5 March, 2015, during high malaria transmission season, survey teams evaluated the 105 participating facilities and assessed HW adherence to the latest national malaria treatment guidelines. During the survey, six facilities in Chikwawa and Nsanje could not be accessed due to poor road conditions during the rainy season and were, therefore, replaced by six facilities from Phalombe district.
Data were collected by four survey teams via questionnaires in CommCare version 2.24.0 (Dimagi, Inc) using ASUS Nexus 7 Android tablets (Taipei, Taiwan). Each team visited one HF for a full day during the working week (Monday to Friday) and randomly selected one OPD (if the facility had more than one) and conducted patient exit interviews, HW interviews and HF assessments.
All patients attending selected OPDs between 08:00 and 16:00 h on the day of the survey comprised the sampling frame. Patients were screened for eligibility after selection using systematic sampling with a skip interval determined by patient volume 1 week prior, calculated to yield approximately 20 patients/HF day. The first patient within the skip interval was randomly selected. If a selected patient did not meet eligibility criteria, investigators approached the next patient using the pre-determined skip interval. Selected patients were enrolled if they met eligibility criteria which were that it was their first visit to the facility for the current illness and they or their caregivers provided written informed consent. All HWs performing clinical consultations in the selected OPDs were eligible for interviews and were assigned unique identification numbers. Enrolled patients were given study cards on which HWs placed their identification numbers and recorded patient diagnoses during the clinical encounter.
Patient exit interviews were completed at the end of the patient’s visit. Surveyors asked patients (or their caregivers) about current malaria-related symptoms spontaneously reported to the HW, whether HWs had specifically asked about the presence/history of fever, any anti-malarials they had taken at home, their clinical encounter with the HW, any laboratory tests done, and any anti-malarial medications administered, dispensed or prescribed at the HF. If ACT were dispensed to the patients, their knowledge regarding the number of ACT tablets to take for each dose, the number of doses to take per day, and the number of days to take the entire ACT course was evaluated through open-ended questions. Additional patient information was obtained from the patient’s personal health booklet, the individual health record on which their clinical encounter is typically documented at the HF. Surveyors then conducted a brief physical examination, including measurement of axillary temperature and preparation of thick and thin blood smears for subsequent reference laboratory evaluation, on every patient interviewed. If a patient reported fever, or if the surveyor-measured temperature was ≥37.5 °C and the patient had not been prescribed first-line anti-malarials by the HW, a malaria RDT (SD Bioline malaria Pf®, Standard Diagnostics, Inc, Giheng-ku, Republic of Korea) was performed by the survey team and, if positive, the first-line anti-malarial was dispensed to the patient.
At the end of the day, all HWs conducting clinical consultations in the selected OPD on the day of the survey were interviewed. They were asked about their professional training, training in malaria case management, supervision, years of clinical experience, and if they had access to a copy of the latest malaria treatment guidelines dated July 2013. A visual confirmation of the available malaria treatment guidelines was made. Finally, HF assessments were completed for each site. Survey teams asked the facility in-charge about staffing and equipment, and visually verified the presence of malaria RDTs, drug stocks, drinking water for directly observed treatment, and other equipment related to malaria case management on the day of the study.
Malaria case definitions
1. Suspect uncomplicated malaria categories by age and pregnancy status
Children <5 years of age or pregnant women in the first trimester:
History of fevera or measured axillary temperature ≥37.5 °C
Patients ≥5 years of age
History of fevera or measured axillary temperature ≥37.5 °C AND at least one additional sign or symptom suggestive of malaria (i.e., chills, muscle or joint pain, headache, vomiting, diarrhoea, weakness, nausea, dizziness, fatigue or abdominal pain)
2. Suspect severe malaria
Patients with any of the following: history of convulsions, lethargy, no urine output, jaundice, coca-cola-coloured urine, palmar pallor, or vomiting everything
For patients <5 years of age, neck stiffness or unable to drink or breastfeed were also included
Definition of outcomes
Outcomes were based on Malawi’s 2013 malaria treatment guidelines. Appropriate testing was defined as: (1) the patient presented with symptoms of suspect uncomplicated malaria (see Table 1); (2) at a facility with malaria-testing services available the day of the survey; and, (3) the patient was tested for malaria by either RDT or microscopy. Appropriate treatment was defined according to the following categories for suspect uncomplicated malaria patients: (1) attended HFs with malaria tests available, tested negative for malaria and did not receive an ACT; or (2) tested positive and received an ACT; or, (3) attended HFs without malaria tests available and received an ACT (presumptively treated for malaria). Patients were considered to have received an ACT if it had been prescribed, administered or dispensed at the HF prior to interview/enrollment in the study (to distinguish from treatments the study team initiated). Suspect severe malaria patients (see Table 1) were considered to have received appropriate treatment if they received intramuscular (IM) artesunate or IM quinine. In-patient intravenous treatment with artesunate at a larger hospital level should then follow.
Data were analysed in SAS 9.3 (SAS Institute, Inc, Cary, NC, USA) and included weighted descriptive analyses of patient-level attributes adjusting for non-response and the sampling scheme, including clustering at the HF level. In addition unweighted descriptive analyses of HW and HF attributes were performed.
To explore factors associated with appropriate testing and treatment, univariable and multivariable logistic regression modelling was conducted for each outcome, using the SURVEYLOGISTIC procedure, which accounts for the weights and complex survey design, including clustering at the HF level [12, 13]. For the multivariable analysis, plausible effect modifiers were explored using 12 interaction terms and included in the model if significant. Variables were explored as interaction terms if there was plausibility for interaction or if they had been reported as such in peer-reviewed literature. Factors were included in the multivariable model if they had a p < 0.1 in the univariable analysis. The base multivariable model was checked for collinearity and confounding. Covariates were retained in the model as confounders if the odds ratio (OR) of any variable in the base model changed by at least 20%, unless the original variables in the base model had p > 0.05 and remained non-significant after adding potential confounders.
Factors associated with appropriate testing were examined for all suspect uncomplicated malaria patients attending HFs able to test for malaria on the day of the survey visit. However, analysis of factors related to appropriate treatment was limited to presumed uncomplicated malaria patients given the lack of variability (consistently high performance) for patients with positive diagnostic tests (confirmed malaria) and negative tests (not malaria). Considering the relatively small sample size of presumed malaria patients (n = 178), the most stable model with the lowest condition index  was selected after adding different combinations of patient-, HW- and HF-level factors.
Health facility characteristics
Summary characteristics of surveyed outpatient health facilities—Southern Malawi, 2015 (N = 105)
Operation of health facility
Ministry of Health
Health facility type
Microscopy service functional for full day of survey
RDTs in stock for full day of survey
Either microscopy or RDT functional for day of surveya
Haemoglobin testing functional for full day
Infrastructure and equipment available on day of survey
Clean drinking water
Cups for administering oral medications available
Functioning hanging or standing scale
Availability of 2013 malaria treatment guidelines on day of survey
Copy of 2013 national or other reference material on malaria treatment guidelines
Wall flowchart with 2013 malaria treatment guidelines
Anti-malarial drugs in stock for the full day on day of survey
A. First-line treatment for uncomplicated malaria in pregnant women (1st trimester) and children <5 kg
B. First-line treatment for uncomplicated malaria in all other patients
At least one artemether-lumefantrine (AL) formulation
AL 1 × 6 dose-pack (regular or dispersible)
AL 2 × 6 dose-pack (regular or dispersible)
AL 3 × 6 dose-pack
AL 4 × 6 dose-pack
C. Second-line treatment for uncomplicated malaria (treatment failure or when AL is contra-indicated)
Artesunate-amodiaquine (co-formulated or co-blistered)
Any first- or second-line anti-malarial treatment for uncomplicated malaria
D. Pre-referral treatment for severe malaria
Any injectable pre-referral treatment (artesunate or quinine)
Ninety-six (91%) HFs had either the first-line (AL) or second-line (artesunate-amodiaquine (ASAQ)) ACT available for the full day of the survey. The majority of HFs (91%) had at least one AL formulation available, with individual dose-pack availability ranging from 73% for both AL 2 × 6 and AL 4 × 6 dose-packs, 79% for AL 3 × 6, to 84% for AL 1 × 6 dose-packs. ASAQ was in stock at 31% of HFs. Quinine tablets were in stock at 35%, parenteral artesunate at 84% and parenteral quinine at 89% of HFs. Nearly all HFs (98%) had at least one injectable pre-referral treatment in stock.
Health worker characteristics
Summary characteristics of health workers providing outpatient care at surveyed health facilities—Southern Malawi, 2015 (N = 150a)
Cadre of health worker caring for patients in sampled outpatient department
Medical assistant (2 years of formal training plus 1 year internship)
Clinical officer (3 years of formal training plus 1 year internship)
Nurseb (at least 3 years of formal training)
Patient attendant (no formal training)
Pharmacy technician (2 years of formal training)
Health surveillance assistant (6 weeks of formal training)
Training and guidelines
Malaria case management (in-service)c training ≥2013
Malaria case management (on-the-job)d training ≥2013
Either in-service or on-the-job malaria case management training ≥2013
Integrated management of childhood illness (IMCI) training within the last 5 years
Has a copy of the latest malaria treatment guidelines (dated ≥2013)
Received any supervision in the past 6 months
Received at least two supervisory visits in the past 6 months
Supervision visits that included observation of patient consultations
At least one supervisory visit with observation of patient consultations that involved assessing health workers’ knowledge and prescription practices of anti-malarial drugse
29.0 (26.0, 36.0)
Years of experience
4.0 (2.0, 7.0)
Characteristics and outcomes for patients who completed the exit interview—Southern Malawi, 2015
Weighted percent (95% CI)
28.3 (21.8, 34.8)
71.7 (65.2, 78.2)
Suspect malaria classification
Suspect malaria cases (both uncomplicated and severe)
73.4 (70.2, 76.6)
Suspect uncomplicated malaria
95.4 (94.2, 96.6)
Suspect severe malaria
4.6 (3.4, 5.8)
Symptoms spontaneously reported to HW by suspect malaria patients
68.5 (64.0, 73.0)
When patient did not spontaneously report fever, HW asked about fever
51.6 (46.0, 57.2)
33.4 (28.6, 38.2)
16.9 (14.3, 19.5)
5.5 (3.9, 6.9)
Testing for suspect uncomplicated malaria patients who attended HFs with diagnostic tests
Tested by either microscopy or RDT
75.7 (68.9, 82.5)
Positive RDT or microscopy
53.2 (46.0, 60.4)
Medications administered, prescribed or dispensed to confirmed uncomplicated malaria patients
Treated with first- or second-line antimalarial (AM)a
92.7 (85.4, 99.9)
Treated with other anti-malarialb
4.7 (0.0, 11.9)
2.6 (1.2, 4.0)
Medications administered, prescribed or dispensed to presumed uncomplicated malaria patients
Treated with first- or second-line AMa
60.3 (45.1, 75.5)
Treated with other anti-malarialc
2.8 (0.0, 8.3)
36.8 (22.8, 50.8)
Suspect severe malaria
Received recommended pre-referral anti-malariald
5.7 (0.3, 11.0)
Referred or told to get in-patient admission right away
6.9 (1.9, 11.9)
Received pre-referral anti-malarial plus immediate referral/admission
1.6 (0.0, 3.6)
Treated with other anti-malariale
59.6 (46.4, 72.8)
34.7 (22.4, 47.0)
Malaria testing and treatment practices among suspect malaria patients
Of 2096 patients who attended facilities with malaria testing services, 1427 (70%) had suspect uncomplicated malaria and therefore required parasitologic testing. Of those, 76% were tested, over half (53%) of whom tested positive (confirmed malaria). Although most confirmed malaria patients (93%) were appropriately treated, nearly 5% received a non-recommended anti-malarial (quinine, sulfadoxine-pyrimethamine (SP), or AL for pregnant women in the first trimester), and 3% received no anti-malarial. Of 525 patients with negative test results, 96% were not treated with any anti-malarial. Among the 29 patients who received an anti-malarial, 25 received AL, two received quinine, and two received SP (none was pregnant).
Of 246 patients who attended facilities without malaria testing services, 75% had presumed uncomplicated malaria. The first- or second-line anti-malarial was prescribed, administered or dispensed to 60% of them, 3% received SP (none was pregnant), and 37% received no anti-malarial.
Dispensing and dosing practices and patient knowledge among uncomplicated malaria patients who had an ACT dispensed at the HF
Artemisinin combination therapy (artemether-lumefantrine or artesunate-amodiaquine) dispensing, dosing and patient knowledge for uncomplicated malaria patients
Weighted percent (95% CI)
1. ACT dispensing and dosing
Total number of uncomplicated (confirmed and presumed) malaria patients
33.0 (27.2, 38.8)
Received an ACT (AL or ASAQ)a
84.9 (77.2, 92.5)
88.9 (80.1, 97.7)
ACT correctly dosed when dispensedb
94.9 (92.7, 97.2)
Type of ACT dispensed
97.2 (93.3, 100.0)
AL correctly dosed when dispensed
92.5 (88.2, 96.8)
2.8 (0.0, 6.7)
ASAQ correctly dosed when dispensedc
93.6 (3.7, 100.0)
HWs provided patients with the following ACT counselling information
First dose of ACT given at HF
16.8 (3.2, 30.3)
HW explained how to take ACT at home
91.8 (88.7, 94.8)
HW advised what to do in case of vomiting within 30 min of taking ACT
7.5 (4.8, 10.1)
HW instructed to complete all doses of ACT even if he/she feels better
60.9 (52.7, 69.1)
HW instructed to take AL with food, milk or milk containing drinkd
27.9 (20.2, 35.7)
2. Patient ACT dosing knowledge
Correct knowledge regarding all aspects of ACT dosinge
78.1 (72.3, 83.8)
Knows correct amount of ACT (tablet or syrup) to take per dose
85.9 (81.3, 90.6)
Knows total number of days to complete ACT dose
90.6 (86.8, 94.3)
Knows correct number of AL doses to take per day
89.5 (86.0, 93.0)
Most patients with uncomplicated malaria (78%) demonstrated correct knowledge regarding AL dosing, including the amount of drug per dose, the number of doses per day and the total number of days to complete the full dose for patients who received AL (Table 5).
Factors associated with appropriate testing among suspect uncomplicated malaria patients
Factors associated with appropriate testing among suspect uncomplicated malaria patients (N = 1427)
Number of patients
Number tested (weighted %)
Unadjusted OR (95% CI)
Adjusted OR (95% CI)
Patient spontaneously reported these complaints to the HW
Weighted percent (95% CI)
OR (95% CI)
Interaction term included in the model: supervision * 2013 malaria treatment guidelines available
Supervision * Guidelines
75.9 (66.1, 85.8)
2.2 (0.8, 6.6)
Supervision * No guidelines
78.8 (69.5, 88.0)
2.7 (0.9, 8.0)
No supervision * Guidelines
87.4 (77.6, 97.2)
6.2 (1.6, 24.7)
No supervision * No guidelines
56.8 (36.2, 77.4)
Interestingly, the effect of having access to a copy of the 2013 national malaria treatment guidelines on testing differed depending on whether or not the HW had had a supervision visit in the previous 6 months (Table 6). For HWs that were not supervised, the odds of testing was higher among those who had guidelines compared to those who did not. Only 57% of patients seen by HWs who were neither supervised in the previous 6 months nor possessed a copy of the guidelines were tested, compared to 76, 79 and 87% of patients seen by HWs with both supervision and guidelines, supervision but not guidelines, and guidelines but not supervision, respectively.
Of the 289 suspect uncomplicated malaria patients seen by HWs with neither supervision nor guidelines, 46 were seen by HWs whose colleagues at the facility had received some supervision or guidelines and 76% of them were tested for malaria (same testing rate for the rest of the study population). The other 243 patients were seen by HWs who either: (1) worked alone and had received neither supervision nor possessed a copy of the guidelines; or, (2) worked with other HWs who like themselves, had received neither. Only 52% of patients seen by this latter category of HWs were tested. In total, there were 18 HWs located at 16 HFs in this category. There were no observed differences between these 18 HWs and other HWs in terms of age, years of clinical experience, type of formal training, malaria-related training received, or the type of HF where they worked. Furthermore, there were no statistically significant differences in distances of these HFs where HWs had neither recent supervision nor guidelines to their respective district hospitals than between the other facilities and the district hospitals.
Factors associated with appropriate treatment among presumed uncomplicated malaria patients
Factors associated with appropriate treatment among presumed uncomplicated malaria patientsa (N = 178)
Number of patients
Number treated (weighted %)
Unadjusted OR (95% CI)
Adjusted OR (95% CI)
Patient spontaneously reported fever to the HW
Patient temperature (°C)—surveyor measured
HW age (years)
Number of supervision visits
Malaria case-management services, including both diagnostics and treatment, were widely available in outpatient HFs in southern Malawi, representing tremendous progress over the past five years. A national health facility survey in 2011, before RDTs became widely available, found that only 24% of HFs across the country had functional microscopy services and 81% had at least one AL dose-pack in stock , while in this study 90% had diagnostic services and 91% had at least one formulation of AL available. The majority of HWs were adherent to the national malaria treatment guidelines when testing for malaria, evidenced by the 76% of suspect uncomplicated malaria patients who were tested for malaria when tests were available. This proportion is similar to that reported in Kenya when both microscopy and RDT were available at HFs  but higher than that reported in many other malaria high-transmission settings since release of the WHO recommendation for universal access to malaria diagnostic testing [16–22]. Most testing was done using RDTs, likely because they were more widely available on the day of the survey, and microscopy is limited to higher-level facilities in Malawi. The widespread use of RDTs reflects their acceptability and consistent supply as a malaria diagnostic tool since they were introduced in Malawi in 2011.
HWs were more likely to test for malaria when patients spontaneously reported fever, vomiting or headache, and were less likely to test when patients reported a skin problem. A similar association between patient-reported symptoms of fever and skin problem on malaria treatment has been reported in Uganda ; in Vanuatu, patients with a main complaint of fever were more likely to get tested for malaria .
Similar to other studies in Malawi, Central African Republic and Zambia, neither supervision nor guidelines alone were associated with HW practices [23–25]. In this study, analyses identified an interaction between HW supervision in the previous 6 months and access to the latest national malaria treatment guidelines. Unlike most interactions, this did not reflect synergy between these two factors but rather that association between guidelines and testing varied by whether or not the HW received supervision. It is difficult to explain this finding with information in this study, as HWs with neither supervision nor guidelines may possess characteristics that were not measured. A further assessment of these HWs may be needed to support them better, but immediate priority should be given to ensuring that these HWs have at least regular supervision and copies of guidelines.
The vast majority of patients were seen at facilities (91%) with malaria diagnostics available on the day of the survey. When these patients tested positive for malaria, nearly all (93%) received correct treatment for malaria. In contrast, when testing was not available and patients were presumed to have malaria, treatment was sub-optimal, with only 60% of presumed malaria patients receiving a recommended treatment. This suggests that HWs make better malaria treatment decisions based on diagnostic test results. Furthermore, when HWs treated patients for malaria, they followed guidelines in selecting the recommended first- or second-line anti-malarial most of the time. In addition, HWs generally accepted negative test results: only 3% of test-negative (either RDT or microscopy) patients received an anti-malarial. This is much lower than the 31% treatment rate reported in 2011 for microscopy-negative patients  and substantially lower than treatment rates for test-negative patients in studies from Kenya, Tanzania, Uganda, and Burkina Faso [15, 26–28].
Pre-referral treatment for suspect severe malaria was extremely poor. The majority of patients were not given IM artesunate or quinine despite the fact that HWs documented a sign or symptom of severe malaria for over half of them. This is especially concerning since most HWs in the study recently received malaria case management refresher training that focused on treatment of severe malaria. Interestingly, half (53%) of suspect severe malaria patients were given an oral ACT, which may reflect a lack of awareness of severe malaria symptoms or a perception of treatment guidelines as a proposition rather than a recommendation requiring strict adherence. It is also concerning that 35% of suspect severe malaria patients did not get any anti-malarial, as mortality from untreated severe malaria approaches 100% . Pre-referral treatment for suspect severe malaria is critical for patients of all ages; adults >50 years have been reported to have a higher risk of death from severe malaria compared to children <10 years . Encouragingly, a recent study found that when patients are admitted to hospitals with a diagnosis of severe malaria they had high rates of correct treatment at 93% . However, a better understanding of why HWs rarely follow guidelines for managing severely ill patients at the outpatient level is needed.
Furthermore, when HWs did not have access to diagnostic testing, the odds of appropriate treatment increased nearly six-fold for patients who spontaneously reported history of fever to the HW. This finding was similar in Kenya . Despite all patients with suspect malaria presenting with fever or history of fever, fever was spontaneously reported to HWs by only two-thirds of suspect uncomplicated malaria patients and only half of those who did not report fever had the HW ask about it. This highlights an opportunity for targeting malaria-related public health interventions at the patient-HW interaction, encouraging patients to report fever to HWs and reminding HWs to ask about fever. Unlike other studies which have found that lower-level HWs tend to adhere to guidelines better than higher-level cadres [19, 20, 32], an association between HW cadre and malaria testing or treatment was not identified in this study.
Vomiting is a common malaria symptom, therefore having patients understand that they should take another dose in case of vomiting within half-an-hour is important in treating malaria appropriately. Only 8% of patients were advised what to do in case of vomiting within 30 min of taking the ACT. In addition, only 17% of uncomplicated malaria patients who received the drug were given the first dose at the HF. This is a missed opportunity to promote adherence to dispensed medications. Patients have been reported to be more likely to complete all the prescribed doses if they are given the first dose at the HF . Furthermore, opportunities exist in instructing patients to take AL with food and to complete all doses of the ACT even when patients feel better. This study did not explore why HWs miss these important counselling messages when dispensing ACT. With most HFs having access to clean drinking water and cups for administering oral medications on the day of the survey, it was expected that a higher proportion of patients would have taken the first dose at the HF. Perhaps HWs are not fully aware of the importance of directly observing patients taking the first dose and perhaps assume that patients will intuitively know to return to the HF for more ACT doses in case of vomiting within half-an-hour of taking the medication or the workload does not allow enough room for counseling. A thorough qualitative study to understand what drives health workers to provide counseling services may be needed to better understand this. Despite HWs not fully providing all necessary drug counselling messages, most patients expressed good understanding of the correct dosing regimen prescribed.
This study has several limitations. Survey teams did not directly observe patient-HW interactions and relied on patient report, which is subject to recall bias. However, over 95% of patients had their clinical encounter recorded in the health booklet, which was examined by the survey teams. The study was limited to seven districts in southern Malawi that had received malaria case management refresher training in 2014. The results of this study cannot be generalized to the entire nation of Malawi or to districts where HWs had not received the same malaria refresher training. However, HFs in this region are typical of other HFs across Malawi. It is therefore expected that the malaria case-management practices in this region are similar to those for the rest of the country, and previous studies have found no significant regional difference in malaria treatment practices . The presence of survey teams at HFs likely influenced HW practices even though they did not directly observe their work. This may have overestimated appropriate treatment since HWs may have been more likely to follow guidelines under assumed observation. Furthermore, the multivariable analysis for appropriate treatment was limited to 178 presumed malaria patients seen at ten HFs, a small sample size that may have underpowered the analysis.
Finally, the accuracy and validity of RDT results was not evaluated to make sure that HWs followed manufacturer instructions and that the kits were in good condition.
Malawi has shown tremendous progress in malaria case management since the ‘test-and-treat’ policy was implemented in HFs by the MoH. Most HFs have diagnostic test availability, and management of patients who test positive (confirmed malaria) or negative (not malaria) was excellent at 93 and 96%, respectively. However, there is much room for improving management of malaria, especially when testing is not available and when patient symptoms are severe. Targeting public health interventions at the patient-HW interaction to encourage patients to report history of fever to the HW and remind HWs to ask about fever or measure temperature is critical to improving both malaria testing and treatment practices in southern Malawi. In addition, the NMCP could provide extra supervision visits to HWs, offer more support to younger HWs, and eliminate RDT stock-outs by strengthening supply chain management. Finally, immediate attention should be given to improving HW recognition and pre-referral treatment of suspect severe malaria, which was vastly undertreated in this study.
LCS, AKR and DPM developed the protocol and designed the study: LCS, RJN, MK, MS, and AB oversaw data collection; DMw, DMo, AG, RJN, MK, and LCS trained survey teams in data collection; RJN, MK and LCS performed data analysis; RJN and LCS wrote the paper; RJN, DMw, DMo, AG, PT, MK, MS, AB, JVE, AKR, DPM, and LCS reviewed and approved final version of the manuscript. All authors read and approved the final manuscript.
The authors would like to acknowledge the patients and HWs that participated in the study, and the survey teams that collected data. We extend our gratitude to the Malaria Alert Centre, National Malaria Control Programme, and Ministry of Health staff who provided assistance during training and data collection. This study was funded by the President’s Malaria Initiative and the Malaria Branch at the Centers for Disease Control and Prevention through a cooperative research agreement with the Malaria Alert Centre.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used and analysed during the current study available from the corresponding author on reasonable request.
Ethics approval and consent to participate
Written informed consent was obtained from all enrolled patients and health workers before conducting interviews. Caregivers provided consent for all children under 18 years old. Assent was also obtained from seven to 17 years-old patients. Ethical approval (Approval Number 6550) was provided by the US Centers for Disease Control and Prevention (CDC) Institutional Review Board as well as the Ethical Committee of the Malawi College of Medicine.
This study was funded by the President’s Malaria Initiative and the Malaria Branch at the Centers for Disease Control and Prevention through a cooperative research agreement with the Malaria Alert Centre.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- WHO. World Malaria Report. Geneva: World Health Organization; 2015.Google Scholar
- Thwing J, Eisele TP, Steketee RW. Protective efficacy of malaria case management for preventing malaria mortality in children: a systematic review for the Lives Saved Tool. BMC Public Health. 2011;11(Suppl 3):S14.View ArticlePubMedPubMed CentralGoogle Scholar
- WHO. T3: test treat track initiative. Geneva: World Health Organization; 2012.Google Scholar
- Kabaghe AN, Visser BJ, Spijker R, Phiri KS, Grobusch MP, van Vugt M. Health workers’ compliance to rapid diagnostic tests (RDTs) to guide malaria treatment: a systematic review and meta-analysis. Malar J. 2016;15:163.View ArticlePubMedPubMed CentralGoogle Scholar
- CIA. The World Factbook. Africa: Malawi; 2016.Google Scholar
- Ministry of Health National Malaria Control Programme. Malawi malaria indicator survey 2014. Lilongwe; 2014.Google Scholar
- Steinhardt LC, Chinkhumba J, Wolkon A, Luka M, Luhanga M, Sande J, et al. Quality of malaria case management in Malawi: results from a nationally representative health facility survey. PLoS ONE. 2014;9:e89050.View ArticlePubMedPubMed CentralGoogle Scholar
- Steinhardt LC, Chinkhumba J, Wolkon A, Luka M, Luhanga M, Sande J, et al. Patient-, health worker-, and health facility-level determinants of correct malaria case management at publicly funded health facilities in Malawi: results from a nationally representative health facility survey. Malar J. 2014;3:64.View ArticleGoogle Scholar
- Ministry of Health National Malaria Control Programme. Guidelines for the treatment of malaria in Malawi. Lilongwe; 2013.Google Scholar
- Mathanga DP, Halliday KE, Jawati M, Verney A, Bauleni A, Sande J, et al. The high burden of malaria in primary school children in southern Malawi. Am J Trop Med Hyg. 2015;93:779–89.View ArticlePubMedPubMed CentralGoogle Scholar
- WHO Country cooperation strategy at a glance, Malawi. Geneva: World Health Organization; 2014.Google Scholar
- Brumback BA, Bouldin ED, Zheng HW, Cannell MB, Andresen EM. Testing and estimating model-adjusted effect-measure modification using marginal structural models and complex survey data. Am J Epidemiol. 2010;172:1085–91.View ArticlePubMedGoogle Scholar
- Siller C. The Big Four: Analyzing Complex Sample Survey Data Using SAS®, SPSS®, STATA®, and SUDAAN®. http://www2.sas.com/proceedings/sugi31/172-31.pdf. Accessed 01 May 2016.
- Liao D, Valliant R. Condition indexes and variance decompositions for diagnosing collinearity in linear model analysis of survey data. Surv Methodol. 2012;38:189–202.Google Scholar
- Zurovac D, Githinji S, Memusi D, Kigen S, Machini B, Muturi A, et al. Major improvements in the quality of malaria case-management under the “test and treat” policy in Kenya. PLoS ONE. 2014;9:e92782.View ArticlePubMedPubMed CentralGoogle Scholar
- Rowe AK, de Leon GF, Mihigo J, Santelli AC, Miller NP, Van-Dunem P. Quality of malaria case management at outpatient health facilities in Angola. Malar J. 2009;8:275.View ArticlePubMedPubMed CentralGoogle Scholar
- Masanja IM, Selemani M, Amuri B, Kajungu D, Khatib R, Kachur SP, et al. Increased use of malaria rapid diagnostic tests improves targeting of anti-malarial treatment in rural Tanzania: implications for nationwide rollout of malaria rapid diagnostic tests. Malar J. 2012;11:221.View ArticlePubMedPubMed CentralGoogle Scholar
- Mubi M, Kakoko D, Ngasala B, Premji Z, Peterson S, Bjorkman A, et al. Malaria diagnosis and treatment practices following introduction of rapid diagnostic tests in Kibaha District, Coast Region, Tanzania. Malar J. 2013;12:293.View ArticlePubMedPubMed CentralGoogle Scholar
- Zurovac D, Tibenderana JK, Nankabirwa J, Ssekitooleko J, Njogu JN, Rwakimari JB, et al. Malaria case-management under artemether-lumefantrine treatment policy in Uganda. Malar J. 2008;7:181.View ArticlePubMedPubMed CentralGoogle Scholar
- Zurovac D, Guintran JO, Donald W, Naket E, Malinga J, Taleo G. Health systems readiness and management of febrile outpatients under low malaria transmission in Vanuatu. Malar J. 2015;14:489.View ArticlePubMedPubMed CentralGoogle Scholar
- Pulford J, Kurumop SF, Ura Y, Siba PM, Mueller I, Hetzel MW. Malaria case management in Papua New Guinea following the introduction of a revised treatment protocol. Malar J. 2013;12:433.View ArticlePubMedPubMed CentralGoogle Scholar
- Bruxvoort K, Kalolella A, Nchimbi H, Festo C, Taylor M, Thomson R, et al. Getting antimalarials on target: impact of national roll-out of malaria rapid diagnostic tests on health facility treatment in three regions of Tanzania. Trop Med Int Health. 2013;18:1269–82.View ArticlePubMedPubMed CentralGoogle Scholar
- Osterholt DM, Rowe AK, Hamel MJ, Flanders WD, Mkandala C, Marum LH, et al. Predictors of treatment error for children with uncomplicated malaria seen as outpatients in Blantyre district, Malawi. Trop Med Int Health. 2006;11:1147–56.View ArticlePubMedGoogle Scholar
- Rowe AK, Hamel MJ, Flanders WD, Doutizanga R, Ndoyo J, Deming MS. Predictors of correct treatment of children with fever seen at outpatient health facilities in the Central African Republic. Am J Epidemiol. 2000;151:1029–35.View ArticlePubMedGoogle Scholar
- Zurovac D, Rowe AK. Quality of treatment for febrile illness among children at outpatient facilities in sub-Saharan Africa. Ann Trop Med Parasitol. 2006;100:283–96.View ArticlePubMedGoogle Scholar
- Reyburn H, Mbakilwa H, Mwangi R, Mwerinde O, Olomi R, Drakeley C, et al. Rapid diagnostic tests compared with malaria microscopy for guiding outpatient treatment of febrile illness in Tanzania: randomised trial. BMJ. 2007;334:403.View ArticlePubMedPubMed CentralGoogle Scholar
- Nankabirwa J, Zurovac D, Njogu JN, Rwakimari JB, Counihan H, Snow RW, et al. Malaria misdiagnosis in Uganda—implications for policy change. Malar J. 2009;8:66.View ArticlePubMedPubMed CentralGoogle Scholar
- Bisoffi Z, Sirima BS, Angheben A, Lodesani C, Gobbi F, Tinto H, et al. Rapid malaria diagnostic tests vs. clinical management of malaria in rural Burkina Faso: safety and effect on clinical decisions. A randomized trial. Trop Med Int Health. 2009;14:491–8.View ArticlePubMedGoogle Scholar
- WHO. Guidelines for the treatment of malaria. Geneva: World Health Organization; 2015.Google Scholar
- Dondorp AM, Lee SJ, Faiz MA, Mishra S, Price R, Tjitra E, et al. The relationship between age and the manifestations of and mortality associated with severe malaria. Clin Infect Dis. 2008;47:151–7.View ArticlePubMedGoogle Scholar
- Shah MP, Briggs-Hagen M, Chinkhumba J, Bauleni A, Chalira A, Moyo D, et al. Adherence to national guidelines for the diagnosis and management of severe malaria: a nationwide, cross-sectional survey in Malawi, 2012. Malar J. 2016;15:369.View ArticlePubMedPubMed CentralGoogle Scholar
- Zurovac D, Rowe AK, Ochola SA, Noor AM, Midia B, English M, et al. Predictors of the quality of health worker treatment practices for uncomplicated malaria at government health facilities in Kenya. Int J Epidemiol. 2004;33:1080–91.View ArticlePubMedGoogle Scholar
- Mace KE, Mwandama D, Jafali J, Luka M, Filler SJ, Sande J, et al. Adherence to treatment with artemether-lumefantrine for uncomplicated malaria in rural Malawi. Clin Infect Dis. 2011;53:772–9.View ArticlePubMedGoogle Scholar