dc.description.abstract |
Tanzania has high burden of morbidity and mortality caused by malaria which is the leading
cause of outpatients, inpatients, and admissions of children less than five years of age at health
facilities in the country. This burden has been attributed to increasing malaria parasite
resistance to most of the antirnalarials used as monotherapies. Tanzania has amended the
malaria treatment policy twice, the first amendment being in August 2001 when SP replaced
chloroquine and the second being in January 2007 when arternether-lumefantrine (Alu)
replaced SP for the treatment of uncomplicated malaria. The goal of the amendments was to
reduce morbidity, mortality and economic losses and to encourage rational drug use in order to
minimize the development of drug resistance. Resistance can develop if artemisisnin
combination therapies (ACTs) are used unjudiciously as in presumptive diagnosis and
treatment of malaria, which is the case in many health care facilities. There are very few
reports on the quality of clinical practices following implementation of Alu policies in Africa
in general and Tanzania in particular. Furthermore, it is not known what percentage of
children suffering from uncomplicated malaria receive ACTs on clinical grounds while in fact
they have or have no malaria as confirmed by laboratory diagnosis.
The aim of this study was to examine the quality of childhood malaria case management
practices using Alu and the accuracy of clinical malaria diagnosis in settings without
mlcroscopy .
. Health care facility-based, cross-sectional, cluster random sample survey was conducted in 17
government health facilities to examine uncomplicated malaria case management practices
using artemether-lurnefantrine in settings without microscopy in underfives in Kibaha and
Kisarawe districts.
IV
Using structured questionnaires data were collected and analysed from 916 children aged less
than 5 years who were brought to the health facilities with history of fever and/or other
symptoms of malaria. Blood smears to detect the presence of malaria parasites were taken
from the selected children and were subsequently processed and examined in the Medical
Parasitology Laboratory at Muhimbili University of Health and Allied Sciences.
Of the 916 caregivers of under five children, 469 (51.2%) sought care within 24 hours of onset
of symptoms and 572 (64.6%) knew correctly more than 3 uncomplicated malaria symptoms
in underfives. This knowledge was associated with early care seeking (OR= 1.4, 95%CI: l.2-
1.7). Moderate to high socioeconomic status was associated with increasing knowledge of
symptoms of uncomplicated malaria in underfives as well as knowledge on correct use of All!
under directly observed therapy and subsequent use at home (OR=3.6, 95%CI: l.5-9.2).
Malaria was suspected in 846 children (92.4%), 527 of whom (62.3%; 95%CI (58.9-65.6)
were appropriately managed according to IMCI and malaria treatment guidelines. Suspected
malaria cases were more likely to receive appropriate management than those who had not
been diagnosed to have malaria (OR= 36.9, 95%CI: 16 to 118). Presence of fever or history of
fever as main presenting symptom was significantly associated with the quality of
management given to the patients (OR = 20, 95%CI :6-68).
Of 723 children who were prescribed with Alu, 459 (63.5%) were properly counseled. Alu
was more likely to be prescribed in consultations by a clinical officer (OR=1.2, 95%CI: 1.06-
] .8); which took more than 5 minutes (OR=I.9, 95%CI:l.3-3.0), and where Alu alone was
available as an antimalarial (OR= 1.4, 955CI: l.05-l.8) than in consultations by non clinical
officers, which took less than 5 minutes and where alu and other antimalarials where available.
Quality of counselling was associated with the counselling by the clinical officer (OR=I.4,
95%CI: 1.2-1.5) and with the counseling by a provider with above 2 years of working
experience (OR=l.5, 95%CI: l.3-1.7).
v
Of the suspected malaria cases, 179 (26.0 %, 95%CI: 22.8-29.5) had laboratory confirmed
malaria. With PPV=26%, post-test probability of absence of disease in clinically positive
malaria = 74% and NPV = 88.5%, post-test probability of presence of malaria parasites in
clinically negative malaria = 11.5%. LR+ >1 (1.06) and LR- <1 (0.4).
Early care seeking, clinical diagnosis and treatment of malaria using Alu in underfives in
settings without microscopy has not reached the set target of appropriately managing 80%
malaria in children by 2010. A lot ofmisdiagnosis and mistreatment with antimalarials well as
omission of true cases of malaria calls for swift deployment of specific and sensitive
diagnostic facilities. |
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