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Malawi Medical Journal logoLink to Malawi Medical Journal
. 2010 Mar;22(1):12–14. doi: 10.4314/mmj.v22i1.55901

Sentinel surveillance of Lymphatic filariasis, Schistosomiasis, Soil transmitted helminths and Malaria in rural southern Malawi

Kelias Msyamboza 1, Bagrey Ngwira 2, Richard Banda 1, Square Mkwanda 3, Bernard Brabin 4,5,6
PMCID: PMC3345679  PMID: 21618842

Abstract

Background

Baseline prevalence and knowledge, attitude and perception (KAP) survey is a prerequisite for mass drug administration for the control of Lymphatic filariasis (LF) and other neglected tropical diseases.

Methods

In preparation for the first mass drug administration for LF elimination, a baseline survey was conducted in six sentinel sites in the southern Malawi, amongst participants aged five years or more. A standard questionnaire was used to obtain data on socio-demographic factors, ownership and use of bed nets, previous ingestion of ivermectin and KAP toward hydrocele and lymphoedema. Finger prick blood samples were collected from 22:00 to 01:00 hours for LF microscopy, malaria and haemoglobin examination. Stool and urine samples were collected for internal helminths and schistosomiasis respectively.

Results

A total of 1, 903 participants were enrolled. Knowledge on the cause of hydrocele and lymphoedema was low in all the sentinel sites (16%–42%, 10%–24% (respectively). Sexual intercourse with a menstruating woman, bad weather and HIV/AIDS were perceived causes of hydrocele. Microfilaraemia prevalence was 1.5% and varied little between sentinel sites (1.0%–2.1%). Childhood urinary schistosomiasis was common in Phalombe (94.9%) and Blantyre (26.9%).

Conclusion

Integrated approach and understanding of the community KAP is vital or successful implementation of LF elimination programme.

Introduction

Lymphatic filariasis (LF) is the second most common vector-borne parasitic disease after malaria 1 and is the second commonest cause of long-term disability aftermental illness2,3. It is endemic in 83 countries, with more than 1.2 billion people at risk of infection. Some 120 million people are affected worldwide of whom about 40 million are incapacitated and disfigured by the disease4. The common manifestations of LF are hydrocele, lymphoedema and elephantiasis. One-third of people infected with LF live in India, a third in Africa and the remainder in Latin America, the Pacific Islands, Papua New Guinea and South-East Asia1. In 1997, a World Health Assembly resolution called for the elimination of LF. The strategy for LF elimination is focused on interrupting the transmission of the parasite through the use of mass drug administration (MDA), once annually for a period of four to six years5. In addition, since LF is transmitted by mosquitoes, malaria vector control interventions such as insecticide treated nets (ITNs) and in-door residual spray (IRS) are likely to play a significant role on LF elimination. Mapping in 2003 showed LF was endemic in all the districts of Malawi except Chitipa6. It is co-endemic with Onchocerciasis (Oncho) in six districts namely; Mwanza/Neno, Chikwawa, Blantyre, Thyolo, Chiradzulu, and Mulanje/Phalombe79. It is also co-endemic with soil transmitted helminths (STH) and Schistosomiasis(SCH) in these districts1013.

Based on the findings of LF mapping, Malawi qualified for free donation of Mectizan® (Ivermectin) and Albendazole from Merck & Co and GSK respectively through the Global Programme to Eliminate Lymphatic filariasis (GPELF). The Action Plan for elimination of LF was integrated with control of Onchocerciasis, SCH, STH and malaria. In the first year, integrated MDA was implemented in six districts selected because the African Programme for Onchocerciasis Control (APOC) had been operating in these since 1997 and they had well established community structures.

The aim of the present survey was to obtain baseline data on the prevalence of microfilaria, STH, SCH, anaemia and malaria parasitaemia and knowledge, attitude and perceptions of the community toward LF. The data was used for development community specific social mobilisation messages and strategies and monitoring and evaluation of the integrated mass drug administration for the control of LF, Oncho and intestinal worms. The survey was conducted in August 2008.

Materials and Methods

Six sentinel sites were selected in the six Oncho districts in the southern region using WHO guidelines14.

Individuals aged over four years were eligible. Recruitment was conducted from 18:00 hours starting with obtaining informed written consent and demographic data.

Finger prick blood samples for microfilaria were collected between 22.00 and 01.00 hours. Blood samples were collected into heparinised tubes from consenting participants by trained technicians and transported for later processing at Queen Elizabeth Central Hospital, Blantyre, or the Community Health Services Unit, Lilongwe.

In children aged 5 to 14 years, in addition to LF microscopy, a finger prick blood sample was also used for haemoglobin and malaria thick smear examination. Urine and stool samples were collected for examination for schistosomiasis and soil transmitted helminths respectively.

For LF microfilaria microscopy, a Sedgewick counting chamber was used.

Haemoglobin was measured by HemoCue® (Hb 201+ Angelholm Sweden). Malaria slides were prepared with Field's A and B stain and air dried. A malaria slide was considered negative if no asexual parasites were observed in 100 fields. Urine was centrifuged and examined for schistosoma and a wet stool preparation was examined for helminths.

Knowledge, attitudes and perceptions of the community toward LF was obtained from adults aged 15 years or more through individual interviews using a semi-structured questionnaire.

Data was entered in Microsoft excel®, Epi-Info 2004 (Centres for Disease Control and Prevention, Atlanta, Ga) and exported to SPSS (Chicago IL) for analysis. Participants under 14 years were considered children and older participants as adults. Anaemia was defined as haemoglobin <11.0g/dl.

Ethical clearance was granted by the National Health Sciences Research Committee.

Results

A total of 1, 903 participants were enrolled with sample sizes in sentinel sites ranging from 126 in (Blantyre) to 477 in (Thyolo), (table 1). The proportion of males and females were similar. Bed net ownership varied from 11% in Thyolo to 37% in Blantyre, with an average of 17.4% of respondents sleeping under a bed net in the previous night.

Table 1.

Demographic characteristics of participants

Sentinel
site
N Gender% Age % Owns bed net% ITN previous night %
Male Female 5–14 yrs > 14yrs Any ITN
Blantyre 126 60.3 39.7 43.0 57.0 37.3 29.3 18.4
Chikwawa 305 50.3 49.4 64.2 35.8 30.8 29.9 29.2
Chiradzulu 428 43.5 56.5 50.3 49.7 21.0 17.5 14.7
Mwanza 303 44.6 55.4 43.4 56.4 34.0 25.1 23.8
Phalombe 264 48.9 51.1 49.2 50.8 20.4 18.8 16.2
Thyolo 477 46.8 53.2 46.7 53.3 10.9 9.2 8.2
All 1903 47.5 52.5 49.7 50.3 23.1 19.3 17.4

Discussion

Prevalence estimates of lymphatic filiariasis were lower than expected (<3% in all the sentinel sites). Surveys using a rapid diagnostic antigen test have reported higher prevalence with an estimate of 30% in Chikwawa compared to 2.1% prevalence for the same location in the present survey 6. Use of Ivermectin in these areas as part of the Onchocerciasis Control Programme may explain the low prevalence. The observation that the mean prevalence was 1.5% for all survey sites indicates by definition that this area is endemic for LF and that MDA is justifiable.

The required sample size for sentinel site LF testing recommended by WHO is 500 participants. The lower participation in this survey is a limitation which could influence prevalence estimates. Low participation in night surveillance surveys can be problematic. The present survey was hindered by initiation ceremonies for boys (manganje) in the Blantyre area which reduced turnout as manganje was a highly valued traditional ceremony in this community. There were also fears that the survey workers might be practising ‘satanism’. In this view, the routine night travel made survey teams vulnerable to attack and armed police officers were required to escort some survey teams. Poor weather; heavy rains and cold temperatures also influenced low participation in this survey. Knowledge of the common manifestation of LF (hydrocele, lymphoedema, elephantiasis) was poor in contrast to that for manifestations of onchocerciosis (itching, skin nodules, skin thickening) which previously had been reported to be high (94%) in these six districts.15

The lack of specific local names emphasises the importance of developing and intensifying community specific information, education and communication messages in order for integrated MDA to be successful. Lack of knowledge, or misconceptions about LF, have been shown previously to be important factors associated with poor compliance in MDA programmes.1,16, 17

Anaemia was common in children surveyed with the highest prevalence in Chikwawa where malaria is endemic. Use of bed nets on the previous night was less than 40% in all sites. Malaria prevalence was highest in Masanjala (19.5%) where bed net usage on the previous night was 18.4%. S.haematobium was endemic in all sites with almost all children infected who were surveyed in Phalombe (94.9%).

Urinary schistosomiasis in Southern Malawi is a major public health problem and in a survey of 779 adolescent girls in the wet season of 2006 in Chikwawa, 28.4 % reported macroscopic haematuria (18). In contrast, soil-transmitted helminths were less common which is consistent with previous findings in children from this area who had <5% prevalence19.

In conclusion operational limitations to night survey activities may be influenced by cultural factors and therefore timing to avoid ceremonial periods is important. Endemic helminth infections in this area of southern Malawi justify the provision of MDA. Improving access to and use of bed nets must be achieved to reduce LF and malaria transmission. Improving the communities' understanding, knowledge and perceptions of the complications of filariasis, as well as other endemic parasitic diseases, is vital for developing community specific social mobilisation messages and strategies for successful implementation of a programme for elimination of lymphatic filariasis.

Acknowledgements

We are grateful to the District Health Management Teams, Surveyors and chiefs for support they rendered to the survey. We are also grateful to WHO Malawi Country Office and WHO AFRO for financial and technical support.

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