2.Intestinal parasitic infections and anaemia among pregnant women in the highlands of Papua New Guinea.
Phuanukoonnon S ; Michael A ; Kirarock WS ; Pomat WS ; van den Biggelaar AH.
Papua New Guinea medical journal 2013;56(3-4):119-125
This study determined the prevalence of intestinal parasitic infections and associations with risk factors among pregnant women in their second or third trimester in Goroka, Eastern Highlands Province, Papua New Guinea. Among the 201 pregnant women enrolled in this study, 163 (81%) were infected with one or more intestinal parasites. Infections with protozoan parasites (65%) were more prevalent than infections with nematodes (31%); protozoan infections included Entamoeba histolytica (43%), Giardia lamblia (39%) and Pentatrichomonas hominis (14%), and nematode infections included hookworm (18%), Ascaris lumbricoides (14%), Strongyloides stercoralis (3%) and Trichuris trichiura (2%). Factors associated with higher risk of intestinal parasitic infections in pregnancy included being a primigravida for protozoan-only infections and education limited to primary school for nematode infections. Altitude-adjusted haemoglobin levels were assessed at the beginning of labour for 110 women, with 69 (63%) found to be anaemic (haemoglobin < 11 g/dl). There were no associations found between being infected in pregnancy and anaemia.
Adult
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Anemia/*epidemiology
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Feces/parasitology
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Female
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Humans
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Intestinal Diseases, Parasitic/*epidemiology
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Papua New Guinea/epidemiology
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Pregnancy
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Pregnancy Complications, Parasitic/*epidemiology
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Prevalence
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Risk Factors
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Surveys and Questionnaires
3.A neonatal pneumococcal conjugate vaccine trial in Papua New guinea: study population, methods and operational challenges.
Phuanukoonnon S ; Reeder JC ; Pomat WS ; Van den Biggelaar AH ; Holt PG ; Saleu G ; Opa C ; Michael A ; Aho C ; Yoannes M ; Francis J ; Orami T ; Namuigi P ; Siba PM ; Richmond PC ; Lehmann D.
Papua New Guinea medical journal 2010;53(3-4):191-206
Infants in Papua New Guinea (PNG) are at a high risk of invasive pneumococcal disease, and a substantial burden of this falls on children less than six months old. PNG is planning to introduce a pneumococcal conjugate vaccine for infants in the near future, but to make the maximum impact neonatal immunization will have to be considered. To provide evidence on safety and immunogenicity for neonatal and early infant immunization, we undertook an open randomized controlled trial of 7-valent pneumococcal conjugate vaccine (7vPCV). 318 children received 7vPCV at ages 0, 1 and 2 months or at 1, 2 and 3 months or not at all. All children received 23-valent pneumococcal polysaccharide vaccine at age 9 months. This was a large and complex trial: village reporters visited participants weekly during the first year and fortnightly for a further 6 months and nurses monitored self-reported morbidity and collected many thousands of biological samples. The study team was remarkably successful in achieving the study aims, with 18-month follow-up completed on 77% of enrolled children and over 80% of scheduled samples collected. While the results of the trial will be reported elsewhere, this paper discusses the design of the study and dissects out some of the main reasons for its successful completion. Strong community engagement was an essential factor in success and the principles of equitable partnership and service provision led to a strong research partnership. A two-stage consent process, comprising primary assent followed by later informed consent, led to a high drop-out before initial enrolment, but an outstanding retention of those enrolled in the study. We conclude that factors such as strong community participation, reciprocity and a good relationship between the study team and participants are just as important as the technical elements of laboratory testing and data handling in ensuring the success of a vaccine trial in PNG.