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Featured researches published by Kimberly Lindblade.


Environmental Health Perspectives | 2005

Case-control study of an acute aflatoxicosis outbreak, Kenya, 2004

Eduardo Azziz-Baumgartner; Kimberly Lindblade; Karen Gieseker; Helen Schurz Rogers; Stephanie Kieszak; Henry Njapau; Rosemary L. Schleicher; Leslie F. McCoy; Ambrose Misore; Kevin M. DeCock; Carol Rubin; Laurence Slutsker

Objectives: During January–June 2004, an aflatoxicosis outbreak in eastern Kenya resulted in 317 cases and 125 deaths. We conducted a case–control study to identify risk factors for contamination of implicated maize and, for the first time, quantitated biomarkers associated with acute aflatoxicosis. Design: We administered questionnaires regarding maize storage and consumption and obtained maize and blood samples from participants. Participants: We recruited 40 case-patients with aflatoxicosis and 80 randomly selected controls to participate in this study. Evaluations/Measurements: We analyzed maize for total aflatoxins and serum for aflatoxin B1–lysine albumin adducts and hepatitis B surface antigen. We used regression and survival analyses to explore the relationship between aflatoxins, maize consumption, hepatitis B surface antigen, and case status. Results: Homegrown (not commercial) maize kernels from case households had higher concentrations of aflatoxins than did kernels from control households [geometric mean (GM) = 354.53 ppb vs. 44.14 ppb; p = 0.04]. Serum adduct concentrations were associated with time from jaundice to death [adjusted hazard ratio = 1.3; 95% confidence interval (CI), 1.04–1.6]. Case patients had positive hepatitis B titers [odds ratio (OR) = 9.8; 95% CI, 1.5–63.1] more often than controls. Case patients stored wet maize (OR = 3.5; 95% CI, 1.2–10.3) inside their homes (OR = 12.0; 95% CI, 1.5–95.7) rather than in granaries more often than did controls. Conclusion: Aflatoxin concentrations in maize, serum aflatoxin B1–lysine adduct concentrations, and positive hepatitis B surface antigen titers were all associated with case status. Relevance: The novel methods and risk factors described may help health officials prevent future outbreaks of aflatoxicosis.


International Journal of Epidemiology | 2012

Profile: The KEMRI/CDC Health and Demographic Surveillance System—Western Kenya

Frank Odhiambo; Kayla F. Laserson; Maquins Sewe; Mary J. Hamel; Daniel R. Feikin; Kubaje Adazu; Sheila Ogwang; David Obor; Nyaguara Amek; Nabie Bayoh; Maurice Ombok; Kimberly Lindblade; Meghna Desai; Feiko O. ter Kuile; Penelope A. Phillips-Howard; Anna M. van Eijk; Daniel H. Rosen; Allen W. Hightower; Peter Ofware; Hellen Muttai; Bernard L. Nahlen; Kevin M. DeCock; Laurence Slutsker; Robert F. Breiman; John M Vulule

The KEMRI/Centers for Disease Control and Prevention (CDC) Health and Demographic Surveillance System (HDSS) is located in Rarieda, Siaya and Gem Districts (Siaya County), lying northeast of Lake Victoria in Nyanza Province, western Kenya. The KEMRI/CDC HDSS, with approximately 220 000 inhabitants, has been the foundation for a variety of studies, including evaluations of insecticide-treated bed nets, burden of diarrhoeal disease and tuberculosis, malaria parasitaemia and anaemia, treatment strategies and immunological correlates of malaria infection, and numerous HIV, tuberculosis, malaria and diarrhoeal disease treatment and vaccine efficacy and effectiveness trials for more than a decade. Current studies include operations research to measure the uptake and effectiveness of the programmatic implementation of integrated malaria control strategies, HIV services, newly introduced vaccines and clinical trials. The HDSS provides general demographic and health information (such as population age structure and density, fertility rates, birth and death rates, in- and out-migrations, patterns of health care access and utilization and the local economics of health care) as well as disease- or intervention-specific information. The HDSS also collects verbal autopsy information on all deaths. Studies take advantage of the sampling frame inherent in the HDSS, whether at individual, household/compound or neighbourhood level.


Journal of Medical Entomology | 2006

Impact of Sustained Use of Insecticide-Treated Bednets on Malaria Vector Species Distribution and Culicine Mosquitoes

Kimberly Lindblade; John E. Gimnig; Luna Kamau; William A. Hawley; Frank Odhiambo; G. Olang; F.O. ter Kuile; John M. Vulule; Laurence Slutsker

Abstract Insecticide-treated bednets (ITNs) significantly reduce malaria vector populations. Susceptibility to ITNs differs by vector species, and culicine mosquitoes have not been shown to be significantly affected by the use of ITNs. We examined the impact of 2–4 yr of ITN use on malaria vector species distribution and culicine mosquitoes. Routine entomological surveillance was conducted in adjacent areas with and without ITNs from November 1999 to January 2002. Use of ITNs reduced the proportion of Anopheles gambiae Giles relative to Anopheles arabiensis Giles. The number of culicines per house was significantly lower in the ITN area than in the neighboring area. Changes in the An. gambiae sibling species distribution may help to explain apparent mosquito behavioral changes attributed to ITNs. Reductions in culicines by ITNs may have implications for community perceptions of ITN effectiveness and for control of other diseases such as lymphatic filariasis.


Tropical Medicine & International Health | 2005

Use of intermittent preventive treatment for malaria in pregnancy in a rural area of western Kenya with high coverage of insecticide-treated bed nets.

A. M. Eijk; I. E. Blokland; Laurence Slutsker; Frank Odhiambo; John G. Ayisi; H. M. Bles; Daniel H. Rosen; Kubaje Adazu; Kimberly Lindblade

Kenya established intermittent preventive treatment (IPT) with sulfadoxine‐pyrimethamine (SP) for malaria in pregnancy as national policy in 1998. We assessed the coverage of IPT among women who had recently delivered in a rural area of western Kenya with perennial malaria transmission and high coverage with insecticide treated nets (ITNs) through a cross‐sectional, community‐based survey in December 2002. Antenatal clinic (ANC) attendance was high (89.9% of the 635 participating women); 77.5% of attendees visited an ANC before the third trimester and 91.9% made more than one visit. Delivery of SP by the ANC was reported by 19.1% of all women but only 6.8% reported receiving more than one dose. Given the high rate of use of ANC services, if SP were given at each visit after the first trimester, the potential coverage of IPT (two doses of SP) would be 80.3% in this study population. ITNs were used by 82.4% of women during pregnancy, and almost all mothers (98.5%) who slept under an ITN shared the nets with their newborns after delivery. Women who thought malaria in pregnancy caused foetal problems were more likely to have used an ITN (adjusted odds ratio [AOR] 1.6, 95% confidence interval [CI] 1.0–2.4), and to have visited ANC more than once (AOR 2.4, 95% CI 1.2–4.7) compared to women who thought malaria in pregnancy was either not a problem or caused problems for the mother only. These findings illustrate the need for improved IPT coverage in this rural area. Identification and removal of the barriers to provision of IPT during ANC visits can help to increase coverage. In this area of Kenya, health messages stressing that foetal complications of malaria in pregnancy may occur in the absence of maternal illness may improve the demand for IPT.


PLOS ONE | 2014

Age-specific malaria mortality rates in the KEMRI/CDC health and demographic surveillance system in western Kenya, 2003-2010.

Meghna Desai; Ann M. Buff; Sammy Khagayi; Peter Byass; Nyaguara Amek; Annemieke van Eijk; Laurence Slutsker; John M. Vulule; Frank Odhiambo; Penelope A. Phillips-Howard; Kimberly Lindblade; Kayla F. Laserson; Mary J. Hamel

Recent global malaria burden modeling efforts have produced significantly different estimates, particularly in adult malaria mortality. To measure malaria control progress, accurate malaria burden estimates across age groups are necessary. We determined age-specific malaria mortality rates in western Kenya to compare with recent global estimates. We collected data from 148,000 persons in a health and demographic surveillance system from 2003–2010. Standardized verbal autopsies were conducted for all deaths; probable cause of death was assigned using the InterVA-4 model. Annual malaria mortality rates per 1,000 person-years were generated by age group. Trends were analyzed using Poisson regression. From 2003–2010, in children <5 years the malaria mortality rate decreased from 13.2 to 3.7 per 1,000 person-years; the declines were greatest in the first three years of life. In children 5–14 years, the malaria mortality rate remained stable at 0.5 per 1,000 person-years. In persons ≥15 years, the malaria mortality rate decreased from 1.5 to 0.4 per 1,000 person-years. The malaria mortality rates in young children and persons aged ≥15 years decreased dramatically from 2003–2010 in western Kenya, but rates in older children have not declined. Sharp declines in some age groups likely reflect the national scale up of malaria control interventions and rapid expansion of HIV prevention services. These data highlight the importance of age-specific malaria mortality ascertainment and support current strategies to include all age groups in malaria control interventions.


American Journal of Tropical Medicine and Hygiene | 2011

Molecular Insights for Giardia, Cryptosporidium, and Soil-Transmitted Helminths from a Facility-Based Surveillance System in Guatemala

Daniel E. Velasquez; Wences Arvelo; Vitaliano Cama; Beatriz López; Lissette Reyes; Dawn M. Roellig; Geoffrey Kahn; Kimberly Lindblade

We molecularly characterized samples with Giardia, Cryptosporidium, and soil-transmitted helminths from a facility-based surveillance system for diarrhea in Santa Rosa, Guatemala. The DNA sequence analysis determined the presence of Giardia assemblages A (N = 7) and B (N = 12) and, Cryptosporidium hominis (N = 2) and Cryptosporidium parvum (N = 2), suggestive of different transmission cycles. All 41 samples with soil-transmitted helminths did not have the β-tubulin mutation described for benzimidazole resistance, suggesting potential usefulness in mass drug administration campaigns.


BMC Public Health | 2016

The effectiveness of non-pyrethroid insecticide-treated durable wall lining to control malaria in rural Tanzania: study protocol for a two-armed cluster randomized trial

George Mtove; Joseph P. Mugasa; Louisa A. Messenger; Robert Malima; Peter Mangesho; Franklin Magogo; Mateusz M. Plucinski; Ramadhan Hashimu; Johnson Matowo; Donald S. Shepard; Bernard Batengana; Jackie Cook; Basiliana Emidi; Yara A. Halasa; Robert Kaaya; Aggrey Kihombo; Kimberly Lindblade; Geofrey Makenga; Robert Mpangala; Abraham Mwambuli; Ruth Mzava; Abubakary Mziray; George Olang; Richard M. Oxborough; Mohammed Seif; Edward Sambu; Aaron Samuels; Wema Sudi; John Thomas; Sophie Weston


Archive | 2012

Profile: The KEMRI/CDC Health and Demographic Surveillance System—Western

Frank Odhiambo; Kayla F. Laserson; Mary J. Hamel; Daniel R. Feikin; Kubaje Adazu; Sheila Ogwang; David Obor; Nyaguara Amek; Nabie Bayoh; Maurice Ombok; Kimberly Lindblade; Meghna Desai; Penelope A. Phillips-Howard; Daniel H. Rosen; Allen W. Hightower; Peter Ofware; Bernard L. Nahlen; Laurence Slutsker; Robert F. Breiman; John M. Vulule


International Journal of Infectious Diseases | 2010

Population-based surveillance for 2009 pandemic influenza A H1N1 Virus in Guatemala, 2009

Wences Arvelo; Lissette Reyes; Alejandra Estevez; Jennifer Gray; Steve Lindstrom; Alicia M. Fry; Sonja J. Olsen; F. Ardon; Gal Frenkel; B. Gordillo; Kimberly Lindblade


International Journal of Infectious Diseases | 2010

The epidemiology of rotavirus disease among children <5 years of age - Santa Rosa, Guatemala, 2007-2009

Jennifer E. Cortes; Wences Arvelo; B. lopez; Lissette Reyes; B. Gordillo; Umesh D. Parashar; Kimberly Lindblade

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Laurence Slutsker

Centers for Disease Control and Prevention

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Frank Odhiambo

Kenya Medical Research Institute

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Mary J. Hamel

Centers for Disease Control and Prevention

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Bernard L. Nahlen

United States Department of Health and Human Services

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John M. Vulule

Kenya Medical Research Institute

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Kubaje Adazu

Kenya Medical Research Institute

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Nyaguara Amek

Kenya Medical Research Institute

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Daniel H. Rosen

Centers for Disease Control and Prevention

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John E. Gimnig

Centers for Disease Control and Prevention

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Kayla F. Laserson

Centers for Disease Control and Prevention

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