Irene Marete
Moi University
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Featured researches published by Irene Marete.
BMC Pregnancy and Childbirth | 2012
Peter Gisore; Evelyn Shipala; Kevin Otieno; Betsy Rono; Irene Marete; Constance Tenge; Hillary Mabeya; Sherri Bucher; Janet Moore; Edward A. Liechty; Fabian Esamai
BackgroundIdentifying every pregnancy, regardless of home or health facility delivery, is crucial to accurately estimating maternal and neonatal mortality. Furthermore, obtaining birth weights and other anthropometric measurements in rural settings in resource limited countries is a difficult challenge. Unfortunately for the majority of infants born outside of a health care facility, pregnancies are often not recorded and birth weights are not accurately known. Data from the initial 6 months of the Maternal and Neonatal Health (MNH) Registry Study of the Global Network for Women and Childrens Health study area in Kenya revealed that up to 70% of newborns did not have exact weights measured and recorded by the end of the first week of life; nearly all of these infants were born outside health facilities.MethodsTo more completely obtain accurate birth weights for all infants, regardless of delivery site, village elders were engaged to assist in case finding for pregnancies and births. All elders were provided with weighing scales and mobile phones as tools to assist in subject enrollment and data recording. Subjects were instructed to bring the newborn infant to the home of the elder as soon as possible after birth for weight measurement.The proportion of pregnancies identified before delivery and the proportion of births with weights measured were compared before and after provision of weighing scales and mobile phones to village elders. Primary outcomes were the percent of infants with a measured birth weight (recorded within 7 days of birth) and the percent of women enrolled before delivery.ResultsThe recorded birth weight increased from 43 ± 5.7% to 97 ± 1.1. The birth weight distributions between infants born and weighed in a health facility and those born at home and weighed by village elders were similar. In addition, a significant increase in the percent of subjects enrolled before delivery was found.ConclusionsPregnancy case finding and acquisition of birth weight information can be successfully shifted to the community level.
Journal of the Pediatric Infectious Diseases Society | 2013
Matthew Turissini; Winstone M. Nyandiko; Samuel Ayaya; Irene Marete; Ann Mwangi; Victor Chemboi; Lucy Warui; Rachel C. Vreeman
BACKGROUND As antiretroviral therapy (ART) allows the worlds 2.3 million human immunodeficiency virus (HIV)-infected children to grow and thrive, these children need to be informed of their HIV status. Neither the prevalence of disclosure to children nor its impact has been evaluated in most resource-limited settings. METHODS We conducted a prospective assessment of a random sample of HIV-infected children ages 6-14 years enrolled in HIV care at a large referral clinic in Eldoret, Kenya. Clinicians administered questionnaires to children and caregivers independently at routine clinic visits to assess disclosure status, ART adherence, stigma, and depression. Childrens demographic and clinical characteristics were extracted from chart review. We calculated descriptive statistics and performed logistic regression to assess the association between disclosure and other characteristics. RESULTS Two hundred seventy children-caregiver dyads completed questionnaires. The mean child age was 9.3 years (standard deviation 2.6); 49% were male, and 42% were orphans. 11.1% of children had been informed of their HIV status (N = 30). Of those under 10 years, 3.3% knew their status, whereas 9.2% of 10- to 12-year-olds and 39.5% of 13- to 14-year-olds knew they had HIV. Only age was significantly associated with disclosure status in both bivariate analyses (P < .0001) and multiple logistic regression (odds ratio 1.67, 95% confidence interval 1.36-2.05) when considering social demographics, disease stage variables, adherence, stigma measures, and depression. CONCLUSIONS Rates of informing children in western Kenya of their HIV status are low, even among older children. Guiding families through developmentally appropriate disclosure processes should be a key facet of long-term pediatric HIV management.
British Journal of Obstetrics and Gynaecology | 2018
Elizabeth M. McClure; Ana Garces; Sarah Saleem; Janet Moore; Carl Bose; Fabian Esamai; Shivaprasad S. Goudar; Elwyn Chomba; Musaku Mwenechanya; Omrana Pasha; A Tshefu; Ashlesha Patel; Sangappa M. Dhaded; Constance Tenge; Irene Marete; Melissa Bauserman; S Sunder; Bhalchandra S. Kodkany; Wally A. Carlo; Richard J. Derman; Patricia L. Hibberd; Edward A. Liechty; K. M. Hambidge; Nancy F. Krebs; Marion Koso-Thomas; Menachem Miodovnik; Dennis Wallace; Robert L. Goldenberg
We sought to classify causes of stillbirth for six low‐middle‐income countries using a prospectively defined algorithm.
Reproductive Health | 2015
Irene Marete; Constance Tenge; Carolyne Chemweno; Sherri Bucher; Omrana Pasha; Umesh Ramadurg; Shivanand C Mastiholi; Melody Chiwila; Archana Patel; Fernando Althabe; Ana Garces; Janet Moore; Edward A. Liechty; Richard J. Derman; Patricia L. Hibberd; K. Michael Hambidge; Robert L. Goldenberg; Waldemar A. Carlo; Marion Koso-Thomas; Elizabeth M. McClure; Fabian Esamai
BackgroundIt is important when conducting epidemiologic studies to closely monitor lost to follow up (LTFU) rates. A high LTFU rate may lead to incomplete study results which in turn can introduce bias to the trial or study, threatening the validity of the findings. There is scarce information on LTFU in prospective community-based perinatal epidemiological studies. This paper reports the rates of LTFU, describes socio-demographic characteristics, and pregnancy/delivery outcomes of mothers LTFU in a large community-based pregnancy registry study.MethodsData were from a prospective, population-based observational study of the Global Network for Womens and Childrens Health Research Maternal Newborn Health Registry (MNHR). This is a multi-centre, international study in which pregnant women were enrolled in mid-pregnancy, followed through parturition and 42 days post-delivery. Risk for LTFU was calculated within a 95%CI.ResultsA total of 282,626 subjects were enrolled in this study, of which 4,893 were lost to follow-up. Overall, there was a 1.7% LTFU to follow up rate. Factors associated with a higher LTFU included mothers who did not know their last menstrual period (RR 2.2, 95% CI 1.1, 4.4), maternal age of < 20 years (RR 1.2, 95% CI 1.1, 1.3), women with no formal education (RR 1.2, 95% CI 1.1, 1.4), and attending a government clinic for antenatal care (RR 2.0, 95% CI 1.4, 2.8). Post-natal factors associated with a higher LTFU rate included a newborn with feeding problems (RR 1.6, 94% CI 1.2, 2.2).ConclusionsThe LTFU rate in this community-based registry was low (1.7%). Maternal age, maternal level of education, pregnancy status at enrollment and using a government facility for ANC are factors associated with being LTFU. Strategies to ensure representation and high retention in community studies are important to informing progress toward public health goals.Trial registrationRegistration at the Clinicaltrials.gov (ID# NCT01073475).
Reproductive Health | 2015
Sherri Bucher; Irene Marete; Constance Tenge; Edward A. Liechty; Fabian Esamai; Archana Patel; Shivaprasad S. Goudar; Bhalchandra S. Kodkany; Ana Garces; Elwyn Chomba; Fernando Althabe; Mabel Barreuta; Omrana Pasha; Patricia L. Hibberd; Richard J. Derman; Kevin Otieno; K. Michael Hambidge; Nancy F. Krebs; Waldemar A. Carlo; Carolyne Chemweno; Robert L. Goldenberg; Elizabeth M. McClure; Janet Moore; Dennis Wallace; Sarah Saleem; Marion Koso-Thomas
BackgroundThe Global Network for Women’s and Children’s Health Research is one of the largest international networks for testing and generating evidence-based recommendations for improvement of maternal-child health in resource-limited settings. Since 2009, Global Network sites in six low and middle-income countries have collected information on antenatal care practices, which are important as indicators of care and have implications for programs to improve maternal and child health. We sought to: (1) describe the quantity of antenatal care attendance over a four-year period; and (2) explore the quality of coverage for selected preventative, screening, and birth preparedness components.MethodsThe Maternal Newborn Health Registry (MNHR) is a prospective, population-based birth and pregnancy outcomes registry in Global Network sites, including: Argentina, Guatemala, India (Belgaum and Nagpur), Kenya, Pakistan, and Zambia. MNHR data from these sites were prospectively collected from January 1, 2010 – December 31, 2013 and analyzed for indicators related to quantity and patterns of ANC and coverage of key elements of recommended focused antenatal care. Descriptive statistics were generated overall by global region (Africa, Asia, and Latin America), and for each individual site.ResultsOverall, 96% of women reported at least one antenatal care visit. Indian sites demonstrated the highest percentage of women who initiated antenatal care during the first trimester. Women from the Latin American and Indian sites reported the highest number of at least 4 visits. Overall, 88% of women received tetanus toxoid. Only about half of all women reported having been screened for syphilis (49%) or anemia (50%). Rates of HIV testing were above 95% in the Argentina, African, and Indian sites. The Pakistan site demonstrated relatively high rates for birth preparation, but for most other preventative and screening interventions, posted lower coverage rates as compared to other Global Network sites.ConclusionsResults from our large, prospective, population-based observational study contribute important insight into regional and site-specific patterns for antenatal care access and coverage. Our findings indicate a quality and coverage gap in antenatal care services, particularly in regards to syphilis and hemoglobin screening. We have identified site-specific gaps in access to, and delivery of, antenatal care services that can be targeted for improvement in future research and implementation efforts.Trial registrationRegistration at Clinicaltrials.gov (ID# NCT01073475)
American Journal of Perinatology | 2013
Irene Marete; Constance Tenge; Omrana Pasha; Shivaprasad S. Goudar; Elwyn Chomba; Archana Patel; Fernando Althabe; Ana Garces; Elizabeth M. McClure; Sarah Saleem; Fabian Esamai; Bhala Kodkany; José M. Belizán; Richard J. Derman; Patricia L. Hibberd; Nancy F. Krebs; Pierre Buekens; Robert L. Goldenberg; Waldemar A. Carlo; Dennis Wallace; Janet Moore; Marion Koso-Thomas; Linda L. Wright; Edward A. Liechty
AIM To determine the rates of multiple gestation, stillbirth, and perinatal and neonatal mortality and to determine health care system characteristics related to perinatal mortality of these pregnancies in low- and middle-income countries. METHODS Pregnant women residing within defined geographic boundaries located in six countries were enrolled and followed to 42 days postpartum. RESULTS Multiple gestations were 0.9% of births. Multiple gestations were more likely to deliver in a health care facility compared with singletons (70 and 66%, respectively, p < 0.001), to be attended by skilled health personnel (71 and 67%, p < 0.001), and to be delivered by cesarean (18 versus 9%, p < 0.001). Multiple-gestation fetuses had a relative risk (RR) for stillbirth of 2.65 (95% confidence interval [CI] 2.06, 3.41) and for perinatal mortality rate (PMR) a RR of 3.98 (95% CI 3.40, 4.65) relative to singletons (both p < 0.0001). Neither delivery in a health facility nor the cesarean delivery rate was associated with decreased PMR. Among multiple-gestation deliveries, physician-attended delivery relative to delivery by other health providers was associated with a decreased risk of perinatal mortality. CONCLUSIONS Multiple gestations contribute disproportionately to PMR in low-resource countries. Neither delivery in a health facility nor the cesarean delivery rate is associated with improved PMR.
African Health Sciences | 2013
Peter Gisore; B. Rono; Irene Marete; J. Nekesa-Mangeni; Constance Tenge; Evelyn Shipala; Hillary Mabeya; D. Odhiambo; Kevin Otieno; Sherri Bucher; C. Makokha; Edward Liechty; Fabian Esamai
BACKGROUND Mortality of mothers and newborns is an important public health problem in low-income countries. In the rural setting, implementation of community based education and mobilization are strategies that have sought to reduce these mortalities. Frequently such approaches rely on volunteers within each community. OBJECTIVE To assess the perceptions of the community volunteers in rural Kenya as they implemented the EmONC program and to identify the incentives that could result in their sustained engagement in the project. METHOD A community-based cross sectional survey was administered to all volunteers involved in the study. Data were collected using a self-administered supervision tool from all the 881 volunteers. RESULTS 881 surveys were completed. 769 respondents requested some form of incentive; 200 (26%) were for monetary allowance, 149 (19.4%) were for a bicycle to be used for transportation, 119 (15.5%) were for uniforms for identification, 88 (11.4%) were for provision of training materials, 81(10.5%) were for training in Home based Life Saving Skills (HBLSS), 57(7.4%) were for provision of first AID kits, and 39(5%) were for provision of training more facilitators, 36(4.7%) were for provision of free medication. CONCLUSION Monetary allowances, improved transportation and some sort of identification are the main incentives cited by the respondents in this context.
AIDS | 2015
Rachel C. Vreeman; Michael L. Scanlon; Thomas S. Inui; Carole I. McAteer; Lydia J. Fischer; Megan S. McHenry; Irene Marete; Winstone M. Nyandiko
Objective:We sought to better understand how social factors shape HIV disclosure to children from the perspective of caregivers and HIV-infected children in Kenya. Design:We conducted a qualitative study using focus group discussions (FGDs) to gain perspectives of caregivers and children on the social environment for HIV disclosure to children in western Kenya. FGDs were held with caregivers who had disclosed the HIV status to their child and those who had not, and with HIV-infected children who knew their HIV status. Methods:FGD transcripts were translated into English, transcribed, and analyzed using constant comparison, progressive coding, and triangulation to arrive at a contextualized understanding of social factors influencing HIV disclosure. Results:Sixty-one caregivers of HIV-infected children participated in eight FGDs, and 23 HIV-infected children participated in three FGDs. Decisions around disclosure were shaped by a complex social environment that included the caregiver–child dyad, family members, neighbors, friends, schools, churches, and media. Whether social actors demonstrated support or espoused negative beliefs influenced caregiver decisions to disclose. Caregivers reported that HIV-related stigma was prominent across these domains, including stereotypes associating HIV with sexual promiscuity, immorality, and death, which were tied to caregiver fears about disclosure. Children also recognized stigma as a barrier to disclosure, but were less specific about the social and cultural stereotypes cited by the caregivers. Conclusion:In this setting, caregivers and children described multiple actors who influenced disclosure, mostly due to stigmatizing beliefs about HIV. Better understanding the social factors impacting disclosure may improve the design of support services for children and caregivers.
Journal of the International AIDS Society | 2016
Carole I. McAteer; Nhan Ai Thi Truong; Josephine Aluoch; Andrew Roland Deathe; Winstone M. Nyandiko; Irene Marete; Rachel C. Vreeman
HIV‐related stigma impacts the quality of life and care management of HIV‐infected and HIV‐affected individuals, but how we measure stigma and its impact on children and adolescents has less often been described.
BMC Pregnancy and Childbirth | 2016
Sherri Bucher; Olive Konana; Edward A. Liechty; Ana Garces; Peter Gisore; Irene Marete; Constance Tenge; Evelyn Shipala; Linda L. Wright; Fabian Esamai
BackgroundThe high rate of home deliveries conducted by unskilled birth attendants in resource-limited settings is an important global health issue because it is believed to be a significant contributing factor to maternal and newborn mortality. Given the large number of deliveries that are managed by unskilled or traditional birth attendants outside of health facilities, and the fact that there is on-going discussion regarding the role of traditional birth attendants in the maternal newborn health (MNH) service continuum, we sought to ascertain the practices of traditional birth attendants in our catchment area. The findings of this descriptive study might help inform conversations regarding the roles that traditional birth attendants can play in maternal-newborn health care.MethodsA structured questionnaire was used in a survey that included one hundred unskilled birth attendants in western Kenya. Descriptive statistics were employed.ResultsInappropriate or outdated practices were reported in relation to some obstetric complications and newborn care. Encouraging results were reported with regard to positive relationships that traditional birth attendants have with their local health facilities. Furthermore, high rates of referral to health facilities was reported for many common obstetric emergencies and similar rates for reporting of pregnancy outcomes to village elders and chiefs.ConclusionsPotentially harmful or outdated practices with regard to maternal and newborn care among traditional birth attendants in western Kenya were revealed by this study. There were high rates of traditional birth attendant referrals of pregnant mothers with obstetric complications to health facilities. Policy makers may consider re-educating and re-defining the roles and responsibilities of traditional birth attendants in maternal and neonatal health care based on the findings of this survey.