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AnPREG
Causes and Impact of Anemia on Pregnancy Outcome on the Thai-Myanmar Border: Retrospective Analysis
Sponsor study identifier
observational
13,520
1 country
1
Study Start
July 20, 2017
Actual (reported)Primary Completion
July 20, 2017
Actual (reported)Study Completion
July 20, 2018
Actual (reported)The global burden of maternal morbidity and mortality attributable to anemia is staggering, and this is especially true in low-resource settings. A recent review suggests 42% of pregnant women have anemia worldwide (1993-2005) with the vast majority of anemic women (90%) residing in Africa or Asia1; and in Asia, anemia was the second highest cause of maternal mortality2. Anemia was diagnosed in almost one third to one half of women presenting to the Shoklo Malaria Research Unit (SMRU) clinics on the Thai-Myanmar border for antenatal care (ANC) in a 2008 survey3, and anemia at first antenatal visit was associated with a two-fold increase in maternal mortality in this population4. Studies have also shown an association between anemia and small for gestational age infants, preterm delivery, infant and childhood anemia and developmental delays5. The anemia in pregnant women presenting to SMRU clinics is multifactorial, as hemoglobinopathies, Glucose-6-dehydrogenase (G6PD) deficiency, iron, folic acid and B12 deficiency, helminth infection, and malaria are all prevalent in this rural population. Though all of these pathologies can cause anemia, they require different and sometimes conflicting treatment and prevention strategies, interacting in a complex web of causes and effects. Iron supplementation is the mainstay of most anemia control programs, but some women with hemoglobinopathies suffer from potentially fatal iron overload6. Iron supplementation has also been associated with increased risk of malaria7. Some helminth infections are associated with increased rates of anemia and malaria, but others may be protective8. Malaria and G6PD deficiency have complex effects on one another, and some malaria treatments can cause acute and life-threatening hemolysis in G6PD deficient individuals9. Given the high prevalence and diverse causes of anemia in this population, and its potentially dire effects on maternal and infant health and survival, SMRU implemented increased clinical testing for pregnant women in 2012 to inform clinical care at the individual level. Further analysis of these data is urgently needed to improve care on a population scale. We propose to review existing data from ANC records to determine the causes and effects of anemia in this population, and use this information to improve treatment and prevention guidelines. Results would be integrated rapidly into local practice with the potential to have profound impacts on maternal and child health in this region.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
July 20, 2018
Actual (reported)Click on a node to explore related trials.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
May 30, 2017
Actual (reported)June 2, 2017
Actual (reported)July 20, 2017
Actual (reported)July 20, 2017
Actual (reported)July 20, 2018
Actual (reported)Hematology
The contribution of thalassemia/other inherited red blood cell (IRBC) abnormalities to anemia in pregnant refugee and migrant Myanmar women attending antenatal clinics in a low resource setting.
1 year
Hematology
1 year
Serum ferritin
1 year
The risk of maternal morbidities
1 year
Data from approximately 15,548 new pregnant women enrolled to antenatal care from antenatal care (ANC) services of Shoklo Malaria Research Unit (SMRU) clinics during August 2012 to 31-Dec-2016.
Shoklo Malaria Research Unit
Mae Sot, Changwat Tak, 63110, Thailand
13,520 participants (actual enrollment reported by the registry).
First Submitted
May 30, 2017
First Posted
June 2, 2017
Study Start
July 20, 2017
Actual (reported)Contact the study team to confirm eligibility.
Primary Completion
July 20, 2017
Actual (reported)Study Completion
July 20, 2018
Actual (reported)Last Updated
August 31, 2018
Record last verified: 2017-08
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Source: ClinicalTrials.gov.
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