Non-adherence to iron-folic acid medications can occur in the situations or combinations thereof: late or non-initiation of the prescribed treatment, sub-optima implementation of the dosing regimen, or early discontinuation of the treatment (1). Iron deficiency is the most common nutritional disorder in the world and pregnant women are especially at risk (2).
Globally iron deficiency alone accounts for 22% of all anemia deaths. In sub-Saharan Africa, anemia contributed to approximately 28.6% of maternal deaths (4). The most common causes of anemia are poor nutrition, deficiencies of iron, micronutrient deficiencies including folic acid, vitamin A, and vitamin B12 (9). It is estimated to affect 38.2% of pregnant women globally, with the highest prevalence in the WHO regions of South-East Asia at 48.7% and Africa 46.3% (10).
Women of reproductive age are at particular risk because of menstruation, whereas pregnancy and childbirth result in a net iron loss of 580 to 680 mg because of fetal and placental requirements and bleeding during delivery, in young children, rapid expansion in red cell mass results in very high dietary iron requirements (3). It is also responsible for some pregnancy complications, such as neural tube defects, including spinal bifida and anencephaly, fetal malformation, type 2 diabetes, and obesity in the newborn (4, 5).
In Sub-Saharan Africa, the overall prevalence of ≥ 90 days of iron supplementation adherence during pregnancy was only 28.7%. Likewise, there is very low adherence to Iron Folic Acid supplementation among pregnant women, which is 11% in Ethiopia (11). One in every three women had anemia while one in every two had iron and folic acid deficiency, indicating that both folic acid and iron deficiencies constitute the major micronutrient deficiencies in Ethiopian women (8). Iron and folic acid are required for appropriate physiological function, growth, and development, as well as life maintenance. Their demand, like that of many other nutrients, rises during pregnancy, necessitating supplementation to meet daily requirements (6).
In Ethiopia, the coverage of iron supplementation during pregnancy is still low and has not fulfilled the World Health Organization (WHO) standard recommendations (12, 13). Iron folic acid intake among pregnant women is a core process indicator of the global nutrition monitoring framework that helps to halt the burden of iron deficiency anemia worldwide, especially in low-income countries including Ethiopia (7). According to the WHO and Ethiopia’s national guidelines for the control and prevention of micronutrient deficiencies, all pregnant women should receive and consume a standard dose of 60mg iron and 400 mg folic acid daily for 6 months starting from the first month of pregnancy or at the time of their first antenatal visit and three months of postnatal period (8)
Previous studies showed that pregnant women were not fully adhered to their iron folate supplement because of many factors; among factors non-adherent to iron/folate supplementation age, didn’t get nutrition counseling, and women lacking knowledge of anemia were associated with a higher likely hood of non-adherence with IFAS (14). Similarly, factors contributing to iron and folic acid non-adherence were forgetfulness, taking too many pills, not knowing the usefulness of iron and folic acid supplementation, fear of the side effects of the medication including nausea, vomiting, and unpleasant tests of the supplement (15, 16).
Also, misinformation includes; fear to give birth to a big baby, spot-on teeth of children and face of mothers, difficult delivery, not beneficial to babies, mothers experience with no history of having children with neural tube defects, and more bleeding during delivery was associated with low adherence to IFAS (17, 18). Medication non-adherence leads to poor outcomes, which then increase healthcare service utilization and overall healthcare costs (19). Women who failed to consume the iron tablets would experience iron folic acid (IFA) deficiency anemia and associated negative effects on mothers and newborns (4). This indicates the identification of determinants of non-adherence to iron-folic acid supplementation among pregnant women.
Moreover, the identification of determinants of non-adherence to iron-folic acid supplementation among pregnant could be used to take intervention and alleviate the risk of maternal anemia and fetal complication. There is limited evidence on determinants of non-adherence to Iron Folic Acid supplementation and most of the previous studies conducted in Ethiopia were focused on adherence to Iron Folic Acid supplementation and associated factors with cross-sectional study design which can determine exposure and disease at the same time. Therefore, the purpose of this study is to fill this gap and aimed to identify the determinants of non-adherence to iron-folic acid supplementation among pregnant women attending public health facilities in Bishoftu Town, Ethiopia.