Key result
Administering a loading dose of magnesium sulphate at primary care facilities significantly increased the likelihood of patients defaulting from the referral process (adjusted OR 9.27) compared to standard care.
Why the study?
Does administering a loading dose of magnesium sulphate at primary care facilities improve maternal and fetal outcomes in pregnant women with severe pre-eclampsia and eclampsia?
Cohort (n=150)
Open-label
Yes
Does administering a loading dose of magnesium sulphate at primary care facilities improve maternal and fetal outcomes in pregnant women with severe pre-eclampsia and eclampsia?
Odds Ratio: 9.27 (95% CI 3.2–26.85)
Absolute Event Rate: 90.2% vs 55.9%
p-value: p=<0.05
Administering a loading dose of magnesium sulphate for severe pre-eclampsia and eclampsia at primary care facilities is feasible and safe, but it may paradoxically increase the rate of patients defaulting on subsequent referral to higher-level care.
May discourage pre-referral magnesium loading due to higher defaulting; leaves open net maternal-fetal outcome benefits.
Background: Evidence has shown that Magnesium Sulphate (MgSo4) is the gold standard for treating severe pre-eclampsia and eclampsia (SPE/E), and calls for its widespread use at all levels of health service delivery, including the primary care level. Objective: To determine if administering loading dose of MgSo4 on pregnant women with severe preeclampsia and eclampsia at primary care level would improve maternal and fetal outcomes. Method: Two sets of Primary Health Care (PHC) facilities were identified; one served as experimental one and the other as control. The community health extension workers (CHEWs) and the community health officers (CHOs) at the experimental PHCs were trained to administer the loading dose of MgSo4 for patients with SPE/E, in addition to other supportive treatments, before making a referral while the control PHCs did not give MgSo4, and neither administered diazepam as an alternative or no anti-convulsant at all, before making a referral to higher centers. Patients from the experimental and control facilities were prospectively monitored for fetal and maternal outcomes, namely maternal and fetal deaths, and for toxic effects of MgSo4 in the experimental arm. Results: Of the 150 patients recruited, 82 (55%) were in the experimental group and 68 (45%) were in the control group. 90% of the patients in the experimental group defaulted after receiving the loading dose of MgSo4 while the remaining 10% completed the referral process. 44% of those in the control group completed the referral process. There were 3 maternal and 3 perinatal deaths, all in the control group. No adverse outcome (maternal or fetal death) or toxic effect was recorded among the recipients of MgSo4. Conclusion: This study suggests that lower-cadre health care professionals at PHCs can administer the loading dose of MgSo4 to SPE/E patients to improve maternal and fetal survival in critical states, without significant risk of adverse effects. However, the lack of compliance with referral processes remains a huge challenge.
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Ishaku et al. (2013) conducted a cohort in Severe pre-eclampsia and eclampsia (n=150). Magnesium Sulphate (MgSo4) vs. Standard care (diazepam or no anti-convulsant) was evaluated on Defaulting from the referral process (Adjusted OR 9.27, 95% CI 3.20-26.85, p=<0.05). Administering a loading dose of magnesium sulphate at primary care facilities significantly increased the likelihood of patients defaulting from the referral process (adjusted OR 9.27) compared to standard care.
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