Dayicioglu Vedat, Sahinoglu Zeki, Kol Emrah, Kucukbas Mehmet
Department of Perinatology, Zeynep Kamil Women and Children's Disease Education and Research Hospital, Uskudar, Istanbul, Turkey.
Hypertens Pregnancy. 2003;22(3):257-65. doi: 10.1081/PRG-120024029.
We anticipated that the universal use of a standard magnesium sulfate infusion to prevent eclamptic convulsions in preeclamptic patients would result in alterations in circulating magnesium levels that were negatively correlated with the patient's body mass index. We postulated that the highest failure rate with seizure prophylaxis would occur in patients with the highest body mass index.
After discarding 6 patients, this study was performed in 194 of 200 preeclamptic patients admitted to our high risk pregnancy unit between February 2000 and August 2000, who were divided into four groups determined by body mass indices. A standard magnesium sulfate infusion protocol (loading dose 4.5 g/15 minutes followed by 1.8 g/hour) was administered to 194 preeclamptic patients. One hundred and thirty-eight severe preeclamptic patients received magnesium sulfate during both antepartum and postpartum periods. The remaining 56 patients only received the therapy during the postpartum period. Serial serum magnesium levels of each groups were recorded and compared.
The 1.8 g infusion rate produced acceptable magnesium levels in the majority of patients but most were in the lower 50% of the therapeutic range. Levels were lowest in patients with high body mass indices (this group recorded most of the subtherapeutic levels, particularly when patient were infused antepartum). Apart from 13 referred patients who had convulsed prior to admission no eclampsia occurred during the antepartum period while seizures occurred in nine women during the postpartum period. Two hours after the initiation of the therapy, magnesium levels were inversely related to the body mass index (BMI) both during the ante- and postpartum periods (Prepartum; group I: 5.97 mg/dl, group II: 4.90 mg/dl, group III: 4.35 mg/dl, group IV: 3.88 mg/dl; Postpartum; group I: 5.89 mg/dl, group II: 5.71 mg/dl, group III: 4.82 mg/dl and group IV: 4.61 mg/dl, Table 4). Although the lowest levels were detected in patients with high body mass indices, in contrast to our hypothesis, eclamptic seizures occurred in four patients with low body mass indices. Furthermore therapeutic serum magnesium levels were detected in three of these patients. There was no association between treatment failures and body mass or with magnesium levels.
The infusion regimen described herein resulted in therapeutic levels in the majority of patients that correlated inversely with body mass index. However most levels fell within the lower range of what many studies consider "therapeutic" suggesting that maintenance infusion rates of at least 2-2.5 g/hour would be more appropriate. This would be particularly true in patients with body mass indices exceeding 30, where subtherapeutic levels occurred most frequently. The study's limited power prevents conclusions on outcomes but what is of interest is that eclamptic convulsions did not correlate with either body mass index or circulating plasma magnesium levels.
我们预计,对先兆子痫患者普遍使用标准硫酸镁输注来预防子痫抽搐会导致循环镁水平发生变化,且与患者体重指数呈负相关。我们推测,预防癫痫发作的失败率最高会出现在体重指数最高的患者中。
在剔除6例患者后,对200例于2000年2月至2000年8月入住我们高危妊娠病房的先兆子痫患者中的194例进行了研究,这些患者根据体重指数分为四组。对194例先兆子痫患者采用标准硫酸镁输注方案(负荷剂量4.5 g/15分钟,随后1.8 g/小时)。138例重度先兆子痫患者在产前和产后均接受硫酸镁治疗。其余56例患者仅在产后接受治疗。记录并比较各组的系列血清镁水平。
1.8 g/小时的输注速率在大多数患者中产生了可接受的镁水平,但大多数处于治疗范围的下50%。体重指数高的患者镁水平最低(该组记录了大多数低于治疗水平的情况,尤其是患者在产前接受输注时)。除13例入院前已发生抽搐的转诊患者外,产前期间未发生子痫,而产后有9名女性发生了抽搐。治疗开始两小时后,产前和产后期间镁水平均与体重指数呈负相关(产前;I组:5.97 mg/dl,II组:4.90 mg/dl,III组:4.35 mg/dl,IV组:3.88 mg/dl;产后;I组:5.89 mg/dl,II组:5.71 mg/dl,III组:4.82 mg/dl,IV组:4.61 mg/dl,表4)。尽管体重指数高的患者镁水平最低,但与我们的假设相反,4例体重指数低的患者发生了子痫抽搐。此外,其中3例患者检测到治疗性血清镁水平。治疗失败与体重或镁水平之间无关联。
本文所述的输注方案在大多数患者中产生了与体重指数呈负相关的治疗水平。然而,大多数水平落在许多研究认为“治疗性”的较低范围内,这表明维持输注速率至少为2 - 2.5 g/小时可能更合适。对于体重指数超过30的患者尤其如此,这些患者中低于治疗水平的情况最常发生。该研究的效力有限,无法得出关于结局的结论,但有趣的是,子痫抽搐与体重指数或循环血浆镁水平均无关联。