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剖宫产预防脊髓低血压的去甲肾上腺素最佳输注速率:一项采用上下序贯分配的随机对照试验

Optimal Infusion Rate of Norepinephrine for Prevention of Spinal Hypotension for Cesarean Delivery: A Randomized Controlled Trial, Using Up-Down Sequential Allocation.

作者信息

Khatoon Fatima, Kocarev Mitko, Fernando Roshan, Naz Amber, Khalid Fouzia, Ibrahim Abdalla Eynas Omer, Columb Malachy

机构信息

From the Department of Anesthesiology, ICU and Perioperative Medicine, Hamad Medical Corporation, Doha, Qatar.

Department of Anaesthesia, Perioperative and Intensive Care Medicine, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

出版信息

Anesth Analg. 2024 Oct 9. doi: 10.1213/ANE.0000000000007231.

Abstract

BACKGROUND

Norepinephrine has recently been suggested to be as effective as phenylephrine for the prevention of hypotension after spinal anesthesia for cesarean delivery. Moreover, compared to phenylephrine, norepinephrine may be superior in maintaining heart rate (HR) and consequently, cardiac output (CO). A recent study demonstrated that norepinephrine given as a single intravenous bolus is approximately 13 times more potent than phenylephrine. However, it is uncertain whether this finding can be applied when these vasopressors are administered as infusions. Therefore, the optimum infusion rate of norepinephrine remains unknown. We aimed to determine the median effective dose (ED50; defined as the rate of vasopressor infusion required to prevent spinal hypotension in 50% of subjects) of both drugs needed to maintain maternal systolic blood pressure within 20% of the baseline after spinal anesthesia for cesarean delivery and to derive the relative potency ratio.

METHODS

Sixty healthy patients undergoing elective cesarean delivery with standardized spinal anesthesia were randomized into 2 groups. The first patient in group 1 received phenylephrine 1200 µg in normal saline 0.9% w/v 60 mL at 60 mL/h infusion rate (20 µg.min-1). The first patient in group 2 received norepinephrine 96 µg in normal saline 0.9% w/v 60 mL at 60 mL/h infusion rate (1.6 µg.min-1). Using up-down sequential allocation technique, the vasopressor dose for every subsequent patient was determined by the response in the previous patient. If effective, the next patient received a dose reduced by 150 µg of phenylephrine (2.5 µg.min-1) or 12 µg (0.2 µg.min-1) of norepinephrine. If ineffective, the dose for the next patient was increased by the same amount. The ED50s were determined according to the Dixon-Massey formula. Stroke volume (SV), HR, and CO were also measured.

RESULTS

The ED50 was 12.7 µg.min-1 (95% CI, 10.5-14.9) for phenylephrine and 1.01 µg.min-1 (95% CI, 0.84-1.18) for norepinephrine, giving a potency ratio of 12.6 (95% CI, 9.92-15.9). HR, SV, and CO did not differ between the groups.

CONCLUSIONS

Norepinephrine is more potent than phenylephrine by a factor of approximately 13 when administered as infusion for equivalent maternal blood pressure control. Based on these findings, we recommend a variable rate prophylactic infusion of norepinephrine to be initiated at 1.9 to 3.8 µg.min-1 for the management of hypotension during cesarean delivery under spinal anesthesia.

摘要

背景

最近有研究表明,去甲肾上腺素在预防剖宫产脊髓麻醉后低血压方面与去氧肾上腺素效果相当。此外,与去氧肾上腺素相比,去甲肾上腺素在维持心率(HR)及心输出量(CO)方面可能更具优势。最近一项研究表明,静脉单次推注的去甲肾上腺素效力约为去氧肾上腺素的13倍。然而,当这些血管升压药以输注方式给药时,这一发现是否适用尚不确定。因此,去甲肾上腺素的最佳输注速率仍不清楚。我们旨在确定剖宫产脊髓麻醉后将产妇收缩压维持在基线值的20%以内所需的两种药物的半数有效剂量(ED50,即50%的受试者预防脊髓性低血压所需的血管升压药输注速率),并得出相对效价比。

方法

60例接受标准化脊髓麻醉的择期剖宫产健康患者被随机分为两组。第1组的第1例患者以60 mL/h的输注速率(20 μg·min-1)接受含1200 μg去氧肾上腺素的0.9% w/v生理盐水60 mL。第2组的第1例患者以60 mL/h的输注速率(1.6 μg·min-1)接受含96 μg去甲肾上腺素的0.9% w/v生理盐水60 mL。采用上下顺序分配技术,根据前一位患者的反应确定后续每位患者的血管升压药剂量。如果有效,下一位患者接受的剂量减少150 μg去氧肾上腺素(2.5 μg·min-1)或12 μg(0.2 μg·min-1)去甲肾上腺素。如果无效,下一位患者的剂量增加相同的量。根据Dixon-Massey公式确定ED50。同时测量每搏输出量(SV)、HR和CO。

结果

去氧肾上腺素的ED50为12.7 μg·min-1(95% CI,10.5 - 14.9),去甲肾上腺素的ED50为1.01 μg·min-1(95% CI,0.84 - 1.18),效价比为12.6(95% CI,9.92 - 15.9)。两组之间的HR、SV和CO无差异。

结论

在等效控制产妇血压的情况下,以输注方式给药时,去甲肾上腺素的效力比去氧肾上腺素高约13倍。基于这些发现,我们建议在脊髓麻醉下剖宫产期间,以1.9至3.8 μg·min-1的可变速率预防性输注去甲肾上腺素来管理低血压。

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