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在无突破性疼痛的患者中使用10毫升0.1%罗哌卡因和0.5微克/毫升舒芬太尼进行分娩镇痛时最佳程序化间歇性硬膜外推注间隔时间:一项前瞻性随机研究

Optimal Programmed Intermittent Epidural Bolus Interval Timing When Using 10 mL of 0.1% Ropivacaine and 0.5 mcg/mL Sufentanil for Labor Analgesia in Patients Without Breakthrough Pain: A Prospective, Randomized Study.

作者信息

Xu Ding-Chao, Ying Jun, Zhao Jing, Chen Xin-De, Deng Guo-Ping, Zhao Yan-Ping, Xiao Fei

机构信息

Department of Anesthesia, Jiashan First People's Hospital, Jiaxing City, People's Republic of China.

Department of Anesthesia, Jiashan Maternity and Child Care Hospital, Jiaxing City, People's Republic of China.

出版信息

Drug Des Devel Ther. 2024 Dec 3;18:5563-5571. doi: 10.2147/DDDT.S491054. eCollection 2024.

Abstract

BACKGROUND

Interval time, defined as the period of time that effective analgesia can be achieved without the need for patient-controlled epidural analgesia (PCEA), has been investigated as an important parameter for the design of programmed intermittent epidural bolus (PIEB) approaches to labor analgesia. PCEA approaches offer flexibility in the management of labor-related pain while minimizing the risk of patient overdose. Here, the optimal interval between PIEB boluses of 0.1% ropivacaine and 0.5 μg/mL sufentanil was evaluated while using revised criteria to define effective analgesia that allowed for the administration of a rescue PCEA bolus during these intervals.

METHODS

Participants were assigned at random to five different groups with PIEB intervals that ranged from 35 to 55 minutes. Labor epidural analgesia was initiated by administering 15mL of 0.1% ropivacaine with 0.5 μg/mL sufentanil over a 2-minute period. Analgesia was considered effective if there was no additional requirement for manual analgesia or an additional PCEA bolus beyond a maximum of one PCEA bolus between intervals during the first stage of labor. Probit regression analyses were used to estimate the effective PIEB intervals that achieved 50% (EI50) and 90% (EI90) success rates in patients.

RESULTS

The final analysis included 142 patients who underwent PIEB for maintaining analgesia during labor. Intervals of 55, 50, 45, 40, and 35 minutes were associated with analgesia efficacy odds of 82.8% (24/29), 86.2% (25/29), 96.3% (26/27), 100% (29/29), and 100% (28/28), respectively. The respective EI50 and EI90 intervals associated with patients not suffering from breakthrough pain were 62.9 (95% CI 57.2-91.8) and 50.4 (95% CI 45.3-54.9) minutes.

CONCLUSION

Under the condition of this study, the optimal PIEB interval for the administration of 10 mL boluses of 0.1% ropivacaine and 0.5 μg/mL sufentanil is approximately 50 minutes.

摘要

背景

间隔时间定义为无需患者自控硬膜外镇痛(PCEA)即可实现有效镇痛的时间段,已被作为设计用于分娩镇痛的程序化间歇性硬膜外推注(PIEB)方法的一个重要参数进行研究。PCEA方法在分娩相关疼痛管理中提供了灵活性,同时将患者用药过量的风险降至最低。在此,在使用修订标准定义有效镇痛的情况下,评估了0.1%罗哌卡因和0.5μg/mL舒芬太尼PIEB推注之间的最佳间隔时间,该标准允许在这些间隔期间给予补救性PCEA推注。

方法

参与者被随机分配到五组,PIEB间隔时间为35至55分钟。通过在2分钟内给予15mL含0.5μg/mL舒芬太尼的0.1%罗哌卡因开始分娩硬膜外镇痛。如果在分娩第一阶段期间,间隔期间除了最多一剂PCEA推注外,无需额外的手动镇痛或额外的PCEA推注,则认为镇痛有效。使用概率回归分析来估计在患者中实现50%(EI50)和90%(EI90)成功率的有效PIEB间隔时间。

结果

最终分析纳入了142例在分娩期间接受PIEB以维持镇痛的患者。55、50、45、40和35分钟的间隔时间对应的镇痛有效概率分别为82.8%(24/29)、86.2%(25/29)、96.3%(26/27)、100%(29/29)和100%(28/28)。与未经历突破性疼痛的患者相关的EI50和EI90间隔时间分别为62.9(95%CI 57.2 - 91.8)分钟和50.4(95%CI 45.3 - 54.9)分钟。

结论

在本研究条件下,给予10mL 0.1%罗哌卡因和0.5μg/mL舒芬太尼推注的最佳PIEB间隔时间约为50分钟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39ca/11624673/b5f12cc47d56/DDDT-18-5563-g0001.jpg

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