Implementation of a piritramide based patient-controlled analgesia (PCA) as a standard of care for pain control in late abortion induction: A prospective cohort study from a patient perspective

被引:0
作者
Padron, L. Tascon [1 ]
Emrich, N. L. A. [1 ]
Strizek, B. [1 ]
Gass, A. [2 ]
Link, C. [2 ]
Hilbert, T. [2 ]
Klaschik, S. [2 ]
Meissner, W. [3 ]
Gembruch, U. [1 ]
Cruz, J. Jimenez [1 ]
机构
[1] Univ Hosp Bonn, Dept Obstet & Prenatal Med, Venusberg Campus 1, D-53127 Bonn, Germany
[2] Univ Hosp Bonn, Dept Anesthesiol & Intens Care Med, Venusberg Campus 1, D-53127 Bonn, Germany
[3] Univ Hosp Jena, Dept Anesthesiol & Intens Care Med, Dept Palliat Care, D-07740 Jena, Germany
来源
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY-X | 2023年 / 20卷
关键词
Late abortion induction; Medically-indicated termination of pregnancy; Obstetrical pain; Pain management; Patient-controlled analgesia; MEDICAL ABORTION; WOMEN; TERMINATION; PREDICTORS; CHALLENGE; PREGNANCY; ANXIETY;
D O I
10.1016/j.eurox.2023.100251
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To assess whether the implementation of patient-controlled analgesia (PCA) with piritramide using an automatic pump system under routine conditions is effective to reduce pain in late abortion inductionsStudy design: Prospective observational cohort study Setting: Patients requiring medically indicated abortion induction from 14 weeks of pregnancy onwards between July 2019 and July 2020 at the department of Obstetrics and Prenatal Medicine of the Bonn University Hospital in Germany.Methods: Evaluation of pain management after implementation of a PCA system compared with previous nurse-controlled tramadol-based standard under routine conditions. Patients answered a validated pain questionnaire and requirement of rescue analgesics was assessed. Pain intensity and satisfaction were measured on a ten-point numeric rating scale. Main Outcome Measure Maximal pain intensityResults: Forty patients were included. Patients using Piritramide-PCA complained of higher pain sores than those in the standard group (6.90 (+/- 2.34) vs. 4.83 (+/- 2.87), (p < 0.05)). In both groups the level of satisfaction with the analgesia received was comparable (8.00 (+/- 2.45) vs 7.67 (+/- 2.62), (p = 0.7)). Patients in the PCA group suffered more nausea (63.2 % vs 30 % respectively, OR 4.0, 95 % CI 1.05-15.20, p < 0.05) and expressed more the desire for more analgesic support compared to the control group (OR 5.7 (1-33.25), p = 0.05).Conclusion: Women with abortion induction after 14 weeks of gestation suffer from relevant severe pain, which requires adequate therapy. However, addition of PCA does not seem to bring any advantage in patients undergoing this procedure.
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