Effects of patient-controlled analgesia with hydromorphone or sufentanil on postoperative pulmonary complications in patients undergoing thoracic surgery: a quasi-experimental study

BMC Anesthesiol. 2018 Dec 19;18(1):192. doi: 10.1186/s12871-018-0657-7.

Abstract

Objective: To compare the analgesic effects of patient-controlled intravenous analgesia (PCA) with hydromorphone and sufentanil after thoracic surgery on postoperative pulmonary complications (PPCs).

Methods: A total of 142 patients who were scheduled for thoracic surgery were randomly allocated to receive PCA with hydromorphone (group A: experimental group): hydromorphone 0.2 mg/kg + dezocine 0.5 mg/kg + ramosetron 0.6 mg diluted with normal saline to 200 mL; or with sufentanil (group B: control group): sufentanil 3.0μg/kg + dezocine 0.5 mg/kg + ramosetron 0.6 mg diluted with normal saline to 200 mL. The parameters of intravenous analgesia pump were set as background dose 4 ml/h, PCA dose 1 mL, locking time 15 min. Pain NRS (numerical rating scale), Ramsay sedation score, nausea or vomiting score were evaluated at 0 h, 6 h, 12 h, 24 h, 48 h after operation. The cases of PPCs (atelectasis, pulmonary infection, respiratory failure), CRP (C-reaction protein) and inflammatory cells (white cell count and percentage of neutrophils) and blood gas analysis at 12 h after operation, length of ICU and postoperative stay were recorded for each patient.

Results: Data of 136 patients were analyzed. Compared with group B (4[IQR:2,2]), the pain NRS in group A (2[IQR:4,4]) was significantly lower at 6 h after operation (P = 0.000). The CRP in group A (69.79 ± 32.13 mg/L) were lower than group B (76.76 ± 43.42 mg/L) after operation, but the difference was not significant (P = 0.427). No difference of nausea or vomiting was found between group A (7.3%) and group B (5.8%) postoperatively (P = 0.999). The PPCs were happened in 11 patients in group A (16.2%) and 22 patients in group B (32.4%) and the difference between two groups was significant (P = 0.027). Seven patients in group A (10.3%) and eighteen patients in group B (26.5%) had clinical evidence of pneumonia and the difference between two groups was significant (P = 0.014). The length of ICU and postoperative stay in group A were 2.73 h and 1.82 days less than group B respectively but the differences were not significant (P = 0.234, P = 0.186 respectively).

Conclusion: Compared with sufentanil, hydromorphone may provide better postoperative analgesic effect with less pulmonary complications for patients undergoing thoracic surgery, and it may accelerate patients' rehabilitation.

Trial registration: Randomized Controlled Trials ChiCTR1800014282c . Registered 3 January 2018.

Keywords: Hydromorphone; Postoperative analgesia; Postoperative pulmonary complications; Thoracic surgery.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Analgesia, Patient-Controlled / methods
  • Benzimidazoles / administration & dosage
  • Blood Gas Analysis
  • Bridged Bicyclo Compounds, Heterocyclic / administration & dosage
  • Double-Blind Method
  • Female
  • Humans
  • Hydromorphone / administration & dosage*
  • Intensive Care Units / statistics & numerical data
  • Length of Stay
  • Lung Diseases / epidemiology
  • Lung Diseases / etiology
  • Lung Diseases / physiopathology
  • Male
  • Middle Aged
  • Pain, Postoperative / drug therapy
  • Postoperative Complications / epidemiology*
  • Sufentanil / administration & dosage*
  • Tetrahydronaphthalenes / administration & dosage
  • Thoracic Surgical Procedures / methods*

Substances

  • Benzimidazoles
  • Bridged Bicyclo Compounds, Heterocyclic
  • Tetrahydronaphthalenes
  • ramosetron
  • Sufentanil
  • Hydromorphone
  • dezocine

Associated data

  • ChiCTR/ChiCTR1800014282c