Matches in SemOpenAlex for { <https://semopenalex.org/work/W4313201784> ?p ?o ?g. }
- W4313201784 endingPage "101787" @default.
- W4313201784 startingPage "101787" @default.
- W4313201784 abstract "BackgroundPost-caesarean section analgesia is important physiologically and psychologically for both mothers and infants. Patient-controlled analgesia is a well-established method of administering opioids for postoperative pain. However, to date, no study has systematically investigated the effects of opioids administered through intravenous patient-controlled analgesia (IVPCA) or patient-controlled epidural analgesia (PCEA) in parturients who have undergone caesarean section.MethodsThis systematic review and network meta-analysis aimed to evaluate the analgesic and adverse effects of opioids administered via IVPCA or PCEA in parturients who have undergone a caesarean section. PubMed, Embase, Scopus, Web of Science, and Cochrane Library were searched from inception through 02 10, 2022 for relevant records. Randomised controlled trials (RCTs) that compared opioids administered via IVPCA or PCEA and reported outcomes of interest were included. Studies were excluded if the solution for patient-controlled analgesia contained antiemetics and/or other analgesics in addition to opioids. The methodological quality of RCTs was assessed using the revised Cochrane Risk of Bias Tool. Summary data were extracted from each eligible study. The primary outcome was pain intensity, and the secondary outcomes were opioid-related adverse effects. Frequentist network meta-analyses were performed using a contrast-based random-effects model. This study is registered with PROSPERO, CRD42021254040.FindingsTwenty-three studies with 2589 parturients were included. Compared with IVPCA morphine as a reference treatment, PCEA fentanyl had better analgesic effects at 4 h (mean difference [MD] in the visual analogue scale score, −0.75; 95% confidence interval [CI] [-1.16, −0.34]) and 8 h (MD, −0.93; 95% CI [-1.57, −0.28]) and yielded lower odds of developing nausea/vomiting (odds ratio [OR], 0.27; 95% CI [0.09, 0.80]) and sedation/drowsiness (OR, 0.22; 95% CI [0.11, 0.45]). However, PCEA fentanyl may be more likely to cause pruritus than IVPCA treatments.InterpretationConsidering the analgesic efficacy; opioid-induced nausea, vomiting, and sedation; and the well-being of breastfed infants, PCEA fentanyl may be the treatment of choice for post-caesarean section analgesia.FundingThe Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation (TCRD-TPE-111-27)" @default.
- W4313201784 created "2023-01-06" @default.
- W4313201784 creator A5007613086 @default.
- W4313201784 creator A5017009984 @default.
- W4313201784 creator A5021152240 @default.
- W4313201784 creator A5033361976 @default.
- W4313201784 creator A5034098370 @default.
- W4313201784 creator A5044064885 @default.
- W4313201784 creator A5046878341 @default.
- W4313201784 creator A5048978489 @default.
- W4313201784 creator A5054771505 @default.
- W4313201784 creator A5082998619 @default.
- W4313201784 date "2023-02-01" @default.
- W4313201784 modified "2023-09-30" @default.
- W4313201784 title "Effects of opioids administered via intravenous or epidural patient-controlled analgesia after caesarean section: a network meta-analysis of randomised controlled trials" @default.
- W4313201784 cites W127928225 @default.
- W4313201784 cites W1492220811 @default.
- W4313201784 cites W1528409549 @default.
- W4313201784 cites W1617328014 @default.
- W4313201784 cites W1970973333 @default.
- W4313201784 cites W1983737552 @default.
- W4313201784 cites W1984052269 @default.
- W4313201784 cites W1994126626 @default.
- W4313201784 cites W1997992658 @default.
- W4313201784 cites W2001256057 @default.
- W4313201784 cites W2008306532 @default.
- W4313201784 cites W2008635293 @default.
- W4313201784 cites W2010699829 @default.
- W4313201784 cites W2011322150 @default.
- W4313201784 cites W2017133454 @default.
- W4313201784 cites W2035287305 @default.
- W4313201784 cites W2038730069 @default.
- W4313201784 cites W2047314795 @default.
- W4313201784 cites W2047657604 @default.
- W4313201784 cites W2050747296 @default.
- W4313201784 cites W2057919084 @default.
- W4313201784 cites W2065746019 @default.
- W4313201784 cites W2072498020 @default.
- W4313201784 cites W2076722711 @default.
- W4313201784 cites W2085803274 @default.
- W4313201784 cites W2091808438 @default.
- W4313201784 cites W2096104266 @default.
- W4313201784 cites W2101669234 @default.
- W4313201784 cites W2114088498 @default.
- W4313201784 cites W2136838525 @default.
- W4313201784 cites W2144625636 @default.
- W4313201784 cites W2146742652 @default.
- W4313201784 cites W2148601385 @default.
- W4313201784 cites W2155798268 @default.
- W4313201784 cites W2158906680 @default.
- W4313201784 cites W2170892587 @default.
- W4313201784 cites W2318896179 @default.
- W4313201784 cites W2319152161 @default.
- W4313201784 cites W2337981352 @default.
- W4313201784 cites W2400390163 @default.
- W4313201784 cites W2431688088 @default.
- W4313201784 cites W2463598422 @default.
- W4313201784 cites W2538994991 @default.
- W4313201784 cites W2565600523 @default.
- W4313201784 cites W2594362584 @default.
- W4313201784 cites W2726458749 @default.
- W4313201784 cites W2766211624 @default.
- W4313201784 cites W2886021238 @default.
- W4313201784 cites W2889072174 @default.
- W4313201784 cites W2896867593 @default.
- W4313201784 cites W2965390203 @default.
- W4313201784 cites W2970684805 @default.
- W4313201784 cites W2977246579 @default.
- W4313201784 cites W2978795816 @default.
- W4313201784 cites W3024455950 @default.
- W4313201784 cites W3081776148 @default.
- W4313201784 cites W3089744077 @default.
- W4313201784 cites W3116332773 @default.
- W4313201784 cites W3135958199 @default.
- W4313201784 cites W3172202962 @default.
- W4313201784 cites W3177578813 @default.
- W4313201784 cites W4206814417 @default.
- W4313201784 cites W4243747196 @default.
- W4313201784 cites W4321428884 @default.
- W4313201784 doi "https://doi.org/10.1016/j.eclinm.2022.101787" @default.
- W4313201784 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36590790" @default.
- W4313201784 hasPublicationYear "2023" @default.
- W4313201784 type Work @default.
- W4313201784 citedByCount "0" @default.
- W4313201784 crossrefType "journal-article" @default.
- W4313201784 hasAuthorship W4313201784A5007613086 @default.
- W4313201784 hasAuthorship W4313201784A5017009984 @default.
- W4313201784 hasAuthorship W4313201784A5021152240 @default.
- W4313201784 hasAuthorship W4313201784A5033361976 @default.
- W4313201784 hasAuthorship W4313201784A5034098370 @default.
- W4313201784 hasAuthorship W4313201784A5044064885 @default.
- W4313201784 hasAuthorship W4313201784A5046878341 @default.
- W4313201784 hasAuthorship W4313201784A5048978489 @default.
- W4313201784 hasAuthorship W4313201784A5054771505 @default.
- W4313201784 hasAuthorship W4313201784A5082998619 @default.
- W4313201784 hasBestOaLocation W43132017841 @default.
- W4313201784 hasConcept C126322002 @default.
- W4313201784 hasConcept C141071460 @default.