ArticleBJA open2026
Preoperative predictive factors associated with severe postdischarge pain after ambulatory gynaecological laparoscopy: a prospective cohort study.
Article in BJA open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05050708 (Risikofaktorer for Postoperativ Smerte og Kvalme Etter Dagkirurgisk Gynekologisk Laparoskopi), which is not on this map. Not yet cited in PubMed.
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Risikofaktorer for Postoperativ Smerte og Kvalme Etter Dagkirurgisk Gynekologisk Laparoskopi
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5 authors.
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Abstract
Background: Ambulatory surgery patients are at risk of postoperative pain despite modern multimodal pain regimens, and these patients are particularly vulnerable to postdischarge pain due to limited access to medical support. This study explored 24 previously suggested preoperative predictive factors with the primary aim to determine which factors are associated with severe postdischarge pain in women undergoing ambulatory gynaecological laparoscopy with standardised anaesthesia and multimodal pain prophylaxis and treatment. Methods: In this observational prospective single-centre cohort study, women undergoing ambulatory gynaecological laparoscopy were enrolled. All patients received TIVA (propofol/remifentanil) and multimodal pain prophylaxis including paracetamol, nonsteroidal anti-inflammatory drugs, glucocorticoids, and local anaesthesia. Data were collected before surgery, upon discharge from the PACU, and on postoperative day 1. Univariable and multivariable logistic regression analyses were conducted. Results: In the final analyses, 439 patients were included. Four preoperative predictive factors were independently associated with severe postdischarge pain (odds ratio, 95% confidence interval): younger age: 0.95, 0.92-0.97, Conclusions: Postdischarge pain remains a significant problem after ambulatory gynaecological laparoscopies despite adherence to guidelines for analgesic management. Preoperative predictive factors for severe postdischarge pain were younger age, preoperative pain, use of opioids before surgery and expecting severe postoperative pain. Preoperative identification of at-risk patients may allow for individualised pain prophylaxis and treatment. Clinical trial registration: NCT05050708.
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