TY - JOUR
T1 - PROSPECT guideline for total hip arthroplasty
T2 - a systematic review and procedure-specific postoperative pain management recommendations
AU - the PROSPECT Working Group and the European Society of Regional Anaesthesia and Pain Therapy
AU - Anger, M.
AU - Valovska, T.
AU - Beloeil, H.
AU - Lirk, P.
AU - Joshi, G. P.
AU - Van de Velde, M.
AU - Raeder, J.
AU - Joshi, G. P.
AU - Pogatzki-Zahn, E.
AU - Van de Velde, M.
AU - Kehlet, H.
AU - Bonnet, F.
AU - Rawal, N.
AU - Lavand’homme, P.
AU - Beloeil, H.
AU - Raeder, J.
AU - Sauter, A.
AU - Albrecht, E.
AU - Lirk, P.
AU - Freys, S.
AU - Lobo, D.
AU - Volk, T.
AU - Werner, M.
AU - Bonnet, M.
N1 - Funding Information:
PROSPECT is supported by an unrestricted grant from the European Society of Regional Anaesthesia and Pain Therapy. In the past, PROSPECT has received unrestricted grants from Pfizer Inc. New York, NY, USA and Grunenthal, Aachen, Germany. GJ has received honoraria from Baxter and Pacira Pharmaceuticals. FB has received honoraria from Pfizer, The Medicine Company, Abbott France and Nordic Pharma France. HK has received honoraria from Pfizer and Grunenthal. SS’s institution has received research and travel funding and speaking and consulting honoraria from bioCSL, Eli Lilly, Indivior, iX Biopharma and Pfizer. NR has received honoraria from Baxter and Sintetica. MVdV received honoraria from Sintetica, Grunenthal, Vifor Pharma, MSD, Nordic Pharma, CLS Behring, Janssen Pharmaceuticals, Heron Therapeutics and Aquettant. No other or competing interests declared.
Funding Information:
PROSPECT is supported by an unrestricted grant from the European Society of Regional Anaesthesia and Pain Therapy. In the past, PROSPECT has received unrestricted grants from Pfizer Inc. New York, NY, USA and Grunenthal, Aachen, Germany. GJ has received honoraria from Baxter and Pacira Pharmaceuticals. FB has received honoraria from Pfizer, The Medicine Company, Abbott France and Nordic Pharma France. HK has received honoraria from Pfizer and Grunenthal. SS?s institution has received research and travel funding and speaking and consulting honoraria from bioCSL, Eli Lilly, Indivior, iX Biopharma and Pfizer. NR has received honoraria from Baxter and Sintetica. MVdV received honoraria from Sintetica, Grunenthal, Vifor Pharma, MSD, Nordic Pharma, CLS Behring, Janssen Pharmaceuticals, Heron Therapeutics and Aquettant. No other or competing interests declared.
Publisher Copyright:
© 2021 Association of Anaesthetists.
PY - 2021/8
Y1 - 2021/8
N2 - The aim of this systematic review was to develop recommendations for the management of postoperative pain after primary elective total hip arthroplasty, updating the previous procedure-specific postoperative pain management (PROSPECT) guidelines published in 2005 and updated in July 2010. Randomised controlled trials and meta-analyses published between July 2010 and December 2019 assessing postoperative pain using analgesic, anaesthetic, surgical or other interventions were identified from MEDLINE, Embase and Cochrane databases. Five hundred and twenty studies were initially identified, of which 108 randomised trials and 21 meta-analyses met the inclusion criteria. Peri-operative interventions that improved postoperative pain include: paracetamol; cyclo-oxygenase-2-selective inhibitors; non-steroidal anti-inflammatory drugs; and intravenous dexamethasone. In addition, peripheral nerve blocks (femoral nerve block; lumbar plexus block; fascia iliaca block), single-shot local infiltration analgesia, intrathecal morphine and epidural analgesia also improved pain. Limited or inconsistent evidence was found for all other approaches evaluated. Surgical and anaesthetic techniques appear to have a minor impact on postoperative pain, and thus their choice should be based on criteria other than pain. In summary, the analgesic regimen for total hip arthroplasty should include pre-operative or intra-operative paracetamol and cyclo-oxygenase-2-selective inhibitors or non-steroidal anti-inflammatory drugs, continued postoperatively with opioids used as rescue analgesics. In addition, intra-operative intravenous dexamethasone 8–10 mg is recommended. Regional analgesic techniques such as fascia iliaca block or local infiltration analgesia are recommended, especially if there are contra-indications to basic analgesics and/or in patients with high expected postoperative pain. Epidural analgesia, femoral nerve block, lumbar plexus block and gabapentinoid administration are not recommended as the adverse effects outweigh the benefits. Although intrathecal morphine 0.1 mg can be used, the PROSPECT group emphasises the risks and side-effects associated with its use and provides evidence that adequate analgesia may be achieved with basic analgesics and regional techniques without intrathecal morphine.
AB - The aim of this systematic review was to develop recommendations for the management of postoperative pain after primary elective total hip arthroplasty, updating the previous procedure-specific postoperative pain management (PROSPECT) guidelines published in 2005 and updated in July 2010. Randomised controlled trials and meta-analyses published between July 2010 and December 2019 assessing postoperative pain using analgesic, anaesthetic, surgical or other interventions were identified from MEDLINE, Embase and Cochrane databases. Five hundred and twenty studies were initially identified, of which 108 randomised trials and 21 meta-analyses met the inclusion criteria. Peri-operative interventions that improved postoperative pain include: paracetamol; cyclo-oxygenase-2-selective inhibitors; non-steroidal anti-inflammatory drugs; and intravenous dexamethasone. In addition, peripheral nerve blocks (femoral nerve block; lumbar plexus block; fascia iliaca block), single-shot local infiltration analgesia, intrathecal morphine and epidural analgesia also improved pain. Limited or inconsistent evidence was found for all other approaches evaluated. Surgical and anaesthetic techniques appear to have a minor impact on postoperative pain, and thus their choice should be based on criteria other than pain. In summary, the analgesic regimen for total hip arthroplasty should include pre-operative or intra-operative paracetamol and cyclo-oxygenase-2-selective inhibitors or non-steroidal anti-inflammatory drugs, continued postoperatively with opioids used as rescue analgesics. In addition, intra-operative intravenous dexamethasone 8–10 mg is recommended. Regional analgesic techniques such as fascia iliaca block or local infiltration analgesia are recommended, especially if there are contra-indications to basic analgesics and/or in patients with high expected postoperative pain. Epidural analgesia, femoral nerve block, lumbar plexus block and gabapentinoid administration are not recommended as the adverse effects outweigh the benefits. Although intrathecal morphine 0.1 mg can be used, the PROSPECT group emphasises the risks and side-effects associated with its use and provides evidence that adequate analgesia may be achieved with basic analgesics and regional techniques without intrathecal morphine.
KW - analgesia
KW - evidence-based medicine
KW - pain
KW - systematic review
KW - total hip arthroplasty
UR - http://www.scopus.com/inward/record.url?scp=85105072300&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85105072300&partnerID=8YFLogxK
U2 - 10.1111/anae.15498
DO - 10.1111/anae.15498
M3 - Article
C2 - 34015859
AN - SCOPUS:85105072300
SN - 0003-2409
VL - 76
SP - 1082
EP - 1097
JO - Anaesthesia
JF - Anaesthesia
IS - 8
ER -