Society for Obstetric Anesthesia and Perinatology Consensus Statement: Monitoring Recommendations for Prevention and Detection of Respiratory Depression Associated With Administration of Neuraxial Morphine for Cesarean Delivery Analgesia.


Journal

Anesthesia and analgesia
ISSN: 1526-7598
Titre abrégé: Anesth Analg
Pays: United States
ID NLM: 1310650

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 15 5 2019
medline: 6 2 2020
entrez: 15 5 2019
Statut: ppublish

Résumé

The majority of women undergoing cesarean delivery in the United States receive neuraxial morphine, the most effective form of postoperative analgesia for this surgery. Current American Society of Anesthesiologists (ASA) and American Society of Regional Anesthesia and Pain Medicine (ASRA) recommend respiratory monitoring standards following neuraxial morphine administration in the general surgical population that may be too frequent and intensive when applied to the healthy obstetric population receiving a single dose of neuraxial morphine at the time of surgery. There is limited evidence to support or guide the optimal modality, frequency, and duration of respiratory monitoring in the postoperative cesarean delivery patient receiving a single dose of neuraxial morphine. Consistent with the mission of the Society for Obstetric Anesthesia and Perinatology (SOAP) to improve outcomes in pregnancy for women and neonates, the purpose of this consensus statement is to encourage the use of this highly effective analgesic technique while promoting safe practice and patient-centered care. The document aims to reduce unnecessary interruptions from respiratory monitoring in healthy mothers while focusing vigilance on monitoring in those women at highest risk for respiratory depression following neuraxial morphine administration. This consensus statement promotes the use of low-dose neuraxial morphine and multimodal analgesia after cesarean delivery, gives perspective on the safety of this analgesic technique in healthy women, and promotes patient risk stratification and perioperative risk assessment to determine and adjust the intensity, frequency, and duration of respiratory monitoring.

Identifiants

pubmed: 31082964
doi: 10.1213/ANE.0000000000004195
doi:

Substances chimiques

Analgesics, Opioid 0
Morphine 76I7G6D29C

Types de publication

Journal Article Practice Guideline Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

458-474

Commentaires et corrections

Type : CommentIn

Auteurs

Jeanette R Bauchat (JR)

From the Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee.

Carolyn F Weiniger (CF)

Division of Anesthesiology & Critical Care & Pain, Sourasky Medical Center, Tel Aviv, Israel.

Pervez Sultan (P)

Department of Anaesthesia and Perioperative Medicine, University College London Hospital, London, United Kingdom.

Ashraf S Habib (AS)

Department of Anesthesiology, Duke University School of Medicine, Durham, North Carolina.

Kazuo Ando (K)

Department of Anesthesiology, Aichi Medical University, Aichi, Japan.

John J Kowalczyk (JJ)

Department of Anaesthesia, Critical Care and Pain Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

Rie Kato (R)

Division of Anesthesiology, Kitasato University School of Medicine, Kanagawa, Japan.

Ronald B George (RB)

Department of Anaesthesia, Pain Management and Perioperative Medicine, Dalhousie University, IWK Health Centre, Halifax, Nova Scotia, Canada.

Craig M Palmer (CM)

Department of Anesthesiology, University of Arizona College of Medicine, Tucson, Arizona.

Brendan Carvalho (B)

Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California.

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Classifications MeSH