Prolonged duration of action of suxamethonium in pregnant and postpartum patients: A registry study

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Prolonged duration of action of suxamethonium in pregnant and postpartum patients : A registry study. / Dalsten, Helene; Crone, Vera; Steinmetz, Jacob; Rosager, Christine L.; Rasmussen, Lars S.; Vested, Matias.

I: Acta Anaesthesiologica Scandinavica, Bind 68, Nr. 6, 2024, s. 737-744.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Dalsten, H, Crone, V, Steinmetz, J, Rosager, CL, Rasmussen, LS & Vested, M 2024, 'Prolonged duration of action of suxamethonium in pregnant and postpartum patients: A registry study', Acta Anaesthesiologica Scandinavica, bind 68, nr. 6, s. 737-744. https://doi.org/10.1111/aas.14413

APA

Dalsten, H., Crone, V., Steinmetz, J., Rosager, C. L., Rasmussen, L. S., & Vested, M. (2024). Prolonged duration of action of suxamethonium in pregnant and postpartum patients: A registry study. Acta Anaesthesiologica Scandinavica, 68(6), 737-744. https://doi.org/10.1111/aas.14413

Vancouver

Dalsten H, Crone V, Steinmetz J, Rosager CL, Rasmussen LS, Vested M. Prolonged duration of action of suxamethonium in pregnant and postpartum patients: A registry study. Acta Anaesthesiologica Scandinavica. 2024;68(6):737-744. https://doi.org/10.1111/aas.14413

Author

Dalsten, Helene ; Crone, Vera ; Steinmetz, Jacob ; Rosager, Christine L. ; Rasmussen, Lars S. ; Vested, Matias. / Prolonged duration of action of suxamethonium in pregnant and postpartum patients : A registry study. I: Acta Anaesthesiologica Scandinavica. 2024 ; Bind 68, Nr. 6. s. 737-744.

Bibtex

@article{381a91d12455464197fc87f06b8b55d6,
title = "Prolonged duration of action of suxamethonium in pregnant and postpartum patients: A registry study",
abstract = "Background: Suxamethonium is hydrolysed by butyrylcholinesterase (BChE) and a low BChE activity can result in a prolonged duration of action of suxamethonium. The BChE activity is reduced during pregnancy and postpartum period by up to 33%. However, it can also be reduced by mutations in the BChE gene. In this study, we assessed BChE activity and mutations in the BChE gene in pregnant and postpartum patients with prolonged duration of action of suxamethonium. It was hypothesised that at least 30% of patients with a low BChE activity did not have a mutation in the BChE gene. Methods: In this registry study we focused on pregnant and postpartum patients with a history of prolonged duration of action of suxamethonium referred to the Danish Cholinesterase Research Unit (DCRU) between March 2007 and January 2023. Primary outcome was the proportion of patients without a mutation among patients with a low BChE activity. Secondary outcomes were the proportion of patients with a low BChE activity and the proportion of patients with a mutation out of the total number of patients. Results: A total of 40 patients were included and among patients with a low BChE activity, 6% (95% CI: 1%–21%) did not have a mutation. Out of the total number of included patients referred to the DCRU, 90% (95% CI: 76%–97%) had a mutation and 94% (95% CI: 80%–99%) had a low BChE activity. Conclusion: Among pregnant and postpartum patients with a history of prolonged duration of action of suxamethonium and a low BChE activity, 6% did not have a mutation in the BChE gene. Our findings suggest that during pregnancy and postpartum clinically relevant prolonged duration of action of suxamethonium rarely occurs in genotypically normal patients.",
keywords = "butyrylcholinesterase, neuromuscular blockade, postpartum, pregnancy, pseudocholinesterase, suxamethonium",
author = "Helene Dalsten and Vera Crone and Jacob Steinmetz and Rosager, {Christine L.} and Rasmussen, {Lars S.} and Matias Vested",
note = "Publisher Copyright: {\textcopyright} 2024 The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation.",
year = "2024",
doi = "10.1111/aas.14413",
language = "English",
volume = "68",
pages = "737--744",
journal = "Acta Anaesthesiologica Scandinavica",
issn = "0001-5172",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Prolonged duration of action of suxamethonium in pregnant and postpartum patients

T2 - A registry study

AU - Dalsten, Helene

AU - Crone, Vera

AU - Steinmetz, Jacob

AU - Rosager, Christine L.

AU - Rasmussen, Lars S.

AU - Vested, Matias

N1 - Publisher Copyright: © 2024 The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation.

PY - 2024

Y1 - 2024

N2 - Background: Suxamethonium is hydrolysed by butyrylcholinesterase (BChE) and a low BChE activity can result in a prolonged duration of action of suxamethonium. The BChE activity is reduced during pregnancy and postpartum period by up to 33%. However, it can also be reduced by mutations in the BChE gene. In this study, we assessed BChE activity and mutations in the BChE gene in pregnant and postpartum patients with prolonged duration of action of suxamethonium. It was hypothesised that at least 30% of patients with a low BChE activity did not have a mutation in the BChE gene. Methods: In this registry study we focused on pregnant and postpartum patients with a history of prolonged duration of action of suxamethonium referred to the Danish Cholinesterase Research Unit (DCRU) between March 2007 and January 2023. Primary outcome was the proportion of patients without a mutation among patients with a low BChE activity. Secondary outcomes were the proportion of patients with a low BChE activity and the proportion of patients with a mutation out of the total number of patients. Results: A total of 40 patients were included and among patients with a low BChE activity, 6% (95% CI: 1%–21%) did not have a mutation. Out of the total number of included patients referred to the DCRU, 90% (95% CI: 76%–97%) had a mutation and 94% (95% CI: 80%–99%) had a low BChE activity. Conclusion: Among pregnant and postpartum patients with a history of prolonged duration of action of suxamethonium and a low BChE activity, 6% did not have a mutation in the BChE gene. Our findings suggest that during pregnancy and postpartum clinically relevant prolonged duration of action of suxamethonium rarely occurs in genotypically normal patients.

AB - Background: Suxamethonium is hydrolysed by butyrylcholinesterase (BChE) and a low BChE activity can result in a prolonged duration of action of suxamethonium. The BChE activity is reduced during pregnancy and postpartum period by up to 33%. However, it can also be reduced by mutations in the BChE gene. In this study, we assessed BChE activity and mutations in the BChE gene in pregnant and postpartum patients with prolonged duration of action of suxamethonium. It was hypothesised that at least 30% of patients with a low BChE activity did not have a mutation in the BChE gene. Methods: In this registry study we focused on pregnant and postpartum patients with a history of prolonged duration of action of suxamethonium referred to the Danish Cholinesterase Research Unit (DCRU) between March 2007 and January 2023. Primary outcome was the proportion of patients without a mutation among patients with a low BChE activity. Secondary outcomes were the proportion of patients with a low BChE activity and the proportion of patients with a mutation out of the total number of patients. Results: A total of 40 patients were included and among patients with a low BChE activity, 6% (95% CI: 1%–21%) did not have a mutation. Out of the total number of included patients referred to the DCRU, 90% (95% CI: 76%–97%) had a mutation and 94% (95% CI: 80%–99%) had a low BChE activity. Conclusion: Among pregnant and postpartum patients with a history of prolonged duration of action of suxamethonium and a low BChE activity, 6% did not have a mutation in the BChE gene. Our findings suggest that during pregnancy and postpartum clinically relevant prolonged duration of action of suxamethonium rarely occurs in genotypically normal patients.

KW - butyrylcholinesterase

KW - neuromuscular blockade

KW - postpartum

KW - pregnancy

KW - pseudocholinesterase

KW - suxamethonium

U2 - 10.1111/aas.14413

DO - 10.1111/aas.14413

M3 - Journal article

C2 - 38522946

AN - SCOPUS:85189554899

VL - 68

SP - 737

EP - 744

JO - Acta Anaesthesiologica Scandinavica

JF - Acta Anaesthesiologica Scandinavica

SN - 0001-5172

IS - 6

ER -

ID: 393840130