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Page 1
Pseudocholinesterase Deficiency.
Trujillo R, West WP. Trujillo R, et al. 2023 Jul 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Jul 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 31082076 Free Books & Documents.
Pseudocholinesterase deficiency, also known as butyrylcholinesterase deficiency, refers to a rare acquired or inherited defect in the pseudocholinesterase enzyme produced by the liver. ...
Pseudocholinesterase deficiency, also known as butyrylcholinesterase deficiency, refers to a rare acquired or in …
Pseudocholinesterase deficiency in ophthalmology: a systematic review.
Cheng T, Curley M, Barmettler A. Cheng T, et al. Orbit. 2024 Jun;43(3):429-437. doi: 10.1080/01676830.2023.2166083. Epub 2023 Jan 20. Orbit. 2024. PMID: 36661099 Review.
We report the first case of pseudocholinesterase deficiency in a Bengali person and the first systematic review of pseudocholinesterase deficiency in ophthalmology. This review analyzed the epidemiology, etiologies, presentation, evaluation, and treatm …
We report the first case of pseudocholinesterase deficiency in a Bengali person and the first systematic review of pseudoch …
Pseudocholinesterase Deficiency: What the Proceduralist Needs to Know.
Robles A, Michael M, McCallum R. Robles A, et al. Am J Med Sci. 2019 Mar;357(3):263-267. doi: 10.1016/j.amjms.2018.11.002. Epub 2018 Nov 10. Am J Med Sci. 2019. PMID: 30578021 Review.
Pseudocholinesterase deficiency is a rare genetic as well as an acquired disorder that affects the body's ability to metabolize choline esters such as succinylcholine and mivacurium. It can be inherited as an autosomal recessive trait, occurring in approximately 1 i …
Pseudocholinesterase deficiency is a rare genetic as well as an acquired disorder that affects the body's ability to metaboliz …
Pseudocholinesterase Deficiency Considerations: A Case Study.
Cornelius BW, Jacobs TM. Cornelius BW, et al. Anesth Prog. 2020 Sep 1;67(3):177-184. doi: 10.2344/anpr-67-03-16. Anesth Prog. 2020. PMID: 32992329 Free PMC article.
Pseudocholinesterase deficiency, sometimes called butyrylcholinesterase deficiency, is a rare disorder in which the neuromuscular blocking drugs succinylcholine and mivacurium cannot be metabolized properly in the blood plasma. ...Anesthesia providers …
Pseudocholinesterase deficiency, sometimes called butyrylcholinesterase deficiency, is a rare disorder in which …
Pseudocholinesterase deficiency: a comprehensive review of genetic, acquired, and drug influences.
Soliday FK, Conley YP, Henker R. Soliday FK, et al. AANA J. 2010 Aug;78(4):313-20. AANA J. 2010. PMID: 20879632 Review.
Pseudocholinesterase deficiency is an inherited or acquired condition in which the metabolism of succinylcholine, mivacurium, or ester local anesthetics is potentially impaired. ...
Pseudocholinesterase deficiency is an inherited or acquired condition in which the metabolism of succinylcholine, mivacurium, …
A case of pseudocholinesterase deficiency in the PACU.
Leadingham CL. Leadingham CL. J Perianesth Nurs. 2007 Aug;22(4):265-71; quiz 272-4. doi: 10.1016/j.jopan.2007.05.005. J Perianesth Nurs. 2007. PMID: 17666297 Review.
This article will provide the perianesthesia nurse with the fundamental understanding of the physiology, laboratory diagnostic interpretation, and nursing interventions needed to deliver evidence-based, high-quality care to patients diagnosed with pseudocholinesterase d …
This article will provide the perianesthesia nurse with the fundamental understanding of the physiology, laboratory diagnostic interpretatio …
Pseudocholinesterase deficiency.
Glasgow JF, Elwood JH. Glasgow JF, et al. J Ir Med Assoc. 1968 Aug;61(374):269-72. J Ir Med Assoc. 1968. PMID: 5664914 No abstract available.
Butyrylcholinesterase deficiency.
Delacour H, Dedome E, Courcelle S, Hary B, Ceppa F. Delacour H, et al. Ann Biol Clin (Paris). 2016 Jun 1;74(3):279-85. doi: 10.1684/abc.2016.1141. Ann Biol Clin (Paris). 2016. PMID: 27237801 Free article. Review. English.
Hereditary pseudocholinesterase deficiency discovery after electroconvulsive therapy.
Pradhan BK, van Helmond N, Mitrev LV, Andonakakis AA. Pradhan BK, et al. BMJ Case Rep. 2021 Jan 18;14(1):e239206. doi: 10.1136/bcr-2020-239206. BMJ Case Rep. 2021. PMID: 33462045 Free PMC article.
Inherited pseudocholinesterase deficiency refers to an uncommon defect in the butyrylcholinesterase enzyme which can result in prolonged muscle paralysis due to delayed breakdown of choline ester paralytic anaesthetic agents. ...Investigated post-ECT, she was found …
Inherited pseudocholinesterase deficiency refers to an uncommon defect in the butyrylcholinesterase enzyme which can result in …
Pseudocholinesterase Deficiency - Is Succinylcholine Still Needed to Facilitate Endotracheal Intubation?
Kurnutala LN, Rugnath N. Kurnutala LN, et al. Cureus. 2020 Sep 29;12(9):e10721. doi: 10.7759/cureus.10721. Cureus. 2020. PMID: 33150117 Free PMC article.
Pseudocholinesterase (butyrylcholinesterase) deficiency is an inherited or acquired condition in which the serum pseudocholinesterase levels are absent or lower than normal. ...In this article, we would like to discuss a case report of prolonged intubation and venti …
Pseudocholinesterase (butyrylcholinesterase) deficiency is an inherited or acquired condition in which the serum pseudocholine …
202 results