Evidence map›Paper›PMID 40078265›Full record

ArticleCureus2025

Prolonged Neuromuscular Blockade Following Succinylcholine Administration and the Clinical Importance of Family History: A Case Report.

Gordon Hubbell, Stewart Slomowitz, Imani Thornton

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Gordon HubbellAnesthesiology, HCA Florida Westside Hospital, Plantation, USA.
Stewart SlomowitzAnesthesiology, HCA Florida Westside Hospital, Plantation, USA.
Imani ThorntonAnesthesiology, HCA Florida Westside Hospital, Plantation, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When evaluating the etiology of delayed emergence from anesthesia, several differential diagnoses must be considered, with family history often being an overlooked factor. This case report highlights the clinical significance and diagnostic challenges of one such differential - pseudocholinesterase deficiency (PD). PD is a known defect in the pseudocholinesterase enzyme that may be either inherited or acquired. This deficiency impairs the metabolism of certain pharmacologic agents, including succinylcholine, a short-acting depolarizing neuromuscular blocking agent widely used in operating rooms to facilitate endotracheal intubation. As a result, affected individuals experience prolonged neuromuscular blockade, with recovery times varying significantly and initial diagnosis often proving difficult. Although not uncommon, PD is insidious, and most individuals with this deficiency remain undiagnosed until they or a family member experience prolonged emergence from anesthesia. Laboratory tests such as the dibucaine inhibition test can quantify the deficiency, as demonstrated in this case. This report describes a 90-year-old female who was found to have heterozygous atypical PD after experiencing significantly delayed recovery - lasting eight hours - following succinylcholine administration during hip arthroplasty in the lateral position. The diagnosis was made clinically through the process of elimination and later confirmed by the dibucaine inhibition test. Postoperatively, it was revealed that several of the patient's family members had previously experienced delayed emergence from anesthesia, suggesting an inherited form of PD that was previously unknown to the patient. This case underscores the importance of considering PD in the differential diagnosis of prolonged emergence from anesthesia, highlights the value of a thorough family history, and emphasizes the need for greater awareness among clinicians to prevent life-threatening adverse events.

Indexed as

anesthesia complicationsneuromuscular blockersneuromuscular depolarizing agentspseudocholinesterasepseudocholinesterase deficiency

Identifiers

PMID40078265
PMCPMC11900903

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