Authors
Temebi W Andafa, Sheriffdeen A Adekanmbi, Chijioke M Ugwumba, Woyengidoubara T Angaye, Godbless N Oyinke, Zulikhat Maruwf
Published in
Cureus. Volume 18. Issue 8. Pages e114485. Epub Aug 13, 2026.
Abstract
Neuroleptic malignant syndrome (NMS) is a rare but potentially fatal idiosyncratic reaction to dopamine antagonism, traditionally recognised by hyperthermia, muscular rigidity, autonomic instability, and altered mental status. International consensus and DSM-5 research criteria uniformly require documented repeated hyperthermia to establish a diagnosis. Primary cohort, case-register, pharmacovigilance, and clinical-feature-frequency data document that a clinically important minority of diagnosed patients are afebrile at presentation, and that rigidity precedes measured hyperthermia in the majority who eventually become febrile. This review synthesises the evidence bearing on early recognition of NMS in patients who do not yet meet the fever criterion, and asks what earlier markers, clinical patterns, and management steps are supported by primary evidence. Feature-frequency series show that rigidity and rising creatine kinase (CK) are earlier and more universal markers than measured hyperthermia; pathophysiological modelling is consistent with the view that hyperthermia is a downstream and variable manifestation of the underlying pathophysiological process; and outcome data indicate that delayed recognition tracks with the leading causes of death and disability (respiratory failure, acute kidney injury, rhabdomyolysis). Because all available evidence is retrospective, cohort, pharmacovigilance, or observational in design, conclusions are directional rather than definitive. Awareness of the afebrile presentation, structured attention to rigidity and CK trajectory, and early exclusion of alternative diagnoses are supported by the primary literature as low-cost strategies to shorten the time to recognition. Formal criteria are unchanged; the change proposed here is one of clinical awareness at the bedside.
PMID:
42732346
Bibliographic data and abstract were imported from PubMed on 13 Sep 2026.
Read full publication at:
Please sign in
to see all details.
Advertisement
Stats
- Recommendations n/a n/a positive of 0 vote(s)
- Views 11
- Comments 0