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Paroxysmal sympathetic hyperactivity in children: An updated narrative review
Justin Burton1, Mi Ran Shin1, Annie Abraham2
1Children's National Hospital, WA, DC, USA.
Paroxysmal sympathetic hyperactivity (PSH) is a serious brain injury complication. Early diagnosis and multimodal treatment, including environmental changes and medication, are crucial for better patient outcomes and preventing other health issues.
Area of Science:
- Neurology
- Critical Care Medicine
- Neuroscience
Background:
- Paroxysmal sympathetic hyperactivity (PSH) is a clinical syndrome following brain injuries.
- It presents with potentially life-threatening symptoms like tachycardia, tachypnea, hyperthermia, and hypertension.
- PSH is a diagnosis of exclusion, requiring careful clinical evaluation.
Purpose of the Study:
- To summarize the key features of paroxysmal sympathetic hyperactivity.
- To highlight the importance of early diagnosis and management.
- To emphasize the necessity of a multimodal treatment approach.
Main Methods:
- Clinical diagnosis based on a constellation of signs and symptoms.
- Exclusion of other potential causes for the observed clinical presentation.
- Multimodal management strategies.
Main Results:
- PSH involves symptoms such as tachycardia, tachypnea, hyperthermia, hypertension, diaphoresis, and abnormal posturing.
- It is a clinical diagnosis that requires ruling out other conditions.
- A combination of environmental modifications and pharmacotherapy is essential for treatment.
Conclusions:
- Prompt recognition and management of PSH are vital.
- Early intervention can prevent comorbidities associated with PSH.
- Effective management improves overall patient outcomes following brain injury.
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