Related Experiment Video
Updated: Feb 21, 2026

Quantifying Acute Changes in Renal Sympathetic Nerve Activity in Response to Central Nervous System Manipulations in Anesthetized Rats
Published on: September 11, 2018
Dexmedetomidine attenuates acute paroxysmal sympathetic hyperactivity
Yuan Peng1, Haifeng Zhu2, Haodong Chen3
1Department of Intensive Care Unit and Neurosurgery, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou 215300, P. R. China.
Dexmedetomidine effectively treats acute paroxysmal sympathetic hyperactivity (PSH) attacks after neurosurgery, showing faster recovery of vital signs than propofol. However, it does not prevent PSH recurrence or improve long-term outcomes.
Area of Science:
- Neuroscience
- Anesthesiology
- Critical Care Medicine
Background:
- Paroxysmal sympathetic hyperactivity (PSH) is a critical condition following neurosurgery.
- Effective management of PSH is crucial for patient recovery and prognosis.
Purpose of the Study:
- To evaluate the efficacy of dexmedetomidine compared to propofol in treating PSH after neurosurgery.
- To assess the impact of dexmedetomidine on PSH symptom resolution and patient outcomes.
Main Methods:
- Retrospective study of 72 patients with PSH post-neurosurgery.
- Comparison of dexmedetomidine versus propofol treatment groups.
- Analysis of vital sign recovery, PSH duration, recurrence, and Glasgow Outcome Score (GOS).
Main Results:
- Dexmedetomidine significantly reduced time to normalize hypertension, heart rate, and respiratory rate compared to propofol.
- Higher PSH remission rates and shorter PSH duration were observed with dexmedetomidine.
- Dexmedetomidine did not prevent PSH recurrence; age and Glasgow Coma Score were key predictors.
- No significant difference in 6-month GOS between the groups.
Conclusions:
- Dexmedetomidine is effective in controlling acute PSH episodes post-neurosurgery.
- While improving acute symptom management, dexmedetomidine does not alter long-term patient prognosis compared to propofol.
- Further research into PSH recurrence factors and long-term management strategies is warranted.
More Related Videos
11:08Novel Approach for Simultaneous Recording of Renal Sympathetic Nerve Activity and Blood Pressure with Intravenous Infusion in Conscious, Unrestrained Mice.
Published on: February 14, 2018
08:49Assessing Changes in Volatile General Anesthetic Sensitivity of Mice after Local or Systemic Pharmacological Intervention
Published on: October 16, 2013
Related Concept Videos
Adrenergic Agonists: Therapeutic Uses
Emergency and Intensive Care Unit (ICU) applications: Pressor agents increase blood pressure, heart rate, and contractility in shock and organ failure situations. Dopamine can induce vasodilation and stimulate adrenoceptors. Endogenous catecholamines are effective in treating cardiogenic shock. α2-agonists like clonidine can reverse anesthesia-induced hypertension.
Allergies and...
Adrenergic Agonists: Direct-Acting Agents
These agents can be classified...
Nondepolarizing (Competitive) Neuromuscular Blockers: Pharmacological Actions
Although all competitive neuromuscular blockers are designed...
Direct-Acting Cholinergic Agonists: Pharmacological Actions
Cholinergic Antagonists: Pharmacological Actions
Gastrointestinal Effects: Antimuscarinics reduce gut contractions, increase gastric emptying, and slow intestinal transit. They partly inhibit gastric acid secretion...
Sedatives and Hypnotics Drugs: Miscellaneous Agents
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...