Clinical Sciences/Health Conditions
Satya Sreekar Dachepalli, MD
Senior Resident
All India Institute of Medical Sciences, Bibinagar
Vinukonda, Andhra Pradesh, India
Sreehari R. N R, Jr., MD
Additional Professor
Amrita Institute of Medical Sciences
Kochi, Kerala, India
Ravi Sankaran, MD
Professor and HoD
Amrita Institute of Medical Sciences
Kochi, Kerala, India
Aneurysmal subarachnoid hemorrhage (aSAH) accounts for 85% of spontaneous SAH cases leading to significant morbidity. Delayed cerebral ischemia (DCI), a complication of SAH worsens functional outcomes. This study evaluated the effect of hyperbaric oxygen therapy (HBOT) as an adjuvant to conventional treatment in DCI.
Design:
In this prospective non-randomized clinical trial, 30 patients with DCI post- endovascular coiling for aSAH were allocated to HBOT and control groups based on informed consent. Modified Rankin Scale (mRS), Disability Rating Scale (DRS), Stroke Specific Quality of Life scale (SS-QoL), and Modified Ashworth Scale (MAS) scores were assessed at baseline after coiling and at 1, 3, and 6 months. In the HBOT group, CT Hounsfield units were measured before and after the completion of HBOT sessions.
Results:
Sixteen patients received HBOT while fourteen were controls. The HBOT group showed greater improvement from baseline in mRS and SS-QoL scales across all follow-ups. DRS improvement also favored HBOT at 1 and 3 months, though differences were not statistically significant. Linear mixed-effects regression showed statistically significant improvement in mRS scores in the HBOT group at 3 months (p=0.034). mRS outcomes showed a moderate effect size at 3 months and 6 months. All patients except for one from the HBOT group, and all patients from the control group reported a return to normal tone on MAS at 6-months follow-up. The difference in means of CT Hounsfield units before and after the intervention was 2.46 with a standard deviation of 6.44 (p=0.16).
Conclusion:
HBOT as an adjunct to conventional treatment in DCI patients may accelerate functional recovery, with significant improvement at 3 months and moderate effect size at 3 and 6 months in mRS scores suggesting a clinically meaningful difference.