Health Condition 1: I609- Nontraumatic subarachnoid hemorrhage, unspecified
Conditions
Interventions
Intervention1: NA: NA
Control Intervention1: NA: NA
Sponsors
Post Graduate Institute of Medical Education and Research
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria for the study consisted of several key factors. Participants had to be aged 18 years or above and have radiologically confirmed aneurysmal subarachnoid hemorrhage. Additionally, patients undergoing surgical management for aneurysmal subarachnoid hemorrhage, including those undergoing surgical clipping or endovascular obliteration, were also included. Conversely, patients with aneurysmal subarachnoid hemorrhage who did not undergo clipping or endovascular procedures were excluded from the study.
Exclusion criteria
Exclusion criteria: The study excluded patients who could not be scored on the Glasgow Coma Scale (GCS) upon admission, such as those who were intubated and under sedation before arriving at the central hospital. Additionally, patients who were lost to follow-up during the study period were also excluded. Furthermore, patients or their legal kin who withheld consent for participation in the study were not included.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| functional outcomes assessed using the Modified Rankin Scale (mRS) at discharge, 1 month, and 3 months, and the Glasgow Outcome Scale-Extended (GOSE) at 1 month and 3 months. Neurological status will be evaluated using the Glasgow Coma Scale (GCS) at discharge and any decline of 2 or more points during hospital stay. Mortality will be assessed based on in-hospital death and its cause.Timepoint: enrollment, during hospitalization, and at discharge, with long-term functional recovery evaluated at 1 and 3 months post-ictus. | — |
Secondary
| Measure | Time frame |
|---|---|
| complications, surgical details, biochemical and radiological parameters, hospital stay, long-term functional recovery, and patient demographics and risk factors.Timepoint: enrollment, during hospitalization, and at discharge, with long-term functional recovery evaluated at 1 and 3 months post-ictus. | — |
Countries
India
Contacts
Public ContactDr Ikjot Singh
PGIMER, Chandigarh
Outcome results
None listed