Subarachnoid Hemorrhage (SAH) Clinical Trial
Official title:
Utility of Serum Procalcitonin Levels to Distinguish Systemic Inflammatory Response From Systemic Infection in Febrile Subarachnoid Hemorrhage Patients
Systemic inflammatory response syndrome (SIRS) is characterized by changes in body
temperature, heart rate, respiratory rate, or peripheral blood white cell count, and is
often a heralding manifestation of blood infection (ie., sepsis or bloodstream infection).
SIRS however can occur as a result of a stroke without sepsis. When SIRS occurs after
stroke, patients are subjected to blood cultures and tests to exclude sepsis, and are often
empirically treated with antibiotics potentially leading to a serious gastrointestinal
infection called C. difficile enterocolitis, and bacterial antibiotic resistance.
Development of a blood test that could provide sufficient sensitivity to exclude blood
infection in stroke would therefore prevent numerous tests, cultures, antibiotics, and
costs. In recent years, there has been increasing evidence that procalcitonin (PCT) may
serve as diagnostic marker to distinguish between infectious and non-infectious SIRS. The
investigators hypothesize that PCT can differentiate SIRS after stroke into patients with
infection and those without infection. Such screening tests would provide crucial
information to clinicians that could improve patient care by reducing the number of tests
and antibiotics used, as well as antibiotic-related infections, bacterial resistance and
hospital costs.
Hypothesis: The investigators hypothesize that PCT can be used to define normal (SIRS
without infection) and abnormal values SIRS with infection (i.e., blood, lung, urinary,
spinal fluid) in a population of patients with aneurysmal subarachnoid hemorrhage (SAH).
Specific Aim 1.) To establish normal values of PCT in patients with aneurysmal subarachnoid
hemorrhage and SIRS.
Specific Aim 2.) Derive the sensitivity and positive predictive value of abnormal PCT values
in patients with aneurysmal SAH, SIRS with true systemic infection.
Hypothesis: We hypothesize that PCT can be used to define normal (SIRS without infection)
and abnormal values SIRS with infection (i.e., blood, lung, urinary, spinal fluid) in a
population of patients with aneurysmal subarachnoid hemorrhage (SAH).
Specific Aim 1.) To establish normal values of PCT in patients with aneurysmal subarachnoid
hemorrhage and SIRS.
Specific Aim 2.) Derive the sensitivity and positive predictive value of abnormal PCT values
in patients with aneurysmal SAH, SIRS with true systemic infection.
Stroke is the third leading cause of death in the United States (AHA), A ruptured brain
aneurysm leads to subarachnoid hemorrhage (SAH) which is a common but deadly stroke subtype
(8% of all strokes). SAH one-month mortality is at least 30-40% from a combination of
complications, being either cerebral (seizures, re-bleeding, hydrocephalus, herniation,
coma, brain death) or extra-cerebral (pulmonary edema, myocardial stunning/infarction,
hyponatremia, and SIRS). SIRS after subarachnoid hemorrhage is common, and is associated
with the increased mortality of SAH (Yoshimoto Y). The pathogenesis remains of SIRS after
SAH remains poorly understood, but theorized to be a results of catecholamines (e.g.,
adrenaline) and interleukins leading to increased heart and respiratory rate, increased
peripheral white blood cell count and fever (Wartenberg K). Therefore SIRS after SAH mimics
true systemic infection (e.g., sepsis) even when no true infection exists. Lack of treatment
of true infection in SAH patients for presumptive non-infective SIRS can lead to missed
sepsis and death.
- A prospective, observational study is proposed
- PCT levels will be obtained with daily intensive care unit laboratory values on the
initial day (day #1), day 3, 5, 7, 9, 11, and 13.
- Patients with presumed infection will have the following comprehensive assessment per
ICU standard of care when a SAH patient has a fever (i.e., temperature 38.5 oral or
greater or 38.0 core temperature or greater): two sets of peripheral blood cultures,
one cerebrospinal fluid (CSF) culture,
;
Observational Model: Cohort, Time Perspective: Prospective
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