Journal Article

Nitric Oxide-Based Treatment of Poor-Grade Patients After Severe Aneurysmal Subarachnoid Hemorrhage

Gerss, Joachim, Ehlert-Gamm, Annette, Manthei, Gerd, Hesselmann, Volker, Starekova, Jitka, Flack, Joachim, Gessert, Marie, Ehlert, Angelika

2020

Overview

Background Patients with aneurysmal subarachnoid hemorrhage (aSAH) require close treatment in neuro intensive care units (NICUs). The treatments available to counteract secondary deterioration and delayed ischemic events remain restricted; moreover, available neuro-monitoring of comatose patients is undependable. In comatose patients, clinical signs are hidden, and timing interventions to prevent the evolution of a perfusion disorder in response to fixed ischemic brain damage remain a challenge for NICU teams. Consequently, comatose patients often suffer secondary brain infarctions. The outcomes for long-term intubated patients w/wo pupil dilatation are the worst, with only 10% surviving. We previously added two nitroxide (NO) donors to the standard treatment: continuous intravenous administration of Molsidomine in patients with mild-to-moderate aSAH and, if required as a supplement, intraventricular boluses of sodium nitroprusside (SNP) in high-risk patients to overcome the so-called NO-sink effect, which leads to vasospasm and perfusion disorders. NO boluses were guided by clinical status and promptly reversed recurrent episodes of delayed ischemic neurological deficit. In this study, we tried to translate this concept, the initiation of intraventricular NO application on top of continuous Molsidomine infusion, from awake to comatose patients who lack neurological–clinical monitoring but are primarily monitored using frequently applied transcranial Doppler (TCD). Methods In this observational, retrospective, nonrandomized feasibility study, 18 consecutive aSAH comatose/intubated patients (Hunt and Hess IV/V with/without pupil dilatation) whose poor clinical status precluded clinical monitoring received standard neuro-intensive care, frequent TCD monitoring, continuous intravenous Molsidomine plus intraventricular SNP boluses after TCD-confirmed macrospasm during the daytime and on a fixed nighttime schedule. Results Very likely associated with the application of SNP, which is a matter of further investigation, vasospasm-related TCD findings promptly and reliably reversed or substantially weakened ( p  < 0.0001) afterward. Delayed cerebral ischemia (DCI) occurred only during loose, low-dose or interrupted treatment (17% vs. an estimated 65% with secondary infarctions) in 17 responders. However, despite their worse initial condition, 29.4% of the responders survived (expected 10%) and four achieved Glasgow Outcome Scale Extended (GOSE) 8–6, modified Rankin Scale (mRS) 0–1 or National Institutes of Health Stroke Scale (NIHSS) 0–2. Conclusions Even in comatose/intubated patients, TCD-guided dual-compartment administration of NO donors probably could reverse macrospasm and seems to be feasible. The number of DCI was much lower than expected in this specific subgroup, indicating that this treatment possibly provides a positive impact on outcomes. A randomized trial should verify or falsify our results.

• Publisher: Springer US,Springer Nature B.V
• Subject: Adult / Aged / Aged, 80 and over / Aneurysm, Ruptured - surgery / Aneurysms / Blood pressure / Brain Ischemia - drug therapy / Brain Ischemia - prevention & control / Critical Care Medicine / Diabetes / Edema / Feasibility Studies / Female / Females / Flow velocity / Hemorrhage / Humans / Hypertension / Infusions, Intravenous / Infusions, Intraventricular / Intensive / Intensive care / Internal Medicine / Intracranial Aneurysm - surgery / Ischemia / Male / Medicine / Medicine & Public Health / Middle Aged / Molsidomine - therapeutic use / Neurology / Nitric Oxide Donors - therapeutic use / Nitroprusside - therapeutic use / Original Work / Patients / Retrospective Studies / Rupture, Spontaneous / Stroke / Subarachnoid Hemorrhage - therapy / Thrombosis / Vasospasm, Intracranial - drug therapy / Vasospasm, Intracranial - prevention & control / Veins & arteries