Key result
Neuroendocrine dysfunction, including altered basal cortisol and severe growth hormone deficiency, predicted impaired quality of life, depression, and sleep disturbances in SAH survivors.
Why the study?
Does neuroendocrine dysfunction correlate with impaired quality of life and psychiatric sequelae in aneurysmal subarachnoid haemorrhage survivors?
Observational (n=40)
Does neuroendocrine dysfunction correlate with impaired quality of life and psychiatric sequelae in aneurysmal subarachnoid haemorrhage survivors?
Neuroendocrine disturbances, including altered cortisol and growth hormone levels, may contribute to impaired quality of life, depression, and sleep disturbances in survivors of subarachnoid hemorrhage.
Neuroendocrine dysfunction may contribute to impaired QoL and depression after SAH; leaves open whether replacement improves outcomes.
OBJECTIVE: Patients who have sustained aneurysmal subarachnoid haemorrhage (SAH) often suffer persistent impairments in their quality of life (QoL) and psychological disturbances despite a good neurological outcome. In the light of the high prevalence of partial hypopituitarism in SAH survivors demonstrated in recent investigations, we aimed to determine whether neuroendocrine dysfunction has an impact on QoL and neurobehavioural symptoms in these patients. DESIGN/PATIENTS: QoL, depression and psychological distress were assessed in 40 SAH survivors who had undergone endocrine function testing at least 1 year after the haemorrhage. MEASUREMENTS: QoL was assessed using the Nottingham Health Profile (NHP), the Quality of Life Assessment of Growth Hormone Deficiency in Adults (QoL-AGHDA) and the Short Form-36 questionnaire (SF-36). The Beck Depression Inventory (BDI) and the Impact of Event Scale (IES) were used to evaluate depression and symptoms of current subjective distress in response to the SAH as a stressful life event, respectively. RESULTS: In a stepwise multiple regression analysis, basal cortisol level was included as the first and often only predictor for several QoL domains assessing psychological aspects of well-being and depression whereas physical aspects of QoL were predicted primarily by neurological recovery from the SAH. Severe GH deficiency (GHD) was the first predictor for the criterion NHP subscale 'Energy' and highest stimulated ACTH level in the insulin tolerance test (ITT) was the first predictor for disturbed sleep as assessed with the NHP subscale 'Sleep'. CONCLUSION: Our results provide preliminary data that neuroendocrine disturbances contribute to disturbed QoL, depression and sleeping disturbances in SAH patients.
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Kreitschmann‐Andermahr et al. (2007) conducted an observational in aneurysmal subarachnoid haemorrhage (SAH) (n=40). Neuroendocrine dysfunction was evaluated on Quality of life, depression, and psychological distress. Neuroendocrine dysfunction, including altered basal cortisol and severe growth hormone deficiency, predicted impaired quality of life, depression, and sleep disturbances in SAH survivors.
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