TY - JOUR
PY - 2016//
TI - Can early clinical parameters predict post-traumatic pituitary dysfunction in severe traumatic brain injury?
JO - Acta neurochirurgica
A1 - Nemes, O.
A1 - Kovács, N.
A1 - Szujo, Sz
A1 - Bodis, B.
A1 - Bajnok, L.
A1 - Buki, A.
A1 - Doczi, T.
A1 - Czeiter, E.
A1 - Mezosi, E.
SP - 2347
EP - 2353
VL - 158
IS - 12
N2 - BACKGROUND: Post-traumatic hypopituitarism is a major complication after severe head trauma. The aim of our study was to evaluate the possible role of early clinical parameters in the development of endocrine deficits.
METHODS: Data on endocrine function, on-admission clinical-, laboratory-, and ICU-monitored parameters were available in 63 patients of the surviving 86 severe head injury patients (post-resuscitation GCS under 8) treated at one neurosurgical center during a 10-year period.
RESULTS: Hypopituitarism was diagnosed in 68.3 % of the patients. The most frequently affected pituitary axis was the growth hormone (GH): GH deficiency or insufficiency was present in 50.8 %. Central hypogonadism affected 23.8 % of male patients; hypothyroidism and secondary adrenal failure were found in 22.2 and 9.5 % of the investigated population, respectively. Early onset (within 1 year of brain injury) hypopituitarism was found in 24 patients. No connection was found between the development of hypopituitarism and any of the clinical parameters assessed on-admission or at ICU. Significant correlations were found between early endocrine dysfunctions and surgical intervention (OR: 4.64) and the diagnosis of subdural hematoma (OR: 12). In our population, after road traffic accidents, the development of late-onset hypopituitarism was less prevalent (OR: 0.22).
CONCLUSIONS: Since our results do not indicate any reliable predictive parameter for the development of endocrine dysfunction in a cohort of patients with severe traumatic brain injury, regular endocrine screening of this specific patient population seems obligatory.
Language: en
LA - en SN - 0001-6268 UR - http://dx.doi.org/10.1007/s00701-016-2995-x ID - ref1 ER -