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26.06.2019 | Original Article | Ausgabe 8/2019

Child's Nervous System 8/2019

Anatomical hemispherectomy revisited—outcome, blood loss, hydrocephalus, and absence of chronic hemosiderosis

Zeitschrift:
Child's Nervous System > Ausgabe 8/2019
Autoren:
Sandeep Sood, Mohammed Ilyas, Neena I Marupudi, Eishi Asano, Ajay Kumar, Aimee Luat, Sheena Saleem, Harry T. Chugani
Wichtige Hinweise
Portions of this paper were presented as podium presentations at the 42nd Annual Meeting of the International Society for Pediatric Neurosurgery (ISPN), Rio de Janeiro, Brazil, Nov 9-13, 2014, and the 43rd Annual Meeting AANS/CNS Section on Pediatric Neurological Surgery, Amelia Island, Fl, Dec 2-5, 2014.

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Abstract

Purpose

To evaluate microsurgical trans-sylvian trans-ventricular anatomical hemispherectomy with regard to seizure outcome, risk of hydrocephalus, blood loss, and risk of chronic hemosiderosis in patients with intractable seizures selected for surgery using current preoperative assessment techniques.

Methods

Out of 86 patients who underwent hemispherectomy between February 2000 and April 2019, by a single surgeon, at a tertiary care referral center, 77 patients (ages 0.2–20 years; 40 females) who had an anatomical hemispherectomy were analyzed. Five of these were ‘palliative’ surgeries. One-stage anatomical hemispherectomy was performed in 55 children, two-stage anatomical hemispherectomy after extraoperative intracranial monitoring in 16, and six hemispherectomies were done following failed previous resection. Mean follow-up duration was 5.7 years (range 1–16.84 years). Forty-six patients had postoperative MRI scans.

Results

Ninety percent of children with non-palliative hemispherectomy achieved ILAE Class-1 outcome. Twenty-seven patients were no longer taking anticonvulsant medications. Surgical failures (n = 4) included one patient with previous meningoencephalitis, one with anti-GAD antibody encephalitis, one with idiopathic neonatal thalamic hemorrhage, and one with extensive tuberous sclerosis. There were no failures among patients with malformations of cortical development. Estimated average blood loss during surgery was 387 ml. Ten (21%) children developed hydrocephalus and required a shunt following one-stage hemispherectomy, whereas 10 (50%) patients developed hydrocephalus among those who had extraoperative intracranial monitoring. Only 20% of the shunts malfunctioned in the first year. Early malfunctions were related to the valve and later to fracture disconnection of the shunt. One patent had a traumatic subdural hematoma. None of the patients developed clinical signs of chronic ‘superficial cerebral hemosiderosis’ nor was there evidence of radiologically persistent chronic hemosiderosis in patients who had postoperative MRI imaging.

Conclusion

Surgical results of anatomical hemispherectomy are excellent in carefully selected cases. Post-operative complications of hydrocephalus and intraoperative blood loss are comparable to those reported for hemispheric disconnective surgery (hemispherotomy). The rate of shunt malfunction was less than that reported for patients with hydrocephalus of other etiologies Absence of chronic ‘superficial hemosiderosis’, even on long-term follow-up, suggests that anatomical hemispherectomy should be revisited as a viable option in patients with intractable seizures and altered anatomy such as in malformations of cortical development, a group that has a reported high rate of seizure recurrence related to incomplete disconnection following hemispheric disconnective surgery.

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