TY - JOUR
T1 - Time-to-event analysis of surgically treated posthemorrhagic hydrocephalus in preterm infants
T2 - a single-institution retrospective study
AU - Han, Rowland H.
AU - Berger, Daniel
AU - Gabir, Mohamed
AU - Baksh, Brandon S.
AU - Morales, Diego M.
AU - Mathur, Amit M.
AU - Smyser, Christopher D.
AU - Strahle, Jennifer M.
AU - Limbrick, David D.
N1 - Publisher Copyright:
© 2017, Springer-Verlag GmbH Germany.
PY - 2017/11/1
Y1 - 2017/11/1
N2 - Purpose: The purpose of this study is to report time points relevant to the neurosurgical management of posthemorrhagic hydrocephalus (PHH). Methods: Data were collected retrospectively on 104 preterm infants with intraventricular hemorrhage (IVH) who received neurosurgical intervention for PHH at St. Louis Children’s Hospital from 1994 to 2016. Kaplan-Meier curves were constructed for various endpoints. Results: IVH grade on head ultrasound obtained through routine clinical care was II, III, and IV in 5 (4.8%), 33 (31.7%), and 66 (63.5%) of the patients, respectively. Neither IVH size nor location appeared to affect development of PHH. Days from birth to IVH, ventriculomegaly, temporizing neurosurgical procedure (TNP), and permanent neurosurgical intervention were 2.0 (95% CI 1.7–2.3), 3.0 (2.5–3.5), 24.0 (22.2–25.8), and 101.0 (90.4–111.6), respectively. Grades III and IV IVH did not differ in age at IVH diagnosis (Χ2 (1 d.f.) = 1.32, p = 0.25), ventriculomegaly (Χ2 = 0.73, p = 0.40), TNP (Χ2 = 0.61, p = 0.43), or permanent intervention (Χ2 = 2.48, p = 0.17). Ventricular reservoirs and ventriculosubgaleal shunts were used in 71 (68.3%) and 30 (28.8%), respectively. Eighty (76.9%) of the patients ultimately received a VPS. Five (4.8%) underwent a primary endoscopic third ventriculostomy (ETV), and two (1.9%) had ETV for a revision procedure. Four of the seven ETVs had choroid plexus cauterization. Conclusions: Although most infants who develop IVH and ventriculomegaly will do so within a few days of birth, at-risk infants should be observed for at least 4 weeks with serial head ultrasounds to monitor for PHH requiring surgery.
AB - Purpose: The purpose of this study is to report time points relevant to the neurosurgical management of posthemorrhagic hydrocephalus (PHH). Methods: Data were collected retrospectively on 104 preterm infants with intraventricular hemorrhage (IVH) who received neurosurgical intervention for PHH at St. Louis Children’s Hospital from 1994 to 2016. Kaplan-Meier curves were constructed for various endpoints. Results: IVH grade on head ultrasound obtained through routine clinical care was II, III, and IV in 5 (4.8%), 33 (31.7%), and 66 (63.5%) of the patients, respectively. Neither IVH size nor location appeared to affect development of PHH. Days from birth to IVH, ventriculomegaly, temporizing neurosurgical procedure (TNP), and permanent neurosurgical intervention were 2.0 (95% CI 1.7–2.3), 3.0 (2.5–3.5), 24.0 (22.2–25.8), and 101.0 (90.4–111.6), respectively. Grades III and IV IVH did not differ in age at IVH diagnosis (Χ2 (1 d.f.) = 1.32, p = 0.25), ventriculomegaly (Χ2 = 0.73, p = 0.40), TNP (Χ2 = 0.61, p = 0.43), or permanent intervention (Χ2 = 2.48, p = 0.17). Ventricular reservoirs and ventriculosubgaleal shunts were used in 71 (68.3%) and 30 (28.8%), respectively. Eighty (76.9%) of the patients ultimately received a VPS. Five (4.8%) underwent a primary endoscopic third ventriculostomy (ETV), and two (1.9%) had ETV for a revision procedure. Four of the seven ETVs had choroid plexus cauterization. Conclusions: Although most infants who develop IVH and ventriculomegaly will do so within a few days of birth, at-risk infants should be observed for at least 4 weeks with serial head ultrasounds to monitor for PHH requiring surgery.
KW - Intraventricular hemorrhage
KW - Temporizing neurosurgical procedure
KW - Ventriculomegaly
KW - Ventriculoperitoneal shunt
UR - http://www.scopus.com/inward/record.url?scp=85028985571&partnerID=8YFLogxK
U2 - 10.1007/s00381-017-3588-6
DO - 10.1007/s00381-017-3588-6
M3 - Article
C2 - 28884229
AN - SCOPUS:85028985571
SN - 0256-7040
VL - 33
SP - 1917
EP - 1926
JO - Child's Nervous System
JF - Child's Nervous System
IS - 11
ER -