Prediction of persistent ventricular dilation by initial ventriculomegaly and clot volume in a porcine model.

animal model germinal matrix hemorrhage hydrocephalus intraventricular hemorrhage posthemorrhagic ventricular dilation

Journal

Journal of neurosurgery. Pediatrics
ISSN: 1933-0715
Titre abrégé: J Neurosurg Pediatr
Pays: United States
ID NLM: 101463759

Informations de publication

Date de publication:
01 Mar 2022
Historique:
received: 02 04 2021
accepted: 02 09 2021
medline: 20 11 2021
pubmed: 20 11 2021
entrez: 19 11 2021
Statut: epublish

Résumé

While intraventricular hemorrhage (IVH) is associated with posthemorrhagic ventricular dilation (PHVD), not all infants affected by high-grade IVH develop PHVD. The authors aimed to determine clot-associated predictors of PHVD in a porcine model by varying the amount and rate of direct intraventricular injection of whole autologous blood. Seven 1-week-old piglets underwent craniectomy and injection of autologous blood into the right lateral ventricle. They survived for a maximum of 28 days. MRI was performed prior to injection, immediately postoperatively, and every 7 days thereafter. T1-weighted, T2-weighted, and susceptibility-weighted imaging (SWI) sequences were used to segment ventricular and clot volumes. Spearman correlations were used to determine the relationship between blood and clot volumes and ventricular volumes over time. The maximum ventricular volume was up to 12 times that of baseline. One animal developed acute hydrocephalus on day 4. All other animals survived until planned endpoints. The interaction between volume of blood injected and duration of injection was significantly associated with clot volume on the postoperative scan (p = 0.003) but not the amount of blood injected alone (p = 0.38). Initial postoperative and day 7 clot volumes, but not volume of blood injected, were correlated with maximum (p = 0.007 and 0.014) and terminal (p = 0.014 and 0.036) ventricular volumes. Initial postoperative ventricular volume was correlated with maximum and terminal ventricular volume (p = 0.007 and p = 0.014). Initial postoperative, maximum, and terminal ventricular dilations were associated with the amount of clot formed, rather than the amount of blood injected. This supports the hypothesis that PHVD is determined by clot burden rather than the presence of blood products and allows further testing of early clot lysis to minimize PHVD risk.

Identifiants

pubmed: 34798598
doi: 10.3171/2021.9.PEDS2190
pii: 2021.9.PEDS2190
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

237-244

Auteurs

Grace Y Lai (GY)

1Department of Neurological Surgery, McGaw Medical Center of Northwestern University, Chicago, Illinois.
2Center for Image-Guided Innovation and Therapeutic Intervention and.

William Chu Kwan (W)

2Center for Image-Guided Innovation and Therapeutic Intervention and.
3Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.

Karolina Piorkowska (K)

2Center for Image-Guided Innovation and Therapeutic Intervention and.

Matthias W Wagner (MW)

4Division of Neuroradiology, The Hospital for Sick Children, Toronto, Ontario, Canada; and.

Pouya Jamshidi (P)

5Department of Pathology, McGaw Medical Center of Northwestern University, Chicago, Illinois.

Birgit Ertl-Wagner (B)

3Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
4Division of Neuroradiology, The Hospital for Sick Children, Toronto, Ontario, Canada; and.

Thomas Looi (T)

2Center for Image-Guided Innovation and Therapeutic Intervention and.
3Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.

Adam C Waspe (AC)

2Center for Image-Guided Innovation and Therapeutic Intervention and.
3Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.

James M Drake (JM)

2Center for Image-Guided Innovation and Therapeutic Intervention and.
3Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.

Classifications MeSH