Multicenter Study of Long-Term Outcomes and Quality of Life in PHACE Syndrome after Age 10

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved..

OBJECTIVE: To characterize long-term outcomes of PHACE syndrome.

STUDY DESIGN: Multicenter study with cross-sectional interviews and chart review of individuals with definite PHACE syndrome ≥10 years of age. Data from charts were collected across multiple PHACE-related topics. Data not available in charts were collected from patients directly. Likert scales were used to assess the impact of specific findings. Patient-Reported Outcomes Measurement Information System (PROMIS) scales were used to assess quality of life domains.

RESULTS: A total of 104/153 (68%) individuals contacted participated in the study at a median of 14 years of age (range 10-77 years). There were infantile hemangioma (IH) residua in 94.1%. Approximately one-half had received laser treatment for residual IH, and the majority (89.5%) of participants were satisfied or very satisfied with the appearance. Neurocognitive manifestations were common including headaches/migraines (72.1%), participant-reported learning differences (45.1%), and need for individualized education plans (39.4%). Cerebrovascular arteriopathy was present in 91.3%, with progression identified in 20/68 (29.4%) of those with available follow-up imaging reports. Among these, 6/68 (8.8%) developed moyamoya vasculopathy or progressive stenoocclusion, leading to isolated circulation at or above the level of the circle of Willis. Despite the prevalence of cerebrovascular arteriopathy, the proportion of those with ischemic stroke was low (2/104; 1.9%). PROMIS global health scores were lower than population norms by at least 1 SD.

CONCLUSIONS: PHACE syndrome is associated with long-term, mild to severe morbidities including IH residua, headaches, learning differences, and progressive arteriopathy. Primary and specialty follow-up care is critical for PHACE patients into adulthood.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:267

Enthalten in:

The Journal of pediatrics - 267(2024) vom: 29. Apr., Seite 113907

Sprache:

Englisch

Beteiligte Personen:

Braun, Mitchell [VerfasserIn]
Frieden, Ilona J [VerfasserIn]
Siegel, Dawn H [VerfasserIn]
George, Elizabeth [VerfasserIn]
Hess, Christopher P [VerfasserIn]
Fox, Christine K [VerfasserIn]
Chamlin, Sarah L [VerfasserIn]
Drolet, Beth A [VerfasserIn]
Metry, Denise [VerfasserIn]
Pope, Elena [VerfasserIn]
Powell, Julie [VerfasserIn]
Holland, Kristen [VerfasserIn]
Ulschmid, Caden [VerfasserIn]
Liang, Marilyn G [VerfasserIn]
Barry, Kelly K [VerfasserIn]
Ho, Tina [VerfasserIn]
Cotter, Chantal [VerfasserIn]
Baselga, Eulalia [VerfasserIn]
Bosquez, David [VerfasserIn]
Jain, Surabhi Neerendranath [VerfasserIn]
Bui, Jordan K [VerfasserIn]
Lara-Corrales, Irene [VerfasserIn]
Funk, Tracy [VerfasserIn]
Small, Alison [VerfasserIn]
Baghoomian, Wenelia [VerfasserIn]
Yan, Albert C [VerfasserIn]
Treat, James R [VerfasserIn]
Hogrogian, Griffin Stockton [VerfasserIn]
Huang, Charles [VerfasserIn]
Haggstrom, Anita [VerfasserIn]
List, Mary [VerfasserIn]
McCuaig, Catherine C [VerfasserIn]
Barrio, Victoria [VerfasserIn]
Mancini, Anthony J [VerfasserIn]
Lawley, Leslie P [VerfasserIn]
Grunnet-Satcher, Kerrie [VerfasserIn]
Horii, Kimberly A [VerfasserIn]
Newell, Brandon [VerfasserIn]
Nopper, Amy [VerfasserIn]
Garzon, Maria C [VerfasserIn]
Scollan, Margaret E [VerfasserIn]
Mathes, Erin F [VerfasserIn]

Links:

Volltext

Themen:

Birthmarks
Infantile hemangioma
Journal Article
Multicenter Study
Neurocutaneous
PHACE syndrome
PHACES syndrome

Anmerkungen:

Date Completed 01.04.2024

Date Revised 01.04.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.jpeds.2024.113907

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM36708922X