TY - JOUR
T1 - Multicenter Study of Long-Term Outcomes and Quality of Life in PHACE Syndrome after Age 10
AU - Braun, Mitchell
AU - Frieden, Ilona J.
AU - Siegel, Dawn H.
AU - George, Elizabeth
AU - Hess, Christopher P.
AU - Fox, Christine K.
AU - Chamlin, Sarah L.
AU - Drolet, Beth A.
AU - Metry, Denise
AU - Pope, Elena
AU - Powell, Julie
AU - Holland, Kristen
AU - Ulschmid, Caden
AU - Liang, Marilyn G.
AU - Barry, Kelly K.
AU - Ho, Tina
AU - Cotter, Chantal
AU - Baselga, Eulalia
AU - Bosquez, David
AU - Jain, Surabhi Neerendranath
AU - Bui, Jordan K.
AU - Lara-Corrales, Irene
AU - Funk, Tracy
AU - Small, Alison
AU - Baghoomian, Wenelia
AU - Yan, Albert C.
AU - Treat, James R.
AU - Hogrogian, Griffin Stockton
AU - Huang, Charles
AU - Haggstrom, Anita
AU - List, Mary
AU - McCuaig, Catherine C.
AU - Barrio, Victoria
AU - Mancini, Anthony J.
AU - Lawley, Leslie P.
AU - Grunnet-Satcher, Kerrie
AU - Horii, Kimberly A.
AU - Newell, Brandon
AU - Nopper, Amy
AU - Garzon, Maria C.
AU - Scollan, Margaret E.
AU - Mathes, Erin F.
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/4
Y1 - 2024/4
N2 - 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.
AB - 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.
KW - PHACE syndrome
KW - PHACES syndrome
KW - birthmarks
KW - infantile hemangioma
KW - neurocutaneous
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UR - http://www.scopus.com/inward/citedby.url?scp=85185606798&partnerID=8YFLogxK
U2 - 10.1016/j.jpeds.2024.113907
DO - 10.1016/j.jpeds.2024.113907
M3 - Article
C2 - 38218370
AN - SCOPUS:85185606798
SN - 0022-3476
VL - 267
JO - journal of pediatrics
JF - journal of pediatrics
M1 - 113907
ER -