Ocular Complications in School-Age Children and Adolescents after Allogeneic Bone Marrow Transplantation

Hoehn, Mary Ellen; Vestal, Robert E.; Calderwood, Julie; Gannon, Edwin; Cook, Brittany; Rochester, Richard; Hartford, Christine; Sunkara, Anusha; Kang, Guolian; Walton, R. Christopher

doi:10.1016/j.ajo.2020.01.025

Cited by 10 publications

(2 citation statements)

References 14 publications

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“…In addition, the increased prevalence of ocular complications related or unrelated to oGVHD after transplants has led other authors to advocate for yearly examinations. 19,28 Based on our findings, we advocate for frequent follow-ups, especially in patients with cutaneous, pulmonary, or multiorgan involvement of GVHD.…”

Section: Discussionmentioning

confidence: 79%

“…[16][17][18] In children, smaller studies have identified the presence of malignant disease (eg, leukemias) or an older age as risk factors, 12 but the main independent risk factor remains nonocular chronic GVHD organ involvement. 18,19 A better identification of risk factors should lead to improved screening guidelines in children, who may not communicate ocular complaints spontaneously and may develop ocular complications of GVHD. Accordingly, we sought to study the epidemiology of chronic oGVHD in children diagnosed with nonocular GVHD and to identify independent predictors of oGVHD.…”

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confidence: 99%

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Risk Factors for Ocular Involvement in Pediatric Graft-Versus-Host Disease

Hébert

Archambault

Doyon

et al. 2021

Cornea

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To identify risk factors for ocular graft-versus-host disease (oGVHD) in children with graft-versus-host disease (GVHD).Methods: This retrospective cohort study identified 38 children diagnosed with GVHD who underwent an ophthalmological examination. Survival to onset of oGVHD after transplant was analyzed using Kaplan-Meier analyses with log-rank tests. A multivariable Cox proportional hazards model was run for time to oGVHD using univariate risk factors. Results:The average age was 10.0 6 5.4 years at the time of transplant. Underlying illness was acute lymphoblastic leukemia in 19 (50%) and acute myeloid leukemia in 8 (21%). Nonocular GVHD organ involvement included skin (84%), lungs (16%), intestines (50%), liver (24%), and bone marrow (3%). Fifteen children (39%) had oGVHD, of which 47% were asymptomatic. oGVHD was diagnosed 601 6 878 days after GVHD. A significant association between risk of oGVHD and diagnosis of acute lymphoblastic leukemia (P = 0.10) or acute myeloid leukemia (P = 0.08) was not found. Organ involvement associated with oGVHD included skin (P = 0.03) and lungs (P = 0.02). Survival curves were significantly influenced by GVHD organ involvement (P = 0.02), but not underlying disease (P = 0.51). The adjusted Cox regression model yielded an independent hazard ratio of 8.82 (95% CI: 1.51-51.49; P = 0.016) for the presence of concomitant GVHD involvement of skin, lungs, and another organ.Conclusions: Children with multiorgan GVHD involvement including skin and lung disease are at increased risk for oGVHD. Given the proportion of asymptomatic cases found in this series, regular eye examinations are warranted in this population.

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Section: Discussionmentioning

confidence: 79%