Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors

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Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors. / Jeppesen, Helene; Kielsen, Katrine; Siersma, Volkert; Lindegaard, Jens; Julian, Hanne Olsen; Heegaard, Steffen; Sengeløv, Henrik; Müller, Klaus.

I: Bone Marrow Transplantation, Bind 57, 2022, s. 487–498.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jeppesen, H, Kielsen, K, Siersma, V, Lindegaard, J, Julian, HO, Heegaard, S, Sengeløv, H & Müller, K 2022, 'Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors', Bone Marrow Transplantation, bind 57, s. 487–498. https://doi.org/10.1038/s41409-022-01564-2

APA

Jeppesen, H., Kielsen, K., Siersma, V., Lindegaard, J., Julian, H. O., Heegaard, S., Sengeløv, H., & Müller, K. (2022). Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors. Bone Marrow Transplantation, 57, 487–498. https://doi.org/10.1038/s41409-022-01564-2

Vancouver

Jeppesen H, Kielsen K, Siersma V, Lindegaard J, Julian HO, Heegaard S o.a. Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors. Bone Marrow Transplantation. 2022;57:487–498. https://doi.org/10.1038/s41409-022-01564-2

Author

Jeppesen, Helene ; Kielsen, Katrine ; Siersma, Volkert ; Lindegaard, Jens ; Julian, Hanne Olsen ; Heegaard, Steffen ; Sengeløv, Henrik ; Müller, Klaus. / Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors. I: Bone Marrow Transplantation. 2022 ; Bind 57. s. 487–498.

Bibtex

@article{6385b0afdf93484fab6805ce733ad66e,
title = "Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors",
abstract = "Ocular graft-versus-host disease (oGVHD) contributes substantially to morbidity after allogeneic haematopoietic stem cell transplantation (HSCT) but is sparsely investigated in children. We assessed incidence and risk factors for oGVHD and dry eye disease (DED) in a nationwide, single-centre study of 484 consecutive children receiving HSCT during the period 1980–2016. Ophthalmological examinations were performed before and annually at least until five years after HSCT. Twenty-five patients had DED before transplantation (5.6%). The cumulative incidence was 1.9% for acute oGVHD, 6.0% for chronic oGVHD, 8.7% for new onset DED, and 12.7% for new onset Corneal Fluorescein Staining (CFS). In adjusted Fine-Gray regression models, the use of Busulfan was a risk factor for developing acute oGVHD (HR 5.01, p = 0.03), and malignant disease was a risk factor for developing CFS (HR 2.00, p = 0.047). Younger recipient age was associated with reduced risk of DED when comparing children aged 0–4 years with 10–16 years (HR 0.33, p = 0.03). These data underscore the need of attention to DED and oGVHD in relation to HSCT leading to our recommendation of performing ophthalmic examinations in all children before HSCT, and after HSCT when needed, in order to secure diagnosis and treatment of these complications.",
author = "Helene Jeppesen and Katrine Kielsen and Volkert Siersma and Jens Lindegaard and Julian, {Hanne Olsen} and Steffen Heegaard and Henrik Sengel{\o}v and Klaus M{\"u}ller",
note = "Publisher Copyright: {\textcopyright} 2022, The Author(s), under exclusive licence to Springer Nature Limited.",
year = "2022",
doi = "10.1038/s41409-022-01564-2",
language = "English",
volume = "57",
pages = "487–498",
journal = "Bone Marrow Transplantation",
issn = "0268-3369",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Ocular graft-versus-host disease and dry eye disease after paediatric haematopoietic stem cell transplantation - incidence and risk factors

AU - Jeppesen, Helene

AU - Kielsen, Katrine

AU - Siersma, Volkert

AU - Lindegaard, Jens

AU - Julian, Hanne Olsen

AU - Heegaard, Steffen

AU - Sengeløv, Henrik

AU - Müller, Klaus

N1 - Publisher Copyright: © 2022, The Author(s), under exclusive licence to Springer Nature Limited.

PY - 2022

Y1 - 2022

N2 - Ocular graft-versus-host disease (oGVHD) contributes substantially to morbidity after allogeneic haematopoietic stem cell transplantation (HSCT) but is sparsely investigated in children. We assessed incidence and risk factors for oGVHD and dry eye disease (DED) in a nationwide, single-centre study of 484 consecutive children receiving HSCT during the period 1980–2016. Ophthalmological examinations were performed before and annually at least until five years after HSCT. Twenty-five patients had DED before transplantation (5.6%). The cumulative incidence was 1.9% for acute oGVHD, 6.0% for chronic oGVHD, 8.7% for new onset DED, and 12.7% for new onset Corneal Fluorescein Staining (CFS). In adjusted Fine-Gray regression models, the use of Busulfan was a risk factor for developing acute oGVHD (HR 5.01, p = 0.03), and malignant disease was a risk factor for developing CFS (HR 2.00, p = 0.047). Younger recipient age was associated with reduced risk of DED when comparing children aged 0–4 years with 10–16 years (HR 0.33, p = 0.03). These data underscore the need of attention to DED and oGVHD in relation to HSCT leading to our recommendation of performing ophthalmic examinations in all children before HSCT, and after HSCT when needed, in order to secure diagnosis and treatment of these complications.

AB - Ocular graft-versus-host disease (oGVHD) contributes substantially to morbidity after allogeneic haematopoietic stem cell transplantation (HSCT) but is sparsely investigated in children. We assessed incidence and risk factors for oGVHD and dry eye disease (DED) in a nationwide, single-centre study of 484 consecutive children receiving HSCT during the period 1980–2016. Ophthalmological examinations were performed before and annually at least until five years after HSCT. Twenty-five patients had DED before transplantation (5.6%). The cumulative incidence was 1.9% for acute oGVHD, 6.0% for chronic oGVHD, 8.7% for new onset DED, and 12.7% for new onset Corneal Fluorescein Staining (CFS). In adjusted Fine-Gray regression models, the use of Busulfan was a risk factor for developing acute oGVHD (HR 5.01, p = 0.03), and malignant disease was a risk factor for developing CFS (HR 2.00, p = 0.047). Younger recipient age was associated with reduced risk of DED when comparing children aged 0–4 years with 10–16 years (HR 0.33, p = 0.03). These data underscore the need of attention to DED and oGVHD in relation to HSCT leading to our recommendation of performing ophthalmic examinations in all children before HSCT, and after HSCT when needed, in order to secure diagnosis and treatment of these complications.

U2 - 10.1038/s41409-022-01564-2

DO - 10.1038/s41409-022-01564-2

M3 - Journal article

C2 - 35042981

AN - SCOPUS:85122867035

VL - 57

SP - 487

EP - 498

JO - Bone Marrow Transplantation

JF - Bone Marrow Transplantation

SN - 0268-3369

ER -

ID: 290528022