Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood
Objective: To study visual pathway pathology detected by visual evoked potentials (VEPs) in patients treated with hematopoietic stem cell transplantation (HSCT) in childhood and to determine the impact of adverse ocular findings, somatic diseases, and conditioning regimens on the VEP results. Method...
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doaj-d7787ff979fc46688dccd7109b9fe49f2020-11-24T21:57:37ZengElsevierClinical Neurophysiology Practice2467-981X2017-01-0126771Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhoodAlba Lucia Törnquist0Thomas Andersson1Jacek Winiarski2Marita Andersson Grönlund3Kristina Teär Fahnehjelm4Department of Clinical Neuroscience, Karolinska Institutet and St Erik Eye Hospital, Polhemsgatan 50, SE 112 82 Stockholm, Sweden1Department of Clinical Neurophysiology, Karolinska University Hospital, Huddinge, Stockholm, SwedenDepartment of Clintec, Karolinska Institutet, and Department of Paediatrics, Karolinska University Hospital, Huddinge, Stockholm, SwedenDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, SwedenDepartment of Clinical Neuroscience, Karolinska Institutet and St Erik Eye Hospital, Polhemsgatan 50, SE 112 82 Stockholm, Sweden1; Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden; Department of Paediatric Ophthalmology, St. Erik Eye Hospital, Polhemsgatan 50, SE 112 82 Stockholm, Sweden; Corresponding author at: Department of Paediatric Ophthalmology, St. Erik Eye Hospital, Polhemsgatan 50, 112 82 Stockholm, Sweden.Objective: To study visual pathway pathology detected by visual evoked potentials (VEPs) in patients treated with hematopoietic stem cell transplantation (HSCT) in childhood and to determine the impact of adverse ocular findings, somatic diseases, and conditioning regimens on the VEP results. Methods: Ophthalmological assessments including pattern VEPs were performed in 47 of 79 patients at a median age of 15 years (range 3–21 years) in median 6 years (1–17 years) after HSCT. Somatic data were extracted from medical records. Results: Eight patients of 47 (17%) demonstrated pathological VEPs with prolonged latencies bilaterally (n = 3) or unilaterally (n = 5) at their latest VEP test at an age of 12–18 years. A subnormal visual acuity was present in 8/11 eyes with pathological VEPs: one eye had cataract, six eyes had cataract surgery where of two had developed secondary cataracts. One eye had residual retinopathy of prematurity. Pathological VEPs were associated with decreased visual acuity (p = 0.00019) but not linked to gender, malignant diagnosis or conditioning. Conclusion: VEP recordings showed an association with decreased visual acuity but no relationship with irradiation or chemotherapy in the present study. Significance: VEP recordings might be of clinical value for children with an unexplained subnormal visual acuity undergoing HSCT. Keywords: Hematopoietic stem cell transplantation, Visual acuity, Visual evoked potentialshttp://www.sciencedirect.com/science/article/pii/S2467981X17300033 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alba Lucia Törnquist Thomas Andersson Jacek Winiarski Marita Andersson Grönlund Kristina Teär Fahnehjelm |
spellingShingle |
Alba Lucia Törnquist Thomas Andersson Jacek Winiarski Marita Andersson Grönlund Kristina Teär Fahnehjelm Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood Clinical Neurophysiology Practice |
author_facet |
Alba Lucia Törnquist Thomas Andersson Jacek Winiarski Marita Andersson Grönlund Kristina Teär Fahnehjelm |
author_sort |
Alba Lucia Törnquist |
title |
Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood |
title_short |
Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood |
title_full |
Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood |
title_fullStr |
Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood |
title_full_unstemmed |
Visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood |
title_sort |
visual evoked potentials after hematopoietic allogeneic stem cell transplantation in childhood |
publisher |
Elsevier |
series |
Clinical Neurophysiology Practice |
issn |
2467-981X |
publishDate |
2017-01-01 |
description |
Objective: To study visual pathway pathology detected by visual evoked potentials (VEPs) in patients treated with hematopoietic stem cell transplantation (HSCT) in childhood and to determine the impact of adverse ocular findings, somatic diseases, and conditioning regimens on the VEP results. Methods: Ophthalmological assessments including pattern VEPs were performed in 47 of 79 patients at a median age of 15 years (range 3–21 years) in median 6 years (1–17 years) after HSCT. Somatic data were extracted from medical records. Results: Eight patients of 47 (17%) demonstrated pathological VEPs with prolonged latencies bilaterally (n = 3) or unilaterally (n = 5) at their latest VEP test at an age of 12–18 years. A subnormal visual acuity was present in 8/11 eyes with pathological VEPs: one eye had cataract, six eyes had cataract surgery where of two had developed secondary cataracts. One eye had residual retinopathy of prematurity. Pathological VEPs were associated with decreased visual acuity (p = 0.00019) but not linked to gender, malignant diagnosis or conditioning. Conclusion: VEP recordings showed an association with decreased visual acuity but no relationship with irradiation or chemotherapy in the present study. Significance: VEP recordings might be of clinical value for children with an unexplained subnormal visual acuity undergoing HSCT. Keywords: Hematopoietic stem cell transplantation, Visual acuity, Visual evoked potentials |
url |
http://www.sciencedirect.com/science/article/pii/S2467981X17300033 |
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