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Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study

We aimed to compare ratings of self‐reported and parent‐reported pain sensitivity between early preterm (EP), moderately‐late preterm (MLP), and full‐term (FT) adolescents. For EP adolescents, we aimed to determine whether pain sensitivity was associated with early‐life events. EP (n = 68, response...

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Autores principales: van Dokkum, Nienke H., de Kroon, Marlou L. A., Reijneveld, Sijmen A., Bos, Arend F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975215/
https://www.ncbi.nlm.nih.gov/pubmed/35547596
http://dx.doi.org/10.1002/pne2.12053
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author van Dokkum, Nienke H.
de Kroon, Marlou L. A.
Reijneveld, Sijmen A.
Bos, Arend F.
author_facet van Dokkum, Nienke H.
de Kroon, Marlou L. A.
Reijneveld, Sijmen A.
Bos, Arend F.
author_sort van Dokkum, Nienke H.
collection PubMed
description We aimed to compare ratings of self‐reported and parent‐reported pain sensitivity between early preterm (EP), moderately‐late preterm (MLP), and full‐term (FT) adolescents. For EP adolescents, we aimed to determine whether pain sensitivity was associated with early‐life events. EP (n = 68, response rate 47.4%), MLP (n = 128, response rate 33.0%), and FT (n = 78, response rate 31.1%) adolescents and their parents (n = 277) answered an author‐generated question on pain sensitivity at 14‐15 years of age within a community‐based cohort study. Differences between groups were determined using the chi‐square test for trends. For EP adolescents, we assessed associations of treatment modalities (inotrope treatment, mechanical ventilation, and C‐section) and neonatal morbidities (sepsis/necrotizing enterocolitis, small‐for‐gestational age status, asphyxia, and cerebral pathologies) with adolescent pain sensitivity using logistic regression analyses. Increased pain sensitivity was reported by 18% of EP adolescents, compared with 12% of MLP adolescents, and 7% of FT adolescents (P = 0.033). Parent‐reported pain sensitivity did not differ by gestational age group. For EP adolescents, inotrope treatment was associated with increased pain sensitivity (odds ratio, 5.00, 95% confidence interval, 1.23‐20.4, P = 0.025). No other neonatal treatment modalities or morbidities were associated with pain sensitivity in adolescence. In conclusion, we observed higher proportions of increased pain sensitivity for EP and MLP adolescents. Physicians treating preterm adolescents should be aware of altered pain sensitivity.
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spelling pubmed-89752152022-05-10 Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study van Dokkum, Nienke H. de Kroon, Marlou L. A. Reijneveld, Sijmen A. Bos, Arend F. Paediatr Neonatal Pain Original Researches We aimed to compare ratings of self‐reported and parent‐reported pain sensitivity between early preterm (EP), moderately‐late preterm (MLP), and full‐term (FT) adolescents. For EP adolescents, we aimed to determine whether pain sensitivity was associated with early‐life events. EP (n = 68, response rate 47.4%), MLP (n = 128, response rate 33.0%), and FT (n = 78, response rate 31.1%) adolescents and their parents (n = 277) answered an author‐generated question on pain sensitivity at 14‐15 years of age within a community‐based cohort study. Differences between groups were determined using the chi‐square test for trends. For EP adolescents, we assessed associations of treatment modalities (inotrope treatment, mechanical ventilation, and C‐section) and neonatal morbidities (sepsis/necrotizing enterocolitis, small‐for‐gestational age status, asphyxia, and cerebral pathologies) with adolescent pain sensitivity using logistic regression analyses. Increased pain sensitivity was reported by 18% of EP adolescents, compared with 12% of MLP adolescents, and 7% of FT adolescents (P = 0.033). Parent‐reported pain sensitivity did not differ by gestational age group. For EP adolescents, inotrope treatment was associated with increased pain sensitivity (odds ratio, 5.00, 95% confidence interval, 1.23‐20.4, P = 0.025). No other neonatal treatment modalities or morbidities were associated with pain sensitivity in adolescence. In conclusion, we observed higher proportions of increased pain sensitivity for EP and MLP adolescents. Physicians treating preterm adolescents should be aware of altered pain sensitivity. John Wiley and Sons Inc. 2021-05-11 /pmc/articles/PMC8975215/ /pubmed/35547596 http://dx.doi.org/10.1002/pne2.12053 Text en © 2021 The Authors. Paediatric and Neonatal Pain published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Researches
van Dokkum, Nienke H.
de Kroon, Marlou L. A.
Reijneveld, Sijmen A.
Bos, Arend F.
Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study
title Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study
title_full Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study
title_fullStr Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study
title_full_unstemmed Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study
title_short Self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: A community‐based cohort study
title_sort self‐reported sensitivity to pain in early and moderately‐late preterm‐born adolescents: a community‐based cohort study
topic Original Researches
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975215/
https://www.ncbi.nlm.nih.gov/pubmed/35547596
http://dx.doi.org/10.1002/pne2.12053
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