High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border

Population risks for neonatal hyperbilirubinaemia (NH) vary. Knowledge of local risks permits interventions that may reduce the proportion becoming severe. Between January 2015 and May 2016, in a resource-limited setting on the Thailand-Myanmar border, neonates from 28 weeks’ gestation were enrolled...

Popoln opis

Bibliografske podrobnosti
Main Authors: Thielemans, L, Peerawaranun, P, Mukaka, M, Paw, MK, Wiladphaingern, J, Landier, J, Bancone, G, Proux, S, Elsinga, H, Trip-Hoving, M, Hanboonkunupakarn, B, Htoo, TL, Wah, TS, Beau, C, Nosten, F, McGready, R, Carrara, VI
Format: Journal article
Jezik:English
Izdano: Public Library of Science 2021
_version_ 1826265355617566720
author Thielemans, L
Peerawaranun, P
Mukaka, M
Paw, MK
Wiladphaingern, J
Landier, J
Bancone, G
Proux, S
Elsinga, H
Trip-Hoving, M
Hanboonkunupakarn, B
Htoo, TL
Wah, TS
Beau, C
Nosten, F
McGready, R
Carrara, VI
author_facet Thielemans, L
Peerawaranun, P
Mukaka, M
Paw, MK
Wiladphaingern, J
Landier, J
Bancone, G
Proux, S
Elsinga, H
Trip-Hoving, M
Hanboonkunupakarn, B
Htoo, TL
Wah, TS
Beau, C
Nosten, F
McGready, R
Carrara, VI
author_sort Thielemans, L
collection OXFORD
description Population risks for neonatal hyperbilirubinaemia (NH) vary. Knowledge of local risks permits interventions that may reduce the proportion becoming severe. Between January 2015 and May 2016, in a resource-limited setting on the Thailand-Myanmar border, neonates from 28 weeks’ gestation were enrolled into a prospective birth cohort. Each neonate had total serum bilirubin measurements: scheduled (24, 48, 72 and 144 hours of life) and clinically indicated; and weekly follow up until 1 month of age. Risk factors for developing NH were evaluated using Cox proportional hazard mixed model. Of 1710 neonates, 22% (376) developed NH (83% preterm, 19% term). All neonates born <35 weeks, four in five born 35–37 weeks, and three in twenty born ≥38 weeks had NH, giving an overall incidence of 249 per 1000 livebirths [95%CI 225, 403]. Mortality from acute bilirubin encephalopathy was 10% (2/20) amongst the 5.3% (20/376) who reached the severe NH threshold. One-quarter (26.3%) of NH occurred within 24 hours. NH onset varied with gestational age: at a median [IQR] 24 hours [24, 30] for neonates born 37 weeks or prematurely vs 59 hours [48, 84] for neonates born ≥38 weeks. Risk factors for NH in the first week of life independent of gestational age were: neonatal G6PD deficiency, birth bruising, Sgaw Karen ethnicity, primigravidae, pre-eclampsia, and prolonged rupture of membranes. The genetic impact of G6PD deficiency on NH was partially interpreted by using the florescent spot test and further genotyping work is in progress. The risk of NH in Sgaw Karen refugees may be overlooked internationally as they are most likely regarded as Burmese in countries of resettlement. Given high levels of pathological jaundice in the first 24 hours and overall high NH burden, guidelines changes were implemented including preventive PT for all neonates <35 weeks and for those 35–37 weeks with risk factors.
first_indexed 2024-03-06T20:22:24Z
format Journal article
id oxford-uuid:2e43f917-b13c-4539-b280-3fdd5458a072
institution University of Oxford
language English
last_indexed 2024-03-06T20:22:24Z
publishDate 2021
publisher Public Library of Science
record_format dspace
spelling oxford-uuid:2e43f917-b13c-4539-b280-3fdd5458a0722022-03-26T12:47:57ZHigh levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar borderJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2e43f917-b13c-4539-b280-3fdd5458a072EnglishSymplectic ElementsPublic Library of Science2021Thielemans, LPeerawaranun, PMukaka, MPaw, MKWiladphaingern, JLandier, JBancone, GProux, SElsinga, HTrip-Hoving, MHanboonkunupakarn, BHtoo, TLWah, TSBeau, CNosten, FMcGready, RCarrara, VIPopulation risks for neonatal hyperbilirubinaemia (NH) vary. Knowledge of local risks permits interventions that may reduce the proportion becoming severe. Between January 2015 and May 2016, in a resource-limited setting on the Thailand-Myanmar border, neonates from 28 weeks’ gestation were enrolled into a prospective birth cohort. Each neonate had total serum bilirubin measurements: scheduled (24, 48, 72 and 144 hours of life) and clinically indicated; and weekly follow up until 1 month of age. Risk factors for developing NH were evaluated using Cox proportional hazard mixed model. Of 1710 neonates, 22% (376) developed NH (83% preterm, 19% term). All neonates born <35 weeks, four in five born 35–37 weeks, and three in twenty born ≥38 weeks had NH, giving an overall incidence of 249 per 1000 livebirths [95%CI 225, 403]. Mortality from acute bilirubin encephalopathy was 10% (2/20) amongst the 5.3% (20/376) who reached the severe NH threshold. One-quarter (26.3%) of NH occurred within 24 hours. NH onset varied with gestational age: at a median [IQR] 24 hours [24, 30] for neonates born 37 weeks or prematurely vs 59 hours [48, 84] for neonates born ≥38 weeks. Risk factors for NH in the first week of life independent of gestational age were: neonatal G6PD deficiency, birth bruising, Sgaw Karen ethnicity, primigravidae, pre-eclampsia, and prolonged rupture of membranes. The genetic impact of G6PD deficiency on NH was partially interpreted by using the florescent spot test and further genotyping work is in progress. The risk of NH in Sgaw Karen refugees may be overlooked internationally as they are most likely regarded as Burmese in countries of resettlement. Given high levels of pathological jaundice in the first 24 hours and overall high NH burden, guidelines changes were implemented including preventive PT for all neonates <35 weeks and for those 35–37 weeks with risk factors.
spellingShingle Thielemans, L
Peerawaranun, P
Mukaka, M
Paw, MK
Wiladphaingern, J
Landier, J
Bancone, G
Proux, S
Elsinga, H
Trip-Hoving, M
Hanboonkunupakarn, B
Htoo, TL
Wah, TS
Beau, C
Nosten, F
McGready, R
Carrara, VI
High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border
title High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border
title_full High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border
title_fullStr High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border
title_full_unstemmed High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border
title_short High levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the Thailand-Myanmar border
title_sort high levels of pathological jaundice in the first 24 hours and neonatal hyperbilirubinaemia in an epidemiological cohort study on the thailand myanmar border
work_keys_str_mv AT thielemansl highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT peerawaranunp highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT mukakam highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT pawmk highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT wiladphaingernj highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT landierj highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT banconeg highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT prouxs highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT elsingah highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT triphovingm highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT hanboonkunupakarnb highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT htootl highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT wahts highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT beauc highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT nostenf highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT mcgreadyr highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder
AT carraravi highlevelsofpathologicaljaundiceinthefirst24hoursandneonatalhyperbilirubinaemiainanepidemiologicalcohortstudyonthethailandmyanmarborder