2010
DOI: 10.1093/ije/dyq127
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Cohort Profile: The Nordic Perinatal Bereavement Cohort

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Cited by 42 publications
(58 citation statements)
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“…27 This population-based cohort study 28 . These registers include data on practically all deliveries in Denmark and Sweden, respectively, and the information is collected from medical records in prenatal, delivery and neonatal care.…”
Section: Study Design and Study Populationmentioning
confidence: 99%
See 1 more Smart Citation
“…27 This population-based cohort study 28 . These registers include data on practically all deliveries in Denmark and Sweden, respectively, and the information is collected from medical records in prenatal, delivery and neonatal care.…”
Section: Study Design and Study Populationmentioning
confidence: 99%
“…30 Socio-demographic factors were obtained from the Danish Integrated Database for Longitudinal Labor Market Research (IDA), the Danish Civil Registry System, the Swedish Education Registry and the Swedish Registry of Population and Population Changes. 28 Outcome measurements Data on cancer were obtained from national cancer registries, and the registration and coding practices have been described elsewhere. 31 32 The main outcomes of interest were all incident cancers (ICD-7 codes 104-205, ICD-10 codes C00-97) diagnosed before 15 years of age and the most frequent childhood cancers for which uterine environment has been suggested to play a role: 3 4 6-9 leukaemias (ICD-7 code 204, ICD-10 codes C91-95), lymphomas (ICD-7 code 201-203, ICD-10 code C81-C85), brain and nervous system tumours (ICD-7 code 193, ICD-10 codes C70-C72, C47, C74.1), retinoblastoma (ICD-7 code 192 and PAD 436, ICD-10 code C69.2), Wilms' tumour (ICD-7 code 180 and PAD 886, ICD-10 code C64.9), hepatoblastoma (ICD-7 code 155, ICD-10 code C22), malignant bone tumours (ICD-7 code 196, ICD-10 codes C40-C41) and testicular cancer (ICD-7 code 178, ICD-10 code C62).…”
Section: Study Design and Study Populationmentioning
confidence: 99%
“…We established the nordic Perinatal Bereavement cohort (details have been previously published) 26 using prospectively collected data from national registers in Denmark. every person born in or immigrating to Denmark obtains a unique identification number by which the individual is registered throughout the Danish health care systems, covering information on birth, diseases, familiar constitution, education, and death.…”
Section: Methodsmentioning
confidence: 99%
“…25 In brief, the unique civil personal registration number, which is assigned to all live-born children and new residents, was used to link children to their relatives and to information on birth, death, demographics, social data and various health outcomes from different national registers. Children of mothers with no personal registration number recorded were excluded as they could not be linked to their relatives (n=10 641; 0.17%).…”
Section: Materials and Methods Study Participants And Follow-upmentioning
confidence: 99%