REPORTING OF MALFORMATIONS IN ROUTINE HEALTH REGISTERS

Citation
E. Hemminki et al., REPORTING OF MALFORMATIONS IN ROUTINE HEALTH REGISTERS, Teratology, 48(3), 1993, pp. 227-231
Citations number
10
Categorie Soggetti
Developmental Biology
Journal title
ISSN journal
00403709
Volume
48
Issue
3
Year of publication
1993
Pages
227 - 231
Database
ISI
SICI code
0040-3709(1993)48:3<227:ROMIRH>2.0.ZU;2-W
Abstract
The utility of three national registers-the malformation, birth, and h ospital in-patient discharge registers-in identification of malformati ons among 60,255 children born in 1987 in Finland was compared. Inform ation in the malformation register is collected by specific reporting of physicians; information on the malformed children in the other two registers in 1987 through 1990 was routinely collected and identified by ICD 9-codes (740-759, 7886A). From October 1990 on, the ICD-9 codes were omitted from the birth register and malformation data were asked only in a yes-no question. In 1987, the malformation register include d 1,032, the birth register 3,084 and the inpatient register 2,003 mal formed infants identified up to the age of 1 year. There was underrepr esentation of almost all malformation diagnoses in the malformation re gister. Individual linkage of the three registers showed that the malf ormation register revealed very few cases not recorded in the birth an d the in-patient registers. With the adoption of the new recording met hod in the birth register beginning in October 1990, reports of malfor mation declined by 75%. Our analyses showed that data sources based on diagnoses collected routinely and not requiring an explicit decision on whether or not a problem is a malformation, can be more useful for routine surveillance of occurrence of malformations. (C) 1993 Wiley-Li ss, Inc.