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embryofoetopathie door indometacine (aandoening)
embryofoetopathie door indometacine
Indomethacin embryofetopathy
Embryofetopathy caused by indomethacin
Fetal indomethacin syndrome
Indomethacin embryofetopathy refers to the manifestations that may be observed in a fetus or newborn when the mother has taken indomethacin, a potent prostaglandin inhibitor and tocolytic agent that can cross placenta, during pregnancy. Reported adverse fetal/neonatal effects include decreased renal function resulting in oligohydramnios, closure of the ductus arteriosus, and delayed cardiovascular adaptation at birth. These effects are usually transient and reversible. Indomethacin may also be a risk factor for cerebral injury (periventricular leukomalacia) and necrotizing enterocolitis in preterm infants.
Id715430001
StatusPrimitive
Associated morphologymorfologische afwijking
Causative agentindometacine
Finding sitestructuur van foetus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ86.8
TermOverige congenitale gestoorde-ontwikkelingssyndromen door bekende exogene oorzaken
SNOMED CT to Orphanet simple map1909
SNOMED CT to ICD-10 extended map
TargetQ86.8
RuleTRUE
AdviceALWAYS Q86.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified