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. 2024 Jul 6;29(4):309–318. doi: 10.4103/jiaps.jiaps_53_24

Table 3.

Various clinical combinations and the counseling options which may be recommended to parents based on Management, Outcome, Risk, and Expectation

MORE category MORE combination Example
Continue pregnancy, good or fair prognosis M1 Mild hydronephrosis UTD A1
O1 Isolated soft markers such as choroid plexus cysts, echogenic cardiac foci, echogenic bowel
R1
E1
O2
R2
E2
Shared decision-making M2 Abdominal wall defect (low-risk types - exomphalos minor, perinatal gastroschisis)
PUV/hydronephrosis without oligohydramnios
Esophageal, duodenal, jejunoileal, and anorectal atresias
Meconium ileus
Enteric cysts and duplications
Small intact meningocele
Unilateral hydronephrosis
Craniofacial, extremity, and chest wall deformities
Cystic hygromas
Small sacrococcygeal teratoma, mesoblastic nephroma, etc.
Benign cysts: Ovarian, mesenteric, choledochal, etc.
M4 PUV with complications/oligohydramnios
O3 Myelomeningocele
R2 Exstrophy bladder
E2 Cleft lip and palate
M3 PUV with severe oligohydramnios/anhydramniossss
O3 Severe myelomeningocele/myeloschisis
R2 Severe hydrocephalus
E2 Large CPAM
High-risk CDH
Large sacrococcygeal teratoma
Large cystic hygroma
21 hydroxylase deficiency (Need to follow the evidence on indications/safety/feasibility/efficacy of fetal intervention)
M4 VACTERL
O4 Associated Major heart defect with a system anomaly
R2
E2
Termination is offered, final decision by parents M5 Anencephaly
O5 Bilateral PCKD
R3 Bilateral renal agenesis
E3 Eisenmenger’s syndrome/severe pulmonary hypertension
Severe anomalies associated with confirmed chromosomal abnormalities (e.g., trisomy 13)

MORE: Management, Outcome, Risk, and Expectation, CDH: Congenital diaphragmatic hernia, PUV: Posterior urethral valve, PCKD: PolyCystic kidney disease, CPAM: Congenital pulmonary adenomatoid malformation, UTD A1: Urinary Tract Dilation Classification (Mild Category)