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Predictors of the Outcome at 2 Years in Neonates With Congenital Cytomegalovirus Infection
被引:2
|作者:
Fourgeaud, Jacques
[1
,2
]
Magny, Jean-Francois
[1
,3
]
Couderc, Sophie
[7
]
Garcia, Patricia
[3
,8
]
Maillotte, Anne-Marie
[9
]
Benard, Melinda
[10
]
Pinquier, Didier
[11
]
Minodier, Philippe
[12
]
Astruc, Dominique
[13
]
Patural, Hugues
[14
]
Parat, Sophie
[15
]
Guillois, Bernard
[16
,17
]
Garenne, Armelle
[18
]
Guilleminot, Tiffany
[1
,2
]
Parodi, Marine
[4
]
Bussieres, Laurence
[1
,5
]
Ghout, Idir
[19
]
Ville, Yves
[1
,6
]
Leruez-Ville, Marianne
[1
,2
,20
]
机构:
[1] Univ Paris Cite, URP FETUS 7328, Paris, France
[2] Hosp Necker, AP HP, Virol Lab, Reference Lab Cytomegalovirus Infect, Paris, France
[3] Hop Necker Enfants Malad, AP HP, NICU, Paris, France
[4] Hop Necker Enfants Malad, AP HP, Otol Dept, Paris, France
[5] Hop Necker Enfants Malad, Clin Res Unit, P HP, AP HP, Paris, France
[6] Hop Necker Enfants Malad, AP HP, Matern, Paris, France
[7] Hosp Intercommunal Poissy St Germain, Matern, Poissy, France
[8] Hosp La Conception, AP HM, Neonatol & Intens Care Dept, Marseille, France
[9] CHU Nice, Hosp LArchet, Dept Clin Nutr, Nice, France
[10] Univ Toulouse, Toulouse Univ Hosp, Dept Neonatol, Infin, Toulouse, France
[11] Rouen Univ Hosp, Dept Neonatol, Rouen, France
[12] Hosp Nord, AP HM, Emergency Care Dept, Marseille, France
[13] Strasbourg Univ Hosp, Dept Neonatol, Strasbourg, France
[14] St Etienne Univ Hosp, Dept Neonatol, St Etienne, France
[15] Hosp Cochin, AP HP, Matern, Paris, France
[16] CHU Caen, Dept Neonatol, Caen, France
[17] Univ Caen Normandie, Med Sch, Caen, France
[18] CHRU Brest, Neonatal & Pediat ICU, Brest, France
[19] Cegedim Hlth Data, Boulogne Billancourt, France
[20] Hop Necker Enfants Malad, Virol Lab, 149 rue Sevres, F-75015 Paris, France
来源:
关键词:
HEARING-LOSS;
SEQUELAE;
CHILDREN;
RISK;
D O I:
10.1542/peds.2023-063531
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
BACKGROUND Approximately 20% of neonates with congenital cytomegalovirus (cCMV) develop long-term sequelae. The ability to accurately predict long-term outcomes as early as the neonatal period would help to provide for appropriate parental counseling and treatment indications. With this study, we aimed to identify neonatal predictive markers of cCMV long-term outcomes. METHODS As this study's subjects, we chose neonates diagnosed with cCMV in 13 hospitals throughout France recruited from 2013 to 2017 and evaluated for at least 2 years with thorough clinical, audiology, and imaging evaluations and psychomotor development tests. RESULTS A total of 253 neonates were included, and 3 were later excluded because of the identification of a genetic disorder. A total of 227 were followed up for 2 years: 187/227 (82%) and 34/227 (15%) were infected after a maternal primary or nonprimary infection, respectively, 91/227 (40%) were symptomatic at birth, and 44/227 (19%) had cCMV sequelae. Maternal primary infection in the first trimester was the strongest prognosis factor (odds ratio = 38.34 [95% confidence interval, 5.02-293], P < .001). A predictive model of no risk of sequelae at 2 years of age according to normal hearing loss at birth, normal cerebral ultrasound, and normal platelet count had 98% specificity, 69% sensitivity, and 0.89 area under the curve (95% confidence interval, 0.83-0.96). CONCLUSIONS In the studied population, children with normal hearing at birth, normal platelet count at birth, and a normal cranial ultrasound had no risk of neurologic sequelae and a low risk of delayed unilateral sensorineural hearing loss. The use of this model based on readily available neonatal markers should help clinicians establish a personalized care pathway for each cCMV neonate.
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