Jurnal Diagnostik - Wening CHD
Jurnal Diagnostik - Wening CHD
Jurnal Diagnostik - Wening CHD
P Asy
I
C Echocardiographic
O CHD
Pencarian Literatur
Strategi Pencarian
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Publication dates: 5 years
Latar Belakang
Tujuan
Lokasi Penelitian
Robert Debré University Children’s
Hospital, Paris, France
Desain Uji
monocentric observational prospective
analysis of collected data from September
2008 to March 2017
Metode Penelitian
Kriteria Inklusi
Kriteria Eksklusi
tidak ada
Pemilihan subjek
Data were recorded in a customized database at the time of newborn discharge.
Maternal data included ethnic group, presence of diabetes, or high blood
pressure.
Perinatal data included tocolysis, antenatal antibiotics and
glucocorticoidsexposure, clinical chorioamnionitis defined by maternal fever and
uterine contractions, prolonged membrane rupture (more than 24 h before birth),
analgesia and mode of delivery, gestational age at birth, birthweight, multiple
pregnancy, and APGAR score at 5 min of life.
Biological data included cord blood PCT at birth and CRP serum concentrations
at birth and at 24 h of life (cutoff for elevated CRP was ≥ 10 mg/L), gastric fluid,
blood and cerebrospinal fluid sampling.
The following postnatal complications of prematurity were collected: death,
bronchopulmonary dysplasia (BPD) defined using a standardized oxygen-reduction
test performed at 36 weeks of postmenstrual age, severe intraventricular
hemorrhage (IVH) grade 3 or 4 according to Papile’s classiffication, NEC ≥ 2a
according to Bell’s classification, surgery of patent ductus arteriosus, and LOS
defined by the detection of a bacterial pathogen in the blood after 72 h of life
requiring antibiotic treatment for more than 72 h
Karakteristik dasar dan karakteristik
klinis dari subjek penelitian
Hasil
Kesimpulan
KAJIAN KRITIS JURNAL
BOX I BOX II BOX III
Representativeness Does this (valid) evidence Is the diagnostic test
Was the diagnostic test demonstrate an important available, affordable,
evaluated in an appropriate ability of this test to accurate, and precise in
spectrum of patients (like
accurately distinguish our setting?
those in whom we would
use it in practice)?
patients who do and don't
have a specific disorder? Can we generate a
Ascertainment clinically sensible
Was the reference standard estimate of our patient's
ascertained regardless of pretest probability?
the diagnostic test result?
Will the resulting posttest
Measurement
Was there an independent,
probabilities affect our
blind comparison with a management and help
reference standard? our patient?
Validasi: 1. Was the diagnostic test evaluated in a
representative spectrum of patients (like those in whom
it would be used in practice)?
All extremely preterm neonates born between 240/7 weeks and
276/7 weeks with cord blood PCT lab testing were included in
the
study.
-Methods
Validasi: 2. Was the reference standard applied
regardless of the diagnostic test result?
Ya,
LIKELIHOOD
RATIO
POST-TEST
%
http://araw.mede.uic.edu/cgi-bin/testcalc.pl
Penting
Relevansi 1: Is the diagnostic test available, affordable,
accurate, and precise in our setting?
Ya.
Relevansi 2: Can we generate a clinically sensible
estimate of our patient's pretest probability?