2007
DOI: 10.1007/s00383-007-1980-0
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Relationship between L/T ratio and LHR in the prenatal assessment of pulmonary hypoplasia in congenital diaphragmatic hernia

Abstract: The lung to thorax transverse area ratio (L/T ratio) and the lung area to head circumference ratio (LHR) have been widely used for the assessment of pulmonary hypoplasia in fetal congenital diaphragmatic hernia (CDH). The aim of this study was to evaluate the relationship between the L/T ratio and the LHR, and to clarify the characteristics of these two indicators as prognostic predictors by means of retrospective concurrent measurements from the same subjects with prenatally diagnosed fetal CDH. The medical r… Show more

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Cited by 39 publications
(31 citation statements)
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“…Persistent pulmonary hypertension (PPHN) is intimately associated with the pathophysiology of cardiopulmonary distress in CDH. To predict severity of PPHN and clinical outcome, several parameters such as fetal lung to thorax area ratio [4], liver position [5], fetal pulmonary artery (PA) size [6,7], and postnatal PA size and blood flow [8][9][10] have been reported to be reliable, but most are only assessed at a single point in time either prenatally or postnatally, and their change over time is not usually evaluated.…”
Section: Introductionmentioning
confidence: 99%
“…Persistent pulmonary hypertension (PPHN) is intimately associated with the pathophysiology of cardiopulmonary distress in CDH. To predict severity of PPHN and clinical outcome, several parameters such as fetal lung to thorax area ratio [4], liver position [5], fetal pulmonary artery (PA) size [6,7], and postnatal PA size and blood flow [8][9][10] have been reported to be reliable, but most are only assessed at a single point in time either prenatally or postnatally, and their change over time is not usually evaluated.…”
Section: Introductionmentioning
confidence: 99%
“…A termination of pregnancy was performed in all 5 cases of the high-potential group. Although the pulmonary hypoplasia of the 2 cases of isolated congenital diaphragmatic hernia were predicted to be severe based on the fetal ultrasonography findings [8], the potential for long-term survival in these cases appeared to be relatively high [8]. A fetus with congenital cystic adenomatoid malformation would be more likely to survive based on the contralateral lung size [9].…”
Section: Resultsmentioning
confidence: 96%
“…The cases demonstrating neonatal surgical diseases with active policies included congenital diaphragmatic hernia (n = 23), cystic lung disease (n = 16), intestinal atresia (n = 14), meconium peritonitis (n = 13), omphalocele (n = 11), duodenal atresia (10), ovarian cyst (10), sacrococcygeal teratoma (8), and others (n = 57). Among the 162 cases with active policies, 3 fetuses died in utero and 16 fetuses died after birth.…”
Section: Resultsmentioning
confidence: 99%
“…Of note, LHR normally changes with advancing gestational age; therefore, a fixed cutoff, as initially proposed, can be misleading (Peralta et al, 2005;Ba'ath et al, 2007;Jani et al, 2007;Usui et al, 2007). Therefore, an observed-to-expected (O/E) LHR could be used regardless of the gestational age at which the study was done (Peralta et al, 2005;Jani et al, 2006b, Kilian et al, 2009.…”
Section: Lung To Head Ratiomentioning
confidence: 99%