Skip to main content
Top
Published in: Pediatric Surgery International 12/2008

01-12-2008 | Original Article

Significance of pulmonary artery size and blood flow as a predictor of outcome in congenital diaphragmatic hernia

Authors: Tadaharu Okazaki, Manabu Okawada, Satoko Shiyanagi, Hiromichi Shoji, Toshiaki Shimizu, Toshitaka Tanaka, Satoru Takeda, Kazunari Kawashima, Geoffrey J. Lane, Atsuyuki Yamataka

Published in: Pediatric Surgery International | Issue 12/2008

Login to get access

Abstract

Aim

To determine if pulmonary artery size and blood flow have prognostic value in congenital diaphragmatic hernia (CDH).

Methods

Twenty-eight consecutive left-sided CDH patients treated according to a standard protocol with high frequency oscillatory ventilation (HFOV) + nitric oxide (NO) had right and left pulmonary artery (RPA, LPA) diameters, LPA/RPA diameter (L/R) ratios, and PA blood flows examined by echocardiography (EC) on days 0, 2, and 5 after birth and compared prospectively.

Results

Twenty-two patients (78.6%) survived. Of these, 15 required NO (NO-s), and seven did not (non-NO-s). All six patients that died required NO (NO-d). RPA in the NO-d group was significantly smaller than in the NO-s or non-NO-s groups on day 0 (2.90 ± 0.41 vs. 3.40 ± 0.49 or 4.01 ± 0.43; P < 0.01, respectively). LPA in the NO-d group was significantly smaller than in the non-NO-s on day 0 (2.13 ± 0.45 vs. 3.39 ± 0.34; P < 0.01). L/R ratios in NO subjects were significantly smaller (NO-s 0.74 ± 0.11; NO-d 0.73 ± 0.11) than in non-NO-s subjects (0.84 ± 0.03) on day 0 (P < 0.01). PA diameters and L/R ratios did not change significantly from day 0 to day 5 in all three groups. There was LPA flow on day 0 in all non-NO-s subjects, but none in all NO subjects. In the NO-s group, LPA flow was confirmed in 87% (13/15) on day 2 and in 100% on day 5, however, there was no LPA flow from day 0 to day 5 in any of the NO-d group.

Conclusion

Our data indicate that PA diameters on day 0 and LPA flow are strongly prognostic in left-sided CDH and L/R ratio would appear to be a simple highly reliable indicator of the necessity for NO therapy.
Literature
1.
go back to reference Molenaar JC, Bos AP, Hazebroek FWJ, Tibboel D (1991) Congenital diaphragmatic hernia, what defect? J Pediatr Surg 26:248–254PubMedCrossRef Molenaar JC, Bos AP, Hazebroek FWJ, Tibboel D (1991) Congenital diaphragmatic hernia, what defect? J Pediatr Surg 26:248–254PubMedCrossRef
2.
go back to reference The congenital diaphragmatic hernia study group (2001) Estimating disease severity of congenital diaphragmatic hernia in the first 5 minutes of life. J Pediatr Surg 36:141–145CrossRef The congenital diaphragmatic hernia study group (2001) Estimating disease severity of congenital diaphragmatic hernia in the first 5 minutes of life. J Pediatr Surg 36:141–145CrossRef
3.
go back to reference The congenital diaphragmatic hernia study group (2006) Treatment evolution in high-risk congenital diaphragmatic hernia—ten years’ experience with diaphragmatic agenesis. Ann Surg 244:505–513 The congenital diaphragmatic hernia study group (2006) Treatment evolution in high-risk congenital diaphragmatic hernia—ten years’ experience with diaphragmatic agenesis. Ann Surg 244:505–513
4.
go back to reference Usui N, Okuyama H, Sawai T, Kamiyama M, Kamata S, Fukuzawa M (2007) Relationship between L/T ratio and LHR in the prenatal assessment of pulmonary hypoplasia in congenital diaphragmatic hernia. Pediatr Surg Int 23:971–976PubMedCrossRef Usui N, Okuyama H, Sawai T, Kamiyama M, Kamata S, Fukuzawa M (2007) Relationship between L/T ratio and LHR in the prenatal assessment of pulmonary hypoplasia in congenital diaphragmatic hernia. Pediatr Surg Int 23:971–976PubMedCrossRef
5.
go back to reference Kitano Y, Nakagawa S, Kuroda T, Honna T, Itoh Y, Nakamura T, Morikawa N, Shimizu N, Kashima K, Hayashi S, Sago H (2005) Liver position in fetal congenital diaphragmatic hernia retains a prognostic value in the era of lung-protective strategy. J Pediatr Surg 40:1827–1832PubMedCrossRef Kitano Y, Nakagawa S, Kuroda T, Honna T, Itoh Y, Nakamura T, Morikawa N, Shimizu N, Kashima K, Hayashi S, Sago H (2005) Liver position in fetal congenital diaphragmatic hernia retains a prognostic value in the era of lung-protective strategy. J Pediatr Surg 40:1827–1832PubMedCrossRef
6.
go back to reference Sokol J, Bohn D, Lacro RV, Ryan G, Stephens D, Rabinovich M (2002) Fetal pulmonary artery diameters and their association with lung hypoplasia and postnatal outcome in congenital diaphragmatic hernia. Am J Obstet Gynecol 186:1085–1090PubMedCrossRef Sokol J, Bohn D, Lacro RV, Ryan G, Stephens D, Rabinovich M (2002) Fetal pulmonary artery diameters and their association with lung hypoplasia and postnatal outcome in congenital diaphragmatic hernia. Am J Obstet Gynecol 186:1085–1090PubMedCrossRef
7.
go back to reference Sokol J, Shimizu N, Bohn D, Doherty D, Ryan G, Hornberger LK (2006) Fetal pulmonary artery diameter measurements as a predictor of morbidity in antenatally diagnosed congenital diaphragmatic hernia: a prospective study. Am J Obstet Gynecol 195:470–477PubMedCrossRef Sokol J, Shimizu N, Bohn D, Doherty D, Ryan G, Hornberger LK (2006) Fetal pulmonary artery diameter measurements as a predictor of morbidity in antenatally diagnosed congenital diaphragmatic hernia: a prospective study. Am J Obstet Gynecol 195:470–477PubMedCrossRef
8.
go back to reference Hasegawa S, Kohno S, Sugiyama T (1994) Usefulness of echocardiographic measurement of bilateral pulmonary artery dimensions in congenital diaphragmatic hernia. J Pediatr Surg 29:622–624PubMedCrossRef Hasegawa S, Kohno S, Sugiyama T (1994) Usefulness of echocardiographic measurement of bilateral pulmonary artery dimensions in congenital diaphragmatic hernia. J Pediatr Surg 29:622–624PubMedCrossRef
9.
go back to reference Okazaki T, Kohno S, Hasegawa S, Urushihara N, Yoshida A, Kawano S, Saito A, Tanaka Y (2003) Congenital diaphragmatic hernia: efficacy of ultrasound examination in its management. Pediatr Surg Int 19:176–179PubMed Okazaki T, Kohno S, Hasegawa S, Urushihara N, Yoshida A, Kawano S, Saito A, Tanaka Y (2003) Congenital diaphragmatic hernia: efficacy of ultrasound examination in its management. Pediatr Surg Int 19:176–179PubMed
10.
go back to reference Ochikubo CG, Waffarn F, Turbow R, Kanakriyeh M (1997) Echocardiographic evidence of improved hemodynamics during inhaled nitric oxide therapy for persistent pulmonary hypertension of the newborn. Pediatr Cardiol 18:282–287PubMedCrossRef Ochikubo CG, Waffarn F, Turbow R, Kanakriyeh M (1997) Echocardiographic evidence of improved hemodynamics during inhaled nitric oxide therapy for persistent pulmonary hypertension of the newborn. Pediatr Cardiol 18:282–287PubMedCrossRef
11.
go back to reference Dillon PW, Cilley RE, Mauger D, Zachary C, Meier A (2004) The relationship of pulmonary artery pressure and survival in congenital diaphragmatic hernia. J Pediatr Surg 39:307–312PubMedCrossRef Dillon PW, Cilley RE, Mauger D, Zachary C, Meier A (2004) The relationship of pulmonary artery pressure and survival in congenital diaphragmatic hernia. J Pediatr Surg 39:307–312PubMedCrossRef
12.
go back to reference Okawada M, Okazaki T, Yamataka A, Yanai T, Kato Y, Kobayashi H, Lane GJ, Miyano T (2006) Efficacy of protocolized management for congenital diaphragmatic hernia. A review of 100 cases. Pediatr Surg Int 22:925–930PubMedCrossRef Okawada M, Okazaki T, Yamataka A, Yanai T, Kato Y, Kobayashi H, Lane GJ, Miyano T (2006) Efficacy of protocolized management for congenital diaphragmatic hernia. A review of 100 cases. Pediatr Surg Int 22:925–930PubMedCrossRef
13.
go back to reference O’Tool SJ, Karamanoukian HL, Glick PL (1996) Cardiopulmonary consequences of congenital diaphragmatic hernia. J Pedinatol 16:34–39 O’Tool SJ, Karamanoukian HL, Glick PL (1996) Cardiopulmonary consequences of congenital diaphragmatic hernia. J Pedinatol 16:34–39
14.
go back to reference Buss M, Williams G, Dilley A, Jones O (2006) Prevention of heart failure in the management of congenital diaphragmatic hernia by maintaining ductal patency. A case report. J Pediatr Surg 41:E9–E11PubMedCrossRef Buss M, Williams G, Dilley A, Jones O (2006) Prevention of heart failure in the management of congenital diaphragmatic hernia by maintaining ductal patency. A case report. J Pediatr Surg 41:E9–E11PubMedCrossRef
15.
go back to reference Geggel PL, Murphy JD, Langleben D, Crone RK, Vacanti JP, Reid LA (1985) Congenital diaphragmatic hernia: arterial structural changes and persistent pulmonary hypertension after surgical repair. J Pediatr 107:457–464PubMedCrossRef Geggel PL, Murphy JD, Langleben D, Crone RK, Vacanti JP, Reid LA (1985) Congenital diaphragmatic hernia: arterial structural changes and persistent pulmonary hypertension after surgical repair. J Pediatr 107:457–464PubMedCrossRef
16.
go back to reference Taira Y, Yamataka T, Miyazaki E, Puri P (1998) Comparison of the pulmonary vasculature in newborns and stillborns with congenital diaphragmatic hernia. Pediatr Surg Int 14:30–35PubMedCrossRef Taira Y, Yamataka T, Miyazaki E, Puri P (1998) Comparison of the pulmonary vasculature in newborns and stillborns with congenital diaphragmatic hernia. Pediatr Surg Int 14:30–35PubMedCrossRef
17.
go back to reference Sokol J, Bohn D, Lacro RV, Ryan G, Stephens D, Rabinovitch M (2002) Fetal pulmonary artery diameters and their association with lung hypoplasia and postnatal outcome in congenital diaphragmatic hernia. Am J Obstet Gynecol 186:1085–1090PubMedCrossRef Sokol J, Bohn D, Lacro RV, Ryan G, Stephens D, Rabinovitch M (2002) Fetal pulmonary artery diameters and their association with lung hypoplasia and postnatal outcome in congenital diaphragmatic hernia. Am J Obstet Gynecol 186:1085–1090PubMedCrossRef
18.
go back to reference Sokol J, Shimizu N, Bohn D, Dohrty D, Ryan G, Hornberger LK (2006) Fetal pulmonary artery diameter measurements as a predictor of morbidity in antenatally diagnosed congenital diaphragmatic hernia: a prospective study. Am J Obstet Gynecol 195:470–477PubMedCrossRef Sokol J, Shimizu N, Bohn D, Dohrty D, Ryan G, Hornberger LK (2006) Fetal pulmonary artery diameter measurements as a predictor of morbidity in antenatally diagnosed congenital diaphragmatic hernia: a prospective study. Am J Obstet Gynecol 195:470–477PubMedCrossRef
19.
go back to reference Walsh MC, Stock EK (2001) Persistent pulmonary hypertension of the newborn. Rational therapy based on pathophysiology. Clin Peinatol 28:609–627CrossRef Walsh MC, Stock EK (2001) Persistent pulmonary hypertension of the newborn. Rational therapy based on pathophysiology. Clin Peinatol 28:609–627CrossRef
20.
go back to reference Okuyama H, Kubota A, Oue T, Kuroda S, Ikegami R, Kamiyama M, Kitayama Y, Yagi M (2002) Inhaled nitric oxide with early surgery improves the outcome of antenatally diagnosed congenital diaphragmatic hernia. J Pediatr Surg 37:1188–1190PubMedCrossRef Okuyama H, Kubota A, Oue T, Kuroda S, Ikegami R, Kamiyama M, Kitayama Y, Yagi M (2002) Inhaled nitric oxide with early surgery improves the outcome of antenatally diagnosed congenital diaphragmatic hernia. J Pediatr Surg 37:1188–1190PubMedCrossRef
21.
go back to reference Christou H, Marter J, Wessel DL et al (2000) Inhaled nitric oxide reduces the need for ECMO in infants with persistent pulmonary hypertension of the newborn. Crit Care Med 28:3722–3727PubMedCrossRef Christou H, Marter J, Wessel DL et al (2000) Inhaled nitric oxide reduces the need for ECMO in infants with persistent pulmonary hypertension of the newborn. Crit Care Med 28:3722–3727PubMedCrossRef
22.
go back to reference The national inhaled nitric oxide study group (1997) Inhaled nitric oxide and hypoxic respiratory failure in infants with congenital diaphragmatic hernia. Pediatrics 99:838–845CrossRef The national inhaled nitric oxide study group (1997) Inhaled nitric oxide and hypoxic respiratory failure in infants with congenital diaphragmatic hernia. Pediatrics 99:838–845CrossRef
23.
go back to reference Okazaki T, Sharma HS, McCune SK, Tibboel D (1998) Pulmonary vascular balance in congenital diaphragmatic hernia: enhanced endothelin-1 gene expression as a possible cause of pulmonary vasoconstriction. J Pediatr Surg 33:81–84PubMedCrossRef Okazaki T, Sharma HS, McCune SK, Tibboel D (1998) Pulmonary vascular balance in congenital diaphragmatic hernia: enhanced endothelin-1 gene expression as a possible cause of pulmonary vasoconstriction. J Pediatr Surg 33:81–84PubMedCrossRef
24.
go back to reference Kobayashi H, Puri P (1994) Plasma endothelin levels in congenital diaphragmatic hernia. J Pediatr Surg 29:1258–1261PubMedCrossRef Kobayashi H, Puri P (1994) Plasma endothelin levels in congenital diaphragmatic hernia. J Pediatr Surg 29:1258–1261PubMedCrossRef
25.
go back to reference Shiyanagi S, Okazaki T, Shoji H, Shimizu T, Tanaka T, Takeda S, Lane GJ, Yamataka A (2008) Management of pulmonary hypertension in congenital diaphragmatic hernia: nitric oxide with prostaglandin-E1 vs. nitric oxide alone. Pediatr Surg Int (in press) Shiyanagi S, Okazaki T, Shoji H, Shimizu T, Tanaka T, Takeda S, Lane GJ, Yamataka A (2008) Management of pulmonary hypertension in congenital diaphragmatic hernia: nitric oxide with prostaglandin-E1 vs. nitric oxide alone. Pediatr Surg Int (in press)
Metadata
Title
Significance of pulmonary artery size and blood flow as a predictor of outcome in congenital diaphragmatic hernia
Authors
Tadaharu Okazaki
Manabu Okawada
Satoko Shiyanagi
Hiromichi Shoji
Toshiaki Shimizu
Toshitaka Tanaka
Satoru Takeda
Kazunari Kawashima
Geoffrey J. Lane
Atsuyuki Yamataka
Publication date
01-12-2008
Publisher
Springer-Verlag
Published in
Pediatric Surgery International / Issue 12/2008
Print ISSN: 0179-0358
Electronic ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-008-2266-x

Other articles of this Issue 12/2008

Pediatric Surgery International 12/2008 Go to the issue