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ISRN Critical Care
Volume 2013 (2013), Article ID 857365, 5 pages
Rescue High-Frequency Oscillatory Ventilation for Congenital Diaphragmatic Hernia: What about Lung Histopathology and Necropsy Findings?
1Division of Neonatology, Department of Pediatrics, Hospital de São João, 4200-319 Porto, Portugal
2Serviço de Neonatologia, Departamento de Pediatria, Hospital de São João–Piso 2, Alameda Prof. Hernâni Monteiro, 4200–319 Porto, Portugal
3Division of Pediatric Surgery, Department of Pediatrics, Hospital de São João, 4200-319 Porto, Portugal
4School of Health Sciences, Minho University, 4709-057 Braga, Portugal
5Faculty of Medicine, Porto University, Porto, Portugal
Received 1 October 2012; Accepted 5 November 2012
Academic Editors: M. Bailey and M. El-Khatib
Copyright © 2013 Gustavo Rocha et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Introduction. It is not yet a resolved issue whether HFOV (high-frequency oscillatory ventilation), used as primary mode or as rescue ventilation, has benefit over conventional mechanical ventilation for CDH (congenital diaphragmatic hernia) patients treatment. Purpose. To evaluate the success rate of rescue HFOV for CDH, and the histological characteristics of the lungs, at the autopsy of the deceased patients. Material and Methods. Out of 80 CDH patients, 10 were treated with rescue HFOV. The success of HFOV, histological exam of the lungs of deceased patients, and data on the followup of discharged patients were assessed. Results. Rescue HFOV was started between two hours and four days of life. The success rate of rescue HFOV was 20% (2/10). Autopsy findings along with pulmonary hypoplasia included coarctation of aorta , pneumonia , meconium aspiration , hyaline membranes , severe muscular hypertrophy of medium and small diameter lung arteries , severe lung hypoplasia , pleural effusions , haemorrhagic diatesis , and signs of overwhelming sepsis . The five-years follow up of the two survivors revealed normal growth and neurodevelopment. Conclusions. The results of this study support the idea that rescue HFOV may increase survival of CDH patients, when conventional mechanical ventilation fails.
The underlying pathophysiology of Bochdalek congenital diaphragmatic hernia (CDH) is that of pulmonary insufficiency and persistent pulmonary hypertension secondary to pulmonary hypoplasia. The severity of CDH is related mostly to the degree of hypoplasia, which depends on the size of the defect, the presence of the liver in the chest, and how early in gestation the abdominal contents were displaced .
A standardized postnatal management of infants with CDH, the CDH EURO Consortium Consensus, has been proposed in 2010 . The different centers treating CDH patients use different mechanical ventilation strategies, and most target the use of gentle ventilation and permissive hypercapnia. The actual recommendations include the use of high-frequency oscillatory ventilation (HFOV) if conventional mechanical ventilation (CMV) fails . Although many centers use HFOV as the primary mode of ventilation, it is not yet a resolved issue whether this approach has benefit over CMV. The ongoing multicenter randomized controlled trial, VICI trial, will help to clarify which primary respiratory mode, CMV or HFOV, has the most benefit on CDH patients.
Our center uses HFOV as a rescue ventilation mode for CDH patients. We conducted a study in order to evaluate the success rate of rescue HFOV, and the histological characteristics of the lungs at the autopsy exam of the deceased patients in which rescue HFOV failed.
2. Material and Methods
Cases of CDH were identified in our database, a tertiary referral centre for neonatal surgery. All neonates diagnosed with CDH from January 1997 to December 2010 were included. Analysed data were retrieved from maternal and infant medical records.
Since 2003, the management protocol of CDH has changed, and in 2010 the CDH EURO Consortium Consensus protocol has been adopted. Inhaled nitric oxide (INO, 20 ppm) was routinely used from 2003 after echocardiography and an oxygenation index (mean airway pressure fraction of inspired oxygen 100/partial arterial pressure of oxygen) over 20. Sildenafil has been used in infants with persistent pulmonary hypertension refractory to INO. A policy of delayed surgery after preoperative stabilization was practiced throughout the study period. Rescue HFOV was done using SensorMedics 3100A (Sensor Medics Corporation, Yorba, Linda, CA, USA), after a period of unsuccessful conventional mechanical ventilation.
The position of the liver, side of herniation, degree of pulmonary hypertension, settings of CMV before changing to HFOV, settings used on HFOV, effect of rescue HFOV on the respiratory status of the patient evaluated by blood gases samples, rate of success of HFOV and histological exam of the lungs, and other necropsy findings of those patients whose parents consented to autopsy were analyzed. Data on the followup of discharged patients who benefited from rescue HFOV were also evaluated.
Results are presented in absolute number and percentage of the total sample. Continuous variables are presented in median (minimum and maximum). Mann-Whitney test was used to compare two independent samples and a P value < 0.05 was considered significant.
The study was approved by the institutional research ethics board.
A total of 80 newborns with CDH were treated at our institution during the considered period. The demographics of patient population are reported in Table 1, and the clinical characteristics in Table 2. Rescue HFOV was used in ten patients, Table 3. HFOV was started between two hours and four days of life. The reason for rescue HFOV from CMV was hypercapnia (PaCO2 > 60 mmHg) in five patients (50%) and hypercapnia plus hypoxia (PaCO2 > 60 mmHg plus preductal saturation < 80%) in five patients (50%). Ventilation settings and indexes before and after HFOV are reported in Table 4. After starting on rescue HFOV there was no benefit over oxygenation in any patient, and there was a significant decrease of PaCO2 values, although not to normal values (45 and 60 mmHg) in three patients, and a decrease of PaCO2 values to normal values in five patients. Two (20%) patients survived and were discharged. The rate of success of rescue HFOV in this subgroup of ten patients was 20% (2/10).
The histological findings of the six patients whose parents consented to necropsy are reported in Table 5.
Clinical neonatal characteristics and followup of the two survivors of CDH after rescue HFOV are reported on Table 6.
Our center’s overall survival of CDH was 49% until 2003. Since 2003, the overall survival has raised to 67% with the implementation of new protocols of treatment. HFOV is used as rescue ventilation and according to the results of our study, two patients out of ten (20%) benefited from this respiratory mode.
Many studies in the literature reported that HFOV for preoperative stabilization and for intra- and postoperative respiratory treatment of CDH has been shown to be effective and associated with a superior survival rate when compared to CMV [4–10]. On the other hand, some other well-conducted studies did not show improvement in survival of CDH patients when HFOV was used as rescue or first intension respiratory mode [11–13]. Although some of these studies were performed years ago, in an era where therapies for pulmonary hypertension and CDH treatment protocols were limited, the comparison to CMV did favour HFOV in some studies, and did not in others. It is still an undefined issue whether HFOV has supremacy over CMV for CDH patients.
In our study, two patients benefited from rescue HFOV, and the five years followup does not show neurodevelopmental or other significant disabilities. The other eight patients to whom HFOV was offered as rescue respiratory mode did not survive. Looking at the necropsy findings of the six patients whose parents consented to necropsy we can understand why ventilation was unsuccessful. One patient with a coarctation of aorta not diagnosed prenatally, and other findings such as pneumonia, meconium aspiration, hyaline membranes, severe muscular hypertrophy of medium and small diameter lung arteries, severe lung hypoplasia, pleural effusions, and haemorrhagic diatesis, may explain the CMV and HFOV failure. It seems that the question is how are the lungs of the CDH patients? Are they hypoplastic without other histological findings that may worsen the outcome, or are there other findings that may worsen the diagnosis? In our small series, it seems that the other findings on the lungs, and in one case a coarctation of aorta, could be the explanation to the fatal outcome.
Two out of ten patients who were ventilated with HFOV had a good outcome, suggesting that these lungs probably did not present the ominous findings of the deceased patients. In these two patients rescue, HFOV proved to be superior to CMV.
Although limited by the small number of patients and the significant period of time considered (1997–2010) in which treatment strategies and protocols for CDH have changed, the results of this study support the idea that there is a role for HFOV in CDH, when used as rescue ventilation for selected patients or as first respiratory mode. Also, the results of this study show that we cannot judge the efficacy of one strategy of ventilation, if we do not know the histopathological characteristics of the lung. The reason why in some studies HFOV was, or was not, superior to CMV, could be better explained if a necropsy study and histological assessment of the lung were done.
More studies are needed to establish which respiratory mode, CMV or HFOV, is better for first respiratory treatment of CDH patients. We hope that the ongoing VICI trial may clarify this issue. The results of this study support the idea that HFOV may increase survival of CDH patients, when conventional ventilation fails.
We suggest that all deceased CDH patients should have a necropsy study in order to identify other congenital malformations that may pass undetected on prenatal and postnatal evaluation, and the lung histological findings that may explain the failure of the respiratory mode. In randomized studies comparing CMV and HFOV, the necropsy study is of great importance and should be part of the study, when comparing the failure of each respiratory mode.
- K. P. Lally, P. A. Lally, R. E. Lasky et al., “Defect size determines survival in infants with congenital diaphragmatic hernia,” Pediatrics, vol. 120, no. 3, pp. e651–e657, 2007.
- I. Reiss, T. Schaible, L. van den Hout et al., “Standardized postnatal management of infants with congenital diaphragmatic hernia in Europe: the CDH EURO consortium consensus,” Neonatology, vol. 98, no. 4, pp. 354–364, 2010.
- J. M. Abu-Shaweesh, “Respiratory disorders in preterm and term infants,” in Fanaroff and Martin's Neonatal-Perinatal Medicine, Diseases of the Fetus and Infant, R. J. Martin, A. A. Fanaroff, and M. C. Walsh, Eds., pp. 1141–1170, Elsevier Mosby, St. Louis, Mo, USA, 9th edition, 2011.
- D. Miguet, O. Claris, A. Lapillonne, A. Bakr, J. P. Chappuis, and B. L. Salle, “Preoperative stabilization using high-frequency oscillatory ventilation in the management of congenital diaphragmatic hernia,” Critical Care Medicine, vol. 22, no. 9, supplement, pp. S77–S82, 1994.
- C. Reyes, L. K. Chang, F. Waffarn, H. Mir, M. J. Warden, and J. Sills, “Delayed repair of congenital diaphragmatic hernia with early high- frequency oscillatory ventilation during preoperative stabilization,” Journal of Pediatric Surgery, vol. 33, no. 7, pp. 1010–1016, 1998.
- L. Desfrere, P. H. Jarreau, M. Dommergues et al., “Impact of delayed repair and elective high-frequency oscillatory ventilation on survival of antenatally diagnosed congenital diaphragmatic hernia: first application of these strategies in the more “severe” subgroup of antenatally diagnosed newborns,” Intensive Care Medicine, vol. 26, no. 7, pp. 934–941, 2000.
- A. Cacciari, G. Ruggeri, M. Mordenti et al., “High-frequency oscillatory ventilation versus conventional mechanical ventilation in congenital diaphragmatic hernia,” European Journal of Pediatric Surgery, vol. 11, no. 1, pp. 3–7, 2001.
- L. Migliazza, C. Bellan, D. Alberti, A. Auriemma, G. Burgio, and G. L. E. A. Colombo, “Retrospective study of 111 cases of congenital diaphragmatic hernia treated with early high-frequency oscillatory ventilation and presurgical stabilization,” Journal of Pediatric Surgery, vol. 42, no. 9, pp. 1526–1532, 2007.
- V. Datin-Dorriere, E. Walter-Nicolet, V. Rousseau et al., “Experience in the management of eighty-two newborns with congenital diaphragmatic hernia treated with high-frequency oscillatory ventilation and delayed surgery without the use of extracorporeal membrane oxygenation,” Journal of Intensive Care Medicine, vol. 23, no. 2, pp. 128–135, 2008.
- G. Y. T. Ng, C. Derry, L. Marston, M. Choudhury, K. Holmes, and S. A. Calvert, “Reduction in ventilator-induced lung injury improves outcome in congenital diaphragmatic hernia?” Pediatric Surgery International, vol. 24, no. 2, pp. 145–150, 2008.
- K. Azarow, A. Messineo, R. Pearl, R. Filler, G. Barker, and D. Bohn, “Congenital diaphragmatic hernia—a tale of two cities: the Toronto experience,” Journal of Pediatric Surgery, vol. 32, no. 3, pp. 395–400, 1997.
- J. M. Wilson, D. P. Lund, C. W. Lillehei, and J. P. Vacanti, “Congenital diaphragmatic hernia—a tale of two cities: the Boston experience,” Journal of Pediatric Surgery, vol. 32, no. 3, pp. 401–405, 1997.
- S. Kamata, N. Usui, S. Ishikawa et al., “Prolonged preoperative stabilization using high-frequency oscillatory ventilation does not improve the outcome in neonates with congenital diaphragmatic hernia,” Pediatric Surgery International, vol. 13, no. 8, pp. 542–546, 1998.
- G. Rocha, M. Rodrigues, and H. Guimarães, “Respiratory distress syndrome of the preterm neonate—placenta and necropsy as witnesses,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 24, no. 1, pp. 148–151, 2011.
- S. Costa, M. Rodrigues, M. J. Centeno et al., “Diagnosis and cause of death in a neonatal intensive care unit—how important is autops?” Journal of Maternal-Fetal and Neonatal Medicine, vol. 24, no. 5, pp. 760–763, 2011.