- Open Access
High-frequency oscillatory ventilation and short-term outcome in neonates and infants undergoing cardiac surgery: a propensity score analysis
Critical Care volume 15, Article number: R259 (2011)
Experience with high-frequency oscillatory ventilation (HFOV) after congenital cardiac surgery is limited despite evidence about reduction in pulmonary vascular resistance after the Fontan procedure. HFOV is recommended in adults and children with acute respiratory distress syndrome. The aim of the present study was to assess associations between commencement of HFOV on the day of surgery and length of mechanical ventilation, length of Intensive Care Unit (ICU) stay and mortality in neonates and infants with respiratory distress following cardiac surgery.
A logistic regression model was used to develop a propensity score, which accounted for the probability of being switched from conventional mechanical ventilation (CMV) to HFOV on the day of surgery. It included baseline characteristics, type of procedure and postoperative variables, and was used to match each patient with HFOV with a control patient, in whom CMV was used exclusively. Length of mechanical ventilation, ICU stay and mortality rates were compared in the matched set.
Overall, 3,549 neonates and infants underwent cardiac surgery from January 2001 through June 2010, 120 patients were switched to HFOV and matched with 120 controls. After adjustment for the delay to sternal closure, duration of renal replacement therapy, occurrence of pulmonary hypertension and year of surgery, the probability of successful weaning over time and the probability of ICU delivery over time were significantly higher in patients with HFOV, adjusted hazard ratios and 95% confidence intervals: 1.63, 1.17 to 2.26 (P = 0.004). and 1.65, 95% confidence intervals: 1.20 to 2.28 (P = 0.002) respectively. No association was found with mortality.
When commenced on the day of surgery in neonates and infants with respiratory distress following cardiac surgery, HFOV was associated with shorter lengths of mechanical ventilation and ICU stay than CMV.
High-frequency oscillatory ventilation (HFOV) is an established treatment for acute respiratory distress in preterm neonates. However, there is no evidence that it improves outcome in term or near-term neonates with pulmonary disease . HFOV is considered as a rescue therapy in children with severe acute respiratory distress syndrome (ARDS), but to date there is lack of evidence to support it [2, 3]. HFOV is also used to achieve lung recruitment and improve oxygenation when recruitment maneuvers have failed, as part of the "open lung" and lung protective ventilation strategies in adults with severe ARDS; early initiation of HFOV has been associated with improved outcome [4–6]. Mild acute lung injury occurs in 12% of adults following cardiopulmonary bypass (CPB), and more severe lung injury, indistinguishable from ARDS, in 0.4% [7, 8], as a result of accumulation of excessive extrapulmonary lung water, decreased lung compliance, atelectasis and increased shunting.
Experience with HFOV following cardiac surgery is limited, due to concerns about hemodynamic impairment in animal and human studies [6, 9–13]. However, HFOV has been associated with a significant reduction in pulmonary vascular resistance (PVR) after the Fontan procedure in children . Thought to be beneficial for gas exchange and PVR, the present authors have used HFOV in neonates and infants with respiratory distress following cardiac surgery since January 2007. The aim of the present study was to assess associations between commencement of HFOV on the day of surgery (Day 0) and the length of mechanical ventilation and Intensive Care Unit (ICU) stay, and mortality in this population.
Materials and methods
This retrospective cohort study was conducted at the Necker University Hospital in Paris, France. It was reviewed and approved by the Ethics Committee of the French Society of Thoracic and Cardiovascular Surgery, which waived the requirement for consent to use anonymized records. All parents had provided informed consent to surgery.
Records of all neonates and infants who underwent cardiac surgery between 1 January 2001 and 30 June 2010 were reviewed; patients switched to HFOV on Day 0 were identified as the HFOV group. Those switched to HFOV after Day 0, as a rescue therapy, were not analyzed. The remaining patients were included in the control group. Data for each patient were extracted retrospectively from a prospective database, which is updated daily by the clinical staff. These concerned: demographics, surgical and CPB techniques, short-term outcome variables accounting for the severity of the postoperative illness, such as re-operation, delayed sternal closure, extracorporeal membrane oxygenation (ECMO), acute kidney injury requiring renal replacement therapy (RRT), and hospital-acquired pneumonia , length of mechanical ventilation, length of ICU stay and in-hospital mortality. Normothermic CPB with intermittent warm blood cardioplegia was performed in every patient during the study period, except in cases where deep hypothermic circulatory arrest (DHCA) was indicated . Pulmonary arterial pressure was measured in every patient, either continuously by a catheter inserted into the pulmonary artery by the end of surgery, or by serial echocardiography. Persistent pulmonary hypertension was noted whenever it occurred during the postoperative course, and inhaled nitric oxide was administered .
All patients were initially commenced on pressure controlled conventional mechanical ventilation (CMV) using a SERVO-300 (Siemens-Elema AB, Sweden) before 2002, then a SERVO-i ventilator (Maquet GmbH&Co.KG, Rastatt, Germany). This was set to provide a positive end expiratory pressure of 2 cmH2O, a tidal volume of 6 to 8 ml Kg-1, and a fraction of inspired oxygen, which was dependent upon the underlying cardiac disease. In the event of severe respiratory failure, recruitment maneuvers by stepwise increase in the mean airway pressure were applied. The patients were switched to HFOV when hypoxemia and acidosis occurred despite increasing alveolar ventilation on CMV, when the tidal volume exceeded 10 ml kg-1, or when there was evidence of pulmonary hypertension and right ventricular failure. The decision to switch was made by the attending intensivist. A SLE 2000 or a SLE 5000 HFO ventilator (SLE Ltd, South Croydon, UK) was used. This was set to a mean airway pressure (Paw) of 12 cmH2O, an inspiratory to expiratory ratio of 33%, and an oscillation frequency of 8 Hz. Amplitude was adapted to achieve adequate chest wall vibrations. All parameters were adjusted to achieve optimal inflation, a PaCO2 of 35 to 45 mmHg and a pH > 7.35. The adequacy of the PaO2 level was judged according to the underlying cardiac disease. Patients were switched back to CMV when these conditions had been achieved with an oscillation frequency ≥10 Hz and a mean Paw ≤10 cmH2O. Sedation was achieved through a continuous infusion of midazolam and morphine. Whenever possible, muscular relaxants were avoided and spontaneous breathing was maintained. Catecholamine support (milrinone and epinephrine), fluid support and diuretics were administered as appropriate to achieve hemodynamic stability and a negative fluid balance. All patients were weaned from mechanical ventilation when the underlying indication had resolved and following a successful one-hour trial of spontaneous breathing with a continuous positive pressure of 2 cmH2O and a pressure support of 10 cmH2O.
After testing for normality, baseline characteristics of the two groups were compared using Student's t or Mann-Whitney tests for continuous variables and χ2 or Fisher's exact tests for categorical variables.
The hypothesis tested was that patients switched to HFOV had shorter length of mechanical ventilation and ICU stay and lower mortality rates. To control for the bias due to selection of patients switched to HFOV, 1:1 propensity score matching was carried out . Logistic regression was used to develop a propensity score quantifying the probability for each patient undergoing surgery since January 2007 to be switched to HFOV. This included all baseline and post-operative variables accounting for severity of illness found to be different between groups in univariate analysis (P < 0.10), and the "HFOV index". Given the large number of surgical procedures and the absence of guidelines for HFOV in this context, an empirical "HFOV index" was attributed to each procedure. This accounted for the influence of each specific procedure being performed on the probability to be switched to HFOV afterwards, and was calculated as the prevalence of HFOV per procedure between January 2007 and June 2010.
In accordance with previous authors, length of mechanical ventilation and length of ICU stay were modeled as censored variables in survivors, with weaning from mechanical ventilation and ICU delivery as censoring events . The probability of successful weaning from mechanical ventilation over time and the probability of ICU delivery over time were calculated for each group using the Kaplan-Meier method, and compared using the log-rank test. Results were confirmed using a multivariable Cox proportional-hazards model, controlling for variables related to length of ICU stay following pediatric cardiac surgery in a previous study , variables unbalanced after matching (P < 0.10), for the propensity score and the year of surgery. Adjusted Hazard ratios (HR) with 95% confidence intervals were estimated.
The R statistical package, "Design" and "optmatch" libraries  were used for the analyses.
Overall, 3,549 neonates and infants underwent cardiac surgery during the study period. Life support was withdrawn from four patients with obstructed total anomalous pulmonary venous connection and one patient with severe pulmonary hypoplasia, with hopeless prognosis secondary to pulmonary lymphangienctasia. Another two patients died periprocedural, leaving 3,542 cases to be analyzed. The number of patients, their length of mechanical ventilation and ICU stay across the study period are shown in Figures 1 and 2.
Patient characteristics are shown in Table 1. The 120 neonates and infants switched to HFOV on Day 0 were younger and smaller, had undergone more complex surgery and had experienced more severe postoperative illness. Patients switched to HFOV had longer durations of both mechanical ventilation, median 7 days, inter-quartile ranges (IQR) 5 to 11 vs. 1 day, IQR 0.3 to 4 in controls (P < 0.001), and ICU stay, median 11 days, IQR 7 to 15.7 vs. 4 days, IQR 3 to 7 (P < 0.001). The median duration of HFOV was 4 days, IQR 2 to 7. The in-hospital mortality rates for the two groups were similar, 8.3% in patients switched to HFOV vs. 4.8% in controls (P = 0.08).
Table 2 shows the most prevalent procedures and their "HFOV indexes", range 0 to 0.82, median 0.04, IQR 0.03 to 0.08. Table 3 shows the variables included in the propensity score. When data were missing, the median of the respective variable was used (< 5% of all information concerning CPB technique was missing). The propensity score model was well calibrated (Hosmer Lemeshow test, P = 0.14) and discriminated well between patients on HFOV and the others (c index = 0.82). Patients were more likely to be switched to HFOV on Day 0 if they were small, had undergone a procedure with high "HFOV index", required CPB and DHCA, had hemodynamic impairment precluding closure of the sternum or required RRT on Day 0. Patients commenced on postoperative ECMO were not matched due to their high mortality rate (39.1%).
Matching resulted in two well-balanced groups of 120 patients respectively: the HFOV and the CMV groups (Table 1). The HFOV group had shorter durations of mechanical ventilation, 7 days, IQR 5 to 11 vs 9 days, IQR 5 to 17 in the CMV group (P = 0.03), shorter durations of ICU stay, 11 days, IQR 5 to 17 vs 14 days, IQR 9 to 22 (P = 0.009), a higher prevalence of pulmonary hypertension, 36.7%, compared to 23.3% (P = 0.03) and a similar prevalence of hospital-acquired pneumonia, 49.2% in the HFOV group compared to 47.5% in the CMV group (P = 0.80). Ten patients in the HFOV group (8.3%) died during ICU stay, compared to 18 in the CMV group (15.8%) (P = 0.08). Median follow-up was 411 days, IQR 32 to 3,060, 18 patients (15.8%) died during follow-up in the HFOV group, compared to 22 in the CMV group (18.3%) (P = 0.66).
Kaplan-Meier plots of the probability of successful weaning from mechanical ventilation over time are shown in Figure 3. The median length of mechanical ventilation was 7 days in the HFOV group, IQR 5 to 11, and 9 days in the CMV group, IQR 5 to 17 (P = 0.01). Four patients in the HFOV group underwent mechanical ventilation for ≥ 30 days. Of these, one developed tracheal stenosis and underwent slide tracheoplasty, another required tracheostomy. Ten patients in the CMV group underwent mechanical ventilation for ≥ 30 days. Of these, two developed tracheal stenosis, one of whom died, one developed oeso-tracheal fistula and died, and seven developed chronic lung disease, of whom four required tracheostomy and two died. Kaplan-Meier plots of the probability of ICU delivery over time are shown in Figure 4. The median length of ICU stay was 11 days in the HFOV group, IQR 7.2 to 15.7 and 14 days in the CMV group, IQR 9 to 22 (P = 0.002). Differences between length of ventilation and ICU stay were found significant with a statistical power of 0.77 and 0.89, respectively.
Cox proportional-hazards regression analysis, adjusted for the delay to sternal closure, duration of RRT, occurrence of pulmonary hypertension and year of surgery, showed that patients in the HFOV group had a higher probability of successful weaning over time, adjusted HR 1.63; 95% confidence interval (CI) 1.17 to 2.23 (P = 0.004) (Table 4). The probability of ICU delivery over time was also higher in the HFOV group, adjusted HR 1.65, 95% CI 1.20 to 2.28 (P = 0.002) (Table 4). Longer delay to sternal closure was independently associated with longer length of mechanical ventilation and ICU stay.
The present study reports experience with HFOV in a population of neonates and infants with respiratory distress following several cardiac surgery procedures. Previous findings reported from randomized trials of HFOV in term or near-term neonates with pulmonary disease showed no benefit in terms of 28-day mortality , and our findings were similar. But, unlike previous research on elective use of HFOV, length of mechanical ventilation and length of stay were reduced among patients with a similar severity of illness when they were switched to HFOV on the day of surgery.
HFOV and PVR
The most common reasons for late weaning from mechanical ventilation following congenital cardiac surgery are a low cardiac output state or a respiratory complication. Even when ventricular function is well preserved and no residual anatomical lesion is present, a low cardiac output may result from inadequate pulmonary blood flow, secondary to elevated PVR. Maintenance of cardiac output by fluid challenge, to ensure adequate preload, leads to extravascular fluid accumulation, pleural and pericardial effusions, pulmonary interstitial edema and decreased compliance. The loss of intravascular volume must be replaced to maintain cardiac output, which may initiate a vicious cycle, and should, therefore, be avoided.
PVR is multifactorial after CPB [22, 23] and highly sensitive to changes in intra-thoracic pressure  and acidosis . Changes in intra-thoracic pressure have been extensively investigated in the Fontan procedure, where high-frequency ventilation has been found to be associated with an increase of up to 25% in cardiac output and led to halve PVR and mean Paw . Although HFOV is known to be effective in settings leading to hypoxemia, the use has been described in reports of asthma and severe bronchiolitis to treat respiratory acidosis [26, 27]. According to Babik et al. , CPB is responsible for an obstructive process in the bronchi, leading to bronchospasm and acidosis. Bronchospasm is also a frequent postoperative finding in patients with a large preoperative left to right shunt . Thus, the use of HFOV to treat respiratory acidosis in an attempt to decrease PVR after CPB appears justified. In the present study, when switching to HFOV, ventilation frequency was initially set to 8 Hz to promote decarboxylation and, thus, rapidly increase pH. But the retrospective design of the present study rendered collection of reliable data concerning PVR, Paw and gas exchanges impossible. Nevertheless, documented pulmonary hypertension was more prevalent in the HFOV group (before or after transition to HFOV) even after propensity score matching, showing that the HFOV group was still more severely ill. Therefore, the shorter durations of mechanical ventilation in the HFOV group suggested a beneficial effect of HFOV on PVR.
Usually, HFOV involves slightly higher mean Paw values than CMV, and low cardiac output may occur due to increased pleural pressure and reduced venous return. Studies of HFOV in animal models of ARDS have reported hemodynamic impairment when high airway pressures were applied [9–11]. Studies of adults [6, 12, 13] and infants [29, 30] switched from CMV to HFOV have found effects such as increased pulmonary artery occlusion pressure, increased central venous pressure, and small decreases in cardiac output and stroke volume index, although it was unclear whether these changes were clinically relevant.
By contrast, sedation may lead to excessive venous vasodilatation and impaired venous return following cardiac surgery, whereas spontaneous breathing maintains a negative pleural pressure, facilitates venous return and improves cardiac output. Spontaneous ventilation can be maintained easily in neonates and small children on HFOV without increasing the work of breathing [31, 32], thus allowing reduced sedation.
Reliable evaluation of hemodynamic consequences when changing ventilatory settings is impossible in a retrospective study. The low mean Paw HFOV strategy employed in the present study may have allowed the preservation of hemodynamic stability in these patients. Furthermore, if a long delay to sternal closure and a long duration of RRT were considered markers of hemodynamic impairment, then switching to HFOV may have resulted in hemodynamic improvement in the present cohort, since both the delay to sternal closure and the duration of RRT were slightly reduced in the HFOV group (Table 1).
The present study was retrospective and, thus, the validity of the results must be viewed with caution. Attempts were made to minimize bias related to selection of patients switched to HFOV through propensity score matching. Even though, and despite adjustment for the year of surgery, the choice of historical controls cannot rule out bias related to improvements in surgical and medical management of congenital heart diseases throughout the study period. Besides, the choice of transition to HFOV was made by the attending intensivist, and, despite the propensity score methodology employed, we cannot rule out residual bias related to pre-held beliefs about HFOV's performance. Furthermore, analysis of ventilation parameters and hemodynamic consequences were lacking. Because of the various intra-cardiac shunting patterns in the study population, oxygenation indexes were not analyzed. Future studies should address these limitations.
When commenced on the day of surgery, HFOV was associated with a shorter duration of mechanical ventilation and ICU stay in this population of neonates and infants with respiratory distress following congenital cardiac surgery. No association was observed between the use of HFOV and mortality.
HFOV has been shown to be associated with lower pulmonary vascular resistance after the Fontan procedure.
The present study found the use of HFOV to be associated with shorter length of mechanical ventilation and ICU stay in neonates and infants with respiratory distress following several cardiac procedures.
Since our pathophysiological inferences are drawn from observational results, the beneficial effect of HFOV needs to be confirmed by interventional studies.
acute respiratory distress syndrome
conventional mechanical ventilation
- Day 0:
day of surgery
deep hypothermic circulatory arrest
extracorporeal membrane oxygenation
high-frequency oscillatory ventilation
intensive care unit
pulmonary vascular resistance
renal replacement therapy
total anomalous pulmonary venous connection
ventricular septal defect.
Henderson-Smart DJ, De Paoli AG, Clark RH, Bhuta T: High frequency oscillatory ventilation versus conventional ventilation for infants with severe pulmonary dysfunction born at or near term. Cochrane Database Syst Rev 2009, CD002974.
Randolph AG: Management of acute lung injury and acute respiratory distress syndrome in children. Crit Care Med 2009, 37: 2448-2454.
Randolph AG, Meert KL, O'Neil ME, Hanson JH, Luckett PM, Arnold JH, Gedeit RG, Cox PN, Roberts JS, Venkataraman ST, Forbes PW, Cheifetz IM, Pediatric Acute Lung Injury and Sepsis Investigators Network: The feasibility of conducting clinical trials in infants and children with acute respiratory failure. Am J Respir Crit Care Med 2003, 167: 1334-1340. 10.1164/rccm.200210-1175OC
Diaz JV, Brower R, Calfee CS, Matthay MA: Therapeutic strategies for severe acute lung injury. Crit Care Med 2010, 38: 1644-1650. 10.1097/CCM.0b013e3181e795ee
Finkielman JD, Gajic O, Farmer JC, Afessa B, Hubmayr RD: The initial Mayo Clinic experience using high-frequency oscillatory ventilation for adult patients: a retrospective study. BMC Emerg Med 2006, 6: 2. 10.1186/1471-227X-6-2
Mehta S, Granton J, MacDonald RJ, Bowman D, Matte-Martyn A, Bachman T, Smith T, Stewart TE: High-frequency oscillatory ventilation in adults: the Toronto experience. Chest 2004, 126: 518-527. 10.1378/chest.126.2.518
Rady MY, Ryan T, Starr NJ: Early onset of acute pulmonary dysfunction after cardiovascular surgery: risk factors and clinical outcome. Crit Care Med 1997, 25: 1831-1839. 10.1097/00003246-199711000-00021
Milot J, Perron J, Lacasse Y, Letourneau L, Cartier PC, Maltais F: Incidence and predictors of ARDS after cardiac surgery. Chest 2001, 119: 884-888. 10.1378/chest.119.3.884
Roosens CD, Ama R, Leather HA, Segers P, Sorbara C, Wouters PF, Poelaert JI: Hemodynamic effects of different lung-protective ventilation strategies in closed-chest pigs with normal lungs. Crit Care Med 2006, 34: 2990-2996.
Nakagawa R, Koizumi T, Ono K, Tsushima K, Yoshikawa S, Kubo K, Otagiri T: Cardiovascular responses to high-frequency oscillatory ventilation during acute lung injury in sheep. J Anesth 2007, 21: 340-347. 10.1007/s00540-007-0508-z
David M, Gervais HW, Karmrodt J, Depta AL, Kempski O, Markstaller K: Effect of a lung recruitment maneuver by high-frequency oscillatory ventilation in experimental acute lung injury on organ blood flow in pigs. Crit Care 2006, 10: R100. 10.1186/cc4967
David M, von Bardeleben RS, Weiler N, Markstaller K, Scholz A, Karmrodt J, Eberle B: Cardiac function and haemodynamics during transition to high-frequency oscillatory ventilation. Eur J Anaesthesiol 2004, 21: 944-952.
Derdak S, Mehta S, Stewart TE, Smith T, Rogers M, Buchman TG, Carlin B, Lowson S, Granton J: High-frequency oscillatory ventilation for acute respiratory distress syndrome in adults: a randomized, controlled trial. Am J Respir Crit Care Med 2002, 166: 801-808. 10.1164/rccm.2108052
Meliones JN, Bove EL, Dekeon MK, Custer JR, Moler FW, Callow LR, Wilton NC, Rosen DB: High-frequency jet ventilation improves cardiac function after the Fontan procedure. Circulation 1991, 84: III364-368.
Hospital-acquired pneumonia in adults: diagnosis, assessment of severity, initial antimicrobial therapy, and preventive strategies. A consensus statement, American Thoracic Society, November 1995 Am J Respir Crit Care Med 1996, 153: 1711-1725.
Pouard P, Mauriat P, Ek F, Haydar A, Gioanni S, Laquay N, Vaccaroni L, Vouhe PR: Normothermic cardiopulmonary bypass and myocardial cardioplegic protection for neonatal arterial switch operation. Eur J Cardiothorac Surg 2006, 30: 695-699. 10.1016/j.ejcts.2006.07.032
Journois D, Baufreton C, Mauriat P, Pouard P, Vouhe P, Safran D: Effects of inhaled nitric oxide administration on early postoperative mortality in patients operated for correction of atrioventricular canal defects. Chest 2005, 128: 3537-3544. 10.1378/chest.128.5.3537
Rosenbaum PR: Observational Studies. 2nd edition. New York: Springer; 2002.
Kollef MH, Shapiro SD, Silver P, St John RE, Prentice D, Sauer S, Ahrens TS, Shannon W, Baker-Clinkscale D: A randomized, controlled trial of protocol-directed versus physician-directed weaning from mechanical ventilation. Crit Care Med 1997, 25: 567-574. 10.1097/00003246-199704000-00004
Brown KL, Ridout DA, Goldman AP, Hoskote A, Penny DJ: Risk factors for long intensive care unit stay after cardiopulmonary bypass in children. Crit Care Med 2003, 31: 28-33. 10.1097/00003246-200301000-00004
The R Project for Statistical Computing[http://www.r-project.org]
Apostolakis E, Filos KS, Koletsis E, Dougenis D: Lung dysfunction following cardiopulmonary bypass. J Card Surg 2010, 25: 47-55. 10.1111/j.1540-8191.2009.00823.x
Babik B, Asztalos T, Petak F, Deak ZI, Hantos Z: Changes in respiratory mechanics during cardiac surgery. Anesth Analg 2003, 96: 1280-1287.
Moore JP, Hainsworth R, Drinkhill MJ: Phasic negative intrathoracic pressures enhance the vascular responses to stimulation of pulmonary arterial baroreceptors in closed-chest anaesthetized dogs. J Physiol 2004, 555: 815-824. 10.1113/jphysiol.2003.057968
Chang AC, Zucker HA, Hickey PR, Wessel DL: Pulmonary vascular resistance in infants after cardiac surgery: role of carbon dioxide and hydrogen ion. Crit Care Med 1995, 23: 568-574. 10.1097/00003246-199503000-00024
Berner ME, Hanquinet S, Rimensberger PC: High frequency oscillatory ventilation for respiratory failure due to RSV bronchiolitis. Intensive Care Med 2008, 34: 1698-1702. 10.1007/s00134-008-1151-3
Duval EL, van Vught AJ: Status asthmaticus treated by high-frequency oscillatory ventilation. Pediatr Pulmonol 2000, 30: 350-353. 10.1002/1099-0496(200010)30:4<350::AID-PPUL13>3.0.CO;2-2
Yau KI, Fang LJ, Wu MH: Lung mechanics in infants with left-to-right shunt congenital heart disease. Pediatr Pulmonol 1996, 21: 42-47. 10.1002/(SICI)1099-0496(199601)21:1<42::AID-PPUL7>3.0.CO;2-S
Laubscher B, van Melle G, Fawer CL, Sekarski N, Calame A: Haemodynamic changes during high frequency oscillation for respiratory distress syndrome. Arch Dis Child Fetal Neonatal Ed 1996, 74: F172-176. 10.1136/fn.74.3.F172
Simma B, Fritz M, Fink C, Hammerer I: Conventional ventilation versus high-frequency oscillation: hemodynamic effects in newborn babies. Crit Care Med 2000, 28: 227-231. 10.1097/00003246-200001000-00038
van Heerde M, van Genderingen HR, Leenhoven T, Roubik K, Plotz FB, Markhorst DG: Imposed work of breathing during high-frequency oscillatory ventilation: a bench study. Crit Care 2006, 10: R23. 10.1186/cc3988
Rimensberger PC: Allowing for spontaneous breathing during high-frequency oscillation: the key for final success? Crit Care 2006, 10: 155. 10.1186/cc4993
The authors declare that they have no competing interests.
MB contributed to the scope and design of the study, obtaining permission for data use, analyzing and interpreting the data, and drafting and revising the manuscript. SG contributed to the scope of the study, to the research concept, and to revising the manuscript. PM and PP contributed both to the scope of the study and to revising the manuscript. All authors have read and approved the manuscript for publication.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
About this article
Cite this article
Bojan, M., Gioanni, S., Mauriat, P. et al. High-frequency oscillatory ventilation and short-term outcome in neonates and infants undergoing cardiac surgery: a propensity score analysis. Crit Care 15, R259 (2011). https://doi.org/10.1186/cc10521
- Mechanical Ventilation
- Propensity Score
- Renal Replacement Therapy
- Intensive Care Unit Stay
- Pulmonary Vascular Resistance