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* From the Pulmonary Division and Respiratory ICU (Drs. T. Todisco, Baglioni, Eslami, Scoscia, C. Todisco, and Dottorini), "R. Silvestrini" Hospital, Perugia; and Internal Medicine Department (Mr. Bruni), University of Perugia, Perugia, Italy.
Correspondence to: Stefano Baglioni, MD, FCCP, Pulmonary Division and Respiratory Intensive Care Unit, "R. Silvestrini" Hospital, Via Dottori 1, 06100, Perugia, Italy; e-mail: Stefano. Baglioni5{at}tin.it
| Abstract |
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Setting: RICU at "R. Silvestrini" Hospital in Perugia, Italy.
Patients and methods: One hundred fifty-two consecutive patients were included in the study and treated with iron lung as first choice or, when contraindicated or not tolerated, with NPPV using a nasal or facial mask. After 2 h of noninvasive mechanical ventilation (NIMV), the patients were reevaluated; in case of clinical deterioration, patients receiving NPV were switched to NPPV. When NPPV as a first or second line of treatment failed the patients were intubated.
Measurements and results: One hundred fifty-two patients received NIMV, 97 with iron lung as the first choice of treatment, and 55 with NPPV. Six patients treated with NPV were switched to NPPV during the first 2 h of treatment. Twenty-five patients required IMV. The success rate of the integrated use of NIMV (NPV plus NPPV) was 81.6%, compared to that of NPV (83.5%) and NPPV (70.5%). Twenty-one patients (13.8%) required tracheostomy; the duration of hospital stay was significantly lower in patients treated with NIMV only. Thirty patients required mechanical ventilation at home. Few severe complications were observed in patients receiving IMV.
Conclusions: The integrated use of two NIMV techniques is effective in patients with acute exacerbation of CRF. In most cases intubation and tracheostomy were avoided, thus reducing the complication rate of mechanical ventilation.
Key Words: acute respiratory failure chronic respiratory failure negative pressure ventilation noninvasive positive-pressure ventilation respiratory ICU
| Introduction |
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After a long period of disuse, except in a single center with an uncontrolled study population, the benefit of negative pressure ventilation (NPV) with iron lung and poncho wrap in hypercapnic respiratory failure has been recently described.141516 In a case-control study,17 the authors suggested that NPV may be comparable to invasive mechanical ventilation (IMV) for efficacy in the treatment of ARF due to COPD exacerbations. In a multicenter study,18 NPV was found to be comparable for efficacy to NPPV in COPD exacerbations. We began using the iron lung 15 years ago as first-choice treatment and NPPV with nasal or full face mask as an alternative in patients with acute-on-chronic respiratory failure. As no study has taken into consideration the integrated use of NPV and NPPV in the treatment of ARF, we evaluated whether the use of an integrated protocol of NPV and NPPV19 could prevent IMV, and reduce tracheostomy and related complications in patients admitted to our respiratory ICU (RICU) for exacerbation of chronic respiratory failure (CRF). The length of hospital stay and need for home mechanical ventilation were recorded.
| Materials and Methods |
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7.30, and need of mechanical ventilation. Exclusion criteria were invasive ventilation in emergency department before RICU admission, previous tracheotomy, CNS disease unrelated to respiratory failure, and end-stage cancer. Lung function test was performed using a Morgan body plethysmograph (P.K. Morgan; Kent, UK) before discharge in 120 collaborative patients. All patients received standard medical treatment for underlying disease and the condition precipitating acute exacerbation of CRF. Informed consent was obtained prior to study inclusion from patients or next of kin.
Study Design
At RICU admission, the patients were assessed and treated with NIMV using the iron lung as first choice, or NPPV with nasal or full face mask when NPV was contraindicated or not tolerated. Exclusion criteria for iron lung treatment are reported in Table 1 . After 2 h, patients were reevaluated (physical examination, arterial blood gas [ABG] analysis). In the case of significant clinical deterioration (see criteria for intubation below) or absolute intolerance of the noninvasive ventilation modality, NPV patients were switched to NPPV and NPPV patients to IMV. The study protocol is shown in Figure 1
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A capnograph used during iron lung ventilation by nasal cannula proved useful in this condition to observe the shape of the capnographic curve and to follow the trend of ETCO2 during mechanical ventilation, as the absolute value of ETCO2 correlates poorly with arterial PaCO2. Any significant variations of ETCO2 were verified by ABG analysis. When there was an improvement in two consecutive analyses (pH > 7.30 and PaCO2 < 70 mm Hg), the hours of ventilation were progressively reduced until it was possible to discontinue ventilation. Forty-eight hours prior to discharge, ventilatory support was discontinued. Oxygen was supplied by nasal prongs or Venturi mask with high fraction of inspired oxygen (FIO2) in the case of severe hypoxemia; SaO2 was maintained at
90%. When the patient could not be completely weaned from NIMV, he was sent home with a ventilator.
NPPV was provided with a volume-cycled ventilator (Monnal DCC; Taema; Antony, France; or EOLE 3XO; Saime; Savigny Le Temple, France) in assist/control mode, low trigger ( 2 cm H2O) with a tidal volume of 10 to 15 mL/kg (ideal body weight) adjusted to obtain sufficient expiratory volume and comfort for the patient. A positive end-expiratory pressure (4 to 5 cm H2O) was used when indicated. Oxygen supplementation was administered through the ventilator circuit to maintain SaO2
90%. The treatment schedule was progressively reduced using the same criteria as for NPV ventilation until mechanical ventilation could be withdrawn.
Criteria for Intubation
The following criteria described by Brochard and coworkers5 modified according to our experience were used: respiratory arrest, respiratory pauses with loss of consciousness or gasping for air, HR < 50 beats/min with loss of alertness, and hemodynamic instability with systolic arterial BP < 70 mm Hg, and PO2 < 45 mm Hg despite ventilation and oxygen therapy. The presence of any one of these criteria was an indication for intubation.
Treatment With IMV
After endotracheal intubation (sedation was achieved using IV midazolam), the patient was connected to the same type of ventilator used for NPPV delivering a tidal volume of 8 to 10 mL/kg, controlled modality in the first hours of ventilation, followed by alternating current modality. The patients were weaned using the method of single day T-tube trial lasting 2 h, as previously described.20 The weaning attempt was considered a failure when patients had PaO2/FIO2 <150 and/or a RR > 40 breaths/min, and/or a HR > 150 beats/min or new onset of arrhythmia, agitation, anxiety, or diaphoresis.
Monitoring
Noninvasive monitoring was used in all patients. Spirometric data and physical examination (respiratory muscle activity) were also recorded.
Tracheostomy Criteria
After 8 to 12 days of IMV (except in diseases that excluded possibility of weaning) and after three failed weaning attempts, patients underwent surgical tracheostomy. We used a tracheostomy/failed attempts time schedule according to guidelines that are being drawn up by an interdisciplinary committee (RICU, ICU, thoracic surgery, and ear, nose, and throat specialists) in our hospital.
Six patients in the NPV group and one patient in the NPPV group who could not be weaned from noninvasive ventilation, after a trial with noninvasive PPV, underwent surgical tracheostomy. Despite good ABG analysis findings during NIMV, these patients did not tolerate mechanical ventilation suspension for more than a few hours. They were allowed to choose between intubation and IMV or immediate tracheostomy, and they decided for the second choice of treatment. Patients were temporarily intubated before tracheostomy. The reasons for weaning failure in these patients were malnutrition and severe emphysema with limited autonomy of spontaneous ventilation.
Home Ventilation
Patients in the NIMV group who could not discontinue mechanical ventilation continued NIMV plus long-term oxygen therapy at home, following the scheme used in the last days of hospitalization.
Statistical Analysis
The primary end point was improvement in ABG analysis value during NIMV. Secondary end points were evaluation of mortality rate during hospital stay, the need for IMV and tracheotomy, length of hospitalization, and complication rate. Results are expressed as mean and SD. Groups were compared using the unpaired or paired t test as appropriate;
2 was used to compare frequency distributions. Failure rate was death or need of endotracheal ventilation for NIMV and death from IMV.
| Results |
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Of the 152 patients admitted, 97 patients were treated with NPV by iron lung as first choice, and 55 patients were treated with NPPV by nasal or full face mask when iron lung treatment was contraindicated. Six patients (6.1%) treated with NPV were changed to noninvasive PPV due to failure of iron lung during the first 2 h of treatment.
The characteristics of patients treated with NPV or NPPV were quite similar; only PaCO2 at RICU admission was significantly higher in the NPV group (Table 2 ). ABG analysis and RR improved significantly in most patients after 2 h of noninvasive treatment (Table 3 ). Success rate of the integrated use of NIMV (NPV plus NPPV) was 81.6%, while that of NPV and NPPV was 83.5% and 70.5%, respectively.
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One hundred thirty-nine patients survived and were discharged (91.4%). Thirteen patients admitted with hypercapnic-induced coma were treated with iron lung; 11 patients (85%) responded well and were discharged; 2 patients required IMV. The length of hospital stay was 12.4 ± 4.5 days in the NPV group, 14.2 ± 10.8 days in the NPPV group, (NS) 19.2 ± 16 days for IMV group (p < 0.01 vs NPV and NPPV); 30 patients needed home mechanical ventilation (27 patients with NPPV and 3 patients with NPV, poncho wrap), 11 in the NPV group and 19 in NPPV group (p < 0.001).
Twenty-one patients (13.8%) underwent tracheotomy because of the impossibility to wean: 14 patients after a period of IMV and 7 patients (6 patients with iron lung, and 1 patient with NPPV) after NIMV. The patients treated only with NIMV had fewer major complications: three pneumothorax (2.2%; two with NPPV and one with NPV); two ventilator-associated pneumonia (VAP, 1.6%) both from the NPPV group; one multiorgan failure (0.08%) from the NPV group; and seven aspirations (four with NPV, and three with NPPV) [5.1%]. However, the patients treated with IMV had a higher rate of major complications: one pneumothorax (4%), three VAPs (12%), three multiorgan failures (12%), five cardiac complications (20%), and one tracheal stenosis (4%). The total rate of major complications was 56% for IMV and 9.5% for NIMV (p < 0.01). Minor undesirable effects of the two noninvasive techniques are shown in Table 4 . We also evaluated the frequency of failure of NIMV in our group of patients, according to the disease leading to CRF (COPD, chest wall disease, neuromuscular disease, and lung fibrosis), and found no significant difference (Fig 2 ).
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| Discussion |
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IMV is very effective treatment for respiratory failure but can be associated with many complications, especially in patients requiring prolonged intubation. Complications included laryngeal and tracheal trauma with potential long-term effects, such as stenosis. In addition, sinusitis and VAP can occur during IMV. The incidence of complications is closely related to the duration of invasive ventilation, particularly the acquisition of VAP.21
Difficult weaning is often a problem in patients with COPD who undergo invasive ventilation. To avoid these problems and reduce hospital stay, many ICUs perform tracheostomy precociously, leading to high human and social costs due to this artificial airway. In the last 10 years, many studies have reported positive results regarding NIMV treatment for exacerbation of CRF primarily in patients with COPD.
The iron lung is our first choice of treatment for several reasons. Patients with acute exacerbation of CRF often present inspiratory muscle weakness, rapid shallow breathing, and excessive CO2 retention. The iron lung improves the performance of respiratory muscles and restores sufficient respiratory compensation.16 Furthermore, many patients in the early phase of ARF are restless and do not tolerate NPPV with nasal or full face mask, whereas with the iron lung these patients receive ventilation effectively. Tracheobronchial secretions are often a problem in patients treated with NIMV and require efficient cleaning of the airways (with catheter or fiberoptic bronchoscope). This is achieved more easily when the iron lung is used.22 Noncontrolled studies232425 indicate a better survival rate when patients with COPD and ARF are treated with the iron lung vs IMV. Using controlled ventilation via iron lung, patients with COPD in hypercapnic-induced coma can be safely treated.26
The recent introduction of NPV with a microprocessor-based thermistor trigger affords assisted NPV, improves the synchrony between patient and ventilator, and reduces the incidence of upper airway collapse.27 When the iron lung is contraindicated, impracticable due to the subjects characteristics or ineffective after 2 h of treatment, the use of intermittent positive pressure ventilation with an oral or full face mask may avoid endotracheal intubation. In our series, the number of complications was similar between the two modalities of noninvasive ventilation. In the NPPV group, a significant percentage of patients acquired nasal skin pressure necrosis; in the iron lung group, meteorism and vomiting were the most frequent complications. Use of nasal gastric drainage and prokinetic drugs can avoid these complications in the majority of patients. Long-term home ventilation was required in a significant number of patients, especially in the NPPV group. There was a higher number of early failures in the NPPV group, while the success rate was higher in the NPV group. Although many centers prefer pressure support ventilator for this type of patient, in this study we used volume-cycled ventilators in the NPPV group because this is the standard nurse-operated equipment in our RICU, which has resulted in highly satisfactory results since its introduction.
One study limitation could be patient selection on inclusion. In particular, those in need of immediate intubation were not included in the study. Another could be that the use of NMV, particularly iron lung ventilation, requires an expert medical and paramedic team able to switch immediately to IMV when necessary.
In our opinion, despite the aforementioned limitations, the possibility of using negative and positive noninvasive pressure ventilators in a RICU as part of the first line-treatment of ARF due to exacerbations of CRF can increase the possibility of resolving exacerbations without invasive procedures. In our series, 81.6% of the patients who had severe respiratory acidosis due to COPD exacerbations or other chronic lung diseases were treated successfully without invasive ventilation and with a very low complication rate. Our patients had a relatively short hospital stay, considering the severity of the clinical conditions on RICU admission, also by organizing, when indicated, long-term mechanical ventilation at home in patients with difficult weaning. The use of the iron lung as first choice of treatment in 64% of patients admitted to the study with a success rate of 83% confirms the efficacy of this device in the treatment of exacerbation of CRF.
| Footnotes |
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Received for publication May 13, 2003. Accepted for publication December 10, 2003.
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