![Intrapulmonary Percussion with Autogenic Drainage and Ventilator-Associated Gram-Negative Infection: a Pilot Study](https://data.docslib.org/img/3a60ab92a6e30910dab9bd827208bcff-1.webp)
Netherlands Journal of Critical Care Submitted July 2015; Accepted December 2015 ORIGINAL ARTICLE Intrapulmonary percussion with autogenic drainage and ventilator-associated Gram-negative infection: A pilot study H. Spapen, M. Borremans, M. Diltoer, J. De Regt, C. Bruggemans, P.M. Honoré Intensive Care Department, University Hospital, Vrije Universiteit Brussels, Brussels, Belgium Correspondence H. Spapen – [email protected] Keywords - chest physiotherapy, intrapulmonary percussive ventilation, assisted autogenic drainage, infection-related ventilator-associated complications, gram-negative Abstract Background Background Intrapulmonary percussive ventilation with assisted autogenic CPT in mechanically ventilated patients primarily aims to drainage physiotherapy (IPV-AADP) is a compelling form facilitate clearance of airway secretions in an attempt to of chest physiotherapy (CPT) in mechanically ventilated prevent lung atelectasis, tracheobronchial infection, and critically ill patients. We evaluated the effect of IPV-AADP on ventilator-associated pneumonia (VAP).[1,2] For this purpose, the occurrence of Gram-negative infection-related ventilator- ICU physiotherapists have a large armamentarium of physical associated complications (IVACs). and mechanical means at their disposal. However, CPT-driven secretion management is not standardised among ICUs and Methods varies from simply providing appropriate humidification and Patients requiring mechanical ventilation for at least 48 as-needed airway suctioning to a more complex ‘multimodality’ hours were randomly assigned to receive either IPV-AADP, approach including percussion, manual or ventilator conventional CPT (CoCPT) or no CPT (NoCPT). Standard hyperinflation, chest wall vibrations, postural drainage, and rib- institutional prevention measures of ventilator-associated cage compression. infection were guaranteed in all subjects. The study endpoint Intrapulmonary percussive ventilation (IPV) delivers very was the presence of IVACs as documented according to the small bursts of tidal volume within a frequency range of 60- Centers of Disease Control 2011 Working Group guidelines. 600 cycles/minute. By providing a convective front of gas to the Statistical analysis used non-parametric tests for independent distal airways, IPV provides a more homogenous distribution samples and Fisher’s exact test to compare treatment groups. of alveolar ventilation, promotes alveolar recruitment, helps to Results: Forty-five patients (24 males, 21 females) were enrolled ‘unstick’ mucus in small and middle-sized airways, and propels with 15 subjects included in each study arm. IPV-AADP patients secretions cephalad to the central airways.[3] Encouraging results were younger (46±17 years) than CoCPT (62±18 years) and with IPV have been obtained in patients with cystic fibrosis.[4] NoCPT (64±16 years) subjects (p=0.014; IPV-AADP vs. CoCPT For more than 20 years, IPV physiotherapy has replaced all other and NoCPT) but APACHE II scores were comparable between forms of CPT in our ICU. With few exceptions, this technique is the groups (20±8, 23±10 and 21±6 respectively for IPV-AADP, routinely performed in all intubated and mechanically ventilated CoCPT and NoCPT subjects, p=NS). Gram-negative IVACs patients, regardless of their underlying clinical condition. were diagnosed in two patients (13%) in the IPV-AADP group, The efficacy of IPV could be enhanced by combining it with seven patients (47%) in the CoCPT group and seven patients autogenic drainage. Essentially, autogenic drainage is a (47%) in the NoCPT group (p=0.10; IPV-AADP vs. CoCPT and ‘concentration intensive’ respiratory self-drainage technique NoCPT). that explores and utilises the most optimal expiratory airflow to mobilise secretions.[5] It consists of three phases: loosening Conclusion peripheral secretions by breathing at low lung volumes, In this small pilot study, adjunctive IPV-AADP tended to collecting secretions from central airways by breathing at low to decrease the occurrence of ventilator-associated Gram-negative mid lung volumes, and finally expelling secretions by breathing at infection as compared with CoCPT and NoCPT. mid to high lung volumes. Today, it is used to treat patients with 6 NETH J CRIT CARE - VOLUME 24 - NO 2 - MARCH 2016 Netherlands Journal of Critical Care Intrapulmonary percussion with autogenic drainage and ventilator-associated Gram-negative infection: A pilot study large amounts of thick mucus. In assisted autogenic drainage, USA) using pulsatile percussions between 80 and 350 cycles the respiratory physiotherapist uses exhaled air to remove per minute. Gas was delivered at adjustable pressure through mucus from the airways of more severely ill patients who are a non-gated sliding venturi connected to the endotracheal not capable of performing autogenic drainage independently. tube. A pressure-controlled tidal volume breath was insufflated Combining IPV with assisted autogenic drainage physiotherapy at regular time intervals to ensure adequate CO2 elimination. (IPV-AADP) might represent a more powerful form of CPT FiO2 and PEEP levels were kept identical to those used on the than the currently used ‘multimodality’ techniques for adjuvant ventilator. For assisted autogenic drainage, gentle bimanual prevention of respiratory infection in mechanically ventilated compression was progressively exerted on the patient’s thorax critically ill patients. We therefore assessed the effect of and maintained at a level where secretions could be ‘heard and providing either no CPT (NoCPT), conventional CPT (CoCPT) felt’. Subsequently, IPV-generated expiratory flow was used to or IPV-AADP on the occurrence of Gram-negative infection- expel the collected secretions. At the end of each IPV-AADP related ventilator-associated complications (IVACs) in this session, endotracheal suction was performed. population. In all three groups, identical standardised measures for prevention of ventilator-associated tracheobronchitis or Methods pneumonia were undertaken: ventilation with at least 5 cm H2O The study was approved by the Health Research Ethics PEEP, no routine change of ventilator circuits, humidification Committee of the University Hospital Brussels (B.U.N. using a heat-moisture device, semi-recumbent body 14320084389). Oral informed consent to initiate the study positioning at an angle of at least 25°, continuous maintenance was obtained from the patient’s next-of-kin. Mechanically of endotracheal tube cuff pressure at 30 cm H2O, periodic ventilated medical, surgical and/or trauma patients with verification of residual gastric volume, daily dental hygiene, negative tracheobronchial cultures were consecutively enrolled. oral cleaning with 1% chlorhexidine every eight hours, a strict Exclusion criteria for the study were: presence of lung infiltrates, sedation protocol aiming at minimal sedation according to a ventilation for less than 48 hours, community-acquired or plain dedicated sedation score and ensuring daily ‘wake-up’ calls. aspiration pneumonia, nosocomial or healthcare-acquired All patients received H2-blockers until adequate enteral infection, immunosuppressive disease, neutropenia, any form nutrition was achieved. Specific types of endotracheal tubes of immunosuppressive therapy including steroids, worse short- (e.g. subglottic aspiration, silver-coated) or cuff material (e.g. term prognosis, or a contraindication for IPV-AADP (i.e. polyurethane) were not used. Patients received no selective undrained pneumothorax, post sternotomy or thoracotomy, rib digestive decontamination treatment. fractures). During the study, all patients were ventilated in the Study endpoint was a documented Gram-negative IVAC. IVACs pressure-controlled mode (Evita XL, Dräger Medical). Inspired were defined according to the Centres of Disease Control 2011 oxygen fraction and positive end-expiratory pressure (PEEP) Working Group guidelines.[6] Briefly, on or after calendar Day 3 were adapted to obtain a PaO2 ≥60 mmHg. Inspiratory pressure of mechanical ventilation and within two calendar days before aimed at tidal volumes of 6-8 ml/kg and was limited at 30 cm or after the onset of worsening oxygenation, patients had to have H2O. Patients were randomly assigned according to a computer- either fever >38°C or a white blood cell count ≥12,000/mm³ or steered permuted block design to receive NoCPT, CoCPT or ≤4000/mm³ and a new antimicrobial agent started for at least IPV-AADP treatment. CoCPT consisted of expiratory chest four days. Additionally, the following criteria had to be met: wall percussion and vibration, positioning, rib springing, aerosol at least one purulent respiratory secretion specimen collected therapy, and airway suctioning. The NoCPT group underwent from the lungs, bronchi, or trachea containing ≥25 neutrophils passive mobilisation, aerosol therapy and tracheobronchial and ≤10 squamous epithelial cells per low power field (or aspiration. Aerosols contained 4 ml hypertonic saline 3% and corresponding semi-quantitative results) and a positive Gram- occasionally ipratroprium bromide, and were administered negative culture (qualitative, semi-quantitative or quantitative) three times daily by metered-dose inhalators connected to a of sputum, endotracheal aspirate or bronchoalveolar lavage spacer. Closed suction was performed for no longer than 15 fluid. IVACs were considered early-onset when they were seconds using pressures ranging from 90-120 mmHg. IPV- diagnosed during the first four days of mechanical ventilation
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