Scholarly article on topic 'The acute effects of body position strategies and respiratory therapy in paralyzed patients with acute lung injury'

The acute effects of body position strategies and respiratory therapy in paralyzed patients with acute lung injury Academic research paper on "Medical engineering"

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Academic research paper on topic "The acute effects of body position strategies and respiratory therapy in paralyzed patients with acute lung injury"

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The acute effects of body position strategies and respiratory therapy in paralyzed patients with acute lung injury

Kenneth Davis Jr, Jay A Johannigman, Robert S Campbell, Ann Marraccini, Fred A Luchette, Scott B Frame and Richard D Branson

University of Cincinnati, Cincinnati, Ohio, USA

Correspondence: Kenneth Davis Jr, MD, University of Cincinnati, Department of Surgery, 231 Bethesda Avenue, Cincinnati, OH 45267-0558, USA. Tel: +1 513 558 3850; fax: +1 513 558 3747; e-mail:

Received: 28 September 2000 Critical Care 2001, 5:81-87

Revisions requested: 14 November 2000 Revisions received: 15 December 2000

AccePted: 26 December 2000 © 2001 Davis et al, licensee BioMed Central Ltd

Published: 29 January 2001 (Print ISSN 1364-8535; Online ISSN 1466-609X)


Background: Routine turning of critically ill patients is a standard of care. In recent years, specialized beds that provide automated turning have been introduced. These beds have been reported to improve lung function, reduce hospital-acquired pneumonia, and facilitate secretion removal. This trial was designed to measure the physiological effects of routine turning and respiratory therapy in comparison with continuous lateral rotation (CLR).

Methods: The study was a prospective, quasi-experimental, random assignment, trial with patients serving as their own controls. Paralyzed, sedated patients with acute respiratory distress syndrome were eligible for study. Patients were randomized to receive four turning and secretion management regimens in random sequence for 6 h each over a period of 24 h: (1) routine turning every 2 h from the left to right lateral position; (2) routine turning every 2 h from the left to right lateral position including a 15-min period of manual percussion and postural drainage (P&PD); (3) CLR with a specialized bed that turned patients from left to right lateral position, pausing at each position for 2 min; and (4) CLR with a specialized bed that turned patients from left to right lateral position pausing at each position for 2 min, and a 15-min period of percussion provided by the pneumatic cushions of the bed every 2 h.

Results: Nineteen patients were entered into the study. There were no statistically significant differences in the measured cardiorespiratory variables. There was a tendency for the ratio of partial pressure of arterial oxygen to fractional inspired oxygen concentration (PaO2/FIO2) to increase (174 ±31 versus 188 ±36; P =0.068) and for the ratio of deadspace to tidal volume 2Vd/Vt) to decrease (0.62 ±0.18 versus 0.59 ±0.18; P =0.19) during periods of CLR, but these differences did not achieve statistical significance. There were statistically significant increases in sputum volume during the periods of CLR. The addition of P&PD did not increase sputum volume for the group as a whole. However, in the four patients producing more than 40 ml of sputum per day, P&PD increased sputum volume significantly. The number of patient turns increased from one every 2 h to one every 10 min during CLR.

Conclusion: The acute effects of CLR are undoubtedly different in other patient populations (spinal cord injury and unilateral lung injury). The link between acute physiological changes and improved outcomes associated with CLR remain to be determined.

Keywords: continuous lateral rotation, hypoxemia, mechanical ventilation, paralysis, positioning, secretion removal, sedation

ARDS = acute respiratory distress syndrome; CLR = continuous lateral rotation; FIO2 = fractional inspired oxygen concentration; ICU = intensive care unit; PaCO2 = partial pressure of arterial CO2; PaO2 = partial pressure of arterial oxygen; PeCO2 = mixed expired CO2 concentration; PEEP = positive end-expiratory pressure; P&PD = percussion and postural drainage; REE = resting energy expenditure; RQ = respiratory quotient; Vd/Vt = ratio of deadspace to tidal volume; VCO2 = CO2 production; VO2 = oxygen consumption.


The complications of bed rest have been known for nearly a century [1]. Routine care of mechanically ventilated patients typically involves a regimen of body position changes to aid in the prevention of skin breakdown, to enhance secretion clearance, and to improve ventilation/ perfusion relationships [2,3]. In the recent past, specialized beds have been introduced that automatically turn patients on a much more frequent basis independently of caregiver availability. Several clinical trials have suggested that this type of rotational or 'kinetic' therapy might reduce the incidence of hospital-acquired pneumonia and reduce the duration of stay in an intensive care unit (ICU) [4-9]. Each of these studies can be criticized for design errors, and these specialized beds are not in routine use at present. Interestingly, little work has been performed to evaluate the physiological effects of rotational therapy. In fact, a recent paper was the first to evaluate gas exchange during short periods of rotation in comparison with the supine position [10].

We designed a study to evaluate the acute physiological effects of rotational therapy in a group of critically ill, paralyzed, mechanically ventilated patients with acute respiratory distress syndrome (ARDS) over a 24-h period.

Materials and methods

The study was approved by the Institutional Review Board of the University of Cincinnati, and informed consent was obtained from the next of kin. Inclusion criteria included (1) patients with ARDS as defined by the North American-European Consensus document [11], (2) a requirement for sedation and paralysis for medical management, and (3) the presence of a pulmonary artery catheter. Patients were excluded from the study if they were hemodynami-cally unstable, defined as having a systolic blood pressure of less than 90 mmHg despite vasopressor support, or undergoing supraventricular arrhythmias. Patients with head injuries requiring intracranial pressure monitoring, with unstable spinal injuries, and with rib fractures were also excluded. Additionally, any patient judged to be at risk from routine turning as determined by the attending surgeon was also excluded.


All patients had previously been diagnosed with ARDS, were chemically paralyzed, and were sedated. Paralysis was monitored with routine train-of-four monitoring. ARDS was defined in accordance with the consensus definition of having a ratio of partial pressure of arterial oxygen to fractional inspired oxygen concentration (PaO2/FIO2) of less than 200, bilateral infiltrates on the anterior-posterior chest radiograph, normal cardiac filling pressures (wedge pressure less than 18 mmHg), and a causative factor. Chest radiographs were interpreted by the attending radiologist. Table 1 lists characteristics of the patients in the

study. All patients were ventilated with pressure-control ventilation. Positive end-expiratory pressure (PEEP) was set to maintain oxygen saturation at more than 93% and the tidal volume was set between 8 and 10 ml/kg. Tidal volume was reduced to maintain peak airway pressures of less than 40 cmH2O. Respiratory rate was adjusted to maintain a pH of more than 7.30. Inspiratory to expiratory time ratio was less than 1:1. Inspiratory time was set to increase mean airway pressure, to allow a period of zero flow during inspiration, and to avoid intrinsic PEEP.

Study design

Patients were randomized to receive four turning and secretion management regimens in random sequence for 6 h each over a period of 24 h. Sequence was determined by a random-number table, varying the assignment of management regimens equally. These regimens included (1) routine turning by the ICU staff every 2 h from the left lateral to the right lateral position; (2) routine turning by the ICU staff every 2 h from the left lateral to the right lateral position including a 15-min period of manual percussion and postural drainage (P&PD) by the respiratory therapists; (3) continuous lateral rotation (CLR) with a specialized bed (Effica; Hill-Rom, Batesville, Indiana, USA) that turned patients from left to right lateral position, pausing at each position for 2 min; and 4) CLR with a specialized bed (Effica) that turned patients from left to right lateral position, pausing at each position for 2 min, and a 15-min period of percussion provided by the pneumatic cushions of the bed every 2 h. P&PD was done 60-90 min into the 2-h turn regimen.


Routine cardiorespiratory monitoring was accomplished in accordance with ICU protocol. Continuous monitoring of the electrocardiogram with lead II, systolic, diastolic, and mean arterial blood pressures from indwelling radial catheters, and pulse oximetry were accomplished. Systolic, diastolic, and mean pulmonary artery pressures and central venous pressure were also monitored continuously. These variables were recorded hourly from cardiovascular monitors (Sirecust; Siemens, Danvers, Massachusetts, USA).

All pressure monitoring systems were calibrated in accordance with the manufacturer's specifications and the zero reference was verified before data collection. Every 3 h, measurements of pulmonary capillary wedge pressure (PCWP) were made and cardiac output was determined from thermodilution curves with iced saline in triplicate. At the 3-h time point, arterial and pulmonary artery blood was drawn for measurements of blood gases, pH, and oxygen saturation. Samples were drawn, iced, and analyzed within 5 min by using standard blood gas (Corning, Medfield, Massachusetts, USA) and co-oximeters (OSM-3; Radiometer, Westlake, Ohio, USA). This time point was

Table 1

Characteristics of patients enrolled in the study

Patient Gender Age Diagnosis Static Cl Qs/Qt (%) PEEP fio2 DOV (h)

1 F 33 Multiple trauma, multiple long bone fractures - indirect ARDS 34 28 10 0.50 18

2 M 26 Liver laceration, ruptured spleen - indirect ARDS 26 31 12 0.55 10

3 M 62 Ruptured bladder, sepsis - indirect ARDS 38 21 10 0.60 15

4 M 44 Pancreatitis, sepsis 31 37 15 0.50 20

5 M 59 Aspiration pneumonia - direct ARDS 37 24 10 0.60 9

6 F 67 Intra-abdominal sepsis, perforated bowel - indirect ARDS 25 33 15 0.65 13

7 M 41 Gun shot wound to abdomen - indirect ARDS 29 21 18 0.60 10

8 M 19 Multiple trauma - indirect ARDS 28 19 10 0.45 9

9 F 72 Perforated gastric ulcer, sepsis - indirect ARDS 35 24 12 0.50 18

10 M 66 Perforated colon, sepsis - indirect ARDS 33 35 15 0.60 16

11 F 57 Aspiration pneumonia - direct ARDS 33 21 10 0.60 14

12 M 63 Aspiration pneumonia - direct ARDS 38 23 10 0.55 6

13 F 30 Multiple stab wounds - indirect ARDS 29 27 14 0.5 15

14 M 70 Liver resection - indirect ARDS 25 30 16 0.5 5

15 M 38 Mesenteric artery occlusion, ischemic bowel - indirect ARDS 24 29 18 0.6 19

16 M 48 Pancreatitis - indirect ARDS 29 23 15 0.70 12

17 F 28 Crushed pelvis - indirect ARDS 27 20 12 0.50 20

18 M 60 Perforated gastric ulcer, aspiration pneumonia - direct ARDS 38 22 10 0.60 13

19 F 55 Esophagectomy, pneumonia - indirect ARDS 36 29 10 0.70 17

N = 19 12 M, 49 ± 17 31.3 ± 26.1 ± 12.7 ± 0.57 ± 13.6 ±

7 F 4.8 5.3 2.9 0.07 4.5

DOV, duration of ventilation; Qs/Qt, venous admixture; FIO2, fractional inspired oxygen concentration.

chosen to allow a 1-h period of rest after suctioning and P&PD. All measurements were made with the patient in the supine position to prevent positional effects on the results. All patients were ventilated with a Puritan-Bennett 7200ae (Puritan-Bennett, Carlsbad, California, USA). Airway pressures and tidal volume were recorded directly from the ventilator's digital display. All patients were ventilated by using pressure control ventilation. Pressure was limited to less than 40 cmH2O and tidal volume targets were 8 ml/kg. Intrinsic PEEP was measured with an expiratory pause of 2.0 s and displayed by the ventilator's intrinsic PEEP maneuver. Static pulmonary compliance was measured during the delivery of a volume-controlled, constant-flow breath by recording inspiratory plateau pressure after a 1.0-s pause, total PEEP and exhaled tidal volume. Static compliance was calculated as static compliance (ml/cmH2O) = tidal volume/plateau pressure - total PEEP.

Continuous measurements of oxygen consumption (VO2), CO2 production (VCO2), respiratory quotient (RQ), and resting energy expenditure (REE) were accomplished with an open-circuit indirect calorimeter with the use of the

dilutional principle (DeltaTrac' Sensormedics, Yorba Linda, California, USA) [12,13]. VO2, VCO2, RQ, and REE were averaged on a minute-to-minute basis and saved to a personal computer for later analysis. Mixed expired CO2 concentration (PeCO2) was also measured and used along with the partial pressure of arterial CO2 (PaCO2) to determine the ratio of deadspace to tidal volume (Vd/Vt). Vd/Vt was calculated with the Bohr equation, Vd/Vt = PdaCOt 2 - PeCO2/PaCO2. d t

Routine care

Patients continued to receive routine care including bathing, mouth care, suctioning, and measurement of hourly vital signs. Every effort was made to maintain continuous rotation during the study period. No patient had received continuous rotation before the start of the study. Additionally, routine procedures were accomplished more than 2 h before blood gas data were obtained. Suctioning was accomplished as needed in the judgement of the nursing and respiratory therapy staff. Indications for suc-tioning included rhonchi on auscultation, audible secretion noises, patient coughing, and the presence of a sawtooth

Table 2

Mean values for cardiorespiratory variables during the four 6-h periods studied

Cardiorespiratory variable Manual turning Manual turning + P&PD Continuous rotation Continuous rotation + P&PD

Mean VO2 (ml/min) 299 ± 88 323 ± 114 288 ± 79 302 ± 97

Mean VCO2 (ml/min) 269 ± 71 294 ± 69 260 ± 73 272 ± 77

Mean PIP (cmH2O) 38 ± 9 40 ± 9 36 ± 10 38 ± 8

Mean Pplat (cmH2O) 34 ± 7 37 ± 6 33 ± 6 34 ± 6

Mean Vt (ml) 733 ±104 710 ± 119 751 ± 96 745 ±113

Vd/Vt (%) 0.62 ± 0.18 0.63 ± 0.23 0.59 ± 0.18 0.64 ± 0.19

Cardiac output (litres/min) 7.4 ± 2.3 7.8 ± 2.7 7.1 ± 2.2 7.4 ± 2.7

Turns per 6 h 2.5 ± 0.4 3.0 ± 0.2 41 ± 8* 43 ± 20*

Values are means ± SD of data recorded every hour for the study period, except Vd/Vv which was every 3 h. PIP, peak inspiratory pressure; P&PD, percussion and postural drainage; Pplat, inspiratory plateau pressure; VO2, oxygen consumption; VCO2, CO2 production.

pattern in the expiratory waveform in the absence of ventilator circuit condensate. A suctioning procedure was also accomplished following P&PD. Suctioning was done with a sterile, open-circuit technique with a single-use disposable suction catheter. Patients were pre-oxygenated before suctioning and manually ventilated with a self-inflating bag in between suction catheter passes. Normal saline was instilled at the discretion of the surgical ICU staff in an attempt to thin secretions. The volume of secretions aspirated were collected in a sputum trap and recorded. Suctioning was performed after each P&PD period or at the time that P&PD would have been accomplished.

All data were collected prospectively by the researchers (RDB and RSC), who were present throughout the 24-h study period. Changes in ventilator settings were limited to temporary increases in inspired oxygen concentrations to alleviate hypoxemia (pulse oximetry saturation less than 90%).

Statistical analysis

All data were collected and analyzed with commercially available data management and statistical software. All data are shown as means ± SD. Data were analyzed with analysis of variance for repeated measures and Tukey's test for post hoc analysis.


All patients completed the 24-h trial period. There were no statistically significant differences in the measured car-diorespiratory variables (Table 2). There was a tendency for PaO2/FIO2 to increase (174 ±31 versus 188 ±36; P =0.068) and Vd/Vt to decrease (0.62 ±0.18 versus 0.59 ±0.18; P =0.19) during periods of CLR, but these differences did not achieve statistical significance. There were no changes in PaCO2 during the study (Fig. 1). Airway pressures were unchanged during the study period

Figure 1

Changes in PaO2 and PaCO2 during the four study periods.

and cardiac output was unaffected. VO2 and VCO2 tended to be higher during the periods of P&PD than without, although this difference was similarly not statistically significant. Results for the cardiorespiratory measurements are shown in Table 2.

There were statistically significant increases in sputum volume during the periods of CLR (Table 3). The addition of P&PD did not increase sputum volume for the group as a whole. However, in the four patients producing more than 40 ml of sputum per day, P&PD increased sputum volume significantly (Table 3). The number of patient turns increased from one every 2 h to one every 10 min during CLR.

During P&PD, all patients showed a rise in VO2 and VCO2 associated with the procedure. In each case, the increase in VO2 and VCO2 during manual P&PD was greater than that during P&PD provided by the bed. In one case, P&PD

Table 3

Effects of P&PD on sputum production, effects of percussion and postural drainage (P&PD) on oxygen consumption (VO2), and number of patient turns during the four 6-h study periods

Manual turning + Continuous rotation +

Variable Manual turning P&PD Continuous rotation P&PD

Sputum volume (ml) 13 ± 7 15 ± 5 23 ± 9* 25 ± 9*

Sputum volume, high production (ml) 18 ± 8 27 ± 13+ 26 ± 14 30 ± 11*

Change in VO2 during P&PD (%) NA [+] 22 ± 8+ NA [+] 7 ± 4

Turns per 6 h 2.5 ± 0.4 3.0 ± 0.2 41 ± 8 43 ± 10

Sputum volume is the total volume for each 6-h period; high production refers to patients with a sputum production of more than 40 ml/day. NA, not applicable. Change in VO2 is the percentage change from previous period without P&PD. *, P< 0.05 versus manual turning periods. f, P< 0.001 versus manual turning periods. *, P < 0.05 versus times without P&PD.

with the bed was associated with multi-focal premature ventricular contractions and 'whip' artefact on the pulmonary artery pressure tracing. The intensity of the percussion was reduced and this problem was eliminated.


Turning regimens are an essential part of the routine management of mechanically ventilated patients. Position changes are thought to reduce atelectasis, enhance fluid mobilization, prevent skin breakdown, improve oxygenation, and decrease the incidence of hospital-acquired pneumonia [4-9]. This study was designed to study the acute effects of CLR in comparison with manual turning, in paralyzed patients with ARDS. Our study was designed to identify the underlying physiological changes that might be related to the positive outcomes attributed to position changes. The major findings of the study are as follows: (1) blood gases are unaffected by a short period (6 h) of CLR, (2) secretion clearance is enhanced by CLR, and (3) P&PD results in an increase in sputum volume only in patients with excessive secretions. These findings are specific to this population of critically ill, paralyzed, surgical patients with ARDS. Extrapolation of these findings to other patient populations should be made with caution.

Few studies have attempted to elucidate the underlying physiological changes that might be responsible for positive outcomes seen with the use of CLR. Bein et al [10] recently compared the effects of a 20 min period of rotation to 20 min in the supine position in 10 ARDS patients. They found an increase in PaO2/FIO2 from 1 74 ± 82 to 217 ±137 and decrease in intrapulmonary shunt from 23 ±14% to 19.1 ±15%. Using the multiple inert-gas elimination technique they attributed this improvement in gas exchange to a decrease in the amount of low ventilation/perfusion (V/Q) lung units and increase in normal V/Q units. In this study, measurements for the rotation periods were made with the patient in an extreme lateral position. This differs from our design. Bein et al also found that patients with more severe lung disease (Murrary Lung

injury score more than 2.5) did not respond to rotational therapy, whereas those with less severe disease (less than 2.5) had significant changes in PaO2/FIO2. This can be explained by the changes in ARDS with time, as the lung evolves from a wet, heavy, atelectatic lung to a brittle fibrotic lung [12]. Early in ARDS, postural changes including CLR and prone positioning can be effective in altering the distribution of ventilation and blood flow [13-15]. In late ARDS, pathophysiological changes seem to render postural changes largely ineffective.

Nelson and Anderson [16] have shown previously that steep lateral positioning can result in either an improvement or a worsening of oxygenation. In their study of ten patients with apparent bilateral lung disease, steep positioning resulted in a decrease in PaO2 in four patients and an increase in PaO2 in six patients. These measurements were made in the extreme lateral position. They found that continuous rotation returned blood gas values to those in the supine position. These authors also suggested that extreme changes in lateral posture were associated with adverse effects on hemodynamics in comparison with continuous rotation. Bein et al [1 7] have also reported adverse hemodynamic effects in patients placed in the extreme lateral position. They suggested that the left lateral position resulted in a hyperdynamic state and that the right lateral position decreased right ventricular preload, resulting in hypotension. The measurement of plasma atrial natriuretic peptide indicated that these changes were due to the gravitational effects on the dis-tensibility of the right heart. However, patients in this study were not solely patients with ARDS. We did not ascertain any significant hemodynamic effects during continuous rotation or manual turning. In many cases, pain associated with manual turning resulted in transient tachycardia and hypertension. Our findings did not reveal the magnitude of changes in gas exchange seen by others. However, PaO2/FIO2 increased in every patient after a period of rotation (188 ± 47 versus 174 ± 48, range 8-29) in our study. However, this difference was not statistically significant.

Position changes in unilateral lung disease have long been shown to be of value [18]. Placing the 'good lung' lower results in improved ventilation perfusion matching and an increase in oxygenation due to the gravitational effects on blood flow. More recently, the use of prone positioning has been shown to improve oxygenation in ARDS by improving distribution of ventilation through changes in regional pleural pressure gradients [14,15,19,20]. These two positioning techniques alter ventilation perfusion relationships through very different mechanisms. Prone positioning uses the shape and size of the dorsal lung compared with the ventral lung to improve the distribution of ventilation in bilateral lung disease. Extreme lateral positioning attempts to alter perfusion through the effects of gravity.

The process of routine turning is steeped in tradition, follows common-sense guidelines, and has some historical prescedent [21,22]. Lambert and colleagues determined that the immobilized postoperative patient was prone to atelectasis in the dependent lung. Chulay et al

[22] found that turning the patient at 2-h intervals during the first 24 h after coronary artery bypass surgery decreased the incidence of fever and shortened ICU stay compared with patients remaining in the supine position. Routine turning also follows the normal pattern of sleep, where the average person changes posture every 12 min

[23]. On the basis of this evidence, routine body position changes to prevent pulmonary complications have become a standard of care. Additionally, turning is important for decreasing skin breakdown and contributing to the mobilization of fluid.

We did find that the use of CLR significantly increased the number of times that the patients were turned each hour. During scheduled turning every 2 h by the staff, turns occurred only every 3 h. This finding is related in part to the study design, but is also related to the availability of staff. Turning patients can be difficult owing to the severity of illness, patient size, patient weight, and the presence of traction, indwelling lines, and ancillary equipment surrounding the bed. During the 2-h manual turning portion of the study, turning was accomplished less frequently owing to the workload of ICU staff. During continuous rotation, patients were turned from left to right six times per hour. Clearly, when used appropriately, a rotational bed facilitates patient turning and reduces nursing workload spent performing this task.

We also demonstrated improved secretion clearance in patients during CLR that were unrelated to P&PD. Compared with manual turning, continuous rotation seems to facilitate secretion clearance in paralyzed patients. This finding might be specific to paralyzed patients who are unable to cough. Changes in body position are an important part of postural drainage and this is most likely to be the mechanism through which secretion clearance is

enhanced. Acutely, improved secretion clearance might be responsible for the reported decrease in pneumonia during prolonged use of CLR [5-8]. Interestingly, the addition of percussion to the postural drainage occurring during CLR failed to increase secretion clearance in our patient population. However, previous work has questioned the use of P&PD in patients without increased secretion production [24-26]. Four of our patients demonstrated high volumes of secretions (40 ml/day); in each of the four, P&PD increased secretion clearance. This finding is not wholly unexpected. Our results suggest that routine P&PD is unnecessary. However, patients with excessive secretions seem to benefit from a combination of continuous rotation and P&PD. Whether this increase in secretion clearance alters outcomes cannot be determined from our 24-h study.

The metabolic cost of P&PD had been previously described [27]. Horiuchi et al [28] have measured a 40% increase in VO2 during P&PD in postoperative surgical patients. This effect has been attributed to both a stresslike and an exercise-like response of the patient to P&PD. In this most recent investigation, these authors found that VO2 was increased both by manual turning into the lateral decubitus position and by the administration of percussion. When vecuronium was given before the procedure, these changes in VO2 were abated. The authors suggested that both patient muscle activity and increased sympathetic output contribute to the increase in VO2 seen during P&PD. Interestingly, our patients tolerated turning and percussion by the bed better than manual turning and percussion. The change in VO2 during P&PD provided by the bed was much lower than that seen during manual techniques. This might be related to the abrupt changes that occur with manual turning, and pain associated with manual hand clapping on the chest wall.

The study design and 24-h trial period impose significant limitations on the results. Because we attempted to determine physiological changes, a short study period was required. It might be that several days of CLR is required before the identification of beneficial effects. Our design cannot answer this question. All measurements were made by the same two investigators in an attempt to limit measurement errors. However, during a 24-h period, changes in lung mechanics as a consequence of disease progression/resolution might have occurred. We attempted to limit these confounding variables by randomizing the sequence of regimens. Variations in blood gases over time in a given patient have been reported and demonstrate significant variation based on timing [29]. We attempted to standardize the collection of data to coincident events, to prevent variability.

This investigation found that, whereas PaO2 improved slightly during periods of rotation, no significant increases

in gas exchange were identified between manual turning every 2 h and CLR. There were no adverse hemodynamic effects of either turning procedure. Continuous rotation did increase secretion clearance compared with manual turning, but the addition of percussion did not further improve secretion removal. In patients with large secretion volumes, P&PD did increase secretion clearance. P&PD was better tolerated when delivered by the bed in comparison with manual turning, as judged by the change in VO2. The acute effects of CLR are undoubtedly different in other patient populations. The link between acute physiological changes and improved outcomes associated with CLR remain to be determined.


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