<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJAnes</journal-id><journal-title-group><journal-title>Open Journal of Anesthesiology</journal-title></journal-title-group><issn pub-type="epub">2164-5531</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojanes.2023.131001</article-id><article-id pub-id-type="publisher-id">OJAnes-122736</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Comparison of Arterial Oxygenation between 60% O&lt;sub&gt;2&lt;/sub&gt; CPAP and 100% O&lt;sub&gt;2&lt;/sub&gt; CPAP during One-Lung Ventilation: A Prospective Randomized Controlled Study
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yuko</surname><given-names>Yamada</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kumiko</surname><given-names>Tanabe</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kiyoshi</surname><given-names>Nagase</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hiroki</surname><given-names>Iida</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Anesthesiology and Pain Medicine, Gifu University Graduate School of Medicine, Gifu, Japan</addr-line></aff><aff id="aff2"><addr-line>Anesthesiology and Pain Relief Center, Central Japan International Medical Center, Minokamo, Gifu, Japan</addr-line></aff><pub-date pub-type="epub"><day>30</day><month>01</month><year>2023</year></pub-date><volume>13</volume><issue>01</issue><fpage>1</fpage><lpage>14</lpage><history><date date-type="received"><day>19,</day>	<month>December</month>	<year>2022</year></date><date date-type="rev-recd"><day>28,</day>	<month>January</month>	<year>2023</year>	</date><date date-type="accepted"><day>31,</day>	<month>January</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution-NonCommercial International License (CC BY-NC).http://creativecommons.org/licenses/by-nc/4.0/</license-p></license></permissions><abstract><p>
 
 
  <b>Background:</b> One-lung ventilation (OLV) is generally adopted for thoracic surgery. The systemic application of a high fraction of inspiratory oxygen (F
  <sub>1</sub>O
  <sub>2</sub>) and continuous positive airway pressure (CPAP) to the non-ventilated lung is useful for preventing arterial oxygen desaturation. The adverse effects of elevated F
  <sub>1</sub>O
  <sub>2</sub> include oxidative lung injury, resorption atelectasis and coronary and peripheral vasoconstriction. It is preferable to avoid hyperoxemia in patients with complications such as chronic obstructive pulmonary disease, idiopathic pneumonia, and bleomycin-treated lungs. We aimed to determine whether the application of 60% O
  <sub>2</sub> CPAP to the non-ventilated lung is sufficient to provide adequate oxygenation with 60% O
  <sub>2</sub> to the ventilated lung. 
  <b>Methods:</b> A total of 70 patients scheduled to receive elective thoracic surgery requiring OLV were recruited. Left double-lumen tubes were applicable in all surgeries. Patients were randomly allocated to one of two groups, to receive either 60% O
  <sub>2</sub> CPAP (60% CPAP group, n = 35), or 100% O
  <sub>2</sub> CPAP (100% CPAP group, n = 35) at a setting of 2 - 3 cmH
  <sub>2</sub>O, applied to the non-ventilated lung. Arterial blood gas analyses were obtained at the following stages: RA, spontaneous breathing under room air (RA); TLV, during total lung ventilation (TLV) prior to the initiation of OLV; T5, 5 min after the initiation of OLV; T15, 15 min after the initiation of OLV; T30, 30 min after the initiation of OLV. 
  <b>Results:</b> The PaO
  <sub>2</sub> value in 60% CPAP group vs. 100% CPAP group at each measurement were as follows: RA (mean [standard deviation: SD], 89.7 [8.2] mmHg vs. 85.8 [11.9] mmHg); TLV (277.9 [52.9] mmHg vs. 269.2 [44.0] mmHg); T5 (191.4 [67.9] mmHg vs. 192.3 [66.0] mmHg); T15 (143.2 [67.3] mmHg vs. 154.7 [60.8] mmHg) and T30 (95.6 [32.0] mmHg vs. 112.5 [36.5] mmHg), respectively. Among the five measurement points, T30 was the only time point at which the 100% CPAP group showed a significantly greater PaO
  <sub>2</sub> value than the 60% CPAP group (p = 0.0495). The SaO
  <sub>2</sub> at T30 in the 100% CPAP group (97.4 [2.0]%) was also significantly greater than that in the 60% CPAP group (96.3 [2.2]%, p = 0.039). No differences were found between the groups regarding changes to the overall PaO
  <sub>2</sub> values (p = 0.44) and SaO
  <sub>2</sub> values (p = 0.23) during the study period. 
  <b>Conclusions:</b> Oxygenation could be safely maintained in relatively healthy patients with 60% O
  <sub>2</sub> OLV and 60% O
  <sub>2</sub> CPAP. The application of 60% O
  <sub>2</sub> CPAP during OLV for patients who are not suited to exposure to high F
  <sub>1</sub>O
  <sub>2</sub> may be an alternative form of respiratory management.
 
</p></abstract><kwd-group><kwd>CPAP</kwd><kwd> Double-Lumen Tube</kwd><kwd> Hyperoxemia</kwd><kwd> Hypoxemia</kwd><kwd> One-Lung Ventilation</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>One-lung ventilation (OLV) is performed to separate the non-ventilated lung from the ventilated lung in thoracic surgery. Collapse of the surgical lung improves access to the surgical field [<xref ref-type="bibr" rid="scirp.122736-ref1">1</xref>]. Intrapulmonary shunt may decrease oxygenation during OLV due to the collapse of the non-ventilated lung. The application of a high fraction of inspiratory oxygen (F<sub>I</sub>O<sub>2</sub>) in order to avoid hypoxemia increases atelectatic areas in the ventilated lung [<xref ref-type="bibr" rid="scirp.122736-ref2">2</xref>]. The incidence of hypoxemia during OLV was slightly enhanced (3% - 10%) [<xref ref-type="bibr" rid="scirp.122736-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref5">5</xref>]. Managements for preventing arterial oxygen desaturation during OLV include using high F<sub>I</sub>O<sub>2</sub>, continuous positive airway pressure (CPAP) to the non-ventilated lung, positive end-expiratory pressure (PEEP) to the ventilated lung, and repeated inflation of the non-ventilated lung [<xref ref-type="bibr" rid="scirp.122736-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref6">6</xref>]. CPAP may potentially reduce mechanical stress by keeping the alveoli open, allowing gas exchange and diverting blood away from the collapsed lung [<xref ref-type="bibr" rid="scirp.122736-ref2">2</xref>]. However, high-pressure CPAP has hemodynamic implications for the non-ventilated lung, causing overexpansion of the non-ventilated lung, which limits surgical access [<xref ref-type="bibr" rid="scirp.122736-ref3">3</xref>]. Thus, to avoid hypoxemia, 100% O<sub>2</sub> is routinely used in the application of CPAP to the non-ventilated lung instead of high-pressure CPAP.</p><p>Higher level F<sub>I</sub>O<sub>2</sub> is routinely used during OLV to minimize the risk of developing hypoxemia [<xref ref-type="bibr" rid="scirp.122736-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref7">7</xref>]. The effects of progressive hypoxemia, particularly in individuals with coexisting cardiovascular, cerebrovascular, or pulmonary disease, undoubtedly pose a greater risk of compromised circulation [<xref ref-type="bibr" rid="scirp.122736-ref8">8</xref>]. On the other hand, the adverse effects of hyperoxemia and the application of high F<sub>I</sub>O<sub>2</sub> include resorption atelectasis, coronary and peripheral vasoconstriction, cardiac output decrease, and direct harm to lung through oxidative stress [<xref ref-type="bibr" rid="scirp.122736-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref12">12</xref>]. Hyperoxemia directly damages the lung in patients with chronic obstructive pulmonary disease (COPD), idiopathic pneumonia and bleomycin-treated lungs through oxidative stress [<xref ref-type="bibr" rid="scirp.122736-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref15">15</xref>]. Cancer patients have a higher oxidative burden and may have less antioxidant capacity [<xref ref-type="bibr" rid="scirp.122736-ref16">16</xref>]. Lower level F<sub>I</sub>O<sub>2</sub> at 0.6 can maintain oxygenation during OLV, and it is less than an inflammatory response, lung edema, thickening of the alveolar wall, or acute injury will occur, in comparison to higher level F<sub>I</sub>O<sub>2</sub> at 1.0% [<xref ref-type="bibr" rid="scirp.122736-ref7">7</xref>]. Therefore, the respiratory management that minimizes F<sub>I</sub>O<sub>2</sub> levels during OLV is deemed desirable. However, it is currently unclear whether a lower F<sub>I</sub>O<sub>2</sub> CPAP can be safely applied to the non-ventilated lung with a lower F<sub>I</sub>O<sub>2</sub> to the ventilated lung in the clinical setting.</p><p>We aimed to determine whether the application of lower F<sub>I</sub>O<sub>2</sub> CPAP to the non-ventilated lung is sufficient to provide adequate oxygenation.</p></sec><sec id="s2"><title>2. Methods</title><sec id="s2_1"><title>2.1. Study Population</title><p>This prospective randomized, controlled study was approved by the university’s institutional review board (IRB: 29-29) and written informed consent was obtained from all subjects who participated in the trial. The trial was registered prior to patient enrollment at the University Hospital Medical Information Network in Japan (UMIN 000028137, Principal investigator: Yuko Yamada, Date of registration: July 7, 2017). The study population included patients scheduled to undergo elective video-assisted thoracotomy requiring OLV from July 2017 to August 2019. The inclusion criteria were age &gt;20 years, American Society of Anesthesiologists physical status of 1 - 3 and OLV lasting &gt;45 min. The exclusion criteria were body mass index ≥30 kg/m<sup>2</sup>, severe respiratory dysfunction and interstitial lung disease. A decline in pulse oximetric saturation (SpO<sub>2</sub>) to &lt;90% measured by pulse oximetry was the indication for interruption of the study; cases in which this occurred were excluded. This article adheres to the applicable Consolidated Standards of Reporting Trials (CONSORT) guidelines.</p></sec><sec id="s2_2"><title>2.2. Group Allocation</title><p>Patients were randomly assigned to one of two groups, receiving either 60% O<sub>2</sub> CPAP (60% CPAP group, n = 35), or 100% O<sub>2</sub> CPAP (100% CPAP group, n = 35). The allocation ratio was 1:1, and a random allocation sequence was performed using sealed opaque envelopes for the purpose of allocation concealment.</p></sec><sec id="s2_3"><title>2.3. Anesthesia and Double-Lumen Tube Intubation</title><p>After the arrival of patients in the operating room, standard monitoring was used. An intraarterial canula was inserted under local anesthesia. A thoracic epidural catheter was placed at the T7 level and a test dose was administered. No further epidural medications were administered until the end of the study period. Anesthesia was induced with propofol, remifentanil, and rocuronium, and maintained with propofol, remifentanil and rocuronium. All patients were intubated with left-sided double-lumen tubes (DLTs) (Broncho-Cath<sup>TM</sup>, Mallinckrodt Medical Ltd., Athlone, Ireland) for both right- and left-sided surgery. An appropriate DLT size was determined based on the diameter of the left mainstem bronchus, measured on preoperative chest computed tomography [<xref ref-type="bibr" rid="scirp.122736-ref17">17</xref>].<sup> </sup>The proper position of the DLT was confirmed by fiberoptic bronchoscopy in both the supine and lateral positions. The bronchial cuff of the DLT was positioned, allowing the cephalad surface to be visible just below the carina. The lungs of all patients were ventilated with 60% oxygen. A tidal volume of 6 - 8 mL/kg (predicted body weight) was applied with PEEP of 4 cm H<sub>2</sub>O. The respiratory rate was 10 - 15 breaths/min. Systolic blood pressure was maintained within 20% of the preoperative value by the intravenous administration of inotropic agents (ephedrine or phenylephrine). Cardiac output (CO) was monitored continuously using a FloTrac/Vigileo<sup>TM</sup> (Edwards Lifesciences) system.</p></sec><sec id="s2_4"><title>2.4. Lung Separation and CPAP Application</title><p>Ventilatory variables were kept constant during the study, both during total lung ventilation (TLV) and OLV. The bronchial cuff was connected to a cuff inflator via a three-way stopcock, and then was inflated to a pressure of 20 cm H<sub>2</sub>O. OLV was initiated just after the pleura was opened. The non-ventilated lung was exposed to the atmosphere, thus allowing deflation to reach atmospheric pressure. The ventilated lung was ventilated with 60% oxygen during OLV. Patients were randomly allocated to one of two groups, which received either 60% O<sub>2</sub> CPAP (60% CPAP group, n = 35), or 100% O<sub>2</sub> CPAP (100% CPAP group, n = 35) at a setting of 2 - 3 cm H<sub>2</sub>O, which was applied to the non-ventilated lung via a CPAP adaptor with a fresh gas flow of 5 l/min using a Broncho-Cath<sup>TM</sup> CPAP system (Mallinckrodt Medical Ltd., Athlone, Ireland). CPAP was applied for a period of 3 min after the initiation of OLV. During OLV, the cuff pressure monitor was attached using a tube to the gas-sampling site of the patient end of the CPAP system to verify the CPAP level.</p></sec><sec id="s2_5"><title>2.5. Measurements</title><p>Blood gas was measured using a commercially available blood gas analyzer (ABL 700 analyzer; Radiometer, Copenhagen, Denmark). Hemodynamic variables, peak inspiratory pressure (PIP), SpO<sub>2</sub> and arterial blood gas analyses were performed at the following stages: 1) RA, spontaneous breathing under room air (RA); 2) TLV, during TLV prior to the initiation of OLV in the lateral position; 3) T5, 5 min after the initiation of OLV; 4) T15, 15 min after the initiation of OLV; and 5) T30, 30 min after the initiation of OLV (<xref ref-type="fig" rid="fig1">Figure 1</xref>). All measurements, with the exception of RA, were taken in a lateral position. Hypoxemia was defined as arterial partial pressure of oxygen (PaO<sub>2</sub>) &lt;60 mmHg, or SpO<sub>2</sub> was maintained at &lt;90%. Concurrently, thoracic surgeons were asked to comment on the quality of lung collapse after the opening of the chest. The condition of lung collapse was assessed as follows: 0 = impossible surgical access; 1 = poor</p><p>surgical access; 2 = fair operative field; and 3 = good operative field. Thoracic surgeons were blinded to the group assignments.</p></sec><sec id="s2_6"><title>2.6. Outcome Variables</title><p>The primary outcome of this study was the PaO<sub>2</sub> values of the two groups at 30 min after the initiation of OLV (T30). The secondary outcomes were the differences between the groups in the changes in PaO<sub>2</sub> and arterial oxygen saturation (SaO<sub>2</sub>).</p></sec><sec id="s2_7"><title>2.7. Sample Size Estimation</title><p>A type I error estimate of 5% (alpha = 0.05) and a power (1-beta) of 90% were set. The sample size calculation was based on the assumption that the difference in the PaO<sub>2</sub> value of the 2 groups was 25 mmHg, and that the standard deviation (SD) of the groups was 30, according to a previous report [<xref ref-type="bibr" rid="scirp.122736-ref18">18</xref>]. It was estimated that a minimum of 63 patients would be required. To compensate for possible dropouts, the enrollment of 70 patients (i.e., 35 patients per group) was planned.</p></sec><sec id="s2_8"><title>2.8. Statistical Analysis</title><p>All data were analyzed using the SPSS&#174; software program, version 23 (SPSS Inc., Chicago, IL, USA). The characteristics of patients are summarized as the mean [SD] for continuous variables. Frequencies and percentages are shown for categorical variables. For the analysis of the primary outcome variables, the mean PaO<sub>2</sub> of the two groups were compared using Student’s t-test with a two-sided significance level of 0.05. The primary result was considered statistically significant when the P value was &lt; 0.05. The analyses of arterial blood gas (pH, PaCO<sub>2</sub>, SaO<sub>2</sub>), SpO<sub>2</sub>, PIP and hemodynamic variables were the same as in the primary analysis.</p><p>For the analysis of the secondary outcome variables, a two-way repeated measures analysis of variance was used to assess the difference between the groups. The secondary results were considered statistically significant when the P value was &lt; 0.05.</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Participants</title><p>Seventy patients were enrolled in this study from July 2017 to Aug 2019 (<xref ref-type="fig" rid="fig2">Figure 2</xref>). The perioperative demographic patient profiles and operative details are summarized in <xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="table" rid="table2">Table 2</xref>. Of these 70 patients, 2 patients were excluded from the analysis. Almost all patients (except for 1 lung carcinoid) underwent lung cancer surgery. In these two cases, there was extensive pleural adhesion of the non-ventilated lung and the lung collapse was interrupted. The remaining 68 patients (n = 34 in each group) completed the study (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p></sec><sec id="s3_2"><title>3.2. Primary Outcome</title><p>The PaO<sub>2</sub> value measured at T30 in the 100% CPAP group (mean [SD], 112.5 [36.5] mmHg) was significantly higher than that in the 60% CPAP group (95.6 [32.0] mmHg, p = 0.0495) (<xref ref-type="fig" rid="fig3">Figure 3</xref>(a)).</p></sec><sec id="s3_3"><title>3.3. Secondary Outcome</title><p>No difference was found between the groups regarding changes to the overall PaO<sub>2</sub> values during study period (p = 0.44). SaO<sub>2</sub> measured at T30 in the 100%</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Patients’ characteristic</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >60% CPAP-group</th><th align="center" valign="middle" >100% CPAP-group</th></tr></thead><tr><td align="center" valign="middle" >Number of patients</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >34</td></tr><tr><td align="center" valign="middle" >Age (years), mean (SD)</td><td align="center" valign="middle" >63.0 (10.5)</td><td align="center" valign="middle" >66.7 (10.4)</td></tr><tr><td align="center" valign="middle" >Male, n (%)</td><td align="center" valign="middle" >15 (44.1)</td><td align="center" valign="middle" >16 (47.1)</td></tr><tr><td align="center" valign="middle" >Height (cm), mean (SD)</td><td align="center" valign="middle" >159.4 (8.7)</td><td align="center" valign="middle" >160.2 (9.4)</td></tr><tr><td align="center" valign="middle" >Weight (kg), mean (SD)</td><td align="center" valign="middle" >57.0 (12.7)</td><td align="center" valign="middle" >59.0 (10.2)</td></tr><tr><td align="center" valign="middle" >ASA class, I/II/III, n</td><td align="center" valign="middle" >9/25/0</td><td align="center" valign="middle" >11/23/0</td></tr><tr><td align="center" valign="middle" >Never smoker, n (%)</td><td align="center" valign="middle" >16 (47.1)</td><td align="center" valign="middle" >16 (47.1)</td></tr><tr><td align="center" valign="middle" >FEV1/FVC (%), mean (SD)</td><td align="center" valign="middle" >75.2 (5.3)</td><td align="center" valign="middle" >74.4 (6.9)</td></tr><tr><td align="center" valign="middle" >FVC, % of the predicted, mean (SD)</td><td align="center" valign="middle" >108.1 (13.0)</td><td align="center" valign="middle" >112.5 (13.0)</td></tr><tr><td align="center" valign="middle" >Side of surgery, left/right, n (%)</td><td align="center" valign="middle" >15 (44.1)/19 (55.9)</td><td align="center" valign="middle" >22 (64.7)/12 (35.3)</td></tr></tbody></table></table-wrap><p>Values presented as the mean (standard deviation) or number (proportion). Abbreviations: ASA, American Society of Anesthesiologists; CPAP, continuous positive airway pressure; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; SD, standard deviation.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Operative details</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >60% CPAP-group</th><th align="center" valign="middle" >100% CPAP-group</th></tr></thead><tr><td align="center" valign="middle" >Number of patients</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >34</td></tr><tr><td align="center" valign="middle" >Duration of OLV (min), mean (SD)</td><td align="center" valign="middle" >162.8 (47.8)</td><td align="center" valign="middle" >166.6 (63.3)</td></tr><tr><td align="center" valign="middle" >Duration of surgery (min), mean (SD)</td><td align="center" valign="middle" >190.7 (47.6)</td><td align="center" valign="middle" >193.4 (65.1)</td></tr><tr><td align="center" valign="middle" >Conditions for surgery, 0/1/2/3, n (%)</td><td align="center" valign="middle" >0 (0)/6 (17.6)/ 23 (67.6)/5 (14.7)</td><td align="center" valign="middle" >0 (0)/9 (26.5)/ 19 (55.9)/6 (17.6)</td></tr><tr><td align="center" valign="middle" >Type of surgery, n (%)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Partial resection</td><td align="center" valign="middle" >2 (5.9)</td><td align="center" valign="middle" >3 (8.8)</td></tr><tr><td align="center" valign="middle" >Segmentectomy or wedge resection</td><td align="center" valign="middle" >13 (38.2)</td><td align="center" valign="middle" >7 (20.6)</td></tr><tr><td align="center" valign="middle" >Lobectomy</td><td align="center" valign="middle" >19 (55.9)</td><td align="center" valign="middle" >24 (70.6)</td></tr></tbody></table></table-wrap><p>Values presented as the mean (standard deviation) or number (%). Abbreviations: CPAP, continuous positive airway pressure; OLV, one lung ventilation; SD, standard deviation.</p><p>CPAP group (97.4 [2.0] %) was higher than that in the 60% CPAP group (96.3 [2.2] %, p = 0.039); however, there was no difference between the two groups regarding changes to the overall SaO<sub>2</sub> values during study period (p = 0.23) (<xref ref-type="fig" rid="fig3">Figure 3</xref>(b)).</p></sec><sec id="s3_4"><title>3.4. Comparison of Physiologic Variables</title><p>The hemodynamic variables, and the results of PIP, SpO<sub>2</sub> and arterial blood gas</p><p>analyses (pH, PaO<sub>2</sub>, PaCO<sub>2</sub>, SaO<sub>2</sub>) are presented in <xref ref-type="table" rid="table3">Table 3</xref>. There were no patients with hypoxemia during the study period. PaCO<sub>2</sub> values in both groups were maintained at approximately 40 mmHg.</p></sec><sec id="s3_5"><title>3.5. The Condition of Surgical Field</title><p>The surgeons assessed the condition of the surgical field as poor surgical access in 6 patients from the 60% CPAP group and 9 patients from the 100% CPAP group. In these patients, the surgical fields did not interfere to the extent that visibility was disturbed due to the application of CPAP. All surgeries were completed</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Blood gas analysis and hemodynamic data</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >RA</th><th align="center" valign="middle" >TLV</th><th align="center" valign="middle" >T5</th><th align="center" valign="middle" >T15</th><th align="center" valign="middle" >T30</th></tr></thead><tr><td align="center" valign="middle" >pH<sub> </sub></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >7.44 (0.03) 7.43 (0.02)</td><td align="center" valign="middle" >7.37 (0.03) 7.36 (0.03)</td><td align="center" valign="middle" >7.38 (0.04) 7.38 (0.03)</td><td align="center" valign="middle" >7.39 (0.04) 7.39 (0.03)</td><td align="center" valign="middle" >7.4 (0.04) 7.4 (0.04)</td></tr><tr><td align="center" valign="middle" >PaO<sub>2</sub> (mm Hg)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >*</td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >89.7 (8.2) 85.8 (11.9)</td><td align="center" valign="middle" >277.9 (52.9) 269.2 (44.0)</td><td align="center" valign="middle" >191.4 (67.9) 192.3 (66.0)</td><td align="center" valign="middle" >143.2 (67.3) 154.7 (60.8)</td><td align="center" valign="middle" >95.6 (32.0) 112.5 (36.5)</td></tr><tr><td align="center" valign="middle" >SaO<sub>2</sub> (%)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >*</td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >97.1 (1.0) 96.7 (1.5)</td><td align="center" valign="middle" >99.6 (0.5) 99.7 (0.2)</td><td align="center" valign="middle" >99.0 (0.9) 99.1 (1.0)</td><td align="center" valign="middle" >97.7 (2.2) 98.3 (1.9)</td><td align="center" valign="middle" >96.3 (2.2) 97.4 (2.0)</td></tr><tr><td align="center" valign="middle" >S<sub>p</sub>O<sub>2</sub> (%)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >98.8 (1.3) 98.4 (1.5)</td><td align="center" valign="middle" >100 (0) 99.9 (0.2)</td><td align="center" valign="middle" >99.8 (0.6) 99.8 (0.6)</td><td align="center" valign="middle" >98.9 (1.9) 99.1 (1.5)</td><td align="center" valign="middle" >97.7 (2.2) 98.4 (1.9)</td></tr><tr><td align="center" valign="middle" >PaCO<sub>2</sub> (mm Hg)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >38.1 (3.2) 38.7 (2.9)</td><td align="center" valign="middle" >45.2 (3.7) 46.3 (3.7)</td><td align="center" valign="middle" >43.6 (3.9) 44.5 (4.2)</td><td align="center" valign="middle" >42.7 (3.9) 42.9 (4.2)</td><td align="center" valign="middle" >41.9 (3.9) 41.8 (4.2)</td></tr><tr><td align="center" valign="middle" >PIP (cm H<sub>2</sub>O)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >16.8 (1.9) 16.4 (1.6)</td><td align="center" valign="middle" >22.7 (3.9) 23.1 (2.9)</td><td align="center" valign="middle" >22.8 (4.1) 23.0 (3.1)</td><td align="center" valign="middle" >23.2 (3.9) 23.6 (3.3)</td></tr><tr><td align="center" valign="middle" >Cardiac index (L/min/m<sup>2</sup>)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >2.6 (0.5) 2.5 (0.6)</td><td align="center" valign="middle" >2.8 (0.6) 2.6 (0.5)</td><td align="center" valign="middle" >2.8 (0.6) 2.7 (0.7)</td><td align="center" valign="middle" >3.0 (0.6) 2.8 (0.6)</td></tr><tr><td align="center" valign="middle" >Heart rate (beats/min)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >74.8 (11.4) 72.7 (12.1)</td><td align="center" valign="middle" >65.0 (9.9) 66.1 (11.0)</td><td align="center" valign="middle" >65.9 (9.4) 65.7 (9.7)</td><td align="center" valign="middle" >70.4 (11.1) 68.2 (9.7)</td><td align="center" valign="middle" >74.7 (10.6) 71.3 (12.3)</td></tr><tr><td align="center" valign="middle" >Mean arterial pressure (mmHg)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >60% CPAP-group 100% CPAP-group</td><td align="center" valign="middle" >104.4 (12.9) 102.2 (13.1)</td><td align="center" valign="middle" >73.1 (8.8) 75.7 (10.3)</td><td align="center" valign="middle" >81.1 (9.6) 80.5 (9.5)</td><td align="center" valign="middle" >77.0 (10.1) 77.4 (10.0)</td><td align="center" valign="middle" >73.4 (7.3) 72.9 (10.3)</td></tr></tbody></table></table-wrap><p>Values presented as the mean (standard deviation). *P &lt; 0.05. Abbreviations: CPAP, continuous positive airway pressure; OLV, one lung ventilation; RA, room air; TLV, total lung ventilation; PIP, peak inspiratory pressure.</p><p>without interruption. In both groups, CPAP was applied safely. The quality of lung collapse was similar between the groups. None of the patients was graded as 0, where interference is maximal (<xref ref-type="table" rid="table2">Table 2</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>In the present study, we compared arterial oxygenation with the application of 60% O<sub>2</sub> CPAP or 100% O<sub>2</sub> CPAP to the non-ventilated lung during 60% O<sub>2</sub> OLV. In our previous study, the lowest PaO<sub>2</sub> value was obtained at 30 min after the initiation of OLV [<xref ref-type="bibr" rid="scirp.122736-ref19">19</xref>]. Therefore, in the present study, we investigated PaO<sub>2</sub> values up to 30 min after the initiation of 60% O<sub>2</sub> OLV. The minimum time required to complete pulmonary artery ligation was 30 min after the initiation of OLV. Among the five PaO<sub>2</sub> values, 30 min after the initiation of OLV was only one time point at which 100% O<sub>2</sub> CPAP was associated with a significantly greater value than 60% O<sub>2</sub> CPAP. However, no difference was found between groups regarding changes to the overall PaO<sub>2</sub> values throughout the study period. Our results suggested that 100% O<sub>2</sub> CPAP would be more applicable for maintaining oxygenation than 60% O<sub>2</sub> CPAP.</p><p>SaO<sub>2</sub> obtained from 30 min after the initiation of OLV also showed significantly greater readings for 100% O<sub>2</sub> CPAP than 60% O<sub>2</sub> CPAP. There was no difference between the groups regarding changes to the overall SaO<sub>2</sub> values during the study period. The relationship between PaO<sub>2</sub> and SaO<sub>2</sub> is represented by the oxygen–hemoglobin dissociation curve. PaO<sub>2</sub> is the amount of oxygen dissolved in the blood. SaO<sub>2</sub> is the percentage of hemoglobin bound to oxygen. Our study showed statistically significant differences between the groups in both PaO<sub>2</sub> and SaO<sub>2</sub>, however these small differences would reflect no advantage within the clinical situation. In this present study, no patients were presented with hypoxia. The present results indicated that 60% O<sub>2</sub> OLV with 60% O<sub>2</sub> CPAP was at least able to maintain oxygenation without exposure to high F<sub>I</sub>O<sub>2</sub>, and as such may be applied safely in clinical use.</p><p>SpO<sub>2</sub> is a parameter that can be non-invasively measured in routine practice and is substituted for SaO<sub>2</sub> in the clinical setting. In this present study, there was no significant difference in the SpO<sub>2</sub> values of the groups, despite the significant differences in PaO<sub>2</sub> and SaO<sub>2</sub> at the 30 min measurement point. The margin of error of SpO<sub>2</sub> is considered to be within 2% to 3% of the SaO<sub>2</sub> [<xref ref-type="bibr" rid="scirp.122736-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref22">22</xref>]. The small difference in SaO<sub>2</sub> values (1.1%) may have had no effect on the difference in SpO<sub>2</sub> values.</p><p>High systemic O<sub>2</sub> delivery is associated with an increased risk of serious adverse effects, including reabsorption atelectasis, decreased capillary perfusion, and cellular oxygen consumption, as well as decreased cardiac output and decreased coronary and cerebral blood flow [<xref ref-type="bibr" rid="scirp.122736-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref24">24</xref>]. Hyperoxia-induced damage due to the production of free radicals is more prominent in the lung, as the lung tissue is continuously exposed to oxygen. There is some evidence suggesting that patients who undergo thoracic surgery may be more susceptible to lung injury from hyperoxia than conventionally thought [<xref ref-type="bibr" rid="scirp.122736-ref25">25</xref>]. Rabbits receiving F<sub>I</sub>O<sub>2</sub> 0.6 during OLV showed a lower inflammatory response in the lung and less lung injury in comparison to rabbits receiving F<sub>I</sub>O<sub>2</sub> 1.0 [<xref ref-type="bibr" rid="scirp.122736-ref26">26</xref>]. It is reasonable to attempt to reduce inspired oxygen concentrations in order to protect vulnerable organs in high-risk patients such as those with COPD, idiopathic pneumonia, or bleomycin-treated lungs [<xref ref-type="bibr" rid="scirp.122736-ref7">7</xref>]. No patients in either of our groups developed hyperoxia-induced respiratory or cardiovascular complications. In the absence of clinical complications, our present study could not determine whether high F<sub>I</sub>O<sub>2</sub> is truly harmful to the lung function. At least, minimizing F<sub>I</sub>O<sub>2</sub> would be a method for avoiding hyperoxia-induced damage in the compromised lung. The lower threshold for SpO<sub>2</sub> is still unknown; however, there is international consensus regarding the achievement of a minimal SpO<sub>2</sub> value of ≥90% with moderate F<sub>I</sub>O<sub>2</sub> levels of 0.4 - 0.6 in OLV [<xref ref-type="bibr" rid="scirp.122736-ref27">27</xref>]. Our study showed that the application of 60% O<sub>2</sub> CPAP can assist in minimizing F<sub>I</sub>O<sub>2</sub> levels to avoid hypoxemia in patients with a normal lung function. Further studies are required to analyze patients with significantly decreased lung function.</p><p>Several management protocols for preventing arterial oxygen desaturation during OLV have been put forward. Repeated inflation of the non-ventilated lung (lung recruitment) is one management for preventing hypoxemia. However, lung recruitment following complete collapse of the lung results in ischemia-reperfusion injury, inducing inflammatory cytokine production in the collapsed lung [<xref ref-type="bibr" rid="scirp.122736-ref2">2</xref>]. Meanwhile, CPAP maintains the patency of non-ventilated alveoli, minimizing the shunt fraction and attenuating the inflammatory cytokine release [<xref ref-type="bibr" rid="scirp.122736-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref28">28</xref>]. A potential limitation of CPAP includes the overexpansion of the non-ventilated lung, which subsequently interferes with surgical access [<xref ref-type="bibr" rid="scirp.122736-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref30">30</xref>]. In the previous study, 6.7% - 30% of patients showed disturbed visibility with CPAP at 5 cm H<sub>2</sub>O [<xref ref-type="bibr" rid="scirp.122736-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref30">30</xref>]. In this study, the application of low-level CPAP (2 - 3 cm H<sub>2</sub>O) to the non-ventilated lung was shown to be feasible for preventing desaturation during OLV without unnecessary lung distention. The method was simple and applicable in all patients. Thus, low-level CPAP is a preferable respiratory management for avoiding hypoxemia and should be attempted first.</p><p>Interaction of the shunt fraction, cardiac output, oxygen expenditure, venous saturation, and hemoglobin levels may affect oxygenation [<xref ref-type="bibr" rid="scirp.122736-ref31">31</xref>]. The shunt fraction during OLV is estimated to be in the order of 20% - 30% of the cardiac output [<xref ref-type="bibr" rid="scirp.122736-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.122736-ref32">32</xref>]. The cardiac output must be maintained for adequate oxygenation, due to the negative effect of low mixed venous oxygen tensions on oxygen delivery in the setting of a high shunt fractions [<xref ref-type="bibr" rid="scirp.122736-ref32">32</xref>]. Age, pH, carbon dioxide, temperature, CO are the principal non-pharmalogical variables that influence hypoxic pulmonary vasoconstriction [<xref ref-type="bibr" rid="scirp.122736-ref32">32</xref>]. In the present study, there were no significant differences in the above-mentioned factors that affect hypoxic pulmonary vasoconstriction.</p></sec><sec id="s5"><title>5. Limitations</title><p>The side of the surgery is an important factor in predicting hypoxemia during OLV [<xref ref-type="bibr" rid="scirp.122736-ref33">33</xref>]. Patients undergoing left thoracotomy show better PaO<sub>2</sub> values during OLV than those undergoing right thoracotomy, since the left lung normally receives 10% less CO than the right lung [<xref ref-type="bibr" rid="scirp.122736-ref34">34</xref>]. In our study, there were no significant differences related to side of the surgery between the groups. Thus, differences based on the side of surgery likely only had a slight effect on our results.</p></sec><sec id="s6"><title>6. Conclusion</title><p>In relatively healthy patients, oxygenation could be safely maintained with 60% O<sub>2</sub> OLV and 60% O<sub>2</sub> CPAP. The application of 60% O<sub>2</sub> CPAP during OLV for patients who are not suited to exposure to high F<sub>I</sub>O<sub>2</sub> may be an alternative form of respiratory management.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s8"><title>Cite this paper</title><p>Yamada, Y., Tanabe, K., Nagase, K. and Iida, H. (2023) A Comparison of Arterial Oxygenation between 60% O<sub>2</sub> CPAP and 100% O<sub>2</sub> CPAP during One-Lung Ventilation: A Prospective Randomized Controlled Study. Open Journal of Anesthesiology, 13, 1-14. https://doi.org/10.4236/ojanes.2023.131001</p></sec></body><back><ref-list><title>References</title><ref id="scirp.122736-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Karzai, W. and Schwarzkopf, K. (2009) Hypoxemia during One-Lung Ventilation: Prediction, Prevention, and Treatment. 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