109 research outputs found

    Polling-Based Downlink Communication Protocol for LoRaWAN using Traffic Indication

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    ํ•™์œ„๋…ผ๋ฌธ (์„์‚ฌ)-- ์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› : ๊ณต๊ณผ๋Œ€ํ•™ ์ปดํ“จํ„ฐ๊ณตํ•™๋ถ€, 2019. 2. ๊น€์ข…๊ถŒ.LPWAN (Low Power Wide Area Network) technologies such as LoRa and SigFox are emerging as a technology of choice for the Internet of Things (IoT) applications where tens of thousands of untethered devices are deployed over a wide area. In such operating environments, energy conservation is one of the most crucial concerns and network protocols adopt various power saving schemes to lengthen device lifetimes. For example, to avoid idle listening, LoRaWAN restricts downlink communications. However, the confined design philosophy impedes the deployment of IoT applications that require asynchronous downlink communications. In this thesis, we design and implement an energy efficient downlink communication mechanism, named TRILO, for LoRaWAN. We aim to make TRILO be energy efficient while obeying an unavoidable trade-off that balances between latency and energy consumption. TRILO adopts a beacon mechanism that periodically alerts end-devices which have pending downlink frames. We implement the proposed protocol on top of commercially available LoRaWAN components and confirm that the protocol operates properly in real-world experiments. Experimental results show that TRILO successfully transmits downlink frames without losses while uplink traffic suffers from a slight increase in latency because uplink transmissions should halt during beacons and downlink transmissions. Computer simulation results also show that the proposed scheme is more energy efficient than the legacy LoRaWAN downlink protocol.์ „๋ ฅ ๊ณต๊ธ‰์ด ์ œํ•œ์ ์ธ ์ˆ˜ ๋งŒ๊ฐœ์˜ ๋””๋ฐ”์ด์Šค๋“ค์„ ์ด์šฉํ•˜์—ฌ ๋„“์€ ์ง€์—ญ์„ ๋ฐ”ํƒ•์œผ๋กœ ์šด์˜๋˜๋Š” ์‚ฌ๋ฌผ์ธํ„ฐ๋„ท ์‹œ์Šคํ…œ์„ ๊ตฌ์ถ•ํ•˜๋Š” ๋ฐ์— ์žˆ์–ด์„œ LoRa, SigFox์™€ ๊ฐ™์€ ์ €์ „๋ ฅ ๊ด‘์—ญ ๋„คํŠธ์›Œํฌ ๊ธฐ์ˆ (LPWA)์ด ์ฃผ๋ชฉ๋ฐ›๊ณ  ์žˆ๋‹ค. ์ด๋Ÿฌํ•œ ์‹œ์Šคํ…œ ํ™˜๊ฒฝ์—์„œ ์—๋„ˆ์ง€ ์ ˆ์•ฝ์€ ์ค‘์š”ํ•œ ๊ด€์‹ฌ์‚ฌ ์ค‘ ํ•˜๋‚˜์ด๋ฉฐ ๋„คํŠธ์›Œํฌ ํ”„๋กœํ† ์ฝœ๋“ค์€ ๋‹ค์–‘ํ•œ ์ ˆ์ „ ๋ฐฉ์‹์„ ์ฑ„ํƒํ•˜์—ฌ ๋””๋ฐ”์ด์Šค์˜ ์ˆ˜๋ช…์„ ๋ณด์žฅํ•˜๋ ค ํ•˜๊ณ  ์žˆ๋‹ค. ์˜ˆ๋ฅผ ๋“ค์–ด, ๋ถˆํ•„์š”ํ•œ ๋Œ€๊ธฐ ์ฒญ์ทจ๋กœ ์ธํ•œ ์—๋„ˆ์ง€ ์†์‹ค์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•ด์„œ LoRaWAN์€ ๋‹ค์šด๋งํฌ ํ†ต์‹ ์„ ์ œํ•œํ•˜๊ณ  ์žˆ๋Š”๋ฐ, ์ด๋Ÿฌํ•œ ์„ค๊ณ„ ์ฒ ํ•™์€ ๋น„๋™๊ธฐ์ ์ธ ๋‹ค์šด๋งํฌ ํ†ต์‹ ์„ ํ•„์š”๋กœ ํ•˜๋Š” IoT ์• ํ”Œ๋ฆฌ์ผ€์ด์…˜์˜ ์š”๊ตฌ ์‚ฌํ•ญ์„ ์ถฉ์กฑ์‹œํ‚ค์ง€ ๋ชปํ•˜๋Š” ๋ฌธ์ œ์ ์„ ๊ฐ€์ง€๊ณ  ์žˆ๋‹ค. ๋”ฐ๋ผ์„œ ๋ณธ ๋…ผ๋ฌธ์—์„œ๋Š” LoRaWAN์—์„œ ๋‹ค์šด๋งํฌ๋ฅผ ํšจ๊ณผ์ ์œผ๋กœ ์ปจํŠธ๋กคํ•  ์ˆ˜ ์žˆ๋„๋ก TRILO๋ผ๋Š” ์—๋„ˆ์ง€ ํšจ์œจ์ ์ธ ๋‹ค์šด๋งํฌ ํ†ต์‹  ๋ฉ”์ปค๋‹ˆ์ฆ˜์„ ์„ค๊ณ„ํ•˜๊ณ  ๊ตฌํ˜„ํ•˜์˜€๋‹ค. TRILO๋Š” ๋‹ค์šด๋งํฌ ํ”„๋ ˆ์ž„์ด ํŒฌ๋”ฉ๋˜์–ด ์žˆ๋Š” ์—”๋“œ ๋””๋ฐ”์ด์Šค๋“ค์˜ ๋ฆฌ์ŠคํŠธ ์ •๋ณด๋ฅผ ์ฃผ๊ธฐ์ ์œผ๋กœ ๋„คํŠธ์›Œํฌ์— ์•Œ๋ฆฌ๋Š” ๋น„์ฝ˜ ๋ฉ”์ปค๋‹ˆ์ฆ˜์„ ์ฑ„ํƒํ•˜์˜€๊ณ , ์„œ๋ฒ„์™€ ๋””๋ฐ”์ด์Šค๋“ค์ด ๊ฐ๊ฐ ์ •ํ•ด์ง„ ์ˆœ์„œ์— ๋”ฐ๋ผ ๋‹ค์šด๋งํฌ ์ „์†ก ๋ฐ ์ˆ˜์‹ ์„ ์Šค์ผ€์ค„๋งํ•˜๋„๋ก ํ•˜์˜€๋‹ค. ์„ค๊ณ„ํ•œ ํ”„๋กœํ† ์ฝœ์ด ์ œ๋Œ€๋กœ ๋™์ž‘ํ•˜๋Š”์ง€ ๊ฒ€์ฆํ•˜๊ธฐ ์œ„ํ•ด์„œ ๊ธฐ์กด LoRaWAN์˜ ๊ตฌ์„ฑ ์š”์†Œ ์œ„์— ์ œ์•ˆ๋œ ํ”„๋กœํ† ์ฝœ์„ ๊ตฌํ˜„ํ•œ ํ›„ ์‹ค์ œ ํ…Œ์ŠคํŠธ ๋ฒ ๋“œ๋ฅผ ๊ตฌ์ถ•ํ•˜์—ฌ์„œ ์‹คํ—˜์„ ์ง„ํ–‰ํ•˜์˜€๋‹ค. ์‹คํ—˜ ๊ฒฐ๊ณผ์— ๋”ฐ๋ฅด๋ฉด TRILO๋Š” ๊ธฐ์กด ํ”„๋กœํ† ์ฝœ์˜ ์—…๋งํฌ ํ†ต์‹  ์„ฑ๋Šฅ์„ ์ €ํ•ดํ•˜์ง€ ์•Š์œผ๋ฉด์„œ๋„ ์ถ”๊ฐ€์ ์ธ ๋‹ค์šด๋งํฌ ํ”„๋ ˆ์ž„์„ ์†์‹ค ์—†์ด ์„ฑ๊ณต์ ์œผ๋กœ ์ „์†ก ๋ฐ ์ˆ˜์‹ ํ•˜์˜€๊ณ , ์ปดํ“จํ„ฐ ์‹œ๋ฎฌ๋ ˆ์ด์…˜ ๊ฒฐ๊ณผ ๋˜ํ•œ ์ œ์•ˆ๋œ ๊ธฐ๋ฒ•์ด ๊ธฐ์กด์˜ LoRaWAN ๋‹ค์šด๋งํฌ ํ”„๋กœํ† ์ฝœ๋ณด๋‹ค ๋” ์—๋„ˆ์ง€ ํšจ์œจ์ ์œผ๋กœ ๋™์ž‘ํ•˜๋Š” ๊ฒƒ์„ ๋ณด์—ฌ์ฃผ์—ˆ๋‹ค.ABSTRACT ........................................................................................................... โ…ฐ CONTENTS ........................................................................................................... โ…ฒ LIST OF FIGURES ............................................................................................ โ…ณ LIST OF TABLES .............................................................................................. โ…ต CHAPTER โ… : Introduction ................................................................................ 1 CHAPTER โ…ก: Related Work ............................................................................. 8 CHAPTER โ…ข: A Primer on LoRa and LoRaWAN .................................. 11 CHAPTER โ…ฃ: Downlink Communications Scheme .................................. 17 4.1 Comparison of Two Polling Schemes ..................................... 19 4.2 Proposed Downlink Communications Scheme ....................... 26 CHAPTER โ…ค: Implementation ........................................................................ 28 CHAPTER โ…ฅ: Evaluation ................................................................................. 31 6.1 Experimental Results .................................................................... 32 6.2 Simulation Results ......................................................................... 37 CHAPTER โ…ฆ: Discussion ................................................................................. 42 CHAPTER โ…ง: Conclusion ................................................................................. 45 BIBLIOGRAPHY ................................................................................................... 47 ์ดˆ๋ก ........................................................................................................................... 51Maste

    Effects of Positive End-Expiratory Pressure on Pulmonary Oxygenation and Biventricular Function during One-Lung Ventilation: A Randomized Crossover Study

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    Although the application ofย positiveย end-expiratoryย pressureย (PEEP) can alter cardiopulmonary physiology duringย one-lungย ventilationย (OLV), these changes have not been clearly elucidated. Thisย studyย assessed theย effectsย of different levels of PEEP onย biventricularย function, as well asย pulmonaryย oxygenationย during OLV. Thirty-six lung cancer patients received one PEEP combination of six sequences, consisting of 0 (PEEP_0), 5 (PEEP_5), and 10 cmH2O (PEEP_10), using aย crossoverย design during OLV. The ratio of arterial oxygen partialย pressureย to inspired oxygen fraction (P/F ratio), systolic and diastolic echocardiographic parameters were measured at 20 min after the first, second, and third PEEP. P/F ratio at PEEP_5 was significantly higher compared to PEEP_0 (pย = 0.014), whereas the P/F ratio at PEEP_10 did not show significant differences compared to PEEP_0 or PEEP_5. Left ventricular ejection fraction (LV EF) and right ventricular fractional area change (RV FAC) at PEEP_10 (EF,ย pย < 0.001; FAC,ย pย = 0.001) were significantly lower compared to PEEP_0 or PEEP_5. RV E/E' (pย = 0.048) and RV myocardial performance index (pย < 0.001) at PEEP_10 were significantly higher than those at PEEP_0 or PEEP_5. In conclusion, increasing PEEP to 10 cmH2O decreasedย biventricularย function, especially on RVย function, with no further improvement onย oxygenationย compared to PEEP 5 cmH2O during OLV.ope

    Decreased S-nitrosylation of tissue transglutaminase contributes to age-related increases in vascular stiffness

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    RATIONALE: Although an age-related decrease in NO bioavailability contributes to vascular stiffness, the underlying molecular mechanisms remain incompletely understood. We hypothesize that NO constrains the activity of the matrix crosslinking enzyme tissue transglutaminase (TG2) via S-nitrosylation in young vessels, a process that is reversed in aging. OBJECTIVE: We sought to determine whether endothelium-dependent NO regulates TG2 activity by S-nitrosylation and whether this contributes to age-related vascular stiffness. METHODS AND RESULTS: We first demonstrate that NO suppresses activity and increases S-nitrosylation of TG2 in cellular models. Next, we show that nitric oxide synthase (NOS) inhibition leads to increased surface and extracellular matrix-associated TG2. We then demonstrate that endothelium-derived bioactive NO primarily mediates its effects through TG2, using TG2(-/-) mice chronically treated with the NOS inhibitor l-N(G)-nitroarginine methyl ester (L-NAME). We confirm that TG2 activity is modulated by endothelium-derived bioactive NO in young rat aorta. In aging rat aorta, although TG2 expression remains unaltered, its activity increases and S-nitrosylation decreases. Furthermore, TG2 inhibition decreases vascular stiffness in aging rats. Finally, TG2 activity and matrix crosslinks are augmented with age in human aorta, whereas abundance remains unchanged. CONCLUSIONS: Decreased S-nitrosylation of TG2 and increased TG activity lead to enhanced matrix crosslinking and contribute to vascular stiffening in aging. TG2 appears to be the member of the transglutaminase family primarily contributing to this phenotype. Inhibition of TG2 could thus represent a therapeutic target for age-associated vascular stiffness and isolated systolic hypertension.ope

    Driving pressure guided ventilation

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    Protective ventilation is a prevailing ventilatory strategy these days and is comprised of small tidal volume, limited inspiratory pressure, and application of positive end-expiratory pressure (PEEP). However, several retrospective studies recently suggested that tidal volume, inspiratory pressure, and PEEP are not related to patient outcomes, or only related when they influence the driving pressure. Therefore, this review introduces the concept of driving pressure and looks into the possibility of driving pressure-guided ventilation as a new ventilatory strategy, especially in thoracic surgery where postoperative pulmonary complications are common, and thus, lung protection is of utmost importance.ope

    The effects of arginase inhibitor on lung oxidative stress and inflammation caused by pneumoperitoneum in rats

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    BACKGROUND: Pneumoperitoneum-induced oxidative stress and organ injury are known to be associated with nitric oxide (NO) inactivation. Because arginase competes with NO synthase (NOS) for a common substrate, L-arginine, arginase inhibition may increase NO bioavailability. Therefore, we evaluated the ability of the arginase inhibitor, 2 (S)-amino-6-boronohexanoic acid (ABH), to attenuate pneumoperitoneum-induced decrease of NO bioavailability and lung injury. METHODS: Thirty rats were randomly divided into the following groups: 1) the PP-ABH group received a subcutaneous injection of ABH (5 mg/kg) 1 h before induction of pneumoperitoneum (insufflation to intraperitoneal pressure of 15 mmHg for 60 min); 2) the PP group received saline by subcutaneous injection 1 h before induction of pneumoperitoneum; and 3) the control group received saline by subcutaneous injection before a sham procedure with no gas insufflation. After desufflation, blood was collected to determine levels of plasma nitrite, NOS, inflammatory cytokines, and malondialdehyde, a marker of oxidative stress. Lung tissue was obtained for histological evaluation. RESULTS: We found that plasma nitrite levels were lower in the PP group and higher in the PP-ABH group, compared with controls (P <0.01 and P <0.05, respectively). In the PP group, endothelial NOS activity was decreased and inducible NOS activity was increased compared with the PP-ABH and control groups. Malondialdehyde levels increased 3-fold in the PP group and 2-fold in the PP-ABH group compared with controls. Tumor necrosis factor-ฮฑ, interleukin-6, and interleukin-1รŸ levels were elevated in the PP group compared to the control group, but the increase in cytokine production was attenuated or blocked in the PP-ABH group. Lung injury scores were 4.8-fold higher in the PP group and 2-fold higher in the PP-ABH group compared with controls (P <0.001 and P <0.01, respectively). DISCUSSION: Pneumoperitoneum decreases NO bioavailability and increases the inflammation cytokines, resulting in organ injuries. Inhibition of arginase activity could maintain NO bioavailability by attenuating pneumoperitoneum-induced changes in NOS activity. In addition, arginase inhibition attenuated the oxidative stress and inflammation and decreased the severity of lung injury caused by pneumoperitoneum. CONCLUSIONS: By increasing NO bioavailability and suppressing oxidative stress and inflammation, pretreatment with an arginase inhibitor may protect against lung injury caused by pneumoperitoneum.ope

    Effects of Iloprost on Arterial Oxygenation and Lung Mechanics during One-Lung Ventilation in Supine-Positioned Patients: A Randomized Controlled Study

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    Patients undergoing one-lung ventilation (OLV) in the supine position face an increased risk of intraoperative hypoxia compared with those in the lateral decubitus position. We hypothesized that iloprost (ILO) inhalation improves arterial oxygenation and lung mechanics. Sixty-four patients were enrolled and allocated to either the ILO or control group (n = 32 each), to whom ILO or normal saline was administered. The partial pressure of the arterial oxygen/fraction of inspired oxygen (PaO2/FiO2) ratio, dynamic compliance, alveolar dead space, and hemodynamic variables were assessed 20 min after anesthesia induction with both lungs ventilated (T1) and 20 min after drug nebulization in OLV (T2). A linear mixed model adjusted for group and time was used to analyze repeated variables. While the alveolar dead space remained unchanged in the ILO group, it increased at T2 in the control group (n = 30 each) (p = 0.002). No significant differences were observed in the heart rate, mean blood pressure, PaO2/FiO2 ratio, or dynamic compliance in either group. Selective ILO nebulization was inadequate to enhance oxygenation parameters during OLV in the supine position. However, it favorably affected alveolar ventilation during OLV in supine-positioned patients without adverse hemodynamic effects.ope

    Cerebral Oxygenation during Laparoscopic Surgery: Jugular Bulb versus Regional Cerebral Oxygen Saturation

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    PURPOSE: We hypothesized that regional cerebral oxygen saturation (rSO2) could replace jugular bulb oxygen saturation (SjvO2) in the steep Trendelenburg position under pneumoperitoneum. Therefore, we evaluated the relationship between SjvO2 and rSO2 during laparoscopic surgery. MATERIALS AND METHODS: After induction of anesthesia, mechanical ventilation was controlled to increase PaCO2 from 35 to 45 mm Hg in the supine position, and the changes in SjvO2 and rSO2 were measured. Then, after establishment of pneumoperitoneum and Trendelenburg position, ventilation was controlled to maintain a PaCO2 at 35 mm Hg and the CO2 step and measurements were repeated. The changes in SjvO2 (rSO2) -CO2 reactivity were compared in the supine position and Trendelenburg-pneumoperitoneum condition, respectively. RESULTS: There was little correlation between SjvO2 and rSO2 in the supine position (concordance correlation coefficient=0.2819). Bland-Altman plots showed a mean bias of 8.4% with a limit of agreement of 21.6% and -4.7%. SjvO2 and rSO2 were not correlated during Trendelenburg-pneumoperitoneum condition (concordance correlation coefficient=0.3657). Bland-Altman plots showed a mean bias of 10.6% with a limit of agreement of 23.6% and -2.4%. The SjvO2-CO2 reactivity was higher than rSO2-CO2 reactivity in the supine position and Trendelenburg- pneumoperitoneum condition, respectively (0.9 ยฑ 1.1 vs. 0.4 ยฑ 1.2% mm Hg(-1), p=0.04; 1.7 ยฑ 1.3 vs. 0.5 ยฑ 1.1% mm Hg(-1), p<0.001). CONCLUSION: There is little correlation between SjvO2 and rSO2 in the supine position and Trendelenburg-pneumoperitoneum condition during laparoscopic surgery.ope

    Effects of milrinone on jugular bulb oxygen saturation and cerebrovascular carbon dioxide reactivity in patients undergoing coronary artery bypass graft surgery

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    BACKGROUND: Jugular bulb oxygen saturation (Sjv(o(2))) is a surrogate marker for global cerebral oxygenation. The effect of milrinone on Sjv(o(2)) and the cerebrovascular carbon dioxide reactivity (CCO2R) was investigated. METHODS: Thirty patients scheduled for coronary artery bypass graft surgery (CABG) were studied prospectively. After sternotomy, normoventilation (at T(1); Pa(co(2))=4.7-5.0 kPa) and hyperventilation (at T(2); Pa(co(2))=3.3-3.7 kPa) were induced and the changes in Sjv(o(2)) (DeltaSjv(o(2))) and Pa(co(2)) (DeltaPa(co(2))), and DeltaSjv(o(2))/DeltaPa(co(2)) (CCO(2)R) were measured. After normoventilation was re-established (at T(3)), milrinone 50 microg kg(-1) was given (at T(4)), followed by hyperventilation (at T(5)), and DeltaSjv(o(2)), DeltaPa(co(2)) and CCO(2)R were measured. RESULTS: After milrinone administration at normoventilation (T(3) and T(4)), cardiac index and mixed venous oxygen saturation increased, while mean arterial pressure and systemic vascular resistance index decreased, without a significant change in Sjv(o(2)). Before milrinone administration (T(1) and T(2)), hyperventilation decreased Pa(co(2)) and Sjv(o(2)), and DeltaSjv(o(2)) showed positive linear correlation with DeltaPa(co(2)). After milrinone administration (T(4) and T(5)), hyperventilation decreased Pa(co(2)) and Sjv(o(2)), and DeltaSjv(o(2)) showed positive linear correlation with DeltaPa(co(2)). There was no significant difference in CCO(2)R before and after milrinone administration (13.3 (5.7)% kPa(-1) and 12.3 (3.9)% kPa(-1), respectively). CONCLUSIONS: Although milrinone induced significant haemodynamic changes, Sjv(o(2)) and CCO(2)R were unchanged during its administration.ope

    Hemodynamic Effects of Vecuronium, Pancuronium and Rocuronium during O2-Midazolam-Fentanyl Anesthesia in Patients with Coronary Artery Disease or Valvular Heart Diseases

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    Background: This study was designed to evaluate the hemodynamic effects of vecuronium, pancuronium and rocuronium in patients with coronary artery disease (CABG) or valvular heart disease (VHD). Methods: With IRB approval, 121 patients (61 patients with CABG and 60 patients with VHD) were randomly divided into a vecuronium, pancuronium and rocuronium group, respectively. Midazolam and fentanyl were administered and then 3 times of ED95 of a muscle relaxant (vecuronium, 0.12 mg/kg; pancuronium, 0.12 mg/kg; or rocuronium, 0.9 mg/kg) was injected. Additional dose of fentanyl was given and the patient was intubated. Hemodynamic variables were measured before the induction of anesthesia, just prior and 1 min after the administration of the muscle relaxant, just before intubation, 5 and 10 min after intubation. Results: The number of patients enrolled in the CABG-vecuronium, CABG-pancuronium, CABG- rocuronium, VHD-vecuronium, VHD-pancuronium, and VHD-rocuronium was 20, 20, 21, 19, 20, and 21 respectively. Each of 10, 4, 4, 5, 1, and 1, respectively, were treated for hypotension or bradycardia during the induction of anesthesia. The heart rate (HR) changed significantly only in the CABG- vecuronium group compared with the control value. All three muscle relaxants decreased mean systemic artery pressure (MAP) significantly in both CABG and VHD patients. The decrease in HR and MAP were significantly greater in CABG-vecuronium and VHD-vecuronium than in CABG-pancuronium and VHD-pancuronium, respectively. The decrease in HR was also greater in VHD-vecuronium than in VHD-rocuronium. Cardiac index (CI) decreased in CABG-vecuronium and all VHD patients. The decrease in CI was greater in CABG-vecuronium than in CABG-pancuronium but it was not significantly different among the three muscle relaxants in VHD patients๏ผŽ Conclusions: While pancuronium and rocuronium exerted minimal hemodynamic effects, vecuronium reduced HR and MAP more significantly than pancuronium in both CABG and VHD patients, and CI also decreased more significantly with vecuronium in CABG patients.ope

    Effects of Iloprost on Oxygenation during One-Lung Ventilation in Patients with Low Diffusing Capacity for Carbon Monoxide: A Randomized Controlled Study

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    The protective mechanism of hypoxic pulmonary vasoconstriction during one-lung ventilation (OLV) is impaired in patients with a low diffusing capacity for carbon monoxide (DLCO). We hypothesized that iloprost inhalation would improve oxygenation and lung mechanics in patients with low DLCO who underwent pulmonary resection. Forty patients with a DLCO &lt; 75% were enrolled. Patients were allocated into either an iloprost group (ILO group) or a control group (n = 20 each), in which iloprost and saline were inhaled, respectively. The partial pressure of arterial oxygen/fraction of inspired oxygen (PaO2/FiO2) ratio, pulmonary shunt fraction, alveolar dead space, dynamic compliance, and hemodynamic parameters were assessed 20 min after the initiation of OLV and 20 min after drug administration. Repeated variables were analyzed using a linear mixed model between the groups. Data from 39 patients were analyzed. After iloprost inhalation, the ILO group exhibited a significant increase in the PaO2/FiO2 ratio and a decrease in alveolar dead space compared with the control group (p = 0.025 and p = 0.042, respectively). Pulmonary shunt, dynamic compliance, hemodynamic parameters, and short-term prognosis were comparable between the two groups. Selective iloprost administration during OLV reduced alveolar dead space and improved oxygenation while minimally affecting hemodynamics and short-term prognosis.ope
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