• Tuberculosis and Respiratory Diseases
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• 제42권5호
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• pp.723-730
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• 1995

Background: Noninvasive ventilation has been used extensively for the treatment of patients with neuromuscular weakness or restrictive chest wall disorders complicated by hypoventilatory respiratory failure. Recently, noninvasive positive pressure ventilation has been used in patients with alveolar hypoventilation, chronic obstructive pulmonary disease(COPD), and adult respiratory distress syndrome. Sanders and Kern reported treatment of obstructive sleep apnea with a modification of the standard nasal CPAP device to deliver seperate inspiratory positive airway pressure(IPAP) and expiratory positive airway pressure(EPAP). Bi-level positive airway pressure(BiPAP) unlike nasal CPAP, the unit delivers a different pressure during inspiration from that during expiration. The device is similar to the positive pressure ventilator or pressure support ventilation. Method and purpose: Bi-level positive airway pressure(BiPAP) system(Respironics, USA) was applied to seven patients with acute respiratory failure and three patients on conventional mechanical ventilation. Results: 1) Two of three patients after extubation were successfully achieved weaning from conventional mechanical ventilation by the use of BiPAP ventilation with nasal mask. Five of seven patients with acute respiratory failure successfully recovered without use of conventional mechanical ventilation. 2) $PaO_2$ 1hour after BiPAP ventilation in acute respiratory failure patients significantly improved more than baseline values(p<0.01). $PaCO_2$ 1hour after BiPAP ventilation in acute respiratory failure patients did not change significantly more than baseline values. Conclusion: Nasal mask BiPAP ventilation can be one of the possible alternatives of conventional mechanical ventilation in acute respiratory failure and supportive method for weaning from mechanical ventilation.

• 대한의용생체공학회:의공학회지
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• 제40권5호
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• pp.215-221
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• 2019

The respiratory medical device is a medical device that delivers optimal oxygen or a certain amount of humidification to a patient by delivering artificial respiration to a patient through a machine when the patient has lost the ability to breathe spontaneously. These include respirators for use in chronic obstructive pulmonary disease and anesthesia or emergency situations, and positive airway pressure devices for treating sleep apnea, and as the population of COPD (chronic obstructive pulmonary disease) and elderly people worldwide surge, the market for the respiratory medical devices it is getting bigger. As the demand for both airway pressure devices, there is a problem that the ventilator standard is applied because the reference standard has not been established. Therefore, the boundaries between the items are blurred due to the purpose, intended use, and method of use overlapping similar items in a respiratory medical device. In addition, for both airway pressure devices, there is a problem that the ventilator standard is applied because the reference standard has not been established. Therefore, in this study, we propose clear classification criteria for the respiratory medical devices according to the purpose, intended use, and method of use and provide safety and performance evaluation guidelines for those items to help quality control of the medical devices. And to contribute to the rapid regulating and improvement of public health. This study investigated the safety and performance test methods through the principles of the respiratory medical device, national and international standards, domestic and international licensing status, and related literature surveys. The results of this study are derived from the safety and performance test items in the individual ventilator(ISO 80601-2-72), the International Standard for positive airway pressure device (ISO 80601-2-70), The safety and performance of humidifiers (ISO 80601-2-74) and the safety evaluation items related to home healthcare environment (IEC 60601-1-11), In addition, after reviewing the guidelines drawn up through expert consultation bodies including manufacturers and importers, certified test inspection institutions, academia, etc., the final guidelines were established through revision and supplementation. Therefore, in this study, we propose guidelines for evaluating the safety and performance of the respiratory medical device in accordance with growing technology development.

• The Journal of Korean Physical Therapy
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• 제16권1호
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• pp.1-13
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• 2004

Airway clearance technique are used to aid in mucus clearance in a variety of disease states. In this review I discuss airway physiology including airway mucus, action of airways, and airway resistance and review the literature and theory regarding forced expiratory technique, active cycle of breathing technique, and autogenic drainage. Also, I look at the appropriate device such as positive expiratory pressure mask(PEP mask), Flutter, and HFCWO(Vest system) which can be applied in the field of respiratory physical therapy. This study is provided as the basic resource regarding the application method of respiratory physical therapy.

• Journal of Oral Medicine and Pain
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• 제39권2호
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• pp.35-45
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• 2014

Many therapeutic modalities including continuous positive airway pressure, surgery, and oral appliances are used to treat patients with sleep-disordered breathing. However, there are no definitive treatment modalities for individual patients due to various causes of sleep-disordered breathing. Clinicians should have select best options for individual patients and it is quite challenging process. Oral appliances attracted clinical attention for its convenience and safety. Several designs of oral appliances are introduces such as soft palate lifter, tongue retaining device, and various appliances which aimed to mandibular advancement. Among these oral appliances, mandibular advancement devices (MADs) are considered the most excellent based on their effectiveness and patient tolerance. Although MADs are not guarantee dramatic outcome and less consistent than continuous positive airway pressure, they offer several advantages over continuous positive airway pressure and surgical methods, including non-invasiveness, silence, portability, and tolerability, simplicity. Therefore, general dental practitioner who had passed sleep dental curriculum or coursework can treat the patients with sleep problems. This article reviews the history, clinical indications, suggested mechanism of actions, various positive effects and several side effects, factors predicting a favorable outcome, determining amounts of mandibular advancement, compliance and long-term efficacy of MADs use.

• 대한치과의사협회지
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• 제53권4호
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• pp.259-265
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• 2015

Recently, oral appliances for treating snoring and obstructive sleep apnea are widely used. Among various appliances, mandibular advancement devices are most effective without serious side effects. Advancement of mandible keep airway open and decrease snoring and/or obstructive apnea events. They can be used as stand-alone therapy or an adjunct to continuous positive air pressure for lowering air pressure. Oral appliances should be applied by dentists who have knowledges and experiences on occlusion and temporomandibular disorders and manage of side effects.

• Clinical and Experimental Pediatrics
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• 제63권1호
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• pp.3-7
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• 2020

High-flow nasal cannula (HFNC) is a relatively safe and effective noninvasive ventilation method that was recently accepted as a treatment option for acute respiratory support before endotracheal intubation or invasive ventilation. The action mechanism of HFNC includes a decrease in nasopharyngeal resistance, washout of dead space, reduction in inflow of ambient air, and an increase in airway pressure. In preterm infants, HFNC can be used to prevent reintubation and initial noninvasive respiratory support after birth. In children, flow level adjustments are crucial considering their maximal efficacy and complications. Randomized controlled studies suggest that HFNC can be used in cases of moderate to severe bronchiolitis upon initial low-flow oxygen failure. HFNC can also reduce intubation and mechanical ventilation in children with respiratory failure. Several observational studies have shown that HFNC can be beneficial in acute asthma and other respiratory distress. Multicenter randomized studies are warranted to determine the feasibility and adherence of HFNC and continuous positive airway pressure in pediatric intensive care units. The development of clinical guidelines for HFNC, including flow settings, indications, and contraindications, device management, efficacy identification, and safety issues are needed, particularly in children.

• 수면정신생리
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• 제13권1호
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• pp.27-32
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• 2006

목 적：이 연구는 폐쇄성 수면무호흡증의 치료에 사용되는 지속적 상기도 양압술(nCPAP)의 순응도를 조사하고, 순응도를 좌우하는 요인을 파악하여 치료에 도움이 되게 하고자 시행되었다. 방 법：1995년 1월부터 1999년 4월까지 서울대학교병원 신경정신과 수면다원검사실에서 nCPAP 처방압력 측정 검사를 받은 모든 환자 120명을 대상으로 하였다. 환자들의 의무기록을 열람하여 연령, 성별, 학력, 체중, 신장, 호흡장애지수, 평균 산소포화도, nCPAP 처방 압력, 이비인후과 수술여부, 주간 졸림 여부, 고혈압의 병력 등을 조사하였고, 환자들을 외래에서 직접 면담하거나 주소지로 전화하여 nCPAP의 구입여부, 현재 nCPAP 치료 여부, 사용기간, nCPAP 중단 이유 등을 조사하였다. 결 과：대상 환자 120명 중 83명에서 정보를 얻을 수 있었다. 83명 중 60명은 nCPAP 기기를 구입하였고 23명은 nCPAP을 구입하지 않았는데, nCPAP 기기를 구입한 환자들은 주간 졸림증이 있었고 학력이 높았다. nCPAP 기기를 구입한 60명 중에 지금까지 사용하고 있는 환자들은 26명(43.3%)이었고 나머지 34명(56.7%)은 사용을 중단하였는데, 가장 큰 중단 사유는 마스크의 불편(26.5%)이었고, 그밖에 소리가 시끄러움(17.6%), 다른 방법으로 해결(17.6%), 코가 막히고 입이 마름(11.8%) 등의 순이었다. 치료를 중단한 환자들 중 25명(73.5%)이 치료를 시작한 후 3개월을 넘기지 못하고 중단하였으며, 31명(91.2%)이 1년 내에 그만 두었다. nCPAP을 6개월 미만으로 사용한 25명(41.7%)과 6개월 이상 사용한 35명(58.3%)간에 성별, 연령, 호흡장애지수, 평균산소포화도, 처방압력, 이비인후과 수술 여부, 체질량지수, 고혈압의 병력, 주간졸림 여부, 학력 등을 비교하였는데, 주간 졸림 여부에서만 의미 있는 차이가 있었고, 나머지 변수에서는 차이가 없었다. 결 론：이 연구를 통해서 우리는 nCPAP 순응도가 외국의 연구에 비해 다소 낮고, 초기 주간 졸림의 여부가 nCPAP의 장기 사용에 의미있는 영향을 미친다는 것을 알게 되었다. 또한 초기 3개월 이상 지속적으로 사용하는 환자들이 장기적으로 사용할 가능성이 높았다. 이 결과를 바탕으로 우리는 폐쇄성 수면무호흡증에 nCPAP 치료를 할 때 환자를 적절히 선택하고 교육을 지속적으로 해야 nCPAP 순응도를 높일 수 있다고 제안한다.

• Tuberculosis and Respiratory Diseases
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• 제43권2호
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• pp.190-200
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• 1996

연구배경 : 장기간 진행된 심한 만성 기도 폐쇄질환 환자에서 합병된 급성 호흡부전의 치료로 기관삽관과 기계호흡이 필요한 경우가 있다. 그러나 기계호흡을 거부하거나 기계호흡의 이탈이 불가능할 것으로 예측되는 환자에서 기관삽관과 기계호흡을 대신할 수 있는 환기법이 필요할 것으로 생각된다. 최근 수면 무호흡질환 환자의 치료로 개발되었던 지속적 기도 양압 치료가 급성 혹은 만성 호흡부전의 치료로 시도되고 있다. 본 연구에서는 급성 호흡부전이 합병된 만성 기도 폐쇄환자에서 비강 마스크를 통한 BiPAP 치료를 실시하여 그 효과를 평가하였다. 방법 : 영남대학교 의과대학 부속병원 내과에 내원한 만성 기도 폐쇄환자 22명을 대상으로 하여, BiPAP 치료군으로 10명의 만성 폐쇄성 폐질 환자와 1명의 기관지 천식환자에게는 대증적 치료 및 BiPAP 치료를 동시에 실시하였고, 대조군으로 11명의 만성 폐쇄성 폐질환자에게는 대증적 치료만 시행하였다. 대증적 치료는 산소 요법, 아미노필린, 부신피질 호르몬 흡입, 베타 agonist 등의 약물을 투여하였고 BiPAP 치료시 mode는 spontaneous timed, 호흡 빈도는 분당 12회에서 20회, IPAP는 $6cmH_2O$에서 $8cmH_2O$, EPAP는 $3cmH_2O$에서 $4cmH_2O$로 설정하였고 사용 기간은 3일간이었다. 치료 효과는 호흡 빈도, modified Borg scale 및 동맥혈 가스소견으로 비교하였다. 결과 : BiPAP 치료군과 대조군 사이에 나이, 치료 시작전 호흡 빈도 동맥혈 가스소견, modified Borg scale 그리고 안정 상태에서 시행한 환기 기능검사 소견은 양군 사이에 차이가 없었다. 호흡빈도와 modified Borg scale은 BiPAP 치료군과 대조군에서 시간의 경과에 따라 모두 유의하게 호전되었으나 두군간의 차이는 없었다. 동맥혈 산소 BiPAP 치료군과 대조군에서 다 같이 치료전에 비해 치료 1일 및 3일후에는 시간에 경과에 따라 호전되었으나 BiPAP 치료군에서는 치료 1일후와 치료 3일후의 소견에도 뚜렷한 호전이 있었던 반면에 대조군에서는 의미있는 차이가 없었다. BiPAP치료군에서는 동맥혈 이산화탄소분압은 치료전과 비교하여 치료 1일후 및 3일후에는 각각 유의하게 감소되었으나 대조군에서는 유의한 감소가 없었다. pH는 BiPAP 치료군에서 치료전과 비교하여 3일후에 의의있게 증가하였으나 대조군에서는 뚜렷한 차이가 없었다. 대조군과 BiPAP치료군의 치료 전후의 평균 동맥혈가스 차이로 두 군간의 비교에서도 동맥혈 산소분압은 치료 3일째, 동맥혈 이산화탄소 분압은 치료 1일째와 3일째, pH는 치료 3일째에 각각 의미있는 (p<0.05) 차이를 보였다. 결론 : 이상의 결과로 중증 만성 폐쇄성 폐질환 환자에서 급성 호흡부전이 발생시 BiPAP 치료는 호흡곤란과 동맥혈 호흡성 가스 소견을 향상시킬 수 있는 보조적인 환기법이 될 수 있겠으며 기관 삽관에 의한 인공호흡을 대신할 수도 있을 것으로 생각된다.

• Clinical Endoscopy
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• 제57권2호
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• pp.196-202
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• 2024

Background/Aims: Hypoxemia is a common side effect of propofol sedation during endoscopy. Applying mild positive airway pressure (PAP) using a nasal mask may offer a simple way to reduce such events and optimize the conditions for diagnostic and therapeutic upper gastrointestinal endoscopies. Methods: We compared overweight patients (body mass index >25 kg/m²) with a nasal PAP mask or standard nasal cannula undergoing upper gastrointestinal endoscopies by non-anesthesiologists who provided propofol sedation. Outcome parameters included the frequency and severity of hypoxemic episodes. Results: We analyzed 102 procedures in 51 patients with nasal PAP masks and 51 controls. Episodes of hypoxemia (oxygen saturation [SpO₂] <90% at any time during sedation) occurred in 25 (49.0%) controls compared to 8 (15.7%) patients with nasal PAP masks (p<0.001). Severe hypoxemia (SpO₂ <80%) occurred in three individuals (5.9%) in both groups. The mean delta between baseline SpO₂ and the lowest SpO₂ recorded was significantly decreased among patients with nasal PAP mask compared to controls (3.7 and 8.2 percentage points difference, respectively). There were significantly fewer airway interventions performed in the nasal PAP mask group (15.7% vs. 41.2%, p=0.008). Conclusions: Using a nasal PAP mask may be a simple means of increasing patient safety and ease of examination.

• Journal of Oral Medicine and Pain
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• 제43권3호
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• pp.61-69
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• 2018

Obstructive sleep apnea (OSA) is a relatively common, but greatly underdiagnosed sleep-related breathing disorder, characterized by recurrent collapse of the upper airway during sleep. OSA has been associated with a variety of cardiometabolic disease, such as hypertension, coronary artery disease, cardiac arrhythmia, cerebrovascular disease and metabolic dysfunction. Neurocognitive impairment, including excessive daytime sleepiness, increased risk of motor vehicle accidents, is also related to OSA. Sleep fragmentation and related arousals during sleep lead to intermittent hypoxia, sympathetic activation, oxidative stress, systemic inflammation and metabolic dysregulation which provide biological plausibility to this pathologic mechanism. Extensive studies demonstrated that OSA is a modifiable risk factor for the above mentioned diseases and oral appliances (OAs), although continuous positive air pressure (CPAP) is a first-line therapy of OSA, are not inferior to CPAP at least in mild OSA, and may be an alternative to CPAP in CPAP-intolerant subjects with OSA. The goal of this article is to provide a current knowledge of pathologic link between OSA and cardiovascular disease, focusing on intermittent hypoxia, sympathetic activation, oxidative stress and metabolic dysregulation. Then, previous epidemiologic studies will be reviewed to understand the causal relationship between OSA and cardiovascular disease. Finally, the effects of OAs will be updated via recent metaanalyses compared to CPAP.