• 제목/요약/키워드: apnea

검색결과 498건 처리시간 0.026초

신생아에서 진단된 Hirschsprung 병을 동반한 congenital central hypoventilation syndrome 1례 (Congenital central hypoventilation syndrome combined with Hirschsprung disease diagnosed in the neonatal period)

  • 최진현;오진희;김종현;고대균;홍승철
    • Clinical and Experimental Pediatrics
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    • 제49권4호
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    • pp.446-450
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    • 2006
  • Congenital central hypoventilation syndrome은 혈중 이산화탄소 증가와 저산소에 대한 자율 신경계와 호흡 조절 기능의 선천성 결함으로 호흡의 저환기가 주로 수면시에 발생하는 질환이다. 이는 신경 이주장애 질환(neurocristopathy)에 속한다고 알려져 있으며 선천성 거대결장 등의 질환과 잘 동반된다. 아직까지 확실한 완치법은 없는 상태이고 환아들은 평생을 환기 보조에 의존하여 생존해야 하며 적절한 환기 보조를 통해서 생존 기간을 연장할 수 있다. 저자들은 출생시부터 반복되는 수면시의 무호흡과 청색증이 있는 환아에서 congenital central hypoventilation 및 선천성 거대 결장이 동반된 1례를 경험하였기에 보고하는 바이다.

Rhesus 및 Cynomolgus 원숭이에서 급성위확장 증례 (Acute Gastric Dilatation in Rhesus (Macaca mulatta) and Cynomolgus (Macaca fascicularis) Monkeys)

  • 이재일;강병철
    • 한국임상수의학회지
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    • 제25권4호
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    • pp.314-316
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    • 2008
  • 급성 위확장은 실험시설에서 사육되고 있는 Macaca 원숭이에서 가장 흔하게 발생하는 응급상황 중에 하나이다. 이 보고서는 사육 원숭이에서 발생한 몇몇 증례를 소개하고자 한다. 급성 위확장증을 보인 원숭이들에는 실험을 위해 원숭이 보정의자에 앉힌 경우나 마취를 한 경우, 그리고 아무런 처치도 하지 않은 경우 등이 있었다. 이환된 동물들은 심한 복부팽만, 탈수, 청색증과 호흡곤란 등을 동반한 혼수 상태를 보였다. 한 증례는 전신장애로 인해 상태가 악화되고 폐사하여 부검을 실시하였다. 나머지 두 증례는 위관과 수액요법으로 응급처치를 한 결과 병증에서 회복되었다. 부검결과, 위의 대부분은 위내 가스와 물 그리고 섭취물로 채워져 있었다. 이 보고서는 영장류에서 급성위확장증의 발생과 관리에 대한 특별한 강조와 더불어 본 질환이 비 특이적인 원인에 의해 발생할 수 도 있음을 시사한다.

소아 위식도 역류에서 시행한 복강경 Nissen식 위바닥 주름술 (Laparoscopic Nissen Fundoplication in Children for Treatment of Gastroesophageal Reflux Disease)

  • 남소현;김대연;김성철;김인구
    • Advances in pediatric surgery
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    • 제13권1호
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    • pp.13-22
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    • 2007
  • Fundoplication is accepted as an effective treatment of gastroesophageal reflux disease. The recent results of laparoscopic fundoplication demonstrated safety and less morbidity, shorter hospital stay and less pulmonary complication compared to the open operation. Laparoscopic fundoplication has been our first choice of operation for gastroesophageal reflux disease since 2003. Among 29 cases, there were 2 conversion cases because of severe distension of transverse colon and hepatomegaly. We studied 27 consecutive patients operated upon from January 2003 through December 2004. There were 15 boys and 12 girls, ages from 1.5 months to 12 years (median 25.3 months). Body weight ranged from 2.9 kg to 37 kg (median 9.8 kg). Neurological abnormalities were present in 23 patients. Indications for surgery included medically refractory reflux associated with vomiting, pneumopathy, otorhinolaryngologic pathology, failure to thrive, esophagitis, apnea and bradycardia. We used 4-5 trocars of 5 mm or 12 mm with $30^{\circ}$ telescope and performed the Nissen technique in all patients. In neurological impaired patients, gastrostomy tube was placed at the time of fundoplication. Median operative time was 130 minutes (70 - 300 minutes). There was no mortality nor intraoperative complication. Twenty-six patients were followed for median of 19 months (8 - 31 months). Four patients (15.4 %), who were all neurological impaired, developed recurrent symptoms of gastroesophageal reflux disease. Two of these patients had reoperation (1 laparoscopic approach, 1 open method). There were significant increases in body weight in 11 patients after fundoplication. Laparoscopic fundoplication is acceptable as a safe and effective method for gastroesophageal reflux disease.

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대구지역 일개 초등학교를 대상으로 한 소아 수면문제에 대한 예비연구 (Preliminary Study of Children's Sleep Problems in an Elementary School in Daegu)

  • 서완석;구본훈;김민지;노영환;성형모;신지현
    • Journal of the Korean Academy of Child and Adolescent Psychiatry
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    • 제19권3호
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    • pp.156-161
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    • 2008
  • Objectives: The purpose of this study was to investigate the prevalence of sleep problems in Korean elementary school children and the differences in sleep problems elated to their school grade and gender. Methods : One public elementary school in Dae-gu, Korea as randomly selected. And, parents who agreed to participate this study were asked to complete a modified version of Tucson Children's Assessment of Sleep Apnea screening questionnaire (TuCASA). Results: The most common sleep problem was 'falling asleep in vehicle (44.2%)' and the prevalence rate of this problem differed by school grade. The prevalence rate of falling asleep while watching TV before 8 P.M. (8.0%), daytime fatigue (21.9%) and nocturnal enuresis during the past 6 months (5.3%) were significantly differed by school grade. The prevalence rate of falling asleep while doing home work, falling sleep during a lesson, snoring and bruxism were 12.6%, 1.0%, 26.7% and 13.2% respectively. Although these rates did not show any differences between grades, snoring as more in boys and daytime fatigue was more in girls. Conclusion: This study demonstrates that many elementary school children may have various sleep problems. Lower grade elementary schoolers had sleep problems which related to euro-developmental factors, whereas higher grade elementary schoolers had sleep problems related to sleep deprivation and stress. Finally, more female schooler showed signs of fatigue or sleepiness than male schoolers.

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신석회화와 소뇌 충부의 무형성을 동반한 Joubert 증후군 1례 (A Case of Joubert Syndrome Associated with Nephrocalcinosis and Agenesis of Cerebellar Vermis)

  • 김지희;신혜경;홍영숙;이주원;김순겸;유기환
    • Childhood Kidney Diseases
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    • 제6권2호
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    • pp.266-271
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    • 2002
  • Joubert 증후군은 소뇌 충부 무형성을 특징으로 하며 근 긴장 저하, 불규칙적인 호흡, 발달 지연, 안진, 망막 이형성, 낭종성 신질환, 간 섬유증, 다지증 등이 동반되는 증후군이다. 이 질환에서는 소뇌 충부의 병변과 신장의 병변이 무작위적으로 함께 나타나기도 하는데, 저자들은 소뇌 충부 무형성, 근 긴장저하, 안진, 무호흡 등이 있어 Joubert 증후군으로 진단받은 환아가 신장 수질 석회화 병변과 만성 신부전으로 진행한 1례를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

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Haddad 증후군 1예 (A Case of Haddad Syndrome)

  • 이민규;김준성;박성종;김기수;김인구;윤종현;김경모
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제8권2호
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    • pp.252-256
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    • 2005
  • 저자들은 청색증, 복부 팽만을 주소로 내원한 생후 2일 된 남아에서 Haddad 증후군, 즉 결장 전체의 무신경절증 형태의 Hirschsprung병을 동반한 선천성 중추성 저환기 증후군 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

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수면의학(睡眠醫學)에 있어서 지필(紙筆) 척도(尺度)의 활용(活用) -과도한 주간 졸음과 일주기리듬의 평가를 중심으로- (Usefulness of Various Questionnaires in the Assessment of Excessive Daytime Sleepiness and Circadian Rhythm)

  • 김무진
    • 수면정신생리
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    • 제1권2호
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    • pp.125-144
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    • 1994
  • 수면의학에서 사용되는 여러 설문지 검사중 과도한 주간졸음과 일주기리듬의 평가를 위한 것들을 소개하고 그 장단점과 특성을 검토하였다. 임상수면의학, 산업의학, 혹은 역학조사에서 이러한 지필척도의 활용이 요구되고 있으나 아직 객관적 타당성이 충분히 검토되지 못했으므로 추후연구가 요구된다. 타당성을 제고할 임상, 혹은 교대근무상황에서의 연구가 더욱 확장되어야 할 것이다.

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Retrospective study of changes in pharyngeal airway space and position of hyoid bone after mandibular setback surgery by cephalometric analysis

  • Cho, Hyun-Woo;Kim, Il-Kyu;Cho, Hyun-Young;Seo, Ji-Hoon;Lee, Dong-Hwan;Park, Seung-Hoon
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제37권
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    • pp.38.1-38.6
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    • 2015
  • Background: The posterior movement of mandible was known as the main cause of the changes in the pharyngeal airway space (PAS) and the postoperative obstructive sleep apnea (OSA). The purpose of this study was to know the changes of PAS and position of hyoid bone. Methods: Lateral cephalographies of 13 patients who had undergone sagittal split ramus osteotomy (SSRO) setback surgery were taken preoperatively (T1), postoperatively within 2 months (T2), and follow-up after 6 months or more (T3). On the basis of F-H plane, diameters of nasopharynx, oropharynx, and hypopharynx were measured. The movements of the soft palate, tongue, and hyoid bone were also measured. Results: The amount of mandible setback was $7.5{\pm}3.8mm$. In the measurements of PAS, there was a statistically significant decrease of $2.8{\pm}2.5mm$ in nasopharynx (P < 0.01), and $1.7{\pm}2.4mm$ in oropharynx (P < 0.01) were observed after surgery. The hypopharynx decreased $1.0{\pm}2.1mm$ after surgery and continuously decreased $1.0{\pm}2.8mm$ at follow-up. The changes in hyoid bone position showed the posterior movement only after surgery and posteroinferior movement at follow-up. Conclusions: The PAS such as nasopharynx, oropharynx, and hypopharynx showed relatively high correlation with the amount of mandibular setback. The change of resistance in upper airway may be important for the prevention of OSA after mandibular setback surgery.

Risk factors of ocular involvement in children with mitochondrial respiratory chain complex defect

  • Chae, Jung-Hyun;Lee, Jung-Hun;Kim, Kyo-Ryung;Byeon, Suk-Ho;Lee, Young-Mock;Kang, Hoon-Chul;Lee, Joon-Soo;Kim, Heung-Dong
    • Clinical and Experimental Pediatrics
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    • 제53권12호
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    • pp.994-999
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    • 2010
  • Purpose: Mitochondrial dysfunction can present with various symptoms depending on the organ it has affected. This research tried to analyze the ophthalmologic symptoms and ophthalmologic examination (OE) results in patients with mitochondrial disease (MD). Methods: Seventy-four patients diagnosed with mitochondrial respiratory chain complex defect with biochemical enzyme assay were included in the study. They were divided into 2 groups based on the OE results by funduscopy and were analyzed on the basis of their clinical features, biochemical test results, morphological analysis, and neuroimaging findings. Results: Thirty-seven (50%) of the 74 MD patients developed ophthalmologic symptoms. Abnormal findings were observed in 36 (48.6%) patients during an OE, and 16 (21.6%) of them had no ocular symptoms. Significantly higher rates of prematurity, clinical history of epilepsy or frequent apnea events, abnormal light microscopic findings in muscle pathology, diffuse cerebral atrophy in magnetic resonance imaging, and brainstem hyperintensity and lactate peaks in magnetic resonance spectroscopy were noted in the group with abnormal OE results. Conclusion: Although the ophthalmologic symptoms are not very remarkable in MD patients, an OE is required. When the risk factors mentioned above are observed, a more active approach should be taken in the OE because a higher frequency of ocular involvement can be expected.

육미지황탕(六味地黃湯)으로 호전시킨 원발성 과수면장애 환자 1례(例) (The Effect of YukMiGiHwangTang on Idiopathic Hypersomnia -1-Case Report-)

  • 김민상;유병찬;김종국;심재철;김종원;최영;김윤식;설인찬;오병열
    • 대한한방내과학회지
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    • 제25권4호
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    • pp.383-390
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    • 2004
  • The most common causes of severe sleepiness beginning or progressively worsening in adults are SLEEP APNEA and RELATED BREATHING DISORDERS DURING SLEEP. Idiopathic hypersomnia is excessive sleeping without obvious cause. Idiopathic hypersomnia diagnosis can be explained as follows: One could be chronically sleepy due to either something wrong with sleep that makes it non-refreshing, or a problem with the brain mechanisms which normally should keep one alert whether caused by primary problems within the brain or its chemistry, or by other factors (such as sedating medications or thyroid problems). A 71-year-old male who had suffered from excessive sleeping was admitted to our department for oriental treatment on 7th of July, 2003. He was diagnosed as an idiopathic hypersomnia for excessive sleeping without obvious cause. Initial treatment modalities with administration of "SoonHwanGi1HoBang(循環器1號方)" were not effective. However, after administration of "YukMiGiHwangTang(六味地黃湯)" desirable effects were seen.

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