• 제목/요약/키워드: First urine

검색결과 289건 처리시간 0.037초

비소 중독 (Arsenic Poisoning)

  • 김양호;이지호;심창선;정경숙
    • 대한임상독성학회지
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    • 제2권2호
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    • pp.67-71
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    • 2004
  • Arsenic poisoning has three types of poisoning. First, acute arsenic poisoning is usually caused by oral intake of large amount of arsenic compound with purpose of homicide or suicide. Second, chronic arsenic poisoning is caused by inhalation of arsenic in the occupational setting or by long-term oral intake of arsenic-contaminated well water. Third, arsine poisoning occurs acutely when impurities of arsenic in non-ferrous metal react with acid. Clinical manifestation of acute arsenic poisoning is mainly gastrointestinal symptoms and cardiovascular collapse. Those of chronic poisoning are skin disorder and cancer. Arsine poisoning shows massive intravascular hemolysis and hemoglobinuria with acute renal failure. Exposure evaluation is done by analysis of arsenic in urine, blood, hair and nail. Species analysis of arsenic is very important to evaluate inorganic arsenic acid and mono methyl arsenic acid (MMA) separated from dimethyl arsenic acid (DMA) and trimethyl arsenic acid (TMA) which originate from sea weed and sea food. Treatment with dimercaprol (BAL) is effective in acute arsenic poisoning only.

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내병외치약물(內病外治藥物)에 관한 문헌적(文獻的) 연구(硏究) (A Study on the External Treatment of Internal Diseases in Medical Classics)

  • 이석재;맹학영;금경수;정헌영;조은희;이시형
    • 대한한의학원전학회지
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    • 제22권2호
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    • pp.139-199
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    • 2009
  • The external treatment of internal diseases was first recorded in Hwangjenaegyeong(黃帝內經), and two hundred and fifty odd cases were found in the Bonchogangmok(本草綱目) and Oechisusebang(外治壽世方). Bonchogangmok(本草綱目) is a technical book devoted to explaining materia media as well as the external treatment of internal diseases. Oechisusebang(外治壽世方) is also a technical book, which make 36 references to the disease patterns of internal medicine. The medicinals employed as external treatment of internal diseases are grouped into 300 classes. These medicinals do not set limits to trees and plants but also uses birds and beasts, reptiles, grains, feces and urine, soil, stone etc., applied to various disease patterns. This study researched the medical texts in order to treat the disease patterns of internal medicine.

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휴대용 방광용적 측정 시스템을 위한 추정 알고리듬 연구 (Estimation Algorithm for Portable Bladder Volume Measurement System)

  • 하재규;송무용
    • 한국음향학회지
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    • 제19권6호
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    • pp.10-16
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    • 2000
  • 휴대용 방광 용적 측정시스템을 위한 새로운 추정 알고리듬을 제안하였다. 먼저 주어진 화상 데이터로부터 방광벽과 소변의 경계 끝점을 추출하고, 이로부터 축의 길이를 계산한 후 필터링하여 단면을 얻는다. 방광의 모양의 불규칙성을 고려하여 종단면과 횡단면 두 개의 데이터로부터 단면을 얻은 후 종단면으로 면적을 구하고 이를 횡단면에 적용하여 부피를 계산한다. 반대의 과정을 거쳐 또 하나의 부피 추정치를 얻고 이를 평균하여 실제 부피를 추정하였다. 제안된 알고리듬과 기존의 추정방법을 비교한 결과 제안된 방법에서 좋은 결과를 얻었다.

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다발성 척추골절을 동반한 비분비형 다발성 골수종 1례 - 증례보고 - (Nonsecretory Multiple Myeloma with Multiple Spine Fracture - Case Report -)

  • 허용석;박관호;지문표;김재오;김정철
    • Journal of Korean Neurosurgical Society
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    • 제30권12호
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    • pp.1435-1438
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    • 2001
  • A case of nonsecretory multiple myeloma in a 66 year-old-woman is reported. At first, she complained severe neck pain and radiologic finding showed C2 pathologic fracture. She complained severe low back pain 4 month later and L1 compression fracture was found. The lumbar MRI showed a 1.4cm-sized round enhancing lesion in the body of T12. Bone marrow aspiration biopsy at L1 spine showed a few polymorphous and small nests of mononuclear cell. L1 lamina bone biopsy showed many abnormal plasma cells. Pathologic diagnosis was multiple myeloma. However, plasma electrophoresis and protein immunoelectrophoresis of serum and urine of patient were normal. So, it is a nonecretory multiple myeloma case and the incidence of nonsecretory multiple myeloma is known to about 1% of all multiple myeloma.

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Oryeong-san has Different Effects on Water and Electrolyte Balance by Routes of Administration

  • Ahn, You-Mee;Kho, Joung-Hyun;Lee, Jae-Yun;Kang, Dae-Gill
    • 동의생리병리학회지
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    • 제26권3호
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    • pp.338-343
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    • 2012
  • Oryeong-san which was first recorded in Shanghanrun describing the treatments of acute febrile disease is one of the frequently used oriental medicines. Oryeong-san has been prescribed for the treatment of symptoms accompanied by edema. The purpose of this study was to examine the diuretic effects of Oryeong-san by different routes of administration. Oryeong-san (100 mg/kg body weight) was administrated by three different routes in Sprague-Dawley rats: intravenous infusion, intraperitoneal injection and oral intake. Oral intake of Oryeong-san significantly increased urinary volume and excretion of $Na^+$, $Cl^-$, and $K^+$ compared to vehicle-treated control group. The effects were concentration-dependent. Intravenously administrated Oryeong-san increased urinary volume and electrolyte excretion but without significance in hydrated (0.02 ml/min/rat for 90 min) anesthetized rats. Similarly, intraperitoneally injected Oryeong-san had no effects on water and urine electrolyte excretion compared with saline control group. These findings suggest that Oryeong-san has different effects on water and electrolyte balance by routes of administration.

Identification of a novel frameshift mutation (L345Sfs*15) in a Korean neonate with methylmalonic acidemia

  • Kim, Young A;Kim, Ji-Yong;Kim, Yoo-Mi;Cheon, Chong Kun
    • Journal of Genetic Medicine
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    • 제14권2호
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    • pp.80-85
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    • 2017
  • Methylmalonic acidemia (MMA) is an autosomal recessive metabolic disorder characterized by an abnormal accumulation of methylmalonyl-CoA and methylmalonate in body fluids without hyperhomocysteinemia. Cardiac disease is a rarely known lethal complication of MMA, herein, we report a Korean neonate diagnosed with MMA on the basis of biochemical and genetic findings, who developed cardiomyopathy, resulting in sudden death. The patient presented vomiting and lethargy at 3 days of age. Initially, the patient had an increased plasma propionylcarnitine/acetylcarnitine concentration ratio of 0.49 in a tandem mass spectrometry analysis and an elevated ammonia level of $537{\mu}mol/L$. Urine organic acid analysis showed increased excretion of methylmalonate. Subsequent sequence analysis of the methylmalonyl-CoA mutase (MUT) gene revealed compound heterozygous mutations c.323G>A (p.Arg108His) in exon 1 and c.1033_1034del (p. Leu345Serfs*15) in exon 4, the latter being a novel mutation. In summary, this is the first case of MMA and cardiomyopathy in Korea that was confirmed by genetic analysis to involve a novel MUT mutation.

Metformin에 추가로 병용되는 SGLT2 inhibitors의 효능과 안전성에 관한 고찰 (A Review on Efficacy and Safety of SGLT2 Inhibitors as Add-on Therapy with Metformin)

  • 정경혜
    • 한국임상약학회지
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    • 제28권3호
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    • pp.243-249
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    • 2018
  • Background: The new type of diabetes treatment, SGLT2 inhibitors, has been approved for monotherapy and combination therapy, but medical insurance is only allowed in combination therapy with metformin, which is the first choice for type 2 diabetes treatment. Methods: The SGLT2 inhibitors prescribed in Korea are dapagliflozin, empagliflozin and ipragliflozin. A review was conducted using Pubmed to evaluate efficacy and safety for these medications with metformin combination therapy. 10 studies were selected by searching for keywords and related references and were reviewed in full. The mechanism of action, pharmacokinetics, and the economics of treatment with SGLT2 inhibitors were examined. Results: SGLT2 inhibitors had moderate glycemic control when added to the treatment of patients with type 2 diabetes who were not being regulated by metformin monotherapy. They also showed positive effects such as weight loss, as well as the lowering of blood pressure. Hypotension and serious side effects were relatively low. However, the risk of genital infection was increased. Conclusion: The SGLT2 inhibitors are a new class of drugs that promote glucose excretion in the urine. They are a good choice for combination therapy with metformin for the treatment of type 2 diabetes, with weight loss and very low risk of serious side effects.

The Health Examinees (HEXA) Study: Rationale, Study Design and Baseline Characteristics

  • Health Examinees (HEXA) Study Group
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권4호
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    • pp.1591-1597
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    • 2015
  • Background: Korea has experienced rapid economic development in a very short period of time. A mixture of traditional and modern risk factors coexists and the rapid change in non-genetic factors interacts with genetic constituents. With consideration of these unique aspects of Korean society, a large-scale genomic cohort study-the Health Examinees (HEXA) Study-has been conducted to investigate epidemiologic characteristics, genomic features, and gene-environment interactions of major chronic diseases including cancer in the Korean population. Materials and Methods: Following a standardized study protocol, the subjects were prospectively recruited from 38 health examination centers and training hospitals throughout the country. An interview-based questionnaire survey was conducted to collect information on socio-demographic characteristics, medical history, medication usage, family history, lifestyle factors, diet, physical activity, and reproductive factors for women. Various biological specimens (i.e., plasma, serum, buffy coat, blood cells, genomic DNA, and urine) were collected for biorepository according to the standardized protocol. Skilled medical staff also performed physical examinations. Results: Between 2004 and 2013, a total of 167,169 subjects aged 40-69 years were recruited for the HEXA study. Participants are being followed up utilizing active and passive methods. The first wave of active follow-up began in 2012 and it will be continued until 2015. The principal purpose of passive follow-up is based on data linkages with the National Death Certificate, the National Cancer Registry, and the National Health Insurance Claim data. Conclusions: The HEXA study will render an opportunity to investigate biomarkers of early health index and the chronological changes associated with chronic diseases.

24개월에 만성 화농성 비루를 주소로 내원하여 진단된 헌터 증후군 1례 (A Case of Hunter Syndrome Presented with Chronic Purulent Rhinorrhea in 24-month-old Boy)

  • 김이안;진장용;박재옥;홍용희
    • 대한유전성대사질환학회지
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    • 제15권3호
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    • pp.160-164
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    • 2015
  • Hunter syndrome(Mucopolysaccharidosis type II, MPS type II) is an X-linked disorder of glycosaminoglycans (GAGs) metabolism caused by an iduronate-2-sulfatase (IDS2) deficiency. A 24-month-old boy visited the department of pediatrics with the chief compliant of chronic purulent rhinorrhea beginning at age one. He had a history of repeated acute otitis media and chronic rhinitis. On physical examination he had a coarse face, enlarged tongue, distended abdomen, joint stiffness, and Mongolian spots at his first visit. The urine GAGs level was elevated at 66.10 mg/mmolCr (reference range, <11.1) and iduronate-2-sulfatase activity in leukocyte was decreased at 0.21 nmol/mg protein/hr (reference range, 18.7-57). Finally with an IDS gene mutational analysis, recombinant known mutation between intron 7 and distal of exon 3 in IDS2 was detected. Recombinant iduronate-2-sulfatase therapy was started without any infusion related reactions. The author highlights the importance of suspecting Hunter syndrome when pediatric patients visit with chronic purulent rhinorrhea which is a common cause of hospital visits for infants and children.

요크셔테리어종 개에서 발생한 임신성 당뇨병 (Gestational Diabetes in a Yorkshire Terrier Dog)

  • 윤원경;서상일;현창백
    • 한국임상수의학회지
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    • 제32권2호
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    • pp.180-182
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    • 2015
  • 3년령의 임신한 요크셔 테리어가 다음, 다뇨를 주증으로 내원하였다. 실험실적 검사를 통해 지속적인 고혈당과 당뇨를 확인하였다. 복부 초음파 검사를 통해 2마리의 죽은 태아가 관찰되었으며 난소자궁적출술을 통해 죽은 태아를 제거하였다. 난소자궁적출술 이후 혈당수치는 정상범위로 돌아왔으며 임상증상과 당뇨도 회복되었다. 실험실적 검사를 기초로 한 추가적인 연구를 통해 이 증례는 임신성 당뇨병으로 진단되었으며 국내에서 최초로 보고된 임신성 당뇨병 증례이다.