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吸入炭疽のスクリーニングアルゴリズム

2001年の米国でのバイオテロリズム事件のように、曝露者が大量に発生した状況下で使用することを前提に作成されたスクリーニングアルゴリズムである。
出典
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1: Conference report on public health and clinical guidelines for anthrax.
著者: Eric Jacob Stern, Kristin Broome Uhde, Sean Vincent Shadomy, Nancy Messonnier
雑誌名: Emerg Infect Dis. 2008 Apr;14(4). doi: 10.3201/eid1404.070969.
Abstract/Text: On March 13-14, 2006, a meeting on anthrax, sponsored by the Centers for Disease Control and Prevention (CDC) in collaboration with the Southeastern Center for Emerging Biologic Threats, was held at Emory University in Atlanta, Georgia, USA. The meeting's agenda included discussion of postexposure prophylaxis (PEP), screening and evaluation, and treatment of the various manifestations of human anthrax. The goal was to convene subject matter experts for a review of research developments and clinical experience with anthrax prophylaxis and treatment and to make consensus recommendations for updating guidelines for PEP, treatment, and clinical evaluation of patients with anthrax. A 2001 conference on guidelines for anthrax has previously been summarized in this journal. This article summarizes the meeting's presentations and discussion. Consensus recommendations are summarized in the Table. Updated CDC guidelines for treatment and prophylaxis of anthrax will be published in detail in other CDC publications and are available on CDC's website at http://www.bt.cdc.gov/agent/anthrax/index.asp.
Emerg Infect Dis. 2008 Apr;14(4). doi: 10.3201/eid1404.070969.

炭疽菌のグラム染色像

炭疽菌は好気性グラム陽性桿菌である。栄養型の状態では鞭毛を欠き運動性がない。
出典
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1: Artenstein Andrew W. Infoctious Diseases. 747-758p Elsevier

皮膚炭疽

浮腫、黒色痂皮を伴う特徴的な潰瘍
出典
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1: G. Raghurama Rao, David H. Walker. Anthrax. Richard L. Guerrant MD, David H. Walker MD and Peter F. Weller MD. Tropical Infectious Diseases: Principles, Pathogens and Practice. Saunders, 2011; 261-264

汚染ヘロイン静注者に発症した重症軟部組織感染

a:初診時の所見で殿部に15×10cmの初発病変を認める。黒色痂皮があり、周辺組織には大きな変化が認めていないが、これは皮膚炭疽として典型的な所見であって、静注者に発症した軟部組織感染症としては非典型的であった。静注者に発症する場合には紫色に変色した皮下出血と著明な浮腫、毛細血管拡張を認めることがより特徴的である。炭疽菌はグラム染色で確認することができる。
b:切除組織では皮下脂肪の浅層が病変の中心であり、浮腫と末梢血管からの出血を伴っており、壊死性筋膜炎の所見とは異なる。壊死性筋膜炎の場合には病変の中心は深層で、微小血管塞栓、混濁液、筋膜融解が生じる。
出典
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1: Anthrax infection in drug users.
Lancet. 2010 Apr 17;375(9723):1345-6. doi: 10.1016/S0140-6736(10)60573-9.

吸入炭疽の胸部X線、および胸部CT画像

吸入炭疽を発症して5日目に病院受診した47歳郵便職員の胸部X線、および胸部CT画像。肺門周囲、肺門下部に進行性両側性浸潤影、縦隔拡大を認める。CT画像では縦隔炎、右に優位な両側胸水を認める。
a:2001年10月21日3時(ER初診時)
b:2001年10月22日5時30分(入院時)
c:2001年10月22日9時
d:2001年10月22日11時(死亡直前)
e:2001年10月22日(死亡直前)
出典
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1: Death due to bioterrorism-related inhalational anthrax: report of 2 patients.
著者: L Borio, D Frank, V Mani, C Chiriboga, M Pollanen, M Ripple, S Ali, C DiAngelo, J Lee, J Arden, J Titus, D Fowler, T O'Toole, H Masur, J Bartlett, T Inglesby
雑誌名: JAMA. 2001 Nov 28;286(20):2554-9.
Abstract/Text: On October 9, 2001, a letter containing anthrax spores was mailed from New Jersey to Washington, DC. The letter was processed at a major postal facility in Washington, DC, and opened in the Senate's Hart Office Building on October 15. Between October 19 and October 26, there were 5 cases of inhalational anthrax among postal workers who were employed at that major facility or who handled bulk mail originating from that facility. The cases of 2 postal workers who died of inhalational anthrax are reported here. Both patients had nonspecific prodromal illnesses. One patient developed predominantly gastrointestinal symptoms, including nausea, vomiting, and abdominal pain. The other patient had a "flulike" illness associated with myalgias and malaise. Both patients ultimately developed dyspnea, retrosternal chest pressure, and respiratory failure requiring mechanical ventilation. Leukocytosis and hemoconcentration were noted in both cases prior to death. Both patients had evidence of mediastinitis and extensive pulmonary infiltrates late in their course of illness. The durations of illness were 7 days and 5 days from onset of symptoms to death; both patients died within 24 hours of hospitalization. Without a clinician's high index of suspicion, the diagnosis of inhalational anthrax is difficult during nonspecific prodromal illness. Clinicians have an urgent need for prompt communication of vital epidemiologic information that could focus their diagnostic evaluation. Rapid diagnostic assays to distinguish more common infectious processes from agents of bioterrorism also could improve management strategies.
JAMA. 2001 Nov 28;286(20):2554-9.

手と頬に発症した皮膚炭疽

a:特徴的な黒色痂皮で周囲にびらん、浮腫を伴っている。
b~d:頬にできた皮膚炭疽の経過を追っている。最初に特徴的な黒色痂皮が形成(b)、翌日に潰瘍化、周囲の浮腫が出現(c)、7日目には病変は改善傾向にあり、浮腫は軽減している(d)。
出典
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1: Anthrax.
N Engl J Med. 1999 Sep 9;341(11):815-26. doi: 10.1056/NEJM199909093411107.

吸入炭疽の胸部X線、および胸部CT画像

胸部X線では縦隔の拡大、右胸水、末梢の含気減少を認める。胸部CT画像では右肺門部リンパ節の腫大、縦隔脂肪織浮腫像、両側胸水を認める。
出典
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1: Clinical presentation of inhalational anthrax following bioterrorism exposure: report of 2 surviving patients.
著者: T A Mayer, S Bersoff-Matcha, C Murphy, J Earls, S Harper, D Pauze, M Nguyen, J Rosenthal, D Cerva, G Druckenbrod, D Hanfling, N Fatteh, A Napoli, A Nayyar, E L Berman
雑誌名: JAMA. 2001 Nov 28;286(20):2549-53.
Abstract/Text: The use of anthrax as a weapon of biological terrorism has moved from theory to reality in recent weeks. Following processing of a letter containing anthrax spores that had been mailed to a US senator, 5 cases of inhalational anthrax have occurred among postal workers employed at a major postal facility in Washington, DC. This report details the clinical presentation, diagnostic workup, and initial therapy of 2 of these patients. The clinical course is in some ways different from what has been described as the classic pattern for inhalational anthrax. One patient developed low-grade fever, chills, cough, and malaise 3 days prior to admission, and then progressive dyspnea and cough productive of blood-tinged sputum on the day of admission. The other patient developed progressively worsening headache of 3 days' duration, along with nausea, chills, and night sweats, but no respiratory symptoms, on the day of admission. Both patients had abnormal findings on chest radiographs. Non-contrast-enhanced computed tomography of the chest showing mediastinal adenopathy led to a presumptive diagnosis of inhalational anthrax in both cases. The diagnoses were confirmed by blood cultures and polymerase chain reaction testing. Treatment with antibiotics, including intravenous ciprofloxacin, rifampin, and clindamycin, and supportive therapy appears to have slowed the progression of inhalational anthrax and has resulted to date in survival.
JAMA. 2001 Nov 28;286(20):2549-53.

汚染ヘロイン静注者に発症した炭疽

a:左の大腿から大陰唇にかけて壊死を起こした女性
b:陰嚢腫大と殿部壊死を起こした男性
c:コンパートメント症候群を来し、皮膚・筋膜壊死部をデブリードマンした後の様子
出典
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1: An overview of anthrax infection including the recently identified form of disease in injection drug users.
著者: Caitlin W Hicks, Daniel A Sweeney, Xizhong Cui, Yan Li, Peter Q Eichacker
雑誌名: Intensive Care Med. 2012 Jul;38(7):1092-104. doi: 10.1007/s00134-012-2541-0. Epub 2012 Apr 24.
Abstract/Text: PURPOSE: Bacillus anthracis infection (anthrax) can be highly lethal. Two recent outbreaks related to contaminated mail in the USA and heroin in the UK and Europe and its potential as a bioterrorist weapon have greatly increased concerns over anthrax in the developed world.
METHODS: This review summarizes the microbiology, pathogenesis, diagnosis, and management of anthrax.
RESULTS AND CONCLUSIONS: Anthrax, a gram-positive bacterium, has typically been associated with three forms of infection: cutaneous, gastrointestinal, and inhalational. However, the anthrax outbreak among injection drug users has emphasized the importance of what is now considered a fourth disease form (i.e., injectional anthrax) that is characterized by severe soft tissue infection. While cutaneous anthrax is most common, its early stages are distinct and prompt appropriate treatment commonly produces a good outcome. However, early symptoms with the other three disease forms can be nonspecific and mistaken for less lethal conditions. As a result, patients with gastrointestinal, inhalational, or injectional anthrax may have advanced infection at presentation that can be highly lethal. Once anthrax is suspected, the diagnosis can usually be made with gram stain and culture from blood or tissue followed by confirmatory testing (e.g., PCR). While antibiotics are the mainstay of anthrax treatment, use of adjunctive therapies such as anthrax toxin antagonists are a consideration. Prompt surgical therapy appears to be important for successful management of injectional anthrax.
Intensive Care Med. 2012 Jul;38(7):1092-104. doi: 10.1007/s00134-012-2...

吸入炭疽のスクリーニングアルゴリズム

2001年の米国でのバイオテロリズム事件のように、曝露者が大量に発生した状況下で使用することを前提に作成されたスクリーニングアルゴリズムである。
出典
imgimg
1: Conference report on public health and clinical guidelines for anthrax.
著者: Eric Jacob Stern, Kristin Broome Uhde, Sean Vincent Shadomy, Nancy Messonnier
雑誌名: Emerg Infect Dis. 2008 Apr;14(4). doi: 10.3201/eid1404.070969.
Abstract/Text: On March 13-14, 2006, a meeting on anthrax, sponsored by the Centers for Disease Control and Prevention (CDC) in collaboration with the Southeastern Center for Emerging Biologic Threats, was held at Emory University in Atlanta, Georgia, USA. The meeting's agenda included discussion of postexposure prophylaxis (PEP), screening and evaluation, and treatment of the various manifestations of human anthrax. The goal was to convene subject matter experts for a review of research developments and clinical experience with anthrax prophylaxis and treatment and to make consensus recommendations for updating guidelines for PEP, treatment, and clinical evaluation of patients with anthrax. A 2001 conference on guidelines for anthrax has previously been summarized in this journal. This article summarizes the meeting's presentations and discussion. Consensus recommendations are summarized in the Table. Updated CDC guidelines for treatment and prophylaxis of anthrax will be published in detail in other CDC publications and are available on CDC's website at http://www.bt.cdc.gov/agent/anthrax/index.asp.
Emerg Infect Dis. 2008 Apr;14(4). doi: 10.3201/eid1404.070969.

炭疽菌のグラム染色像

炭疽菌は好気性グラム陽性桿菌である。栄養型の状態では鞭毛を欠き運動性がない。
出典
img
1: Artenstein Andrew W. Infoctious Diseases. 747-758p Elsevier