CLINICAL STUDY ON DRUG FEVER WITHOUT DRUG ERUPTION
Drug fever without manifestation of so-called drug eruptions was studied so as to clarify its clinical characteristics. Between 1983 and 1988, eight patienus, three men and five women with a mean age of 90 years (range 38-75 years old), were identified according to the following criteria for drug fe...
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Published in | Japanese Journal of National Medical Services Vol. 44; no. 4; pp. 430 - 435 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
Japanese Society of National Medical Services
1990
一般社団法人 国立医療学会 |
Subjects | |
Online Access | Get full text |
ISSN | 0021-1699 1884-8729 |
DOI | 10.11261/iryo1946.44.430 |
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Abstract | Drug fever without manifestation of so-called drug eruptions was studied so as to clarify its clinical characteristics. Between 1983 and 1988, eight patienus, three men and five women with a mean age of 90 years (range 38-75 years old), were identified according to the following criteria for drug fever: (1) It was an unexplained fever under a condition that might itself have caused a febrile state. (2) Fever coincided with the administration of the drug and then improved after discontinuation of the drug without other therapeutic measures. (3) The temperature remained normal thereafter, accompanied with a recovery of general condition from the unexplained fever. (4) There was no so-called drug eruption. Diagnosis was confirmed in four of the eight patients by rechallenge of the causative drugs. All patients had fever caused by the antibiotics which were administered; for infectious diseases in 7, for prophylactic use in 1. Other manifestations occurred in 2 patients (lymphnodes swellings in 2, polyarthritis in 1, and erythema nodosum in 1). Only 3 patients had prior histories of allergy. Fever pattens were high (≥36°C) in 6 patients, medium (38-39°C) in 1, low (<38°C) in 1. Duration of the drugs before the occurrence of drug fever ranged widely from 5 to 34 days. A relative eosinophilia was detected in only 2 patients. Erythrocyte sedimention rate, C-reactive protein and nuclear shift of neutrocytes were not helpful in making a differential diagnosis of drug fever against infectious disease. White blood cell counts ranged from 3500 to 6200/cmm. All intradermal skin tests of causative drugs showed negative. Patch test examined in 2 patients showed negative for both. Drug-induced lymphocyte stimulation test examined in 5 showed positive in 4. Circulating antibodies examined in 2 showed positive in 2. Drug fever disappeared within 24 hours in 5 patents, 3 days in 2 patients, but continued for more than 7 days after the drug discontinuation in 1 patient. Our data showed no specific clinical patterns to confirm the diagnosis of drug fever against the infectious disease. In conclusion, we reconfim that drug fever must be among first considerations for unexplained fever in any patient receiving medications. |
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AbstractList | Drug fever without manifestation of so-called drug eruptions was studied so as to clarify its clinical characteristics. Between 1983 and 1988, eight patienus, three men and five women with a mean age of 90 years (range 38-75 years old), were identified according to the following criteria for drug fever: (1) It was an unexplained fever under a condition that might itself have caused a febrile state. (2) Fever coincided with the administration of the drug and then improved after discontinuation of the drug without other therapeutic measures. (3) The temperature remained normal thereafter, accompanied with a recovery of general condition from the unexplained fever. (4) There was no so-called drug eruption. Diagnosis was confirmed in four of the eight patients by rechallenge of the causative drugs. All patients had fever caused by the antibiotics which were administered; for infectious diseases in 7, for prophylactic use in 1. Other manifestations occurred in 2 patients (lymphnodes swellings in 2, polyarthritis in 1, and erythema nodosum in 1). Only 3 patients had prior histories of allergy. Fever pattens were high (≥36°C) in 6 patients, medium (38-39°C) in 1, low (<38°C) in 1. Duration of the drugs before the occurrence of drug fever ranged widely from 5 to 34 days. A relative eosinophilia was detected in only 2 patients. Erythrocyte sedimention rate, C-reactive protein and nuclear shift of neutrocytes were not helpful in making a differential diagnosis of drug fever against infectious disease. White blood cell counts ranged from 3500 to 6200/cmm. All intradermal skin tests of causative drugs showed negative. Patch test examined in 2 patients showed negative for both. Drug-induced lymphocyte stimulation test examined in 5 showed positive in 4. Circulating antibodies examined in 2 showed positive in 2. Drug fever disappeared within 24 hours in 5 patents, 3 days in 2 patients, but continued for more than 7 days after the drug discontinuation in 1 patient. Our data showed no specific clinical patterns to confirm the diagnosis of drug fever against the infectious disease. In conclusion, we reconfim that drug fever must be among first considerations for unexplained fever in any patient receiving medications. Drug fever without manifestation of so-called drug eruptions was studied so as to clarify its clinical characteristics.Between 1983 and 1988, eight patienus, three men and five women with a mean age of 90 years (range 38-75 years old), were identified according to the following criteria for drug fever: (1) It was an unexplained fever under a condition that might itself have caused a febrile state. (2) Fever coincided with the administration of the drug and then improved after discontinuation of the drug without other therapeutic measures. (3) The temperature remained normal thereafter, accompanied with a recovery of general condition from the unexplained fever. (4) There was no so-called drug eruption.Diagnosis was confirmed in four of the eight patients by rechallenge of the causative drugs. All patients had fever caused by the antibiotics which were administered; for infectious diseases in 7, for prophylactic use in 1. Other manifestations occurred in 2 patients (lymphnodes swellings in 2, polyarthritis in 1, and erythema nodosum in 1). Only 3 patients had prior histories of allergy. Fever pattens were high (≥36°C) in 6 patients, medium (38-39°C) in 1, low (<38°C) in 1. Duration of the drugs before the occurrence of drug fever ranged widely from 5 to 34 days. A relative eosinophilia was detected in only 2 patients. Erythrocyte sedimention rate, C-reactive protein and nuclear shift of neutrocytes were not helpful in making a differential diagnosis of drug fever against infectious disease. White blood cell counts ranged from 3500 to 6200/cmm. All intradermal skin tests of causative drugs showed negative. Patch test examined in 2 patients showed negative for both. Drug-induced lymphocyte stimulation test examined in 5 showed positive in 4. Circulating antibodies examined in 2 showed positive in 2. Drug fever disappeared within 24 hours in 5 patents, 3 days in 2 patients, but continued for more than 7 days after the drug discontinuation in 1 patient. Our data showed no specific clinical patterns to confirm the diagnosis of drug fever against the infectious disease. In conclusion, we reconfim that drug fever must be among first considerations for unexplained fever in any patient receiving medications. いわゆる薬疹を伴わない薬剤熱8例(男性3例, 女性5例)について検討し, その臨床的特徴を見いだそうと試みた. 原因薬剤は全例が抗生物質であつた. 8例のうち4例は誘発テストにて診断を確認した. アレルギー既往歴は3例のみ, 好酸球増多は2例のみに認めた. 熱型は微熱1例, 中等度発熱1例, 高熱6例であつた. 薬剤熱出現までの薬剤投与期間は5日から34日であつた. 血沈は1例を除き全例亢進. CRPは1例を除き全例+3以上. 末梢白血球数は全例が正常ないしやや減少. 核左方移動は5例に認めた. 皮内テストは全例陰性, パッチテストは施行した2例で陰性, 液性抗体は施行した2例で陽性, DLSTは5例中4例で陽性であつた. 薬剤中止後解熱するまでの期間は7例が3日以内であつたが1例は1週間以上を要した. 以上から感染症との鑑別診断の上で臨床的な特異的変化は見い出されず臨床経過の詳細な観察が最も大切であることが再確認された. |
Author | KANAMARU, Minoru KUWABARA, Hidemasa GOTO, Kazuhiro UEHARA, Masahiro CHISHIMA, Joichi KUBOTA, Shozo SAITO, Shozo UEHARA, Mutsumi MASUDA, Jun |
Author_FL | 増田 淳 後藤 和弘 久保田 鐘造 桑原 英真 金丸 稔 斎藤 昭三 植原 睦美 植原 政弘 千島 丈一 |
Author_FL_xml | – sequence: 1 fullname: 桑原 英真 – sequence: 2 fullname: 増田 淳 – sequence: 3 fullname: 金丸 稔 – sequence: 4 fullname: 後藤 和弘 – sequence: 5 fullname: 植原 睦美 – sequence: 6 fullname: 植原 政弘 – sequence: 7 fullname: 千島 丈一 – sequence: 8 fullname: 久保田 鐘造 – sequence: 9 fullname: 斎藤 昭三 |
Author_xml | – sequence: 1 fullname: SAITO, Shozo organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: KANAMARU, Minoru organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: KUBOTA, Shozo organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: MASUDA, Jun organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: UEHARA, Mutsumi organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: UEHARA, Masahiro organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: GOTO, Kazuhiro organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: CHISHIMA, Joichi organization: Department of Internal Medicine, Numata National Hospital – sequence: 1 fullname: KUWABARA, Hidemasa organization: Department of Internal Medicine, Numata National Hospital |
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References | 6) Lipsky BA et al: Drug fever, JAMA, 245: 851, 1981 5) Rahal JJ Jr et al: Adverse reactions to anti-infective agents, Disease-a-Month, 25: 1, 1978 3) Alanis A et al: Adverse reactions associated with the use of oral penicillins and cephalosporins, Med Clin N Amer, 67: 113, 1983 8) Ley AB et al: Circulating antibody directed against penicillins, Science, 127: 1118, 1957 4) 大沼菊夫他: 注射用抗生物質による発熱に関する臨床的研究, Chemotherapy, 33: 562, 1985 9) 溝口靖紘他: 薬物アレルギーの診断におけるリンパ球幼若化反応, 臨免疫, 19, 673, 1987 2) 桑原英真他: 薬剤により血清病型反応を呈したと思われる一例, 臨と研, 64: 2852, 1987 1) Young EJ et al: Drug-induced fever: Cases seen in the evaluation of unexplained fever in a general hospital population, Rev Infect Dis, 4: 69, 1982 7) Parker CVO: Drug therapy, N Engl J Med, 292: 511, 1975 |
References_xml | – reference: 1) Young EJ et al: Drug-induced fever: Cases seen in the evaluation of unexplained fever in a general hospital population, Rev Infect Dis, 4: 69, 1982 – reference: 4) 大沼菊夫他: 注射用抗生物質による発熱に関する臨床的研究, Chemotherapy, 33: 562, 1985 – reference: 6) Lipsky BA et al: Drug fever, JAMA, 245: 851, 1981 – reference: 5) Rahal JJ Jr et al: Adverse reactions to anti-infective agents, Disease-a-Month, 25: 1, 1978 – reference: 7) Parker CVO: Drug therapy, N Engl J Med, 292: 511, 1975 – reference: 9) 溝口靖紘他: 薬物アレルギーの診断におけるリンパ球幼若化反応, 臨免疫, 19, 673, 1987 – reference: 3) Alanis A et al: Adverse reactions associated with the use of oral penicillins and cephalosporins, Med Clin N Amer, 67: 113, 1983 – reference: 8) Ley AB et al: Circulating antibody directed against penicillins, Science, 127: 1118, 1957 – reference: 2) 桑原英真他: 薬剤により血清病型反応を呈したと思われる一例, 臨と研, 64: 2852, 1987 |
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Snippet | Drug fever without manifestation of so-called drug eruptions was studied so as to clarify its clinical characteristics. Between 1983 and 1988, eight patienus,... Drug fever without manifestation of so-called drug eruptions was studied so as to clarify its clinical characteristics.Between 1983 and 1988, eight patienus,... |
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SubjectTerms | adverse reaction antibiotics drug fever 副作用 抗生物質 薬剤熱 |
Title | CLINICAL STUDY ON DRUG FEVER WITHOUT DRUG ERUPTION |
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