SM, INH, PASの臨床耐性限界
スポンサーリンク
概要
- 論文の詳細を見る
To decide the clinical significance of the critical drug resistance concentration, studies were done from two aspects. One was an approach from the distribution of naturally resistant variant of the wild strains and another was the one from the clinical view point. The technique used was the proportion method of Canetti, using 1% Ogawa medium with cork stop.<BR>Proportion of resistant variants to SM, INH and PAS was measured on strains isolated from previously untreated patients. Considering the variation of the proportion between cases in each drug concentration the, variation of the same strain measured at different days or lots (Table 1), and the decreasing trend of the median value of colonies shown in Fig., it seemed reasonable to take 4mcg of SM, 0.1mcg of INH and O.5mcg of PAS as critical concentrations.<BR>For clinical investigation, the grade of drug resistance was divided into 4 categories; that is, sensitive, criteria 1, 2 and 3 as presented in Table 2.<BR>A study was done on cases treated for more than 6 months with 3 major primary drugs and have only one drug resistance of each criteria. Minimal cases were excluded from this study as all of them converted to negative regardless of resistance (Table 3).<BR>According to this study, the treatment failure was found in 0.4% of the sensitive, and 8.3% in criteria 3 among the original treatment group but there was no statistically significant difference, while among the retreatment group, significant difference was found between sensi tive and criteria 2 (Table 6). Accordingly, it seemed to be reasonable to take criteria 2 as a critical concentration from clinical stand points.<BR>Concerning bacillary relapse, temporally or permanent (Table 7), there was a significant difference between sensitive and criteria 3 of the original treatment group and between sensitive and criteria 1 of the retreatment group.<BR>The relation between the period of chemotherapy and resistance was examined from the previous history taken at the time of hospitalization. The number of drug resistant cases according to criteria 3 was too few in number among cases after one year or more treatment with SM, INH and PAS, alone or combinated and resulted in failure (Table 8). Similarily, many of hospitalized cases did not become resistant according to criteria 3 in spite of unsuc cessful treatment (Table 9).<BR>Considering all these facts, we concluded that the clinically significant critical drug resist ance concentration by using 1% Ogawa medium with cork stop is one percent or more of the following drug concentration ; 10mcg of SM, 0.2mcg of INH, and 1mcg of PAS. But it is also recommendable to take 4mcg of SM, 0.1mcg of INH and 0.5mcg of PAS as subcritical concentrations.
- 日本結核病学会の論文
著者
関連論文
- 外来性再感染によると思われる4症例について-4-総括,討論,結論
- 外来性再感染によると思われる4症例について-3-症例4および症例2,3,4の相互関連その他の検討
- 外来性再感染によると思われる4症例について-2-症例3について
- 外来性再感染によると思われる4症例について-1-症例1および症例2について
- 結核性膿胸患者の治療に関する研究
- 燒灼336名について
- ^Hg : グルタチオンによる肺癌シンチグラフィーの臨床的価値
- 肺癌の放射性第2塩化水銀のマクロオートラジオグラムと組織変化の検討 : 関東支部 : 第39回支部活動
- 11.肺癌における放射性水銀の診断的価値 : 第37回支部会 : 関東支部
- RFPを含む3方式による肺結核6ヵ月化療の対照試験 (第2報) : 治療終了後1年目の成績
- RFPを含む3方式による肺結核6ヵ月化療の対照試験 (第1報)
- 外来性再感染によると思われる4症例について : 第4部総括, 討論, 結論
- 外来性再感染によると思われる4症例について : 第3部 症例4および症例2, 3, 4の相互関連その他の検討
- 外来性再感染によると思われる4症例について : 第2部症例3について
- 外来性再感染によると思われる4症例について : 第1部症例1および症例2について
- 一次薬3者併用におけるSM毎日と週2回の比較 : 特に耐性限界を考慮して (第2報)
- RFPの耐性 (後編)
- RFPの耐性 (前編)
- 次薬3者併用におけるSM毎日と週2回の比較 : ―特に耐性限界を考慮しで(第1報)―
- SM, INH, PASの臨床耐性限界
- 抗結核剤の1回および分服法の比較
- Rifampicinによる肺結核の再治療
- Rifampicinによる肺結核の再治療
- Ethambutolによる視力障害
- D-2,2-(Ethylenediimino)di-1-butanol[Ethambutol, Ebutol]の臨床成績
- D-2, 2-(Ethylenediimino)di-1-butanol[Ethambutol,Ebuto1]の臨床成績
- エタンブトールの体内分布とその代謝