Drug-resistant tuberculosis treatment
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- , all-oral, bedaquiline-containing r egimen for multidrug-/ rifampicin-r esistant tuber culosis
- (updat ed rec ommendation)
- Recommendations in the 2019 updat e Recommendations in the curr ent updat e
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or ding but c ombined with s ection abo ve called: Section 3: Rec ommendations on the us e o f longer r egimens for multidr ug/ r ifampicin resist ant tuber culosis) In MDR/RR-TB patients on longer r egimens, a tr eatment duration of 15–17 months af ter cultur e conver sion is suggested for most patients; the duration may be modified accor ding to the patient’ s response to therapy (conditional r ecommendation, ver y low cer tainty in the estimates o f effect). 3.16 In MDR/RR-TB patients on longer r egimens, a tr eatment duration o f 15–17 months af ter cultur e conver sion is suggested for most patients; the duration may be modified accor ding to the patient’ s r esponse to therapy . (Conditional r ecommendation, ver y low cer tainty in the estimates o f effect). (no change to w or ding but c ombined with s ection abo ve called: Section 3: Rec ommendations on the us e o f longer r egimens for multidr ug/ r ifampicin resist ant tuber culosis) In MDR/RR-TB patients on longer r egimens that contain amikacin or str eptomycin, an intensive phase o f 6–7 months is suggested for most patients; the duration may be modified accor ding to the patient’ s r esponse to therapy (conditional r ecommendation, ver y low cer tainty in the estimates o f effect). 3.17 In MDR/RR-TB patients on longer r egimens containing amikacin or str eptomycin, an intensive phase o f 6–7 months is suggested for most patients; the duration may be modified accor ding to the patient’ s r esponse to therapy . (Conditional r ecommendation, ver y low cer tainty in the estimates o f effect. (no change to w or ding but c ombined with s ection abo ve called: Section 2.2: Rec ommendations on the us e o f longer r egimens for multidr ug/ r ifampicin resist ant tuber culosis) Section 4: Use o f the standar dized shor ter MDR-TB r egimen Section 2: Shor ter , all-oral, bedaquiline-containing r egimen for multidrug-/ rifampicin-r esistant tuber culosis In MDR/RR-TB patients who have not been pr eviously treated for mor e than 1 month with second- line medicines used in the shor ter MDR-TB r egimen or in whom r esistance to fluor oquinolones and second-line injectable agents has been excluded, a shor ter MDR-TB r egimen o f 9–12 months may be used instead o f the longer r egimen s (conditional recommendation, low cer tainty in the estimates o f effect). 2.1 A shor ter all-oral bedaquiline-containing r egimen o f 9–12 months duration is r ecommended in eligible patients with confir med multidrug- or rifampicin- resistant tuber culosis (MDR/RR-TB) who have not been exposed to tr eatment with second-line TB medicines used in this r egimen for mor e than 1 month, and in whom r esistance to fluor oquinolones has been excluded. (Conditional r ecommendation, ver y low cer tainty in the evidence). (updat ed rec ommendation) WHO consolidated guidelines on tuberculosis: drug-resistant tuberculosis treatment 95 Recommendations in the 2019 updat e Recommendations in the curr ent updat e Not included in 2019 guidelines Section 4: The bedaquiline, pr et omanid and linezolid (BP aL) r egimen for MDR-TB with additional fluor oquinolone r esistance Not included in 2019 guidelines 4.1. A tr eatment r egimen lasting 6–9 months, composed o f bedaquiline, pr etomanid and linezolid (BP aL), may be used under operational r esear ch conditions in multidrug-r esistant tuber culosis (MDR-TB) patients with TB that is r esistant to fluor oquinolones, who have either had no pr evious exposur e to bedaquiline and linezolid or have been exposed for no mor e than 2 weeks. (Conditional r ecommendation, ver y low cer tainty in the estimates o f effect). (new rec ommendation) Section 5: Monit oring p atient r esponse t o MDR-TB tr eatment using cultur e Section 5: Monit oring p atient r esponse t o MDR-TB tr eatment using cultur e In MDR/RR-TB patients on longer r egimens, the per for mance of sputum cultur e in addition to sputum smear micr oscopy is recommended to monitor tr eatment r esponse. It is desirable for sputum cultur e to be r epeated at monthly inter vals (str ong recommendation, moderate cer tainty in the estimates o f test accuracy). 5.1. In multidrug- or rifampicin-r esistant tuber culosis (MDR/RR-TB) patients on longer r egimens, the per for mance o f sputum cultur e in addition to sputum smear micr oscopy is r ecommended to monitor tr eatment r esponse (str ong recommendation, moderate cer tainty in the estimates o f test accuracy). It is desirable for sputum cultur e to be r epeated at monthly inter vals. (no change) Section 6: S tar t o f antir etr oviral therapy in p atients on second-line antituber culosis r egimens Section 6: S tar t o f antir etr oviral therapy in p atients on second-line antituber culosis r egimens Antir etr oviral therapy is r ecommended for all patients with HIV and DR-TB r equiring second-line antituber culosis drugs, irr espective o f CD4 cell count, as early as possible (within the fir st 8 weeks) following initiation o f antituber culosis tr eatment (str ong recommendation, ver y low-quality evidence). 6.1. Antir etr oviral therapy is r ecommended for all patients with HIV and drug- resistant tuber culosis r equiring second-line antituber culosis drugs, irr espective o f CD4 cell count, as early as possible (within the fir st 8 weeks) following initiation o f antituber culosis treatment . (Str ong r ecommendation, ver y low quality evidence). (no change) Supplementary Table 96 Recommendations in the 2019 updat e Recommendations in the curr ent updat e Section 7: Sur ger y for p atients on MDR-TB tr eatment Section 7: Sur ger y for p atients on MDR-TB tr eatment In patients with RR-TB or MDR-TB, elective par tial lung r esection (lobectomy or wedge r esection) may be used alongside a recommended MDR-TB r egimen (conditional r ecommendation, ver y low cer tainty in the evidence). 7.1. In patients with rifampicin-r esistant tuber culosis (RR-TB) or multidrug- resistant TB (MDR-TB), elective par tial lung r esection (lobectomy or wedge resection) may be used alongside a r ecommended MDR-TB r egimen. (Conditional r ecommendation, ver y low cer tainty in the evidence). (no change) Section 8: Car e and suppor t for p atients with MDR/RR-TB Section 8: Car e and suppor t for p atients with MDR/RR-TB Health education and counselling on the disease and tr eatment adher ence should be pr ovided to patients on TB tr eatment (str ong r ecommendation, moderate cer tainty in the evidence). 8.1 Health education and counselling on the disease and tr eatment adher ence should be pr ovided to patients on tuber culosis (TB) tr eatment. (Str ong r ecommendation, moderate cer tainty in the evidence) (no change) A package o f tr eatment adher ence inter ventions 71 may be o ffer ed to patients on TB tr eatment in conjunction with the selection of a suitable tr eatment administration option (conditional recommendation, low cer tainty in the evidence). 72 8.2 A package o f tr eatment adher ence inter ventions 71 may be o ffer ed to patients on TB tr eatment in conjunction with the selection o f a suitable tr eatment administration option. 72 (no change) 71 Tr eat m ent adhe renc e int er ve ntions inc lude soc ial suppor t suc h as m at erial suppor t (e .g. f ood, financ ial inc ent ive s, t ranspor t f ee s), psyc hologic al suppor t, t rac er s suc h as hom e visit s or digit al healt h c om m unic ations (e.g. SMS, telephone calls), medication monitor and staff education. The inter ventions should be selected based on an assessment of the individual patient’ s needs, pr ovider ’s resour ces and conditions for implementation. 72 Tr eatment administration options include dir ectly obser ved tr eatment (DO T), non-daily DO T, video-obser ved tr eatment (V O T), or unsuper vised treatment. WHO consolidated guidelines on tuberculosis: drug-resistant tuberculosis treatment 97 Download 1.73 Mb. Do'stlaringiz bilan baham: |
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