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Transcript of SA TB Guidelines – The interface with Advanced Clinical Care Dr Kogie Naidoo Head: CAPRISA...
![Page 1: SA TB Guidelines – The interface with Advanced Clinical Care Dr Kogie Naidoo Head: CAPRISA Treatment Research Programme Annual Workshop on Advanced Clinical.](https://reader036.fdocuments.us/reader036/viewer/2022062519/5697bfdf1a28abf838cb2822/html5/thumbnails/1.jpg)
SA TB Guidelines – The interface with Advanced Clinical Care
Dr Kogie NaidooHead: CAPRISA Treatment Research
ProgrammeAnnual Workshop on Advanced Clinical Care
Durban, 20 November 2015
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Presentation Outline• Diagnostic algorithm for DR and DS TB• Retreatment TB: Revised definitions and
treatment regimen• ART initiation in TB patients• Special considerations:
Aluvia with TB treatment Atazanivir in TB Ethambutol in Renal failure Moxifloxacin and streptomycin indications
• TB prevention in HIV infected patients
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Currently available TB Diagnostic tests
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Which initial TB diagnostic test does WHO recommend for HIV + people with suspected TB?
1. Smear Microscopy
2. Xpert MTB/RIF
3. Culture
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Which initial TB diagnostic test does WHO recommend for HIV + people with suspected TB?
1. Smear Microscopy
2. Xpert MTB/RIF
3. Culture
![Page 6: SA TB Guidelines – The interface with Advanced Clinical Care Dr Kogie Naidoo Head: CAPRISA Treatment Research Programme Annual Workshop on Advanced Clinical.](https://reader036.fdocuments.us/reader036/viewer/2022062519/5697bfdf1a28abf838cb2822/html5/thumbnails/6.jpg)
Where GeneXpert (GXP) is available, culture may still be required for:
1. HIV positive TB suspects, who have a negative GXP test
2. TB cases diagnosed as Rifampicin(Rif) resistant on GXP for susceptibility testing of other drugs
3. Despite a Rif susceptible result, the patient is failing treatment and treatment adherence is good and thus resistance to drugs other than Rif is suspected
4. All of the above
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TB SUSPECTSTB and DR-TB contacts, non-contact symptomatic individuals, re-treatment after relapse, failure and default
Collect one sputum specimen at the health facility under supervision
GXP positiveRifampicin susceptible
GXP positiveRifampicin resistant
GXP positiveRifampicin unsuccessful
GXP negative GXP unsuccessful
Treat as TBStart on Regimen 1
Send one specimen for microscopy
Treat as MDR-TBRefer to MDR-TB
Unit
Treat as TB
Start on Regimen 1Collect one specimen for microscopy Culture & DST / LPA
Collect one sputum specimen for a repeat GXP
HIV positive HIV negative
Collect one specimen for culture and LPA or culture and DST (for R and H)Treat with antibiotics and review after 5 daysDo chest x-ray
Treat with antibiotics
Poor response to antibiotics Clinically TB TB on chest x-ray
LPA/ DST results
Resistant to R and H/ R only
Good response
No further follow up
Advise to return when symptoms recur
Poor response
Consider other diagnosis
Refer for further investigation
Treat as MDR-TB
Refer to MDR-TB Unit
Treat as TBStart on Regimen 1Review culture results
Follow up with microscopy
Collect one specimen for microscopy, culture and DST for Rifampicin, Isoniazid, fluoroquinolone and Aminoglycoside
Follow up with microscopy and culture
![Page 8: SA TB Guidelines – The interface with Advanced Clinical Care Dr Kogie Naidoo Head: CAPRISA Treatment Research Programme Annual Workshop on Advanced Clinical.](https://reader036.fdocuments.us/reader036/viewer/2022062519/5697bfdf1a28abf838cb2822/html5/thumbnails/8.jpg)
Where GeneXpert (GXP) is available, culture may still be required for:
1. HIV positive TB suspects, who have a negative GXP test
2. TB cases diagnosed as Rifampicin(Rif) resistant on GXP for susceptibility testing of other drugs
3. Despite a Rif susceptible result, the patient is failing treatment and treatment adherence is good and thus resistance to drugs other than Rif is suspected
4. All of the above
![Page 9: SA TB Guidelines – The interface with Advanced Clinical Care Dr Kogie Naidoo Head: CAPRISA Treatment Research Programme Annual Workshop on Advanced Clinical.](https://reader036.fdocuments.us/reader036/viewer/2022062519/5697bfdf1a28abf838cb2822/html5/thumbnails/9.jpg)
Advantages and Disadvantages of GXP Test
• Detects MTB and Rif resistance
• Rapid TAT• Specific for MTB
complex• Use in CSF, gastric
aspirates, lymph nodes, tissue
• ↓ Risk of cross-contamination & error
• > sensitivity than microscopy
• Cannot be used for monitoring treatment (cannot distinguish between live and dead bacilli)
• Discordant results• Unsuccessful test due
to lab errors, test failure or invalid results. Needs repeat with second specimen
• Expensive • Does not detect INH
resistance
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Retreatment TB Definitions• Previously treated: past TB treatment > 4 weeks
& now either relapse, defaulted, or treatment failure(+/- microscopy; PTB/EPTB)
• Relapse: TB again after previous cure/Rx completion – either true relapse or new infection
• Retreatment after failure: Received full course of treatment and remains or becomes smear or culture positive at the end of the treatment period
• Retreatment after default: completes one month of treatment and returns foll a 2 month treatment interruption
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Streptomycin is indicated for:
1. All categories of DS TB
2. All categories of retreatment TB
3. For patients that cannot tolerate first line TB medication
4. All of the above
5. None of the above
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TB SUSPECTSTB and DR-TB contacts, non-contact symptomatic individuals, re-treatment after relapse, failure and default
Collect one sputum specimen at the health facility under supervision
GXP positiveRifampicin susceptible
GXP positiveRifampicin resistant
GXP positiveRifampicin unsuccessful
GXP negative GXP unsuccessful
Treat as TBStart on Regimen 1
Send one specimen for microscopy
Treat as MDR-TBRefer to MDR-TB
Unit
Treat as TB
Start on Regimen 1Collect one specimen for microscopy Culture & DST / LPA
Collect one sputum specimen for a repeat GXP
HIV positive HIV negative
Collect one specimen for culture and LPA or culture and DST (for R and H)Treat with antibiotics and review after 5 daysDo chest x-ray
Treat with antibiotics
Poor response to antibiotics Clinically TB TB on chest x-ray
LPA/ DST results
Resistant to R and H/ R only
Good response
No further follow up
Advise to return when symptoms recur
Poor response
Consider other diagnosis
Refer for further investigation
Treat as MDR-TB
Refer to MDR-TB Unit
Treat as TBStart on Regimen 1Review culture results
Follow up with microscopy
Collect one specimen for microscopy, culture and DST for Rifampicin, Isoniazid, fluoroquinolone and Aminoglycoside
Follow up with microscopy and culture
![Page 13: SA TB Guidelines – The interface with Advanced Clinical Care Dr Kogie Naidoo Head: CAPRISA Treatment Research Programme Annual Workshop on Advanced Clinical.](https://reader036.fdocuments.us/reader036/viewer/2022062519/5697bfdf1a28abf838cb2822/html5/thumbnails/13.jpg)
Streptomycin is indicated for:
1. All categories of DS TB
2. All categories of retreatment TB
3. For patients that cannot tolerate first line TB medication
4. All of the above
5. None of the above
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TB Treatment if unable to treat with standard first line
Missing drug Possible regimen Duration of treatment
INH Moxifloxacin/ rifampicin/ ethambutol
12 months ±PZA in intensive phase
Rifampicin Moxifloxacin/ INH/ ethambutol
18 months(PZA or streptomycin in intensive phase)
Rifampicin/INH Moxifloxacin/ ethambutol/ streptomycin
18 months
PZA Rifampicin/INH/ ethambutol Nine months
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TB Drugs in Renal failure
• INH, rifampicin, PZA : biliary excretion normal doses
•Streptomycin and ethambutol : can maintain at reduced dose – monitor for uveitis
•Safest regimen: INH, Rifampicin, pyrazinamide X 4 months followed by INH and Rifampicin x 2 months
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Managing TB treatment Interruption
• Less than 1 month: extend treatment for the number of days that patient did not take treatment
• 1-2 months missed: do geneXpert Sensitive: add number of days that patient did not take
treatment. Resistant: stop treatment: refer to MDR-TB unit
• More than 2 months missed (loss to follow up) do geneXpert Sensitive : restart treatment Resistant : refer MDR-TB
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TB Prevalence & Incidence in SA: WHO Global Report 2015
696/100 000
All: 834/100 000HIV+:509/100 000
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Integration of TB HIV Services
• Screening for TB and HIV at same visit• Early initiation of ARVs• Co-management of Drug toxicities common
to both• Consideration of Drug interactions• Early detection and management of TB IRIS• Initiation of INH prophylaxis
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Why start ARVs early?
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How early should ART be initiated?
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Balance of risks and benefitsFor CD4 count <50 cells/mm3 For CD4 ≥50 cells/mm3
Late integrated therapy↓ AIDS or
death↓IRIS
↓drug switches
Early integrated therapy Late integrated therapy
Early integrated therapy has:68% lower AIDS /death rate overshadows - 5-fold higher risk of IRIS- Increasing trend in drug switches
Early integrated therapy has:No discernable benefit in AIDS /death rate- 2-fold higher risk of IRIS- ↑ drug switches
Early integrated therapy
Recommend: Recommend:
Early ART initiation as soon as possible after TB treatment initiation
Defer ART initiation to start of continuation phase of TB therapy
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SA guidelines for HIV-TB co-infected
ACTIVE TB DISEASE, IRRESPECTIVE OF CD4 COUNT
OR CLINICAL STAGE
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• In TB co-infection, start with TB treatment first, followed by ART as soon as possible and within 8 weeks
• If CD4 <50 cells/μl initiate ART within 2 weeks of starting TB treatment, when the patient’s symptoms are improving and TB treatment is tolerated
• If CD4 >50 cells/μl initiate ART within 2-8 weeks of starting TB treatment
• In cryptococcal or TB meningitis: Defer ART initiation for 4-6 weeks
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TB service One-stop service HIV service
NOTo
Referral
HIV testing
ART
CPT
Condoms
Partiallyintegrated
HIV and TB Services provided together
ART
TB diagnosis and treatment
Co-locatedAdjacent
NOTo
Referral
TB screening
IPT
TB diagnosis
TB treatment
TB contact tracing
Partiallyintegrated
Models for integrated TB and HIV services delivery
Integrated service delivery
Source: WHO
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Concerns of co-treating TB and HIV
• Overlapping Toxicity• Drug Interactions• IRIS
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What are the overlapping drug toxicities with TB treatment and ARVs?
1. Liver Injury2. Rash3. Psychosis4. All of the above
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Side-effect Antiretroviral drug TB Therapy
Nausea & vomiting Didanosine, Zidovudine,Ritonavir
Pyrazinamide
Hepatitis NevirapineEfavirenz
RifampicinIsoniazidPyrazinamide
Peripheralneuropathy
StavudineDidanosine
Isoniazid
Rash
PsychosisRenal Toxicity
NevaripineEfavirenz
EFVTenofovir
RifampicinIsoniazidPyrazinamideEthambutol
INH/EthambutolRifampicin
Overlapping Toxicities with co-Rx of HIV and TB
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What are the overlapping drug toxicities with TB treatment and ARVs?
1. Liver Injury2. Rash3. Psychosis4. All of the above
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Case 1
• Mrs AA is HIV + since 2010. She was initially started on TDF / 3TC and EFV.
• In 2014, she was changed to ABC / 3TC and Alluvia due to treatment failure.
• She now presents with night sweats, loss of appetite and abdominal pain.
• The Gene Xpert test on ascitic fluid is positive for Rif sensitive MTB
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How to do you manage further?
1. Start TB Rx, double the dose of Alluvia immediately
2. Start TB Rx, double the dose of Alluvia over 2 weeks
3. Double the dose of Alluvia over 2 weeks then start TB Rx
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How to do you manage further?
1. Start TB Rx, double the dose of Alluvia immediately
2. Start TB Rx, double the dose of Alluvia over 2 weeks
3. Double the dose of Alluvia over 2 weeks then start TB Rx
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Mrs AA improves on TB Rx and completes the course. Her symptoms and signs have resolved, and her exit sputum is negative for AFB. How do you manage further?
1. Reduce Alluvia dose to 2T bd immediately
2. Continue TB Rx for two weeks longer
3. Continue the double dose (4T bd) of Alluvia until 2 weeks after TB Rx is completed
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Mrs AA improves on TB Rx and completes the course. Her symptoms and signs have resolved, and her exit sputum is negative for AFB. How do you manage further?
1. Reduce Alluvia dose to 2T bd immediately
2. Continue TB Rx for two weeks longer
3. Continue the double dose (4T bd) of Alluvia until 2 weeks after TB Rx is completed
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Case 2
• Mr E has been on a second line regimen for a year.
• His regimen includes AZT/3TC/ATZ/rit because he had severe diarrhoea whilst on Aluvia.
• He now presents with fever and productive cough.
• His sputum Gene Xpert is positive for Rif sensitive MTB.
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How do you manage further?
1. Commence TB treatment immediately
2. Double the dose of Atazanavir as you do for Aluvia
3. Atazanavir may not be given to patients on TB treatment. Refer to specialist
4. Stop the ART, treat TB, then restart ART
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How do you manage further?
1. Commence TB treatment immediately
2. Double the dose of Atazanavir as you do for Aluvia
3. Atazanavir may not be given to patients on TB treatment. Refer to specialist
4. Stop the ART, treat TB, then restart ART
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Drug Interactions: 1. RIF and EFV• Previously reported that Rif caused a 30%
decrease in EFV trough concentrations, particularly in patients >50kg.
• An increase in EFV dose recommended by FDA (USA)
• Later reports → clearance of EFV is reduced in black African patients, due to CYP enzyme polymorphisms (therefore drug levels actually increased by 30-50%)
• No increase in EFV dose recommended in SA
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2. RIF and NVP• NVP clearance may vary between ethnic groups
• Standard NVP dose is effective when co-
administered with RIF
• Increased hepatotoxicity, especially during
the first two months of NVP containing ART
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3. RIF and PI• PI metabolized by CYP 3A4: induced by Rifampicin and
inhibited by Ritonavir • Significant reduction of plasma drug levels of most PI’s,
except Ritonavir• LPV/r (Aluvia): Ritonavir boosted Lopinavir (400/100mg)• Increase Ritonavir to 400mg daily to overcome the
enzyme induction – double Aluvia dose Usual 2T BD, increased to 3T BD for 1 wk then 4T BD Maintain escalated dose of PI until 2 wks after TB Rx
completion• Rif accelerated Atazanavir/r metabolism, cannot be
overcome by boosting with Ritonavir Referral to higher centre to change PI or change
Rifampicin to Rifabutin
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TB IRIS
TB diagnosed & treatment started
before ART initiation
No TB diagnosis before ART initiation
ART Initiation
Clinical deterioration of TB as a result of
ART-induced immune recovery =
Paradoxical TB IRIS
Atypical inflammatory presentation of TB as a result of ART-induced immune recovery =
Unmasking IRIS
Lawn Expert Rev Anti Infect Ther, 2011.
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TB IRIS incidence and outcomes
• Unmasking TB IRIS Incidence 4.8% (most common )
• Paradoxical TB-IRIS Incidence 18%• Onset 14 days after ART initiation in 48%• Hospitalisation 25% • Mortality 7%, death attributed to TB IRIS 2%
• Increased mortality in CNS IRIS
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Major TB-IRIS risk factors
• Low CD4 count
• Short interval between TB treatment and ART
• Disseminated TB
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TB IRIS Management
• Double-blind, placebo-controlled RCT• Intervention: Prednisone 1.5mg/kg/day x 2 wks then
0.75mg/kg/day x 2 wks• Primary outcome = hospital days• Findings: Steroid arm - fewer days in hospital and fewer
procedures. IRIS associated mortality same in both arms, except CNS disease
• Excl other causes of patient deterioration: MDR TB etc
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What are the current guidelines for IPT for patients on ART?
1. 36 months IPT for all patients2. 12 months IPT for all patients3. 6 months IPT for all patients4. 36 months IPT for TST positive, 12 months for TST negative, 6 months for TST unknown
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INH Prophylaxis
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What are the current guidelines for IPT for patients on ART?
1. 36 months IPT for all patients2. 12 months IPT for all patients3. 6 months IPT for all patients4. 36 months IPT for TST positive, 12 months for TST negative, 6 months for TST unknown
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Questions
Are patients eligible for more IPT post TB therapy completion?
1. Yes: can be started immediately after TB treatment in all patients
2. No: patients no longer at risk for TB, having just completed TB treatment
3. Yes: can be started immediately after TB treatment but only in patients with documented bacteriologic cure
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Questions
Are patients eligible for more IPT post TB therapy completion?
1. Yes: can be started immediately after TB treatment in all patients
2. No: patients no longer at risk for TB, having just completed TB treatment
3. Yes: can be started immediately after TB treatment but only in patients with documented bacteriologic cure
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Summary• Diagnostic algorithm for DR and DS TB• Retreatment TB: Revised definitions and
treatment regimen• ART initiation in TB patients• Special considerations:
Aluvia with TB treatment Atazanivir in TB Ethambutol in Renal failure Moxifloxacin and streptomycin indications
• TB prevention in HIV infected patients
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Acknowledgements
This training was supported by the Grant or Cooperative Agreement Number U2G GH001142, funded by the Centers for Disease Control and Prevention. Its contents are solely the responsibility of the presenters and do not necessarily represent the official views of the U.S. Centers for Disease Control and Prevention or the U.S. Department of Health and
Human Services