Mdr , xdr,dots strategy
Transcript of Mdr , xdr,dots strategy
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Multidrug resistant tuberculosis, Extended - Drug resistant tuberculosis, DOTS
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A Global Emergency
Kills 5,000 people per day
2.3 million people die each year
Highly prevalent in Pakistan-the estimated
incidence is around 2,50,000 per year
Ranks 6th among the 22 high burden countries of
TB in the world.
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The 22 countries most affected by
tuberculosis are Afghanistan, Bangladesh,
Brazil, Cambodia, China, the Democratic
Republic of Congo, Ethiopia, India,
Indonesia, Kenya, Myanmar, Nigeria,
Pakistan, Peru, the Philippines, Russia, South
Africa, Thailand, Tanzania, Uganda, Vietnam
and Zimbabwe
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Emergence of multi-drug resistant
(MDR-TB), extremely drug resistant
tuberculosis (XDR-TB) and latent TB
have been the major constraints in
the eradication of TB.
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Data from the latest 12 month
period
the highest ever number of infectious
patients – 2.3 million people – were
cured with the launch of DOTS
87% of treated patients being cured
85% global target was exceeded
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estimated half a million MDR-TB cases
occur per year
almost 30 000 were officially reported
6000 known to be treated
but almost 29 ,000 people are expected to
be treated in 2010.
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Eradicating M. tuberculosis infection
Preventing development of drug
resistance
Preventing relapse of infection
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Occur in a patient who has never
received antituberculosis therapy
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The development of resistance during or
following chemotherapy in patients who
previously had drug-susceptible
tuberculosis.
Main cause of primary drug resistance due Main cause of primary drug resistance due
to transmission of resistant strains.to transmission of resistant strains.
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Cases of tuberculosis caused by an
isolate of Mycobacterium
tuberculosis that is resistant to one
of the first-line antituberculosis
drugs: INH, RMP, PZA, EMB, or
streptomycin
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A.Genetic mutations occur spontaneously- confer resistance to Anti-Tuberculous drugs are present in Wild type M tuberculosis isolates occur by chance alone do not depend upon prior drug exposure not linked occur in frequency specific for each drug
1 in 107 for INH 1 in 108 for STM and INH
1 in 1010 for RMP 1 in 1014 for INH & RMP
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Wild TB Strain
Strains with genetic drug resistance
Acquired drug resistance
Primary Drug Resistance
Spontaneous mutation
Selection: Inadequate treatment
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B. Treatment with a Single TB drug-
Due to natrural occurrence of spontaneous mutations, treatment with one drug (or one efective drug) leads to development of resistance .
- drug susceptible bacteria will be killed
- drug resistant bacteria will survive
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1950s-1970s:1950s-1970s: Mycobacterium tuberculosis resistant to Mycobacterium tuberculosis resistant to
INH, streptomycin and / or PASINH, streptomycin and / or PAS 1980s-curreny:1980s-curreny: TB that is resistant at least to INH
and RMP Isolates that are multiply-resistant
to any other combination of anti-TB drugs but not to INH and RMP are not classed as MDR-TB
))
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While community based information is
lacking, laboratory data suggests an
increasing frequency of MDR from 14% in
1999 to 28% in 2004[6] and 47% in 2006[8].
(referemces: 6. utt T, Ahmad RN, Kazmi SY, Rafi N. Multi-drug resistant tuberculosis in Northern Pakistan. J Pak Med Assoc. 2004;54:469–472(PUBMED)
8. rfan S, Hassan Q, Hasan R. Assessment of resistance in multi drug resistant tuberculosis patients. J Pak Med Assoc. 2006;56:397–400. [PubMed]
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MDR Bacilli-resistant to at least INH and RM.
Are the consequence of human error in any of
the following:
prescription of chemotherapy
management of drug supply
case management
process of drug delivery to the
patient
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MDR-TB plus - resistance to one of the fluroquinolones
Ofloxacin Levofloxacin Moxifloxacin AND-resistance to one of the second line injectables
AmikacinKanamycinCapreomycin
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XDR plus cycloserine, PAS, all
injectables
15 TDR isolates identified in IRAN
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Resistance to all major
anti-TB drugs
Treatable but requires
extensive chemotherapy
upto 2 yrs of treatment.
Expensive
Drugs are toxic to the
patient
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Previous treatment especially if prolonged
Contact with drug resistant patient
Country of origin East Europe Former USSR
Middle East South
and SE Asia
Latin America Africa
Age (In MDR area, commoner in children)
HIV (Where MDR common)
Substance abuse and homelessness
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Drug Gene
Rifampicin rpoB
Streptomycin rps
Isoniazid No:
base pairs
katG
inhA
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Programmatic Drugs: InadequateSupply/Quantity
Patients: Inadequate drug intake
Absence of guidance orInappropriate guidelinesNon-compliance with guidelinesInadequate training of health staffNo monitoring of treatmentPoorly organized orfunded TB control programmes
Non-availability ofcertain drugs (stock outsor delivery disruptions)Poor qualityPoor storage conditionsWrong dosages or combination
Poor adherence (orpoor DOT) – lack of Informationnon-availability of free drugsAdverse drug reactionsSocial and economic barriersMalabsorptionSubstance abusedisorders
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Treat with adequate number of drugs to prevent emergence of further resistance
- use more drugs if susceptibility tests pending (often start with 5-6 drugs)
DRUG SELECTION - at least 3 new drugs not previously not
used - those with proven or suspected
susceptibility - as many bactericidal drugs as possible -Any first line drugs with proven
susceptibility Limit toxicity a much as possible
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Step 1
Strep 2
Step 3
Use any
available
plus
One of these
plus
One of these
1st line drugsPZA & EBM
Fluroquinolones
LevofloxacinMoxifloxacin
Injectable agentsAmikacin
Capreomycin Streptomycin
Kanamycin
Oral 2nd line drugs
Cycloserine Ethionamide
PAS3rd line drugs
ImepenemMacrolidesLinezolid
Amoxicillin/Clavulante
Begin with a 1st line agents to which the isolateIs susceptibleAdd a fluroquinolones and an injectable drugBased on susceptibllity
Add 2nd line drugsUntil u have 4-6 drugs to which isolate is susceptible
if there are not 4-6 drugs Available, consider 3rd line in consult with MDRTB experts
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Treat at least 18-24 months after
conversion of the culture to the negative
Continue injectables to at least 6-12 months
after conversion of the culture to the
negative
Shorter therapy for limited, primary or early
disease
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Primarily available for INH & rifampin
gene probe for rpoB ( for Rifampicin)is
available in some countries & this serves
as a useful marker for MDR-TB
If a gene probe (rpoB) test - positive, then it
is reasonable to omit RMP and to use
SHEZ+MXF+cycloserine
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Careful history taking for previous treatment regimens.
Compliance of the drugs in the previous regime
Determine the status of sputum smears at all junctures (in
terms of positivity ,conversions and sensitivities – if available).
Confirmed/ Strongly suspect MDR TB
Counsel the Patient and family members
Send Tissue / sputum for culture and sensitivity testing (if
available)
Start MDR Regimen
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Depends on a number of factors:
How many drugs the organism is resistant to
(the fewer the better),
How many drugs the patient is given (Patients
treated with five or more drugs do better),
Whether an injectable drug is given or not (it
should be given for the first three months at
least),
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The expertise & experience of the physician
responsible
How co-operative the patient is with treatment
(treatment is long, requires persistence &
determination on the part of the patient),
HIV positive or not (HIV co-infection is
associated with an increased mortality
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Hurdles in the success of the treatment
Lack of awareness/misconceptions about
the disease
Late / improper diagnosis
Limited accessibility to diagnostic facilities
Incorrect treatment by doctors
Patients’ non-compliance to treatment
Socio-economic factors
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Dates and chemotherapy Smear results
Culture results
Susceptibilityresults
Radiologicalresults
Clinicalresults
a)Date of diagnosis: ..................
b ) Date of starting first course of chemotherapy:
Drugs taken (dose, frequency, duration) i..e.: H300, 7/7, 6 Months R450, 7/7, 6 Months S1g, 7/7, 2 Months
c) Date of completing or stopping first
course of chemotherapy
d) Date of starting second course of chemotherapy: ……………....................... Drugs taken (dose, frequency, duration) ......., .........., ........
......., .........., ........e) Date of completing second course of chemotherapy: ..........................
f) Date of starting third course of chemotherapy: ........................(to be continued ...)
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Resistance-
Suggested regimen
Length Comments
Isoniazid and PZI
Amik,
RIF,E,Mox
9 months to a year
Anticipate good response
Isoniazid and E
Amik,RIF,
PZI,Mox.
9-12/12
Isoniazid and RIF
Amik,PZI,
E,Mox.
At least 18/12
Consider surgery
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Resistance Suggested regimen
Length Comments
INH,RIF,
PZI
Amik,E,
Mox,Eth,Cy
18-24/12
After cul-ve
Consider surgery
INH,RIF,
PZI,E
Amik,Mox.Eth,Cy,Clar
As above As above
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The top priority is not the management but the prevention of MDR Tuberculosis
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In new cases
Best prevention - give each new case
of sputum positive pulmonary
tuberculosis an effective regimen of
short course chemotherapy with four
drugs at least for 4 months, given
under direct observation
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In the group of TB patients previously treated with one or several courses of chemotherapy & who remain sputum positive (by smear and/or culture), 3 subpopulations can be observed:
• patients excreting bacilli still susceptible to all antituberculosis drugs
• patients excreting bacilli resistant to at least isoniazid, but still susceptible to rifampicin;
• patients excreting bacilli resistant to at least isoniazid and rifampicin
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In patients who have failure after the 1st
course of chemotherapy ( WHO
recommended or any other)– WHO Tx
regimen of 8 months ( using 5 drugs for the 1st
2 months, 4 drugs in the 3rd month and 3 drugs
for the remaining 5 months ( 2
SHRZE/1HRZE/5HRE), given under direct
observation
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Rank
Drugs Average daily dosage
Type of antimycobacterial activity
1
2
3
4
5
6
7
Aminoglycosides
a. Streptomycin
b. Kanamycin/Amikacin
c. Capreomycin
Thioamides
(Ethionamide / rothionamide)
Pyrazinamide
Ofloxacin
Ethambutol
Cycloserine
PAS acid
15 mg/kg
10-20 mg/kg
20-30 mg/kg
7.5-15 mg/kg
15-20 mg/kg
10-20 mg/kg
10-12 g
Bactericidal against actively
multiplying organisms
Bactericidal
Bactericidal at acid pH 7.5-10
Bactericidal
Bacteriostatic
Bacteriostatic
Bacteriostatic
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Aminoglycosides Kanamycin, Amikacin, Capreomycin ( useful in cases with
tubercle bacilli resistant to streptomycin,
amikacin and kanamycin) Thiamides- Ethionamides Prothionamides
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Fluroquinolones Ofloxacin Ciprofloxacin (Complete cross resistance within
the group) Sparfloxacin – should be avoided due
to severe cutaneous side effects ( photo sensitisation)
Norfloxacin should not be used as it does not give adequate serum level
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Cycloserine ( or terizidone)- bactriostatic agent no cross reaction with other ATT limited use due to the high toxicity
Para-aminosalicyclic acid-valuable for preventing resistance to INH-& Streptomycin
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Treat for 6 months or observe without treatmnet
* use drugs source case is sensitive to
* Choose 2: EMB, FQN, PZA Follow for 2 years regardless of
treatment * Chest X-ray and clinical
evaluation
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1970’s Tanzania Dr Karel Styblo strategy
1991 WHO TB a global problem
In 1992 The WHO Global Tuberculosis Program
developed a new strategy-DOTS ( brand
name of the WHO Recommended TB
Control Strtegy)
1993 WHO promoted Styblo’s strategy (DOTS)
Implemented in 200+ countries
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That the highest ever number of infectious
patients – 2.3 million people – were cured.
With 87% of treated patients being cured,
the 85% global target was exceeded for the
first time since it was established in 1991
A total of 53 countries surpassed this
treatment milestone
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Directly
Observed
Treatment
Short-course
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To achieve universal access to high-quality
diagnosis and patient-centered treatment
To reduce suffering and socio-economic burden
associated with TB
To protect the poor and vulnerable populations
from TB, TB/HIV and MDR-TB
To support development of new tools and
enable their timely and effective use
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National TB Control Program adopted DOTS strategy first in 1995
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Political commitment with increased and
sustained financing
Case detection through quality assured
bacteriology
Standardized treatment with supervision and
patient support
An effective drug supply and management system
Monitoring and evaluation system, and impact
measurement
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DIRECTLY OBSERVED TB SHORT COURSE
Comprehensive TB management
strategy Consists of 5
elements Now expanded
Stop TB Strategy
DIRECTLY OBSERVED TREATMENT
A part of the DOTS strategy
Direct supervision of
individual patients to ensure treatment adherence
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Health inspectors
Pharmacists
Malaria field workers
Workplace
supervisors
Railwayschool
teachers
Cured patients
Wife of medical officers
Mid-wife
Self help group
volunteers
Senior dressers
Multi purpose health
workers
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Prompt sputum conversion, cessation
of transmission
Halts generation of resistant (MDR-TB)
strains
Lessening of relapse rates
Early recognition of drug toxicity
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Treatment with properly implemented
DOTS has a success rate exceeding 95%
prevents the emergence of further multi-
drug resistant strains of tuberculosis
The WHO extended the DOTS programme
in 1998 to include the treatment of MDR-
TB (called "DOTS-Plus").
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Country population 163,902,000
Established no. of new TB cases 297,108
Established TB incidence(all cases per one
lakh population)
181
DOTS population coverage (%) 99
Rate of new SS+c ases(per 100.000
population)
81
DOTS caes detection rate
(new SS+ cases) (%)
67
DOTS treatment success rate,2006
(new SS+ cases) (%)
88
New Multidrug resistant TB cases(%) 3.2
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New MDR-TB cases rose from 2.0 percent
in 2003 to 3.2 percent in 2007.
Pakistan accounts for 57 percent of the
MDR-TB burden within WHO’s Eastern
Mediterranean Region.
Extensively drug-resistant TB has not
been reported in the country.
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New developments in eradicating tuberculosis
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May 2009- a new antibiotic
Moxifloxacin has completed
phase II trial and is expected to
reduce the drug regimen by several
months
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Standard TB drugs are dissolved into/adsorbed to fine,
particulate carriers (simple and economical)
Can be given orally (as well as IV), in distinction to
liposomes
Taken up by RES, mononuclear cells and solid organs
Extremely long half-lives (give every 2 weeks?)
More effective sterilizing than std. drug forms
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A new compound exhibiting a completely
new mode of action (inhibition of ATP
synthase) against mycobacteria
The compound is being developed in
phase IIa trials for the treatment of active
tuberculosis as TMC207
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Cytokines IL-2 Gamma-interferon
Immunomodulators Mycobacterium vaccae
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Development of affordable newdrugs, diagnostics and vaccines
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BCG vaccine (for TB) currently administered against infection only reduces the risk of TB in infants but offers no protection against pulmonary TB and infection in adolescence or adulthood.
A new TB vaccine, developed at the Oxford University called MVA85A/AERAS-485 holds promise. It has entered Phase II b trial in April 2009 and is being carried out in South Africa.
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New challenges addressed by new Stop TB
Strategy
Strengthen TB control
Prevent drug resistance
Treat 50 million TB cases
Saves 14 million lives
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