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Issues in TB care  and financing Issues in TB care  and financing

Issues in TB care and financing - PowerPoint Presentation

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Issues in TB care and financing - PPT Presentation

Gesine MeyerRath Health Economics and Epidemiology Research Office HE 2 RO University of the Witwatersrand Boston University BEMF consolidation meeting 15 July 2011 Why TB financing ID: 736251

mdr treatment diagnosis cost treatment mdr cost diagnosis care hiv positive patients xpert culture negative months microscopy 2011 cases

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Slide1

Issues in TB care

and financingGesine Meyer-RathHealth Economics and Epidemiology Research Office (HE2RO)University of the Witwatersrand/ Boston UniversityBEMF consolidation meeting 15 July 2011Slide2

Why TB financing?

HIV care and treatment is better planned and funded than ever before in South AfricaLots of cost and epi data is knownHIV care has ear-marked, national-level funds (Conditional grant)HIV care has own vertical system including own distribution channels for drugsTB diagnosis and treatment uses outdated tools and drugs and produces shoddy outcomesVery few cost data available, not much epi dataTB care is funded at provincial level via Equitable share, like all other provincial programmesTB care is highly localised and integrated into horizontal systemsSlide3

TB issues

UninfectedSuspectCaseCuredMDR

XDR

Cured

PREVENTION

DIAGNOSIS

TB TREATMENT

MDR-TB TREATMENTSlide4

TB prevention

UninfectedSuspectPREVENTIONSlide5

TB preventionEarly HIV diagnosis and ART initiation

HCT: 11.9 million people tested, but no link to TB diagnosis and treatment, not enough link to ARTART initiation at >200 CD4 cells/µl<350 for patients with TB since April 2010Initiation at <500 or irrespective of CD4 cell count?CMX and INH prophylaxis for HIV+vesIPT: INH prophylaxis for 6 mts irrespective of CD4 cell count after excluding active TBINH stock-outs as a result of badly planned demandINH/CMX combination possible but still in developmentSlide6

TB diagnosis

UninfectedSuspectCaseDIAGNOSISSlide7

TB diagnosis: Issues

Coverage: Case findingIntensified Case Finding (ICF) campaign: visited 41,000 families and screened 112,000 contacts since Feb 2011Sensitivity of current diagnostics (smear microscopy)Time to result (culture, LPA, DST)Cost of newer diagnostics (Xpert MTB/RIF, line-probe assay, drug-susceptibility testing)Slide8

TB diagnosis: Current situation

Current algorithm starts with smear microscopySmear microscopy of sputum  technology more than 125 years oldSensitivity of smear microscopy (ability to find TB when it is there) is approximately 70%Sensitivity of smear microscopy in HIV+ population drops to 35-45%Current algorithm depends on culture Culture highly sensitive (considered ‘gold standard’)However, takes 2-6 weeks for resultsHigh rates of contamination, missing resultsSlide9

Possible solution: Xpert MTB/RIF

The Xpert MTB/RIF (Cepheid) test detects TB and rifampicin resistance (indication of MDR-TB) in less than 2 hoursThe sensitivity of Xpert MTB/RIF has been shown to be 86% in a SA demonstration studyHIV status does NOT affect sensitivity of XpertSlide10

Xpert roll-out: Planned timing

FAST SCALE-UP scenario: Full coverage by December 2012 (Ministerial mandate) SLOW SCALE-UP scenario: Full coverage by September 2013FAST SCALE-UP | June 2011 | Dec 2011 | Sept 2011 | Mar 2011 | Dec 2011 | Dec 2012SLOW SCALE-UP | June 2011 | Dec 2011 | Sept 2011 | Mar 2012 | Mar 2013 | Sept 2013

PHASES

| PILOT | FULL PILOT|HIGH CASE| GF XPERT | CONTROL

| DISTRICTS| ALL LABSSlide11

VISIT 3

VISIT 2

VISIT 1

GeneXpert

if negative

if positive

if unsuccessful

RIF resistant/

inconclusive

(MTB+/RIF+)

Sputum microscopy

TB culture

+ LPA +/- DST

TB diagnosis

HIV negative

Antibiotics

if resolved

if failed

if positive

TB diagnosis

if positive

TB diagnosis

Antibiotics

Chest X-ray

TB culture + LPA +/- DST

Chest X-ray

TB culture + LPA +/- DST

if positive

TB diagnosis

if negative

HIV status

HIV positive/

status

unknown

HIV positive/

status

unknown

HIV status

Antibiotics

TB culture + LPA +/- DST

if negative

if positive

TB diagnosis

Patients with suspected pulmonaryMTB

Xpert algorithm

Stop

Chest X-ray

Repeat GeneXpert

Sputum microscopy

TB culture

+ LPA +/- DST

if positive

TB diagnosis

Stop

Stop

HIV negative

HIV positive/

status

unknown

Antibiotics

if positive

TB diagnosis

if positive

TB diagnosis

Sputum microscopy

Antibiotics

Chest X-ray

Chest X-ray

if positive

TB diagnosis

if negative

HIV status

TB culture

+ LPA +/- DST

if negative

Stop

if resolved

if failed

Stop

Patients with TB history

Current guidelines

Patients without TB history

All patients

if un-

successful

HIV negative

HIV status

Antibiotics

TB culture + LPA

if negative

Chest X-ray

Stop

Stop

TB diagnosis

HIV positive

if negative

if positive

TB diagnosis

Sputum microscopy

if positive

Stop

if negative

Stop

if negativeSlide12

Xpert roll-out: Cost input

Cost itemCost in 2011 ZARTB diagnostics

Xpert MTB/RIF test

R190-220

Sputum microscopy (fluorescent microscopy)

R26

TB culture (liquid medium, growth)

R114

TB culture (liquid medium, no growth)

R87

Line probe assay (LPA) for all positive cultures

R189

Drug susceptibility test (DST) (first-line drugs only)

R519

Chest x-ray

R110

Antibiotic

trial

R19

Clinic visit: Nurse

R71

Clinic visit: Physician

R130

TB treatment

- First-line treatment (non- resistant)

R3,441

- Second-line treatment (non-resistant)

R6,806

- RIF monoresistance

R29,677

- INH monoresistance

R6,275

- Multi-drug resistance (outpatient care only)

R29,677Slide13

Xpert roll-out: Results of National TB Cost Model

Xpert leads to an increase of30% in TB cases diagnosed 76% in MDR cases identified39% in number of patients treated55% in the cost of the TB diagnostic programme32% in the outpatient cost of the TB treatment programmeif scaled-up fastUnder the Xpert scenario, 87% of diagnosed patients are diagnosed by Xpert83% are diagnosed after the first visitSlide14

TB treatment

UninfectedSuspectCaseCuredMDRTB TREATMENTSlide15

Patients with diagnosed pulmonaryMTB

Regimen 1(RHZE for 2 months, RH for 4 months)Patients without TB history(New cases)

Regimen 2

(RHZES for 2 months,

RHZE for 1 month,

RHE for 4 months)

Patients with TB history

(

Retreatment cases, old guidelines only

)

RHZE for 2 months,

RH for 4 months

+ OFL for 6 months

Patients with

INH mono-resistance

KNM, ETH, PZA, OFL+ TZ for 6 months

+ ETH, OFL+ TZ for 18 months

Patients with

RIF mono-resistance

Patients with

multi-drug resistant TB (MDR-TB)

KNM, ETH, PZA, OFL + TZ for 6 months

+ ETH, OFL + TZ for 18 months

+ Inpatient care until culture -Slide16

TB treatment: Non-resistant TBCommunity-based treatment

Good coverage, but low quality:Low completion rateLow cure rateHigh MDR and XDR rate2008 NHLS data: 6,219 MDR cases and 576 XDR casesCommunity-based system needs re-strengthening PHC revitalisation Community health-worker framework Intensified case-finding (ICF) campaignSlide17

MDR/ XDR-TB treament

UninfectedSuspectCaseCuredMDR

XDR

Cured

MDR-TB TREATMENTSlide18

MDR-TB treatment: Issues

Cost of drugs and monitoring of side effectsCentralised vs. decentralised care; inpatient vs. community careInfection controlPatient autonomyOperational challengesDrug supply chainsAdministration of daily injectibles for 6 monthsImproving outcomesCure rates between 33% and 45%Default rates up to 70%Death rate at Tugela Ferry after 1 year 75% (2005-2007)Slide19

MDR-TB treatment: Current situation

MDR-TB care differs vastly by provinceKZN: mostly community care; GP: exclusively centralised careCurrent guidelines prescribe inpatient care until culture negative (2 cultures taken 30 days apart)currently at specialised MDR/ XDR hospitals (9 specialised, 11 decrentralised units)73% of known MDR/ XDR cases in 2008 were hospitalisedon average 4 monthsnot enough capacity (1,854 beds in Feb 2010), waiting listat average cost per patient-day equivalent (R 1,069) 4 months cost R163,000Slide20

MDR-TB treatment: Decentralised care

Decentralisation plan for MDR care approved by National Health CouncilRationale:Low capacity and infection risk while waitingNosocomial transmission of MDR/XDR-TBPatients abscond due to lack of recreational facilities, family responsibilities and lack of incomeEven if ambulant, monthly trips to centralised hospitals are difficultDecentralised care is uncoordinated and chaoticSlide21

Planned guidelines:MDR-TB treatment at MDR units in TB hospitals (district and sub-district level) and at PHC clinicsInpatient treatment for 8 weeks or until

2 consecutive sputum smears negativeFollow-up at community level by PHC staff or mobile units and DOTS plus supportersMDR-TB treatment: Decentralised careSlide22

Summary: Cost issues IVery few data available

Cost of diagnosis modelledCost of treatment: 1 study of community-based treatment (Sinanovic et al Int J TB Lung Dis 2003)1 study on cost of care for HIV-co-infected patients (Cleary et al Cost Effect Resource Alloc 2006)No data on cost of MDR careStudies on real cost of Xpert roll-out and on cost of MDR-TB inpatient care plannedSlide23

Summary: Cost issues IIICF

: more suspects (target: 10% growth every year)Xpert: 30% more cases, 76% more MDR cases, 39% more patients on treatmentHigher costICF: lower smear sensitivity in suspectsXpert: more cases treated, lower transmission, less new cases (including of MDR-TB)MDR/XDR-TB treatment decentralised with less inpatient careLower cost