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. Author manuscript; available in PMC: 2011 Jan 28.
Published in final edited form as: Int J Tuberc Lung Dis. 2010 Oct;14(10):1244–1251.

Table 3.

Diagnosis, management and outcomes of pediatric XDR-TB cases

Case 1 Case 2 Case 3 Case 4
Sputum smear result* Positive on 2nd specimen Positive on 4th specimen All 5 specimens negative All 2 specimens negative
Culture result* Positive on 1st specimen Positive on 3rd specimen Positive on 3rd specimen Positive on 2nd specimen
DST result All resistant to INH, RMP, SM, EMB, CFX, KM
Time to DST result, weeks 10 6 13 7.5
Chest radiograph findings at time of XDR-TB diagnosis Right ML infiltrate and right UL cavity Extensive bilateral infiltrates Left UL/LL infiltrates; right perihilar lymphadenopathy Left UL/LL consolidation
Intensive phase regimen Backbone of ETH, PAS, PZA, CS, CM
EMB, CLA, AM/CL CLA, AM/CL EMB, CLA, AM/CL EMB, CLA, AM/CL
Time to culture conversion, weeks§ 13 13 5 8
Medication side effects None None Acute psychosis, likely due to CS and efavirenz Behavioral changes due to CS
Weight gain, kg# 4.8 6.0 6.0 2.8
Change in CD4 count in cells/mm3 (% change in lymphocytes)** +356 (+7.1) (+6.0) Baseline data not available +60 (+6.0)
24-month survival Alive with mild bronchiectasis Thriving Thriving Alive with bronchiectasis and chronic lung disease
XDR-TB treatment outcome Cured Cured Cured Cured
*

Specimens obtained prior to initiation of XDR-TB treatment.

Interval between date of diagnostic sputum sample collection and receipt of DST results showing XDR-TB.

Added during month 5 of treatment due to impending drug shortages.

§

Culture conversion: 2 successive months of sputum cultures without growth of Mycobacterium tuberculosis while on XDR-TB treatment.

Initial culture conversion; Cases 1 and 2 had relapse of XDR-TB following initial culture conversion after defaulting from treatment; Cases 2–4 had an isolated positive sputum culture after culture conversion while remaining on full treatment, then re-converted to negative.

#

Weight gain: measured as difference in weight over 24-month survival period.

**

Measured after 7–15 months of initiating HAART, based on available data.

XDR-TB = extensively drug-resistant tuberculosis; DST = drug susceptibility testing; INH = isoniazid; RMP = rifampin; SM = streptomycin; EMB = ethambutol; CFX = ciprofloxacin; KM = kanamycin; ML = middle lobe; UL = upper lobe; LL = lower lobe; ETH = ethionamide; PAS = para-aminosalicylic acid; PZA = pyrazinamide; CS = cycloserine; CM = capreomycin; CLA = clarithromycin; AM/CL = amoxicillin/clavulanate.