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Search: L773:1537 6591 > (2020-2022) > (2022) > Hesseling Anneke C. > Optimizing Dosing a...

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Optimizing Dosing and Fixed-Dose Combinations of Rifampicin, Isoniazid, and Pyrazinamide in Pediatric Patients With Tuberculosis : A Prospective Population Pharmacokinetic Study

Denti, Paolo (author)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa.
Wasmann, Roeland E. (author)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa.
van Rie, Annelies (author)
Univ Antwerp, Family Med & Populat Hlth, Fac Med, Antwerp, Belgium.
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Winckler, Jana (author)
Stellenbosch Univ, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa.
Bekker, Adrie (author)
Stellenbosch Univ, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa.
Rabie, Helena (author)
Stellenbosch Univ, Dept Paediat & Child Hlth, Cape Town, South Africa.;Stellenbosch Univ, FAMily Ctr Res Ubuntu FAMCRU, Cape Town, South Africa.;Tygerberg Hosp, Cape Town, South Africa.
Hesseling, Anneke C. (author)
Stellenbosch Univ, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa.
van der Laan, Louvina E. (author)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa.;Stellenbosch Univ, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa.
Gonzalez-Martinez, Carmen (author)
Malawi Liverpool Wellcome Trust Clin Res Programm, Blantyre, Malawi.;Univ Liverpool Liverpool Sch Trop Med, Liverpool, Merseyside, England.
Zar, Heather J. (author)
Univ Cape Town, Red Cross War Mem Childrens Hosp, Dept Paediat & Child Hlth, Cape Town, South Africa.;Univ Cape Town, SAMRC Unit Child & Adolescent Hlth, Cape Town, South Africa.
Davies, Gerry (author)
Univ Liverpool, Inst Translat Med, Dept Mol & Clin Pharmacol, Liverpool, Merseyside, England.;Univ Liverpool, Inst Infect & Global Hlth, Dept Clin Infect Microbiol & Immunol, Liverpool, Merseyside, England.
Wiesner, Lubbe (author)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa.
Svensson, Elin, 1985- (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Institutionen för farmaci,Radboud Univ Nijmegen, Radboud Inst Hlth Sci, Dept Pharm, Med Ctr, Nijmegen, Netherlands.;Uppsala Univ, Dept Pharm, Uppsala, Sweden.
McIlleron, Helen M. (author)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa.;Univ Cape Town, Inst Infect Dis & Mol Med, Wellcome Ctr Infect Dis Res Africa CIDRI Africa, Cape Town, South Africa.
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Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa Univ Antwerp, Family Med & Populat Hlth, Fac Med, Antwerp, Belgium. (creator_code:org_t)
2021-10-19
2022
English.
In: Clinical Infectious Diseases. - : OXFORD UNIV PRESS INC. - 1058-4838 .- 1537-6591. ; 75:1, s. 141-151
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background In 2010, the World Health Organization (WHO) revised dosing guidelines for treatment of childhood tuberculosis. Our aim was to investigate first-line antituberculosis drug exposures under these guidelines, explore dose optimization using the current dispersible fixed-dose combination (FDC) tablet of rifampicin/isoniazid/pyrazinamide; 75/50/150 mg, and suggest a new FDC with revised weight bands. Methods Children with drug-susceptible tuberculosis in Malawi and South Africa underwent pharmacokinetic sampling while receiving first-line tuberculosis drugs as single formulations according the 2010 WHO recommended doses. Nonlinear mixed-effects modeling and simulation was used to design the optimal FDC and weight-band dosing strategy for achieving the pharmacokinetic targets based on literature-derived adult AUC(0-24h) for rifampicin (38.7-72.9), isoniazid (11.6-26.3), and pyrazinamide (233-429 mg center dot h/L). Results In total, 180 children (42% female; 13.9% living with human immunodeficiency virus [HIV]; median [range] age 1.9 [0.22-12] years; weight 10.7 [3.20-28.8] kg) were administered 1, 2, 3, or 4 FDC tablets (rifampicin/isoniazid/pyrazinamide 75/50/150 mg) daily for 4-8, 8-12, 12-16, and 16-25 kg weight bands, respectively. Rifampicin exposure (for weight and age) was up to 50% lower than in adults. Increasing the tablet number resulted in adequate rifampicin but relatively high isoniazid and pyrazinamide exposures. Administering 1, 2, 3, or 4 optimized FDC tablets (rifampicin/isoniazid/pyrazinamide 120/35/130 mg) to children < 6, 6-13, 13-20. and 20-25 kg, and 0.5 tablet in < 3-month-olds with immature metabolism, improved exposures to all 3 drugs. Conclusions Current pediatric FDC doses resulted in low rifampicin exposures. Optimal dosing of all drugs cannot be achieved with the current FDCs. We propose a new FDC formulation and revised weight bands. Current pediatric dosing guidelines lead to infant rifampicin exposures much lower than in adults, whereas isoniazid and pyrazinamide exposures are similar. A new fixed-dose combination (FDC) with rifampicin/isoniazid/pyrazinamide 120/35/130 mg and weight bands of < 6, 6-13, 13-20, and 20-25 kg could improve treatment.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

children
first-line tuberculosis treatment
fixed-dose combination
NONMEM
pharmacokinetics

Publication and Content Type

ref (subject category)
art (subject category)

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