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      A Systematic Review on the Effect of HIV Infection on the Pharmacokinetics of First-Line Tuberculosis Drugs

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          Abstract

          Introduction

          Contrasting findings have been published regarding the effect of human immunodeficiency virus (HIV) on tuberculosis (TB) drug pharmacokinetics (PK).

          Objectives

          The aim of this systematic review was to investigate the effect of HIV infection on the PK of the first-line TB drugs (FLDs) rifampicin, isoniazid, pyrazinamide and ethambutol by assessing all published literature.

          Methods

          Searches were performed in MEDLINE (through PubMed) and EMBASE to find original studies evaluating the effect of HIV infection on the PK of FLDs. The included studies were assessed for bias and clinical relevance. PK data were extracted to provide insight into the difference of FLD PK between HIV-positive and HIV-negative TB patients. This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement and its protocol was registered at PROSPERO (registration number CRD42017067250).

          Results

          Overall, 27 studies were eligible for inclusion. The available studies provide a heterogeneous dataset from which consistent results could not be obtained. In both HIV-positive and HIV-negative TB groups, rifampicin (13 of 15) and ethambutol (4 of 8) peak concentration ( C max) often did not achieve the minimum reference values. More than half of the studies (11 of 20) that included both HIV-positive and HIV-negative TB groups showed statistically significantly altered FLD area under the concentration–time curve and/or C max for at least one FLD.

          Conclusions

          HIV infection may be one of several factors that reduce FLD exposure. We could not make general recommendations with respect to the role of dosing. There is a need for consistent and homogeneous studies to be conducted.

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          Most cited references58

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          Official American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America Clinical Practice Guidelines: Treatment of Drug-Susceptible Tuberculosis.

          The American Thoracic Society, Centers for Disease Control and Prevention, and Infectious Diseases Society of America jointly sponsored the development of this guideline for the treatment of drug-susceptible tuberculosis, which is also endorsed by the European Respiratory Society and the US National Tuberculosis Controllers Association. Representatives from the American Academy of Pediatrics, the Canadian Thoracic Society, the International Union Against Tuberculosis and Lung Disease, and the World Health Organization also participated in the development of the guideline. This guideline provides recommendations on the clinical and public health management of tuberculosis in children and adults in settings in which mycobacterial cultures, molecular and phenotypic drug susceptibility tests, and radiographic studies, among other diagnostic tools, are available on a routine basis. For all recommendations, literature reviews were performed, followed by discussion by an expert committee according to the Grading of Recommendations, Assessment, Development and Evaluation methodology. Given the public health implications of prompt diagnosis and effective management of tuberculosis, empiric multidrug treatment is initiated in almost all situations in which active tuberculosis is suspected. Additional characteristics such as presence of comorbidities, severity of disease, and response to treatment influence management decisions. Specific recommendations on the use of case management strategies (including directly observed therapy), regimen and dosing selection in adults and children (daily vs intermittent), treatment of tuberculosis in the presence of HIV infection (duration of tuberculosis treatment and timing of initiation of antiretroviral therapy), as well as treatment of extrapulmonary disease (central nervous system, pericardial among other sites) are provided. The development of more potent and better-tolerated drug regimens, optimization of drug exposure for the component drugs, optimal management of tuberculosis in special populations, identification of accurate biomarkers of treatment effect, and the assessment of new strategies for implementing regimens in the field remain key priority areas for research. See the full-text online version of the document for detailed discussion of the management of tuberculosis and recommendations for practice.
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            Therapeutic drug monitoring in the treatment of tuberculosis: an update.

            Tuberculosis (TB) is the world's second leading infectious killer. Cases of multidrug-resistant (MDR-TB) and extremely drug-resistant (XDR-TB) have increased globally. Therapeutic drug monitoring (TDM) remains a standard clinical technique for using plasma drug concentrations to determine dose. For TB patients, TDM provides objective information for the clinician to make informed dosing decisions. Some patients are slow to respond to treatment, and TDM can shorten the time to response and to treatment completion. Normal plasma concentration ranges for the TB drugs have been defined. For practical reasons, only one or two samples are collected post-dose. A 2-h post-dose sample approximates the peak serum drug concentration (Cmax) for most TB drugs. Adding a 6-h sample allows the clinician to distinguish between delayed absorption and malabsorption. TDM requires that samples are promptly centrifuged, and that the serum is promptly harvested and frozen. Isoniazid and ethionamide, in particular, are not stable in human serum at room temperature. Rifampicin is stable for more than 6 h under these conditions. Since our 2002 review, several papers regarding TB drug pharmacokinetics, pharmacodynamics, and TDM have been published. Thus, we have better information regarding the concentrations required for effective TB therapy. In vitro and animal model data clearly show concentration responses for most TB drugs. Recent studies emphasize the importance of rifamycins and pyrazinamide as sterilizing agents. A strong argument can be made for maximizing patient exposure to these drugs, short of toxicity. Further, the very concept behind 'minimal inhibitory concentration' (MIC) implies that one should achieve concentrations above the minimum in order to maximize response. Some, but not all clinical data are consistent with the utility of this approach. The low ends of the TB drug normal ranges set reasonable 'floors' above which plasma concentrations should be maintained. Patients with diabetes and those infected with HIV have a particular risk for poor drug absorption, and for drug-drug interactions. Published guidelines typically describe interactions between two drugs, whereas the clinical situation often is considerably more complex. Under 'real-life' circumstances, TDM often is the best available tool for sorting out these multi-drug interactions, and for providing the patient safe and adequate doses. Plasma concentrations cannot explain all of the variability in patient responses to TB treatment, and cannot guarantee patient outcomes. However, combined with clinical and bacteriological data, TDM can be a decisive tool, allowing clinicians to successfully treat even the most complicated TB patients.
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              Multidrug-resistant tuberculosis not due to noncompliance but to between-patient pharmacokinetic variability.

              It is believed that nonadherence is the proximate cause of multidrug-resistant tuberculosis (MDR-tuberculosis) emergence. The level of nonadherence associated with emergence of MDR-tuberculosis is unknown. Performance of a randomized controlled trial in which some patients are randomized to nonadherence would be unethical; therefore, other study designs should be utilized. We performed hollow fiber studies for both bactericidal and sterilizing effect, with inoculum spiked with 0.5% rifampin- and isoniazid-resistant isogenic strains in some experiments. Standard therapy was administered daily for 28-56 days, with extents of nonadherence varying between 0% and 100%. Sizes of drug-resistant populations were compared using analysis of variance. We also explored the effect of pharmacokinetic variability on MDR-tuberculosis emergence using computer-aided clinical trial simulations of 10 000 Cape Town, South Africa, tuberculosis patients. Therapy failure was only encountered at extents of nonadherence ≥60%. Surprisingly, isoniazid- and rifampin-resistant populations did not achieve ≥1% proportion in any experiment and did not achieve a higher proportion with nonadherence. However, clinical trial simulations demonstrated that approximately 1% of tuberculosis patients with perfect adherence would still develop MDR-tuberculosis due to pharmacokinetic variability alone. These data, based on a preclinical model, demonstrate that nonadherence alone is not a sufficient condition for MDR-tuberculosis emergence.
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                Author and article information

                Contributors
                +31 503614070 , j.w.c.alffenaar@umcg.nl
                Journal
                Clin Pharmacokinet
                Clin Pharmacokinet
                Clinical Pharmacokinetics
                Springer International Publishing (Cham )
                0312-5963
                1179-1926
                8 November 2018
                8 November 2018
                2019
                : 58
                : 6
                : 747-766
                Affiliations
                [1 ]ISNI 0000 0000 9558 4598, GRID grid.4494.d, Department of Clinical Pharmacy and Pharmacology, , University of Groningen, University Medical Center Groningen, ; PO Box 30.001, 9700 RB Groningen, The Netherlands
                [2 ]ISNI 0000 0004 0407 1981, GRID grid.4830.f, Unit of PharmacoTherapy, -Epidemiology and -Economics, Groningen Research Institute of Pharmacy, , University of Groningen, ; Groningen, The Netherlands
                [3 ]ISNI 0000 0000 9558 4598, GRID grid.4494.d, Department of Health Sciences, , University of Groningen, University Medical Center Groningen, ; Groningen, The Netherlands
                [4 ]ISNI 0000 0000 9558 4598, GRID grid.4494.d, Department of Internal Medicine-Infectious Diseases, , University of Groningen, University Medical Center Groningen, ; Groningen, The Netherlands
                [5 ]ISNI 0000 0004 0407 1981, GRID grid.4830.f, Unit of Pharmacokinetics, Toxicology and Targeting, Groningen Research Institute of Pharmacy, , University of Groningen, ; Groningen, The Netherlands
                [6 ]GRID grid.475435.4, Department of Infectious Diseases, , Rigshospitalet, ; Copenhagen, Denmark
                [7 ]ISNI 0000 0001 2214 904X, GRID grid.11956.3a, Department of Paediatrics and Child Health, , University of Stellenbosch, ; Cape Town, South Africa
                [8 ]ISNI 0000 0004 1937 1151, GRID grid.7836.a, Division of Clinical Pharmacology, Department of Medicine, , University of Cape Town, ; Cape Town, South Africa
                [9 ]ISNI 0000 0004 1767 6138, GRID grid.417330.2, National Institute for Research in Tuberculosis (ICMR), ; Chennai, India
                [10 ]ISNI 0000 0004 0367 5636, GRID grid.416716.3, National Institute for Medical Research, Mwanza Medical Research Centre, ; Mwanza, Tanzania
                [11 ]ISNI 0000 0004 1936 8091, GRID grid.15276.37, College of Medicine and Emerging Pathogens Institutes, , University of Florida, ; Gainesville, FL USA
                [12 ]ISNI 0000 0004 1937 1151, GRID grid.7836.a, Institute of Infectious Diseases and Molecular Medicine, Wellcome Centre for Infectious Diseases Research in Africa, , University of Cape Town, ; Cape Town, South Africa
                [13 ]GRID grid.452470.0, Dignitas International, ; Zomba, Malawi
                [14 ]ISNI 0000 0001 2113 2211, GRID grid.10595.38, Department of Medicine, College of Medicine, , University of Malawi, ; Blantyre, Malawi
                [15 ]ISNI 0000 0001 2113 8111, GRID grid.7445.2, Department of Medicine, , Imperial College London, ; London, UK
                [16 ]ISNI 0000 0004 1795 1830, GRID grid.451388.3, The Francis Crick Institute, ; London, UK
                Article
                716
                10.1007/s40262-018-0716-8
                7019645
                30406475
                efe9f063-b9b4-4f32-a69a-d8cb65771b8b
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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                © Springer Nature Switzerland AG 2019

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