Cutaneous adverse drug reactions to anti-tuberculosis drugs: state of the art and into the future
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Lehloenya, Rannakoe J.
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Univ Cape Town, Dept Med, Div Pulmonol, Lung Infect & Immun Unit, Western Cape, South Africa
Univ Cape Town, UCT Lung Inst, Western Cape, South Africa
Univ Cape Town, Dept Med, Div Dermatol, Western Cape, South AfricaUniv Cape Town, Dept Med, Div Pulmonol, Lung Infect & Immun Unit, Western Cape, South Africa
Lehloenya, Rannakoe J.
[1
,2
,3
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Dheda, Keertan
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Univ Cape Town, Dept Med, Div Pulmonol, Lung Infect & Immun Unit, Western Cape, South Africa
Univ Cape Town, UCT Lung Inst, Western Cape, South Africa
Univ Cape Town, Inst Infect Dis & Mol Med, Western Cape, South Africa
UCL Med Sch, Dept Infect, London, EnglandUniv Cape Town, Dept Med, Div Pulmonol, Lung Infect & Immun Unit, Western Cape, South Africa
Dheda, Keertan
[1
,2
,4
,5
]
机构:
[1] Univ Cape Town, Dept Med, Div Pulmonol, Lung Infect & Immun Unit, Western Cape, South Africa
[2] Univ Cape Town, UCT Lung Inst, Western Cape, South Africa
[3] Univ Cape Town, Dept Med, Div Dermatol, Western Cape, South Africa
[4] Univ Cape Town, Inst Infect Dis & Mol Med, Western Cape, South Africa
First- and second-line anti-tuberculosis drugs are associated with a diverse presentation of cutaneous adverse drug reactions (CADR), ranging from mild to life threatening. An individual drug can cause multiple types of CADR, and a specific type of CADR can be due to any anti-tuberculosis drug, which can make the management of tuberculosis (TB) following CADR challenging. The higher incidence of TB and CADR in HIV-infected persons makes TB-associated CADR a burgeoning problem for clinicians, particularly in high HIV-prevalence settings, This review discusses the pathogenesis, epidemiology, clinical presentation, diagnosis and management of TB-associated CADR. Clinical controversies including its impact on treatment outcomes, challenges in restarting optimal anti-tuberculosis therapy and the timing of highly active antiretroviral therapy initiation in those with HIV coinfection are also discussed. Finally, gaps in the current knowledge of TB-associated CADR have been identified and a research agenda has been proposed.
机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Bastuji-Garin, S
Fouchard, N
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Fouchard, N
Bertocchi, M
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Bertocchi, M
Roujeau, JC
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Roujeau, JC
Revuz, J
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Revuz, J
Wolkenstein, P
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Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, FranceUniv Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Bastuji-Garin, S
Fouchard, N
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Fouchard, N
Bertocchi, M
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Bertocchi, M
Roujeau, JC
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Roujeau, JC
Revuz, J
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机构:Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France
Revuz, J
Wolkenstein, P
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Univ Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, FranceUniv Paris 12, Hop Henri Mondor AP HP, Dept Dermatol, F-94010 Creteil, France