Efficacy and tolerability of desensitization in the treatment of delayed drug hypersensitivities to anti-tuberculosis medications. (February 2019)
- Record Type:
- Journal Article
- Title:
- Efficacy and tolerability of desensitization in the treatment of delayed drug hypersensitivities to anti-tuberculosis medications. (February 2019)
- Main Title:
- Efficacy and tolerability of desensitization in the treatment of delayed drug hypersensitivities to anti-tuberculosis medications
- Authors:
- Ban, Ga-Young
Jeong, Yoon-Jeong
Lee, So-Hee
Shin, Seung-Soo
Shin, Yoo-Seob
Park, Hae-Sim
Kim, Seung-Hyun
Ye, Young-Min - Abstract:
- Abstract: Background: Delayed drug hypersensitivity to first-line anti-tuberculosis medication is a major challenge in tuberculosis treatment. Objective: This study was performed to investigate the efficacy/tolerability of desensitization therapy in treatment of first-line anti-tuberculosis medication hypersensitivity and the usefulness of immunologic evaluation therein. Methods: This study was conducted as a prospective, observational cohort study. Subjects who experienced hypersensitivity reactions, including maculopapular exanthema (MPE) and drug reaction with eosinophilia and systemic symptoms (DRESS), to first-line anti-tuberculosis medications (isoniazid [INH], ethambutol [EMB], rifampin [RFP], and pyrazinamide [PZA]) were enrolled. Patch, intradermal, lymphocyte transformation, and oral provocation tests were performed to determine culprit drugs, which were desensitized with rapid and graded challenge protocols. Breakthrough reactions (BTRs) during or after desensitization were assessed. Results: In total, 31 desensitization treatments (INH, 8; EMB, 8; RFP, 11; PZA, 4) to 12 patients (8 with MPE and 4 with DRESS) were performed. The overall success rate of desensitization was 80.7%. All the study subjects except one completed the full course of anti-tuberculosis treatment. The overall BTR free rate was 64.5%. Sixteen (80%) treatments for MPE and four (36.4%) for DRESS were BTR free ( P = 0.023). Drugs that were positive on any two of three immunologic studies showedAbstract: Background: Delayed drug hypersensitivity to first-line anti-tuberculosis medication is a major challenge in tuberculosis treatment. Objective: This study was performed to investigate the efficacy/tolerability of desensitization therapy in treatment of first-line anti-tuberculosis medication hypersensitivity and the usefulness of immunologic evaluation therein. Methods: This study was conducted as a prospective, observational cohort study. Subjects who experienced hypersensitivity reactions, including maculopapular exanthema (MPE) and drug reaction with eosinophilia and systemic symptoms (DRESS), to first-line anti-tuberculosis medications (isoniazid [INH], ethambutol [EMB], rifampin [RFP], and pyrazinamide [PZA]) were enrolled. Patch, intradermal, lymphocyte transformation, and oral provocation tests were performed to determine culprit drugs, which were desensitized with rapid and graded challenge protocols. Breakthrough reactions (BTRs) during or after desensitization were assessed. Results: In total, 31 desensitization treatments (INH, 8; EMB, 8; RFP, 11; PZA, 4) to 12 patients (8 with MPE and 4 with DRESS) were performed. The overall success rate of desensitization was 80.7%. All the study subjects except one completed the full course of anti-tuberculosis treatment. The overall BTR free rate was 64.5%. Sixteen (80%) treatments for MPE and four (36.4%) for DRESS were BTR free ( P = 0.023). Drugs that were positive on any two of three immunologic studies showed significantly high BTR rates ( P = 0.014), although this was not correlated with desensitization failure rate. Conclusion: Rapid desensitization therapy to multiple anti-tuberculosis medications for delayed drug hypersensitivity was safe and successful. Combination of multiple immunologic evaluations may predict BTR although it needs validation in larger studies. Highlights: The overall success rate of desensitization to anti-tuberculosis medications was 80.7% in the present study. The breakthrough reaction free rate of desensitization to anti-tuberculosis medications was 64.5%. Combination of multiple immunologic evaluations may predict the occurrence of breakthrough reaction. … (more)
- Is Part Of:
- Respiratory medicine. Volume 147(2019)
- Journal:
- Respiratory medicine
- Issue:
- Volume 147(2019)
- Issue Display:
- Volume 147, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 147
- Issue:
- 2019
- Issue Sort Value:
- 2019-0147-2019-0000
- Page Start:
- 44
- Page End:
- 50
- Publication Date:
- 2019-02
- Subjects:
- Desensitization -- Delayed drug hypersensitivity -- Anti-tuberculosis medication
BTR breakthrough reaction -- DRESS drug reaction with eosinophilia and systemic symptoms -- EMB ethambutol -- IM intramuscular injection -- INH isoniazid -- IV intravenous injection -- LTT lymphocyte transformation test -- MPE maculopapular exanthema -- PZA pyrazinamide -- RFP rifampin -- SCAR severe cutaneous adverse reaction -- SImax maximum stimulation index
Chest -- Diseases -- Periodicals
Chest -- Diseases -- Great Britain -- Periodicals
Respiratory organs -- Diseases -- Periodicals
Respiratory Tract Diseases -- Periodicals
Appareil respiratoire -- Maladies -- Périodiques
Thorax -- Maladies -- Périodiques
Appareil respiratoire -- Maladies -- Traitement -- Périodiques
Electronic journals
616.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09546111 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/09546111 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/09546111 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.rmed.2018.12.017 ↗
- Languages:
- English
- ISSNs:
- 0954-6111
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7777.661900
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