APAAACI clinical pathway on direct provocation testing for penicillin allergy delabeling

Author:

Li Philip Hei1,Thong Bernard Yu-Hor2,Pawankar Ruby3,Jeewandara Chandima4,Lobo Rommel Crisenio M.5,Kang Hye-Ryun6,Mahesh Padukudru Anand7,Meng Juan8,Munkhbayarlakh Sonomjamts9,Pham Duy Le10,Rerkpattanapipat Ticha11,Tang Min-Moon12,Yamaguchi Masao13,Abdul Latiff Amir Hamzah14,Rengganis Iris15,Wang Jiu-Yao16,Zhang Luo17,Lucas Michaela1819

Affiliation:

1. Division of Rheumatology and Clinical Immunology, Department of Medicine, Queen Mary Hospital, University of Hong Kong, Hong Kong

2. Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore

3. Department of Pediatrics, Nippon Medical School, Tokyo, Japan

4. Allergy Immunology and Cell Biology Unit, University of Sri Jayewardenepura, Sri Lanka

5. Fe del Mundo Medical Center, Quezon City, Philippines

6. Division of Allergy and Clinical Immunology, Department of Internal Medicine, Seoul National University College of Medicine/Seoul National University Hospital, South Korea

7. Department of Respiratory Medicine, JSS Medical College, JSSAHER, Mysore, Karnataka, India

8. Allergy Center, West China Hospital, Sichuan University, China

9. Department of Pulmonology & Allergology, School of Medicine, Mongolian National University of Medical Sciences, Mongolia

10. Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam

11. Allergy Immunology and Rheumatology Division, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Thailand

12. Department of Dermatology, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia

13. Division of Respiratory Medicine, Third Department of Medicine, Teikyo University Chiba Medical Center, Ichihara-shi, Chiba, Japan

14. Allergy & Immunology Centre Pantai Hospital Kuala Lumpur, Malaysia.

15. Division of Allergy and Clinical Immunology, Department of Internal Medicine, Faculty of Medicine Universitas Indonesia, Cipto Mangunkusumo General Hospital, Jakarta, Indonesia

16. Allergy, Immunology, and Microbiome (A.I.M.) Research Centre, China Medical University Children’s Hospital, Taichung, Taiwan

17. Department of Otolaryngology-Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, China

18. Department of Clinical Immunology, Sir Charles Gairdner Hospital, Perth Children’s Hospital, Perth, Western Australia, Australia

19. Medical School, University of Western Australia, Nedlands, Western Australia, Australia

Abstract

Background: Allergy to penicillin is commonly reported in many countries and is an overwhelming global public health concern. Penicillin allergy labels can lead to the use of less effective antibiotics and can be associated with antimicrobial resistance. Appropriate assessment of suspected penicillin allergy (often including skin testing, followed by drug provocation testing [DPT] performed by allergists) can prevent the unnecessary restriction of penicillin or delabelling. Many countries in the Asia Pacific (AP) have very limited access to allergy services, and there are significant disparities in the methods of evaluating penicillin allergy. Therefore, a clinical pathway for the management of penicillin allergy is essential. Objectives: To develop a risk-stratified clinical pathway for delabeling penicillin allergy, taking into account the distinct epidemiology, patient/sensitization profiles, and disparities of allergy services or facilities within the AP. Methods: A risk-stratified penicillin allergy delabeling clinical pathway was formulated by the Drug Allergy Committee of the Asia Pacific Association of Allergy, Asthma and Clinical Immunology. and members of the Penicillin Allergy Disparities survey in AP each representing one country/region of the AP. The clinical pathway was tested based on a database of anonymized patients who were sequentially referred for and completed penicillin allergy evaluation in Hong Kong. Results: The clinical pathway was piloted employing a “hub-and-spoke” approach to foster multidisciplinary collaboration between allergists and nonallergists. A simulation run of the algorithm on a retrospective Hong Kong cohort of 439 patients was performed. Overall, 367 (84%) of patients were suitable for direct DPT and reduced the need for skin testing or specialist’s care for 357 (97%) skin test-negative individuals. Out of the skin test-negative patients, 345 (94%) patients had a negative DPT. Conclusions: This risk-stratification strategy for direct oral DPT can reduce the need for unnecessary skin testing in patients with low-risk penicillin allergy histories. The hub and spoke model of care may be considered for further piloting and validation in other AP populations that lack adequately trained allergists.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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