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. 2021 May 15;9(5):e04249. doi: 10.1002/ccr3.4249

Which immunosuppressive drug is preferred in the treatment of toxic epidermal necrolysis during COVID‐19 outbreak?

Saeedeh Farajzadeh 1, Najmeh Ahramiyanpour 1,
PMCID: PMC8123742  PMID: 34026201

Abstract

Cyclosporine is an effective and safe immunosuppressant in the management of Toxic epidermal necrolysis (TEN) during COVID‐19 outbreak for patients that intravenous immunoglobulin (IVIG) is contraindicated or is not affordable.

Keywords: calcineurin inhibitors, COVID‐19, cyclosporine, immunosuppressant, toxic epidermal necrolysis


Cyclosporine is an effective and safe immunosuppressant in the management of Toxic epidermal necrolysis (TEN) during COVID‐19 outbreak for patients that intravenous immunoglobulin (IVIG) is contraindicated or is not affordable.

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1. INTRODUCTION

Toxic epidermal necrolysis (TEN) is a serious drug reaction. Its proper cure would be challenging especially during COVID‐19 outbreak because of a dilemma regarding selecting the immunosuppressive drug. In this case presentation, we report a case of TEN who treat successfully with cyclosporine during COVID‐19 outbreak in a referral COVID‐19 hospital.

Toxic epidermal necrolysis (TEN) is a rare drug reaction associated with high mortality rate. 1 TEN presents with erythematous and dusky maculopapular rash that progresses to flaccid blisters, epidermal erosion, necrosis, and skin detachment. 1 , 2 , 3 Drug hypersensitivity is the most common cause of TEN. TEN can be associated with infections, systemic diseases, malignancies, and autoimmune conditions. 4 , 5 , 6 While there is no gold standard treatment for TEN, systemic corticosteroid, intravenous immunoglobulin (IVIG), cyclosporine, and tumor necrosis factor (TNF) inhibitors is optional drugs for the management of TEN. 1 , 2 , 3 , 4

Management of TEN is always challenging especially during COVID‐19 outbreak because use of the immunosuppressive drugs might have both beneficial and harmful effects on COVID‐19 course. 7 As we know there is not any study to compare the effects of different immunosuppressive drugs such as cyclosporine or prednisolone on TEN patients who are predisposed to COVID‐19. Selecting an immunosuppressive drug in a patient with TEN is challenging and troublesome. Here, we report a case of TEN who treat successfully with cyclosporine during COVID‐19 outbreak in a referral corona hospital.

2. CASE SYNOPSIS

A 24‐year‐old man came into the emergency department with a 4 days history of painful generalized dusky rash on his body associated mucosal surface involvement. His past medical history was positive for bipolar mood disorder. He was on carbamazepine and valproate sodium for the last 2 years and lamotrigine during the last 2 weeks.

On arrival to the emergency room, the patient was oriented and his vital signs were stable (Bp: 130/80 mm Hg, pulse rate: 80 beats per minute, temperature: 36.9℃, respiratory rate: 16 per minute, and O2 saturation: 99%). Physical examination described more than 50% of body surface area involvement. Skin lesions were as painful, dusky, and purpuric macules and patches of irregular size and shape on the trunk and extremities. Flaccid blisters with serosal fluid and detached epidermal surface on the neck and chest were detected (Figure 1). The Nikolsky sign was positive. Hemorrhagic crust, lips erosion, erythema of buccal mucosa, conjunctivitis, and facial edema are seen He also complained of photophobia and painful dysphagia. His SCORTEN (SCORs of Toxic Epidermal Necrolysis) was 2.

FIGURE 1.

FIGURE 1

On arrival skin lesions

Laboratory tests revealed exclusively a mild leukopenia while other results were negative or in normal ranges: potassium: 4 mmol/L, serum creatinine: 1.1 mg/dL, serum urea: 12 mmol/L, serum bicarbonate: 22 mmol/L, serum glucose: 10 mmol/L, white blood cells: 3.5 μL, hemoglobin: 13.7 g/dL, platelets: 420 000, aspartate transaminase: 24 U/L, alanine aminotransferase: 16 U/L, albumin: 36 g/L.

The patient was admitted with a diagnosis of TEN into the dermatology ward of Afzalipour hospital, of Kerman University of Medical Sciences, Iran that also is a referral COVID‐19 center hospital in Kerman. Lamotrigine was stopped and he was managed with supportive care, wound care, and thrombotic prophylaxis. As corticosteroid is rather controversial during COVID‐19 outbreak and IVIG which is the first choice of treatment was not afforded for the patient, we worked up to start cyclosporine. The blood pressure, electrolytes, and cholesterol were normal. Therefore, we started cyclosporine 4 mg/kg/day.

Within the first 36 hours after starting cyclosporine, the patient showed a dramatic response to the treatment. No new bullae formation was detected, and there was a reduction in erythema and erosion. The evidence of re‐epithelization was observed on the third day and the Nikolsky sign became negative (Figure 2). Meanwhile, blood pressure and kidneys’ function were normal.

FIGURE 2.

FIGURE 2

Improved skin lesions at day 4 of admission after starting cyclosporine

Eventually, he was discharged after 1 week with prescription of the cyclosporin 2 mg/kg/day for another 1 week. He informed respecting the possibility of relapse. One week later, the patient referred to our clinic. Skin and mucosal lesions improved, and the cyclosporine therapy was discontinued.

3. DISCUSSION

Although systemic corticosteroid, IVIG, cyclosporine, and TNF inhibitors are optional drugs in managing TEN, it is still controversial about the gold standard treatment for TEN. 1 , 4 During COVID‐19 outbreak, the management of TEN has encountered an additive challenge. Because use of the immunosuppressive drug, especially like prednisolone and cyclosporine, is controversial. 8 It seems IVIG is the best option for the management of TEN, because IVIG is human immunoglobulin and can strengthen the immune system. 9

An important issue in patients that IVIG is not affordable, as it is the case in our patient, or is contraindicated, in which one of immunosuppressive drugs can be used in the management of TEN during COVID‐19 outbreak. As we know, there is not any study in COVID‐19 outbreak to compare the effects of different immunosuppressive drugs such as cyclosporine and prednisolone on TEN patients.

Use of corticosteroid, which is the routine choice in treating TEN patients, is controversial in COVID‐19 outbreak especially among critical patients. 10 , 11 Albeit, it appears that corticosteroids can be effective in severe COVID‐19 cases, its routine use is not supported in the literature. 12 , 13 , 14 On the other hand, due to the increasing mortality of seasonal epidemic of influenza among corticosteroid users, administrating corticosteroids in TEN patients would be of concern. 15 Therefore, we discarded the use of corticosteroid.

We decided to start cyclosporine, as it can be a good treatment option in COVID‐19 outbreak due to several reasons. First, in Kirchhof et al 16 cohort study, the relative mortality of TEN patients who were treated with cyclosporine was lower than those with IVIg. Second, cyclosporine might be associated with a rapid re‐epithelialization 17 and reduce duration of hospitalization, 17 , 18 which can reduce the risk of COVID‐19 in critical patients during hospitalization. Third, cyclosporine can inhibit influenza A virus. 19 forth, in vitro studies showed that cyclosporine can inhibit immunophilin pathway and by this way, it can inhibit replication of coronavirus. 8 , 19 , 20 , 21 , 22 Fifth, COVID‐19 mortality is highly linked to the cytokine storm and cyclosporine can be beneficial during the inflammatory phase of COVID‐19. 21 , 22 Sixth, Cavagana et al 22 reported that clinical course of COVID‐19 patients on calcineurin inhibitors (CNIs) is generally mild with a low risk of superinfection. Finally, although cyclosporine is an immunosuppressant agent, infections are not one of its common side effects. 23

4. CONCLUSION

Intravenous immunoglobulin is the best treatment option in the management of TEN during COVID‐19 outbreak. For those IVIG is contraindicated or is not affordable, cyclosporine can be a better choice than other immunosuppressant drugs. As patients on cyclosporine can benefit its antiviral effects and have a shorter hospital admission stay.

CONFLICT OF INTEREST

The authors declare no conflicts of interest.

AUTHOR CONTRIBUTION

SF: involved in follow‐up and visit, data collection, and manuscript review. NA: involved in follow‐up and visit, data collection, and manuscript drafting.

ETHICAL APPROVAL

The subject signed the written informed consent.

ACKNOWLEDGMENTS

Published with written consent of the patient.

Farajzadeh S, Ahramiyanpour N. Which immunosuppressive drug is preferred in the treatment of toxic epidermal necrolysis during COVID‐19 outbreak?. Clin Case Rep. 2021;9:e04249. 10.1002/ccr3.4249

DATA AVAILABILITY STATEMENT

Data are available upon request to the corresponding author, Najmeh Ahramiyanpour MD

REFERENCES

  • 1. Kinoshita Y, Saeki H. A review of toxic epidermal necrolysis management in Japan. Allergol Int. 2017;66(1):36‐41. [DOI] [PubMed] [Google Scholar]
  • 2. Rijal JP, Pompa T, Giri S, Bhatt VR. A case of toxic epidermal necrolysis caused by trimethoprim‐sulfamethoxazole. BMJ Case Rep. 2014;2014:bcr2013203163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Mukasa Y, Craven N. Management of toxic epidermal necrolysis and related syndromes. Postgrad Med J. 2008;84(988):60‐65. [DOI] [PubMed] [Google Scholar]
  • 4. Hasegawa A, Abe R. Recent advances in managing and understanding Stevens‐Johnson syndrome and toxic epidermal necrolysis. F1000Research. 2020;9:612. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Harr T, French LE. Toxic epidermal necrolysis and Stevens‐Johnson syndrome. Orphanet J Rare Dis. 2010;5:39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Charlton OA, Harris V, Phan K, Mewton E, Jackson C, Cooper A. Toxic epidermal necrolysis and steven‐johnson syndrome: a comprehensive review. Adv Wound Care. 2020;9(7):426‐439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Schoot TS, Kerckhoffs A, Hilbrands LB, van Marum RJ. Immunosuppressive drugs and COVID‐19: a review. Front Pharmacol. 2020;11:1333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Poulsen NN, von Brunn A, Hornum M, Blomberg Jensen M. Cyclosporine and COVID‐19: Risk or favorable? Am J Transplant. 2020;20(11):2975‐2982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Dhar S. Intravenous immunoglobulin in dermatology. Indian J Dermatol. 2009;54(1):77‐79. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Li H, Chen C, Hu F, et al. Impact of corticosteroid therapy on outcomes of persons with SARS‐CoV‐2, SARS‐CoV, or MERS‐CoV infection: a systematic review and meta‐analysis. Leukemia. 2020;34(6):1503‐1511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. RECOVERY Collaborative Group , Horby P, Lim WS, et al. Dexamethasone in hospitalized patients with Covid‐19 ‐ preliminary report. N Eng J Med. 2020;384(8):693–704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Yang Z, Liu J, Zhou Y, Zhao X, Zhao Q, Liu J. The effect of corticosteroid treatment on patients with coronavirus infection: a systematic review and meta‐analysis. J Infect. 2020;81(1):e13‐e20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Veronese N, Demurtas J, Yang L, et al. Use of corticosteroids in coronavirus disease 2019 pneumonia: a systematic review of the literature. Front Med (Lausanne). 2020;24(7):170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Russell CD, Millar JE, Baillie JK. Clinical evidence does not support corticosteroid treatment for 2019‐nCoV lung injury. Lancet (London, England). 2020;395(10223):473‐475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Abdollahimajd F, Shahidi‐Dadras M, Robati MR, Dadkhahfar S. Management of pemphigus in COVID‐19 pandemic era; a review article. Arch Acad Emerg Med. 2020;8(1):e51. [PMC free article] [PubMed] [Google Scholar]
  • 16. Kirchhof MG, Miliszewski MA, Sikora S, Papp A, Dutz JP. Retrospective review of Stevens‐Johnson syndrome/toxic epidermal necrolysis treatment comparing intravenous immunoglobulin with cyclosporine. J Am Acad Dermatol. 2014;71(5):941‐947. [DOI] [PubMed] [Google Scholar]
  • 17. Arévalo JM, Lorente JA, González‐Herrada C, Jiménez‐Reyes J. Treatment of toxic epidermal necrolysis with cyclosporin A. J Trauma. 2000;48(3):473‐478. [DOI] [PubMed] [Google Scholar]
  • 18. Kumar R, Das A, Das S. Management of Stevens‐Johnson syndrome‐toxic epidermal necrolysis: looking beyond guidelines!. Indian J Dermatol. 2018;63(2):117‐124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Rudnicka L, Glowacka P, Goldust M, et al. Cyclosporine therapy during the COVID‐19 pandemic. J Am Acad Dermatol. 2020;83(2):e151‐e152. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Gelincik A, Brockow K, Çelik GE, et al. Diagnosis and management of the drug hypersensitivity reactions in coronavirus disease 19: an EAACI position paper. Allergy. 2020;75(11):2775‐2793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Rodriguez‐Cubillo B, de la Higuera M, Lucena R, et al. Should cyclosporine be useful in renal transplant recipients affected by SARS‐CoV‐2? Am J Transplant. 2020;20(11):3173‐3181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Cavagna L, Seminari E, Zanframundo G, et al. Calcineurin inhibitor‐based immunosuppression and COVID‐19: results from a multidisciplinary cohort of patients in Northern Italy. Microorganisms. 2020;8(7):977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Colombo D, Chimenti S, Grossi P, et al. Prevalence of past and reactivated viral infections and efficacy of cyclosporine A as monotherapy or in combination in patients with psoriatic arthritis–synergy study: a longitudinal observational study. Biomed Res Int. 2014;2014:941767. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data are available upon request to the corresponding author, Najmeh Ahramiyanpour MD


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