Skip to main content
Wiley - PMC COVID-19 Collection logoLink to Wiley - PMC COVID-19 Collection
. 2021 Sep 14;61(2):252–256. doi: 10.1111/ijd.15892

Plasmapheresis: a feasible choice for bullous pemphigoid patients infected with SARS‐CoV‐2

Yu Cui 1, Caixia Hu 1, Yi Cheng 1, Xiaomei Han 1, Wenqing Wang 1,
PMCID: PMC8653043  PMID: 34520570

Abstract

Bullous pemphigoid (BP) patients were vulnerable to severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection because they have similar risk factors, so we should pay attention to patients with BP during the epidemic of coronavirus disease‐19 (COVID‐19). As far as treatment is concerned, many strategies for BP were changed during the epidemic. Plasmapheresis not only has been included in the guidelines for BP but also has been used successfully to rescue COVID‐19 patients, especially in severe cases. Therefore, it is a feasible choice for BP patients, especially for refractory BP patients, infected with SARS‐CoV‐2. Apart from these, we have reviewed some points for attention during the plasmapheresis session.

Background

As is well known, a novel coronavirus, initially called 2019‐nCoV, was reported at the end of the year 2019. 1 Then the coronavirus, which was named SARS‐CoV‐2 by the International Committee on Taxonomy of Viruses (ICTV), has spread rapidly worldwide and caused the outbreak of COVID‐19. Globally, as of 3:24 pm CEST, May 20 2021, there have been 169,118,995 confirmed cases of COVID‐19, including 3,519,175 deaths, which were reported to the World Health Organization (WHO). 2

The risk factors for SARS‐CoV‐2 infection and severe outcomes are advanced age and underlying diseases including, but not limited to, diabetes, hypertension, cardiovascular disease, and active cancer. 3 , 4 , 5 Bullous pemphigoid (BP) also occurs in these people, 6 and BP patients are vulnerable to cutaneous, respiratory, multi‐organ, and systemic infections. 7 Therefore, as dermatologists, we should pay special attention to patients with BP during the epidemic.

Introduction of treatment strategies for BP during the epidemic

Bullous pemphigoid, one of the autoimmune blistering diseases (AIBDs), typically presents with tense and mostly clear blisters and erythema. Blisters often appear on the flexural aspects of the limbs and on the abdomen. Almost all patients have severe pruritus. 6

In terms of treatment, for mild BP patients, topical corticosteroids, antibiotics, and nicotinamide are recommended. Topical and systemic corticosteroids and immunosuppressive drugs are suggested for the treatment of moderate BP patients. Meanwhile, for severe BP patients, intravenous immunoglobulin (IVIG), biologic agent, and plasmapheresis might be considered. 8 , 9 , 10

Patients with AIBDs using immunosuppressive drugs which contain azathioprine, mycophenolate mofetil, mycophenolic acid, methotrexate, cyclosporine, cyclophosphamide, and corticosteroids (prednis[ol]one >10 mg/day) are more likely to be infected with SARS‐CoV‐2 and develop more severe COVID‐19. 11 During the pandemic, these drugs should be tapered to the lowest effective dose. 12 However, if patients are positive for SARS‐CoV‐2, these drugs should be temporarily withdrawn, after considering the severity of AIBDs, past medical history, comorbidities, age, and severity of COVID‐19, except corticosteroids, which should be reduced gradually to at least 7.5–10 mg/day to avoid abrupt termination or considerable dose reduction. 11 , 13 , 14 Moreover, some experts found that the low‐dose systemic dexamethasone decreased the mortality rate in COVID‐19 patients who were receiving either invasive mechanical ventilation or oxygen alone at randomization. 15

However, topical corticosteroids, dapsone, sulfapyridine, antibiotics (e.g., doxycycline, tetracycline), antihistamine, colchicine, and normal human IVIG are less likely to increase the risk for infection or more severe COVID‐19. 11 , 13 Fortunately, dapsone, doxycycline, and IVIG also demonstrate beneficial effects on COVID‐19. 16 , 17

If patients using biologic agent have suspected or confirmed SARS‐CoV‐2 infection within 31 days, the next dose should be withdrawn or postponed (based on the potential time of viral shedding). 18 The biologic therapy can be recommended depending on the resolution of illness and/or confirmation of negative PCR testing manifesting no viral shedding 18 (Table 1).

Table 1.

Changes in treatment strategies for bullous pemphigoid during the epidemic 11 , 12 , 13 , 15 , 16 , 17

Drugs During the epidemic Patients are positive for SARS‐CoV‐2
Azathioprine Tapered to the lowest effective dose Temporarily withdrawn
Mycophenolate mofetil Same as above Same as above
Mycophenolic acid Same as above Same as above
Methotrexate Same as above Same as above
Cyclosporine Same as above Same as above
Cyclophosphamide Same as above Same as above
Systemic corticosteroids Reduced gradually to prednis[ol]one ≤10 mg/day Depending on the severity of COVID‐19
Topical corticosteroids Continued Continued
Dapsone Continued Continued
Sulfapyridine Continued Continued
Antibiotics (e.g. doxycycline, tetracycline) Continued Continued
Antihistamine Continued Continued
Colchicine Continued Continued
IVIG Continued Continued
Biologic agent Tapered to the lowest effective dose Withdrawn or postponed

In addition to the above treatments, plasmapheresis, which was proved effective for refractory BP (using systemic corticosteroids and immunosuppressant for 1 month failed to control the disease), has also been included in the guidelines for BP. 8 , 9 , 10

Plasmapheresis

Introduction of plasmapheresis

Plasmapheresis, such as plasma exchange (PE) and double filtration plasmapheresis (DFPP), was a therapeutic option for severe or intractable cases. 19

Therapeutic PE is a procedure in which blood of the patient is passed through a medical device that removes units of whole blood anticoagulated with heparin and isolates plasma from other components of blood. The plasma is removed and substituted with a replacement solution such as colloid solution (e.g., albumin and/or plasma) or a combination of crystalloid/colloid solution. Eventually, the cellular elements are then mixed with the replacement and reinfused. 20 , 21 DFPP is a filter‐based therapeutic procedure that removes pathogenic substances from isolated plasma based on their size, which is mainly determined by molecular weight and three‐dimensional configuration by plasma filters with different pore sizes. 20 In these ways, the pathologic substances such as pathologic autoantibodies, immune complexes, and cytokines will be removed. 21

Indications of plasmapheresis

We have used plasmapheresis along with glucocorticosteroid and/or immunosuppressive agents to treat severe BP patients, and the results were the reduction in serum levels of antiBP180, the alleviation of pruritus, and the disappearance of bulla, which were consistent with our expectations. 22 , 23 Similar outcomes were found in other studies. 24 , 25 When the clinical manifestation appears resistant to oral immunosuppression, or when additional second‐line drugs produce an increasingly unfavorable side effect, it was preferable to consider a trial of plasmapheresis. 24

In addition to BP, plasmapheresis was also used in some severe dermatoses, such as severe psoriasis, connective tissue diseases, pemphigus, drug eruption, and insect and animal bite diseases. 26 , 27 Similarly, in other disciplines, plasmapheresis was used in hematologic disorders, solid organ transplantation, hematopoietic stem cell transplantation, neurologic disorders, renal disorders, fulminant hepatitis, vasculitis, and so on. 20 , 28

Plasmapheresis and COVID‐19

During the epidemic, plasmapheresis was used successfully to rescue COVID‐19 patients, especially severe cases. 29 , 30 , 31 , 32 , 33 , 34

As is known to all, the level of cytokine, coagulation agent, and viral load is the most important parameter to determine the outcome of COVID‐19, 31 particularly the “cytokine storm” that plays an important role in the pathophysiology of the SARS‐CoV‐2 infection in patients. 35 Plasmapheresis can remove toxins and deleterious inflammatory cytokines such as IL‐1, IL‐6, granulocyte‐colony stimulating factor, tumor necrosis factor (TNF), and other inflammatory parameters to alleviate cytokine storm. 32 These cytokines’ levels, such as IL‐1, IL‐6, and TNF‐α, were correlated with the activity of BP. 36 Then removing these cytokines by plasmapheresis is a good strategy not only for COVID‐19 but also for BP patients. Moreover, plasmapheresis also exerts a role in reducing the abnormal coagulation agents. 31 In addition, plasmapheresis could reduce the viral load by eliminating SARS‐CoV‐2 viral particles since they have a diameter of 60–140 nm and are large enough to be eliminated with DFPP. 33 Apart from these, plasmapheresis can promote the suppression of thromboinflammation and amelioration of microangiopathy, thus preventing the development of multisystem organ failure. 34

Based on these reports, experts in our country have included plasmapheresis in the consensus on the diagnosis and treatment of COVID‐19. 37 , 38 In view of obvious benefits for both BP patients and COVID‐19 patients, plasmapheresis should be a feasible choice for BP patients infected with SARS‐CoV‐2. Especially for refractory BP patients infected with SARS‐CoV‐2, the plasmapheresis, which is cheaper than IVIG, is the preferred treatment. 9

Matters need attention

So what should we pay attention to during the plasmapheresis session?

First, when is the appropriate time for the first plasmapheresis session? BP is a chronic disease, and the plasmapheresis usually is given a long time after onset. However, as is demonstrated in reports, the results of plasmapheresis for severe COVID‐19 are highly dependent on timing. For most viral illnesses, viremia peaks in the first week of infection. The patient usually develops a primary immune response on days 10–14, which is followed by the clearance of the virus. 39 Symptomatic COVID‐19 mainly consists of three phases. The first is a starting phase, including the acquisition of the virus and subsequent viremia; the second is the acceleration phase, that is, virus‐induced secondary damage of targeting organs and tissue including the lungs, the heart, the gastrointestinal tract, and even an overall inflammatory storm; and the third phase is the final recovery phase. 40 So, the strategies against COVID‐19 should be given early in the course of the disease, just prior to the acceleration phase. 34 , 40 If clinical deterioration has begun, the first few days of deterioration is also a critical point. 40 Several studies have also shown that the administration of plasmapheresis within 7–14 days of the illness onset could be associated with better outcome. 32 , 39 Second, how much plasma volume is advised? A total of 2–3 liters of plasma is recommended in the plasmapheresis of BP patients, 9 and 1.5 plasma volume was suggested in the PE for severe COVID‐19 patients every time. 38 In another study, 1.2 plasma volume also had a good effect on the condition. 30 In addition, we can use this formula to calculate the plasma volume, the amount of plasma replacement (l) = body weight (kg) × (1/13) × (1−hematocrit/100) and that at least 2 liters of plasma should be administered when plasma is scarce. 41 Third, what is the replacement solution? The choice for replacement solution includes fresh frozen plasma, 5% albumin, or 0.9% saline. 29 , 42 After plasmapheresis, the convalescent plasma from a recovered patient or IVIG could be transfused to the patient immediately. 38 , 43 , 44 Last, the frequency and the number of times of plasmapheresis depend on the patient's condition. We summarized the experience in the treatment of BP and COVID‐19 patients with plasmapheresis in Tables 2 and 3. 22 , 31 , 44 , 45 , 46 , 47

Table 2.

Our experience in the treatment of bullous pemphigoid patients with plasmapheresis 22

Patients' age Time of first plasmapheresis after onset Number of plasmapheresis Frequency of plasmapheresis Volume of each plasmapheresis Outcome
72 4 months Three Every other day 2000 ml Discharge
73 4 months One 2000 ml Discharge
69 20 days Two 2000 ml Discharge
67 0 day Two Once every three days 2000 ml Discharge

Table 3.

The experience in the treatment of COVID‐19 patients with plasmapheresis reported in the literature 31 , 44 , 45 , 46 , 47

Patients' age/gender Time of first plasmapheresis after onset (days) Number of plasmapheresis Frequency of plasmapheresis (days) Volume of each plasmapheresis Outcome
44/male 10 One 3020 ml Discharge
55/male 17 One 3000 ml Discharge
64/male 15 One 2660 ml Discharge
65/female 6 One 4500 ml Discharge
74/male 7 Four 7,9,11,13 About 6600 ml Discharge
50/female 14 Four 14,15,16,17 6000 ml Discharge
53/male 12 Two 3600 ml, 3660 ml Discharge
71/male 9 One 3380 ml Died
62/male 16 Two 3020 ml, 2930 ml Discharge
76/female 17 One 3170 ml Died
67/female 11 Two 3510 ml, 3400 ml Discharge

Although plasmapheresis is safe and effective, special attention should be paid to its possible complications. The common complications include hypocalcemia or hypomagnesemia, hypothermia, transfusion reactions, hypotension, urticarial, infection, bleeding/hematoma, and so on. 21 , 48 , 49 However, after continuous observation in healthcare faculties, these side effects could be closely monitored, thus ensuring patients' safety. 48

It is noteworthy that plasmapheresis merely interrupts or delays the progression of the disease. It only removes the pathogenic substances rapidly, creating opportunities for drug treatment, so in the meantime, etiological treatment should be carried out. Moreover, given that it is an invasive and expensive treatment, the indications should be clarified. 50

Questions: True or False questions (answers provided after references)

  1. The risk factors for SARS‐CoV‐2 infection and BP are different.

  2. BP typically presents with tense and mostly clear blisters and erythema.

  3. During the pandemic, all drugs for BP should be temporarily withdrawn.

  4. Dapsone, doxycycline, and IVIG demonstrate beneficial effects on COVID‐19.

  5. The pathologic substances such as pathologic autoantibodies, immune complexes, and cytokines will be removed by plasmapheresis.

  6. We have used plasmapheresis along with glucocorticosteroid and/or immunosuppressive agents to treat severe BP patients successfully.

  7. Plasmapheresis could not rescue COVID‐19 patients.

  8. Plasmapheresis can remove toxins and deleterious inflammatory cytokines to alleviate cytokine storm.

  9. Plasmapheresis is not a feasible choice for BP patients infected with SARS‐CoV‐2.

  10. The results of plasmapheresis for severe COVID‐19 are highly dependent on timing.

Answers to Questions

  1. False

  2. True

  3. False

  4. True

  5. True

  6. True

  7. False

  8. True

  9. False

  10. True

Conflict of interest: None.

Funding source: None.

References

  • 1. Munster VJ, Koopmans M, van Doremalen N, et al. A novel coronavirus emerging in China – key questions for impact assessment. N Engl J Med 2020; 382: 692–694. [DOI] [PubMed] [Google Scholar]
  • 2. Word Health Organization . WHO Coronavirus Disease (COVID‐19) Dashboard. Available from: https://covid19.who.int/ [accessed on 30 May 2021].
  • 3. Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 2020; 395: 497–506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Booth A, Reed AB, Ponzo S, et al. Population risk factors for severe disease and mortality in COVID‐19: a global systematic review and meta‐analysis. PLoS One 2021; 16: e0247461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Wu Z, McGoogan JM. Characteristics of and important lessons from the coronavirus disease 2019 (COVID‐19) outbreak in China: summary of a report of 72 314 cases from the Chinese center for disease control and prevention. JAMA 2020; 323: 1239–1242. [DOI] [PubMed] [Google Scholar]
  • 6. Schmidt E, Zillikens D. Pemphigoid diseases. Lancet 2013; 381: 320–332. [DOI] [PubMed] [Google Scholar]
  • 7. Ren Z, Narla S, Hsu DY, et al. Association of serious infections with pemphigus and pemphigoid: analysis of the Nationwide Inpatient Sample. J Eur Acad Dermatol Venereol 2018; 32: 1768–1776. [DOI] [PubMed] [Google Scholar]
  • 8. Schmidt E, Sticherling M, Sárdy M, et al. S2k guidelines for the treatment of pemphigus vulgaris/foliaceus and bullous pemphigoid: 2019 update. J Dtsch Dermatol Ges 2020; 18: 516–526. [DOI] [PubMed] [Google Scholar]
  • 9. The Autoimmune Diseases Council of Chinese Dermatologist Association . Expert advice on diagnosis and treatment of bullous pemphigoid. Chin J Dermatol 2016; 49: 384–387. 10.3760/cma.j.issn.0412-4030.2016.06.003 [DOI] [Google Scholar]
  • 10. Feliciani C, Joly P, Jonkman MF, et al. Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. Br J Dermatol 2015; 172: 867–877. [DOI] [PubMed] [Google Scholar]
  • 11. European Academy of Dermatology and Venereology . Guidance from the EADV Task Force Autoimmune Blistering Diseases during the COVID‐19 pandemic. Available from: https://www.eadv.org/covid‐19/task‐force [accessed on 30 May 2021].
  • 12. Shakshouk H, Daneshpazhooh M, Murrell DF, Lehman JS. Treatment considerations for patients with pemphigus during the COVID‐19 pandemic. J Am Acad Dermatol 2020; 82: e235–e236. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Kasperkiewicz M, Schmidt E, Fairley JA, et al. Expert recommendations for the management of autoimmune bullous diseases during the COVID‐19 pandemic. J Eur Acad Dermatol Venereol 2020; 34: e302–e303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. De D, Pandhi D. Use of immunosuppressants/immunomodulators in autoimmune/inflammatory dermatologic diseases during COVID‐19 pandemic—general recommendation based on available evidence. Indian Dermatol Online J 2020; 11: 526–533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. The RECOVERY Collaborative Group . Dexamethasone in hospitalized patients with covid‐19 – preliminary report. N Engl J Med 2021; 384: 693–704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Farouk A, Salman S. Dapsone and doxycycline could be potential treatment modalities for COVID‐19. Med Hypotheses 2020; 140: 109768. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Prete M, Favoino E, Catacchio G, et al. SARS‐CoV‐2 infection complicated by inflammatory syndrome. Could high‐dose human immunoglobulin for intravenous use (IVIG) be beneficial? Autoimmun Rev 2020; 19: 102559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Wang C, Rademaker M, Baker C, Foley P. COVID‐19 and the use of immunomodulatory and biologic agents for severe cutaneous disease: an Australian/New Zealand consensus statement. Australas J Dermatol 2020; 61: 210–216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Yoshida T, Minakuchi H, Takahashi R, et al. Safety and efficacy of plasma exchange via direct femoral vein puncture in autoimmune blistering diseases. J Clin Apher 2020; 35: 172–177. [DOI] [PubMed] [Google Scholar]
  • 20. Padmanabhan A, Connelly‐Smith L, Aqui N, et al. Guidelines on the use of therapeutic apheresis in clinical practice – evidence‐based approach from the Writing Committee of the American Society for Apheresis: the eighth special issue. J Clin Apher 2019; 34(3): 171–354. [DOI] [PubMed] [Google Scholar]
  • 21. Winters JL. Plasma exchange: concepts, mechanisms, and an overview of the American Society for Apheresis guidelines. Hematology Am Soc Hematol Educ Program 2012; 2012: 7–12. [DOI] [PubMed] [Google Scholar]
  • 22. Hu CX, Wang WQ, Wu XG, et al. Clinical analysis and serological antibody level detection of patinets with pemphigus and bullous pemphigoid after plasmapheresis therapy. J Clin Dermatol 2017; 46: 552–555. [Google Scholar]
  • 23. Wang WQ, Hu CX, Wu XG, et al. A retrospective study of 122 cases of bullous pemphigoid. Chin J Derm Venereol 2018; 32: 1153–1157. [Google Scholar]
  • 24. Chang B, Tholpady A, Huang RS, et al. Clinical and serological responses following plasmapheresis in bullous pemphigoid: two case reports and a review of the literature. Blood Transfus 2014; 12: 269–275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Wei L, Lu R, Chen JB. Clinical effect of plasma exchange therapy on severe bullous pemphigoid. Chin J TCM WM Crit Care 2020; 27: 110–113. 10.3969/j.issn.1008-9691.2020.01.030 [DOI] [Google Scholar]
  • 26. Li TN, Sun XJ, Wang Z. Application of plasma exchange on treating severe dermatoses. J Pract Dermatol 2011; 4: 2–4. [Google Scholar]
  • 27. Gao TW, Liao WJ, Li ZN, et al. Treatment of severe dermatoses with plasma transfusion and plasma exchange therapy. J ClinDermatol 2002; 31: 301–302. [Google Scholar]
  • 28. Fernández‐Zarzoso M, Gómez‐Seguí I, de la Rubia J. Therapeutic plasma exchange: review of current indications. Transfus Apher Sci 2019; 58: 247–253. [DOI] [PubMed] [Google Scholar]
  • 29. de Prost N, Bastard P, Arrestier R, et al. Plasma exchange to rescue patients with autoantibodies against type I interferons and life‐threatening COVID‐19 pneumonia. J Clin Immunol 2021; 41: 536–544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Altmayer V, Saheb S, Rohaut B, et al. Therapeutic plasma exchange in a critically ill Covid‐19 patient. J Clin Apher 2021; 36: 179–182. [DOI] [PubMed] [Google Scholar]
  • 31. Balagholi S, Dabbaghi R, Eshghi P, et al. Potential of therapeutic plasmapheresis in treatment of COVID‐19 patients: immunopathogenesis and coagulopathy. Transfus Apher Sci 2020; 59: 102993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Khamis F, Al‐Zakwani I, Al Hashmi S, et al. Therapeutic plasma exchange in adults with severe COVID‐19 infection. Int J Infect Dis 2020; 99: 214–218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Turgutkaya A, Yavaşoğlu İ, Bolaman Z. The application of plasmapheresis for Covid‐19 patients. Ther Apher Dial 2021; 25: 248–249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Memish ZA, Faqihi F, Alharthy A, et al. Plasma exchange in the treatment of complex COVID‐19‐related critical illness: controversies and perspectives. Int J Antimicrob Agents 2021; 57: 106273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Mahmoudi S, Rezaei M, Mansouri N, et al. Immunologic features in coronavirus disease 2019: functional exhaustion of T cells and cytokine storm. J Clin Immunol 2020; 40: 974–976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Ludwig RJ, Schmidt E. Cytokines in autoimmune bullous skin diseases. Epiphenomena or contribution to pathogenesis? G Ital Dermatol Venereol 2009; 144: 339–349. [PubMed] [Google Scholar]
  • 37. General Office of National Health Commission of the People’s Republic of China , Office of National Administration of Traditional Chinese Medicine . Diagnosis and treatment of corona virus disease‐19 (8th trial edition). China Medicine 2020; 15: 1494–1499. 10.3760/j.issn.1673-4777.2020.10.002 [DOI] [Google Scholar]
  • 38. Chinese Society of Nephrology; Professional Committee of Nephrology . Expert consensus on special blood purification technics in patients with corona virus disease 2019. Chin J Intern Med 2020; 59: 847–853. [DOI] [PubMed] [Google Scholar]
  • 39. Cheng Y, Wong R, Soo YOY, et al. Use of convalescent plasma therapy in SARS patients in Hong Kong. Eur J Clin Microbiol Infect Dis 2005; 24: 44–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Cao W, Liu X, Bai T, et al. High‐dose intravenous immunoglobulin as a therapeutic option for deteriorating patients with Coronavirus Disease 2019. Open Forum. Infect Dis 2020; 7: 10.1093/ofid/ofaa102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41. National Clinical Research Center for Infectious Diseases , State Key Laboratory for Diagnosis and Treatment of Infectious Diseases . Expert consensus on the application of artificial liver blood purification system in the treatment of severe and critical COVID‐19 (in Chinese). Chin J Clin Infect Dis 2020; 13: 1–3. 10.3760/cma.j.issn.1674-2397.2020.01.001 [DOI] [Google Scholar]
  • 42. Hashemian SM, Shafigh N, Afzal G, et al. Plasmapheresis reduces cytokine and immune cell levels in COVID‐19 patients with acute respiratory distress syndrome (ARDS). Pulmonology 2020; 10.1016/j.pulmoe.2020.10.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Ragab D, Salah‐Eldin H, Afify M, et al. A case of COVID‐19, with cytokine storm, treated by consecutive use of therapeutic plasma exchange followed by convalescent plasma transfusion: a case report. J Med Virol 2021; 93: 1854–1856. [DOI] [PubMed] [Google Scholar]
  • 44. Shi H, Zhou CM, He PH, et al. Successful treatment of plasma exchange followed by intravenous immunogloblin in a critically ill patient with 2019 novel coronavirus infection. Int J Antimicrob Agents 2020; 56: 105974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Zhang LI, Zhai H, Ma S, et al. Efficacy of therapeutic plasma exchange in severe COVID‐19 patients. Br J Haematol 2020; 190: e181–e183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Keith P, Day M, Choe C, et al. The successful use of therapeutic plasma exchange for severe COVID‐19 acute respiratory distress syndrome with multiple organ failure. SAGE Open Med Case Rep 2020; 8: 1–4. 10.1177/2050313X20933473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. Morath C, Weigand MA, Zeier M, et al. Plasma exchange in critically ill COVID‐19 patients. Crit Care 2020; 24: 481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48. Szczeklik W, Wawrzycka K, Włudarczyk A, et al. Complications in patients treated with plasmapheresis in the intensive care unit. Anaesthesiol Intensive Ther 2013; 45: 7–13. [DOI] [PubMed] [Google Scholar]
  • 49. Sergent SR, Ashurst JV. Plasmapheresis. Treasure Island, FL: StatPearls Publishing, 2021; StatPearls [Internet]. [PubMed] [Google Scholar]
  • 50. Blood Purification Specialist Committee of Pediatric Association in Chinese Medical Doctor Association . Expert consensus documents on clinical application of plasma exchange in pediatrics. Chin J Appl. 2018; 33: 1128–1135. [Google Scholar]

Articles from International Journal of Dermatology are provided here courtesy of Wiley

RESOURCES