- Case Report
Systemic varicella-zoster virus infection in two critically ill patients in an intensive care unit
Virology Journalvolume 10, Article number: 225 (2013)
Varicella-zoster virus (VZV) usually causes localized zoster in adults. However, in immunocompromised patients, it can cause systemic infection accompanied by complications such as pneumonia, encephalitis, and hepatitis. Although most of critically ill patients in intensive care unit (ICU) are immunologically compromised, they are usually not considered to be at risk for systemic VZV infection.
We report two cases of systemic VZV infection occurring in critically ill patients in an ICU. One patient was a 69-year-old man with Streptococcus pneumoniae-induced purpurafulminans, and the other was a 75-year-old woman with severe acute pancreatitis. During the clinical course in the ICU, characteristic vesicles with umbilical fossa appeared diffusely and bilaterally on their face, trunk, and extremities. VZV-specific IgG levels were confirmed to be elevated compared to that of the pre-onset, and a diagnosis of recurrent VZV infection was made in both patients. The patients were treated at the same ICU but did not coincide with each other; therefore a cross-infection was unlikely. They were treated with intravenous acyclovir, but the latter patient eventually died of respiratory failure.
VZV infection can cause a number of serious complications, and can lead to death in some patients. Early detection and proper treatment are needed to prevent the infection from spreading out and save the patients. It might be necessary to consider antiviral prophylaxis against VZV infection for a part of critically ill patients in ICU, although the effectiveness of this approach is yet to be established.
Varicella-zoster virus (VZV) has the potential to cause life-threatening infection in adults, especially in those who are immunocompromised. In addition to specific humoral immunity, cellular-mediated immunity is involved in protection against VZV infection [1–3]. Pneumonia, encephalitis, hepatitis, and disseminated intravascular coagulopathy (DIC) are well-known complications of systemic VZV infection, and the overall mortality rate has been reported to be high in such cases (approximately 30% among renal transplant patients) . Previous studies have reported that transplant recipients, human immunodeficiency virus (HIV)-infected patients, and patients undergoing treatment with tumor necrosis factor-α inhibitors are at an increased risk of developing severe VZV infection [5–7]. Critically ill patients in the intensive care units (ICU) tend to be immunologically weak [8–12] and they are considered to be at a high risk for various opportunistic infections. However, systemic VZV infection has not been considered as such an opportunistic infection in ICU patients and its clinical picture has yet to be well assessed to date. We present 2 cases of systemic VZV infection occurring in critically ill patients in the ICU.
A 69-year-old man presenting with chills, rigor, stomachache, and vomiting was admitted to a hospital in a state of shock. He had undergone bone marrow transplantation and chemotherapy for multiple myeloma 4 years ago and had been administered prednisolone (PSL; 5 mg/day at that time) since then. Physical examination revealed systemic purpuric rash and laboratory tests showed renal impairment, liver disorder, a highly inflammatory state, lactacidemia, and DIC. Computed tomography (CT) demonstrated bilateral hilar shadows and a relatively small spleen. Under the diagnosis of septic shock, DIC, and acute respiratory distress syndrome (ARDS), the patient was admitted to the ICU. His Acute Physiology and Chronic Health Evaluation (APACHE) II score was 26, and his Sequential Organ Failure Assessment (SOFA) score was 10. Streptococcus pneumoniae (serotype 22) was detected in blood cultures and a diagnosis of purpura fulminans caused by S. pneumoniae was made. Despite an intensive care and antibiotic therapy, the purpura and necrotic lesions spread over his face and extremities, and eventually quadruple amputation was needed and actually performed on day 7. Hemodialysis was unavoidable because of renal impairment, and multiple blood transfusions were given due to prolonged pancytopenia. Methylprednisolone 1 mg/kg/day was administered for the treatment of ARDS, and the corticosteroid therapy was gradually tapered to 5 mg/day of PSL, which was the dosage prescribed before admission.
On day 71, vesicles accompanied by umbilical fossa appeared diffusely and bilaterally on his face, trunk, and extremities (Figure 1A, B). Vesicles were in various stages, and a Tzanck preparation of the vesicles showed multinucleated giant cells (Figure 1C). Systemic varicella was suspected due to the appearance of these characteristic vesicles, and the patient was isolated and treated with intravenous acyclovir (reduced amount of 250 mg every 24 h due to renal insufficiency). There were no symptoms or findings suggesting pneumonia, encephalitis, or hepatitis. Although his serum VZV-specific IgM levels were not elevated, the IgG levels were found to be elevated from 13.2 to more than 128 for 3 weeks (Varicella-zoster IgG-EIA, Varicella-zoster IgM-EIA [SEIKEN], DENKA SEIKEN CO., LTD. Tokyo, Japan.). Acyclovir was administered for 7 days and the vesicles gradually formed clusters that were completed after 11 days. His history of VZV vaccination and VZV infection were unknown. Recent contact with VZV patients was unlikely because of his ongoing hospitalization in the ICU.
A 75-year-old woman was admitted to our hospital because of abdominal pain. Her past medical history included coronary artery bypass grafting, aortic valve replacement, atrial fibrillation, diabetes mellitus, obesity (body mass index on admission was approximately 31), and psoriasis vulgaris. She had taken oral steroids for 4 years for the treatment of psoriasis vulgaris and was receiving 4 mg/day of PSL at the time of admission. Contrast-enhanced CT revealed an entirely swollen, poorly marginated pancreas, and she was diagnosed with severe acute pancreatitis. The patient was initially admitted to a general ward, however, respiratory failure worsened, and she was admitted to the ICU and intubated on the following day. Laboratory testing showed severe DIC, and APACHE II and SOFA scores at the time of ICU admission were 20 and 7, respectively.
A few days after the admission to the ICU, the patient’s consciousness was found to be worsened. Head CT revealed multiple cerebral infarctions. Otherwise, her subsequent condition was relatively stable. However, on ICU day 15, expiratory wheezing and vesicles appeared. By the next day, the vesicles distributed bilaterally on her back and buttocks that rapidly spread over her whole body. Systemic varicella was diagnosed due to the characteristic dermatological findings, and the patient was immediately started on intravenous acyclovir (500 mg every 8 h) and topical vidarabine. A liver disorder was detected 3 days after vesicles appeared; transaminase levels were elevated to maximums of 264 IU/L for aspartate aminotransferase and 157 IU/L for alanine aminotransferase. Although the patient's serum VZV-specific IgM levels were found to be not elevated either as the patient in Case 1, the IgG levels were elevated from 8.2 of one week before onset to 120.8 for two weeks. Under the diagnosis of VZV associated pneumonia and hepatitis, she was treated with 7 days of acyclovir. With treatment, respiratory wheezing and liver disorder disappeared, clustering was completed, and then patient left the ICU.
After that, she experienced a relapse of severe respiratory failure at the general ward. However, her family did not authorize intubation because of patient’s unconscious state at this time and eventually she died on hospital day 30. Although no autopsy was performed, chest radiography revealed deteriorated bilateral pulmonary infiltrations, and we clinically speculated that the patient died of VZV pneumonia or ARDS.
A detail of the two cases is summarized in Table 1.
Generally, critically ill patients have reduced cellular immunocompetence . The overproduction of anti-inflammatory cytokines due to a highly inflammatory state causes immunosuppression, known as immunoparalysis [11, 12]. Corticosteroid therapy, which suppresses cellular-mediated immunity, is frequently induced in various situations, and its long-term use often let the patients be immunocompetent state. Both patients presented here were in immunocompromised states due to their primary severe diseases and long period of corticosteroids administration. These conditions were considered being related to the onset of systemic VZV infection. Additionally, in Case 1, the relatively small spleen found by CT (spleen dysfunction is associated with reduction of humoral immunity ), the substantial blood transfusions, and the quadruple amputation were considered the other possible risk factors.
It was not clear whether these 2 cases were of disseminated zoster or varicella. The former is associated with multiple vesicular skin lesions in a generalized distribution affecting a number of distinct dermatomes that do not cross the midline, and the latter involves diffusely distributed several-staged vesicles. It is often difficult to differentiate the one to the other. Although a report of seemingly apparent varicella in an adult exists , atypical recurrent varicella without characteristic clustering have been described in immunocompromised patients [15, 16]. We assumed that the presenting cases were varicella, rather than zoster, because of the dermatological appearance: diffuse and bilaterally distributed, but not closely aggregated.
As shown, systemic VZV infection can be fatal. Therefore, early detection and proper treatment is necessary. The vesicles or blisters are characteristic dermatological findings of VZV infection and can be the best indicator for diagnosis. However, VZV infection can progress without the appearance of typical vesicles, especially in immunocompromised patients [15, 16]. In addition, specific antibodies are not always elevated in such patients [17, 18]. Similarly, VZV pneumonia, the most frequent complication in adults, develops insidiously, usually after the onset of rash as seen in Case 2, and can progress to acute respiratory failure or ARDS. For these reasons, the early detection of systemic VZV infection is mandatory but often difficult. Accordingly, VZV prophylaxis may be required in some of immunosuppressed ICU patients to prevent fatal VZV infection. In bone marrow transplant recipients, the use of antiviral prophylaxis with low-dose oral acyclovir (600 mg daily) or ganciclovir (5 mg/kg 3-times weekly) is well established , but there is no guideline concerning prophylaxis for VZV infection in ICU. Acyclovir is also active against Human simplex virus (HSV) types 1 and 2, and acyclovir resistant HSV has been increasingly described as a problematic pathogen. Especially, the resistant organism has been isolated from a variety of immunocompromised patients (prevalence around 5%), including bone marrow recipients (prevalence reaching 30%), solid organ transplant recipients, and those with the acquired immunodeficiency syndrome (AIDS) [19, 20]. VZV resistance to acyclovir has also been reported in patients with AIDS who had been given chronic acyclovir therapy . Moreover, acyclovir has nephrotoxicity and drug interactions with the other frequently used drugs. We should cautiously determine the indicated patients if considering its use in the ICU setting.
Vaccination, another method of preventing VZV infection, is not possible for critically ill patients in ICU because it is the attenuated live vaccine and therefore contraindicated for immunosuppressed patients.
For VZV-infected immunocompromised patients, early high-dose acyclovir (e.g., 10 mg/kg 3-times daily) has been recommended . In adult patients who progress to pneumonia or ARDS, corticosteroid therapy combined with acyclovir has been shown to reduce the duration of hospital and ICU stay [22, 23]. Both patients described here were treated with 7 days of acyclovir. The therapy successfully treated the patient in Case 1; however, it was failed in Case 2. Although the relevance of the duration of acyclovir therapy to outcome is unclear, the patients should have been treated for longer period considering their impaired immunological state.
VZV is highly contagious; transmission occurs via direct contact with lesions or via respiratory droplets. Localized zoster is considered to transmit only by contact, while the virus can be infected by air-borne transmission in case of disseminated zoster. At present, there are no reliable guidelines available concerning the handling of VZV patients in the ICU. However, since many ICU patients are in a state of immunosuppression, we consider VZV patients should be isolated as soon as possible, and appropriate antiviral treatment should be initiated immediately to prevent the spread of the virus. As for the two patients, although they were treated at the same ICU, there was no chance of cross-contamination since their admission period was totally different and not overlapped.
In summary, systemic VZV infection, although rare, can cause serious and fatal complications in critically ill patients in ICU. Early detection and proper treatment is critical for minimizing mortality and controlling infection. However, the typical dermatological findings of VZV infection and the elevation of specific antibodies can be absent in immunosuppressed patients. Prophylactic antiviral treatment, though not yet an established approach, should be considered, particularly in markedly immunosuppressed ICU patients.
Written informed consent was obtained from the patient or family member for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Cvjetković D, Jovanović J, Hrnjaković-Cvjetković I, Brkić S, Bogdanović M: Reactivation of herpes zoster infection by varicella-zoster virus. Med Pregl 1999, 52: 125-128.
Cohen J: Varicella-Zoster virus replication, pathogenesis, and management. In Fields Virology. Volume 2. 5th edition. Edited by: Knipe DA, Howley PE. San Francisco: Wolters Kluwer Inc; 2006:2773-2818.
Feldman S: Varicella-zoster virus pneumonitis. Chest 1994, 106: 22S-27S. 10.1378/chest.106.1_Supplement.22S
Fehr T, Bossart W, Wahl C, Binswanger U: Disseminated Varicella infection in adult renal allograft recipients: four cases and a review of the literature. Transplantation 2002, 73: 608-611. 10.1097/00007890-200202270-00023
Jantsch J, Schmidt B, Bardutzky J, Bogdan C, Eckardt KU, Raff U: Lethal varicella-zoster virus reactivation without skin lesions following renal transplantation. Nephrol Dial Transplant 2011, 26: 365-368. 10.1093/ndt/gfq542
Chilek K, Routhouska S, Tamburro J: Disseminated varicella zoster virus in an immunized child as the acquired immunodeficiency syndrome-defining illness. Pediatr Dermatol 2010, 27: 192-194. 10.1111/j.1525-1470.2009.00942.x
Becart S, Segaert S: Recurrent Varicella in an Adult Psoriasis Patient Treated with Etanercept. Dermatology 2008, 217: 260-261. 10.1159/000149311
Boomer JS, To K, Chang KC, Takasu O, Osborne DF, Walton AH, et al.: Immunosuppression in patients who die of sepsis and multiple organ failure. JAMA 2011, 306: 2594-2605. 10.1001/jama.2011.1829
Kimura F, Shimizu H, Yoshidome H, Ohtsuka M, Miyazaki M: Immuonosuppression following surgical and traumatic injury. Surg Today 2010, 40: 793-808. 10.1007/s00595-010-4323-z
Schefold JC, Hasper D, Volk HD, Reinke P: Sepsis: time has come to focus on the later stage. Med Hypotheses 2008, 71: 203-208. 10.1016/j.mehy.2008.03.022
Hotchkiss RS, Coopersmith CM, McDunn JE, Ferguson TA: The sepsis seesaw: tilting toward immunosuppression. Nat Med 2009, 15: 496-497. 10.1038/nm0509-496
Frazier WK, Hall MW: Immunoparalysis and adverse outcomes from critical illness. Pediatr Clin North Am 2008, 55: 647-668. 10.1016/j.pcl.2008.02.009
Hancock BW, Bruce L, Dunsmore IR, Ward AM, Richmond J: Follow up studies on the immune status of patients with Hodgkin’s disease after splenectomy and treatment, in relapse and remission. Br J Cancer 1977, 36: 347-354. 10.1038/bjc.1977.199
Ku CH, Liu YT, Christiani DC: Case report: occupationally related recurrent varicella (chickenpox) in a hospital nurse. Environ Health Perspect 2005, 113: 1373-1375. 10.1289/ehp.7766
Nikkels AF, Simonart T, Kentos A, Liesnard C, Sadzot-Delvaux C, Feremans W, et al.: Atypical recurrent varicella in 4 patients with hemopathies. J Am Acad Dermatol 2003, 48: 442-447. 10.1067/mjd.2003.94
Rothwell WS, Gloor JM, Morgenstern BZ, Milliner DS: Disseminated varicella infection in pediatric renal transplant recipients treated with mycophenolate mofetil. Transplantation 1999, 68: 158-161.
Steer CB, Szer J, Sasadeusz J, Matthews JP, Beresford JA, Grigg A: Varicella Zoster infection after allogeneic bone marrow transplantation: incidence, risk factors and prevention with low-dose aciclovir and ganciclovir. Bone Marrow Transplant 2000, 25: 657-664. 10.1038/sj.bmt.1702190
Matsui T, Maruyama F, Miyazaki H, Nomura T, Ezaki K, Hirano M, et al.: Disseminated varicella-zoster virus infection without vesicles in a patient with malignant lymphoma. Rinsho Ketsueki 1992, 33: 483-487.
Englund JA, Zimmerman ME, Swierkosz EM, Goodman JL, Scholl DR, Balfour HH Jr: Herpes simplex virus resistant to acyclovir. A study in a tertiary care center. Ann Intern Med. 1990, 112: 416-422.
Morfin F, Thouvenot D: Herpes simplex virus resistance to antiviral drugs. J Clin Virol 2003, 26: 29-37. 10.1016/S1386-6532(02)00263-9
Boivin G, Edelman CK, Pedneault L, Talarico CL, Biron KK, Balfour HH Jr: Phenotypic and genotypic characterization of acyclovir-resistant varicella-zoster viruses isolated from persons with AIDS. J Infect Dis 1994, 170: 68-75. 10.1093/infdis/170.1.68
Mer M, Richards GA: Corticosteroids in life-threatening varicella pneumonia. Chest 1998, 114: 426-431. 10.1378/chest.114.2.426
Adhami N, Arabi Y, Raees A, Al-Shimemeri A, Ur-Rahman M, Memish ZA: Effect of corticosteroids on adult varicella pneumonia: cohort study and literature review. Respirology 2006, 11: 437-441. 10.1111/j.1440-1843.2006.00870.x
The authors declare that they have no competing interest.
HH mainly drafted the manuscript. MK, TM and FO helped to draft the manuscript. All authors read and approved the final manuscript.