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Cytomegalovirus infection natural history, complications and prognosis

Introduction

Overview

Overview

Primary CMV infection takes place in childhood and early adolescence is asymptomatic. After the resolution of the primary infection CMV is latent in the mononuclear leukocytes. Reactivation in immunocompetent patients presents with mononucleosis like syndrome, but severe infection can occur in elderly and critically ill patients. Common complications of CMV infection in immunocompromised patients include CMV retinitis, CMV colitis, CMV encephalitis, CMV pneumonia and CMV myocarditis. CMV is associated with increased risk of graft versus host disease, myelosuppression, and invasive bacterial and fungal infections increasing morbidity and mortality of the patients.

Natural History, Complications and Prognosis

Natural History, Complications and Prognosis

Natural History

Natural History

Primary CMV infection which occurs in childhood and early adolescence is asymptomatic. After the resolution of the primary infection, CMV is latent in the mononuclear leukocytes. Reactivation of the virus can occur during states of stress and immunosuppression. Reactivation in immunocompetent patients presents with a mononucleosis like syndrome. If left untreated, severe infection can occur in elderly and critically ill patients. They present with clinical manifestations affecting the gastrointestinal tract and the central nervous system. Retinitis and pneumonitis are uncommon in immunocompetent patients when compared to immunocompromised patients. Reactivation of CMV infection in immunocompromised patients results in CMV end organ infection affecting multiple organs.[1]

Complications

Complications

Common complications of CMV infection in immunocompromised patients include:[1]

Complications in critically ill immunocompetent patients include:

Complications of CMV infection in organ transplant patients:[4]

  • Acute allograft rejection and failure
  • Death
Prognosis

Prognosis

CMV disease is common in patients with solid organ transplantation causing significant morbidity and mortality. CMV is associated with increased risk of graft versus host disease, myelosuppression, and invasive bacterial and fungal infections increasing morbidity and mortality of the patients.[5][6]

References

References

  1. ↑ 1.0 1.1 Al-Omari A, Aljamaan F, Alhazzani W, Salih S, Arabi Y (2016). “Cytomegalovirus infection in immunocompetent critically ill adults: literature review”. Ann Intensive Care. 6 (1): 110. doi:10.1186/s13613-016-0207-8. PMCΒ 5095093. PMIDΒ 27813024.
  2. ↑ Makker J, Bajantri B, Sakam S, Chilimuri S (2016). “Cytomegalovirus related fatal duodenal diverticular bleeding: Case report and literature review”. World J Gastroenterol. 22 (31): 7166–74. doi:10.3748/wjg.v22.i31.7166. PMCΒ 4988300. PMIDΒ 27610026.
  3. ↑ Rezaee-Zavareh MS, Tohidi M, Sabouri A, Ramezani-Binabaj M, Sadeghi-Ghahrodi M, Einollahi B (2016). “Infectious and coronary artery disease”. ARYA Atheroscler. 12 (1): 41–9. PMCΒ 4834180. PMIDΒ 27114736.
  4. ↑ Luscalov S, Loga L, Dican L, Junie LM (2016). “Cytomegalovirus infection in immunosuppressed patients after kidney transplantation”. Clujul Med. 89 (3): 343–6. doi:10.15386/cjmed-587. PMCΒ 4990428. PMIDΒ 27547053.
  5. ↑ Ariza-Heredia EJ, Nesher L, Chemaly RF (2014). “Cytomegalovirus diseases after hematopoietic stem cell transplantation: a mini-review”. Cancer Lett. 342 (1): 1–8. doi:10.1016/j.canlet.2013.09.004. PMIDΒ 24041869.
  6. ↑ de la CΓ‘mara R (2016). “CMV in Hematopoietic Stem Cell Transplantation”. Mediterr J Hematol Infect Dis. 8 (1): e2016031. doi:10.4084/MJHID.2016.031. PMCΒ 4928522. PMIDΒ 27413524.

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aravind Kuchkuntla, M.B.B.S[2]