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Brucellosis natural history, complications and prognosis

Introduction

Overview

Overview

If left untreated, patients with brucellosis may progress to develop focal organ complications, relapses or chronic brucellosis.[1] Common complications of brucellosis include granulomatous hepatitis, arthritis, sacroiliitis, meningitis, orchitis, epididymitis uveitis, and endocarditis. The prognosis of brucellosis is good with adequate treatment.

Natural History

Natural History

If left untreated, patients with brucellosis may progress to develop focal organ involvement, relapses and chronic brucellosis.[2]

Complications

Complications

Complications of brucellosis include the following:[3][4][5][6][7][8][9][10][11]

Complications of Brucellosis
Osteoarticular
Cardiovascular
Hepatobiliary complications
Genitourinary Orchitis and epididymitis
Neurological
Gastrointestinal Colitis, ileitis, and spontaneous bacterial peritonitis.
  • Rare cases have been reported.
Respiratory tract
Pregnancy Spontaneous abortion
Cutaneous
Opthalmic Uveitis
  • Most frequent ophtalmic complications[12]
Prognosis

Prognosis

The prognosis of brucellosis is good with treatment. Mortality is less then 1%, usually due to consequence of cardiac involvement or severe neurologic disease.[13]

Reference

Reference

  1. ↑ Brucellosis. CDC. http://wwwnc.cdc.gov/travel/yellowbook/2016/infectious-diseases-related-to-travel/brucellosis. Accessed on February 3, 2016
  2. ↑ Brucellosis. CDC. http://wwwnc.cdc.gov/travel/yellowbook/2016/infectious-diseases-related-to-travel/brucellosis. Accessed on February 3, 2016
  3. ↑ Colmenero JD, Reguera JM, Martos F, SΓ‘nchez-De-Mora D, Delgado M, Causse M; et al. (1996). “Complications associated with Brucella melitensis infection: a study of 530 cases”. Medicine (Baltimore). 75 (4): 195–211. PMIDΒ 8699960.
  4. ↑ Mantur BG, Amarnath SK, Shinde RS (2007). “Review of clinical and laboratory features of human brucellosis”. Indian J Med Microbiol. 25 (3): 188–202. PMIDΒ 17901634.
  5. ↑ Overturf ML, Druihet RE, Fitz A (1979). “The effects of kallikrein, plasmin, and thrombin on hog kidney renin”. J Biol Chem. 254 (23): 12078–83. PMIDΒ 159304.
  6. ↑ Doganay M, Aygen B. Human brucellosis: An overview. Int J Infect Dis 2003; 7:173.
  7. ↑ Young EJ (1995). “Brucellosis: current epidemiology, diagnosis, and management”. Curr Clin Top Infect Dis. 15: 115–28. PMIDΒ 7546364.
  8. ↑ Zamani A, Kooraki S, Mohazab RA, Zamani N, Matloob R, Hayatbakhsh MR; et al. (2011). “Epidemiological and clinical features of Brucella arthritis in 24 children”. Ann Saudi Med. 31 (3): 270–3. doi:10.4103/0256-4947.81543. PMCΒ 3119967. PMIDΒ 21623056.
  9. ↑ Mousa AM, Bahar RH, Araj GF, Koshy TS, Muhtaseb SA, al-Mudallal DS; et al. (1990). “Neurological complications of brucella spondylitis”. Acta Neurol Scand. 81 (1): 16–23. PMIDΒ 2330811.
  10. ↑ Pappas G, Bosilkovski M, Akritidis N, Mastora M, Krteva L, Tsianos E (2003). “Brucellosis and the respiratory system”. Clin Infect Dis. 37 (7): e95–9. doi:10.1086/378125. PMIDΒ 13130417.
  11. ↑ Herrick JA, Lederman RJ, Sullivan B, Powers JH, Palmore TN (2014). “Brucella arteritis: clinical manifestations, treatment, and prognosis”. Lancet Infect Dis. 14 (6): 520–6. doi:10.1016/S1473-3099(13)70270-6. PMCΒ 4498663. PMIDΒ 24480149.
  12. ↑ FAO/WHO/OIE Brucellosis in humans and animals. WHO (2006). http://www.who.int/csr/resources/publications/Brucellosis.pdf Accessed on February 3, 2016
  13. ↑ Brucellosis “Dennis Kasper, Anthony Fauci, Stephen Hauser, Dan Longo, J. Larry Jameson, Joseph Loscalzo”Harrison’s Principles of Internal Medicine, 19e Accessed on December 9th, 2017

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2] Danitza LukacVishal Devarkonda, M.B.B.S[3]