Leptospirosis
Leptospirosis
Leptospirosis
DOI: 10.5812/ircmj.16030
Published online 2014 October 5. Research Article
*Corresponding Author: Alireza Davoudi, Department of Infectious Diseases and Tropical Medicine, Antimicrobial Resistance Research Center, Mazandaran University of Medical
Sciences, Sari, IR Iran. Tel: +98-1232316319, Fax: +98-1232316319, E-mail: eiy_iran@yahoo.com
Received: November 9, 2013; Revised: January 21, 2014; Accepted: February 24, 2014
1. Background
Leptospirosis is a zoonotic infection in humans and ani- penetration of tissue barriers, including invasion to the
mals caused by Leptospira species of the spirochete fam- central nervous system and aqueous humor of the eye.
ily (1). There are two stages in the disease process. The first Transendothelial migration of spirochetes is facilitated
phase occurs during the active leptospira infection named by a systemic vasculitis, accounting for a broad spectrum
as bacteriemic or septicemic phase. In this phase, flu-like of clinical illness (2, 7). Severe vascular injury can be de-
symptoms (including fever, severe headache, myalgia, veloped, leading to pulmonary hemorrhage, ischemia of
chills, nausea and vomiting, conjunctival suffusion, ab- the renal cortex and tubular-epithelial cell necrosis, and
dominal pain, anorexia, coughing and sore throat) occur destruction of the hepatic architecture, resulting in jaun-
for more than 5-7 days. The second phase, immunologic, dice and liver cell injury, with or without necrosis (2, 8-11).
occurs immediately after the bacteriemic phase or 1-3 days Immune-mediated mechanisms have been postulated
after asymptomatic period. Patient's symptoms vary in to affect the severity of symptoms and immune mecha-
this phase. Many patients have mild fever, headache, vom- nisms, including circulating immune complexes, anticar-
iting and rash. Aseptic meningitis is most common in the diolipin antibodies, and antiplatelet antibodies, but their
second phase. Ten percent of patients with leptospirosis significance has not been proven yet (2). Old age, pneumo-
are affected by a severe form of disease or Weil's syndrome nia, renal failure, and thrombocytopenia are associated
(with a mortality rate of 5-40%) (2). Common symptoms of with a bad prognosis (1). Thrombocytopenia occurs in the
this syndrome are due to liver, kidney and blood vessels absence of disseminated intravascular coagulation and
involvement. Symptoms of this severe disease occur af- may accompany progressive renal dysfunction (2).
ter 3 to 7 days and include persistent jaundice, decreased
2. Objectives
urine output, anemia, rash, hypotension, shock, changes
in consciousness, skin and mucosal hemorrhagic lesions
and pulmonary hemorrhage (1-6). On entering the body, In this study, we investigated the role of corticosteroids
there is widespread hematogenous dissemination and to improve thrombocytopenia due to leptospirosis.
Copyright © 2014, Iranian Red Crescent Medical Journal; Published by Kowsar. This is an open-access article distributed under the terms of the Creative Commons
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Alian S et al.
Moderate
2-censored
15 19 34 0.8
Sever 13 9 22
Cum Survuval
Total
0.6
28 28 56
0.4
subgroup) and three in the control group (all in the
severe thrombocytopenia subgroup). One died due
to acute renal failure and others died due to multi- 0.2
Hospitalizationb
Cum Survuval
4.916 0.027
0.6
Case 5.241 5.000
0.4
Control 6.231 6.000
Table 4. Demographic Characteristics and Frequency of Clinical and Laboratory Findings in the Groups a
Group/Analysis Variable Received Corticosteroid Group Not-received Corticosteroid P-Value Total
Group Frequency
Number of Patients 28 28 56 (100)
Moderate Thrombocytopenia 15 19 34 (60.7)
Severe Thrombocytopenia 13 9 22 (39.2)
Gender 0.789
Female 14 13
Male 14 15
Age 49.75 ± 8.45 46.68 ± 11.26 0.254
Kidney involvement 5 (17.9) 5 (17.9) 1.000
Lung involvement 5 (17.9) 6 (21.4) 0.737
Liver involvement 9 (32.1) 12 (42.9) 0.408
Intubation 4 (14.2) 4 (14.2) 1.000
Mortality 2 (7.1) 3 (10.7) 0.500
ICU admission, Mean Rank 28.02 28.98 0.758
Dialysis
Platelet Consumption, Mean Rank 27.79 29.21 0.568
Durationb 0.003
Mean 4.41 ± 0.197 5.72 ± 0.318
Median 4 ± 0.215 5 ± 0.255
Hospitalizationc 0.028
Mean 5.24 ± 0.244 6.23 ± 0.329
Median 5 ± 0.221 6 ± 0.297
Rural 24 (85.7) 24 (85.7) 48 (85.7)
Farmer 24 (85.7) 25 (89.2) 49 (87.5)
Weakness 28 (100) 28 (100) 56 (100)
Fever 28 (100) 28 (100) 56 (100)
Anorexia 20 (71) 20 (71) 40 (71.4)
Myalgia 25 (89.28) 24 (85.71) 49 (87.5)
Arthralgia 20 (71.42) 20(71.42) 40 (71.4)
N/V 9 (32.1) 7 (25) 16 (28.5)
Cough 6 (21.4) 5 (17.8) 11 (19.6)
Headache 7 (25) 7 (25) 14 (25)
Abdominal pain 5 (17.8) 5 (17.8) 10 (17.8)
Hemoptysis 1 (3.5) 2 (7.1) 3 (5.35)
Diarrhea 2 (7.1) 2 (7.1) 4 (7.1)
Hypotension 3 (10.7) 3 (10.7) 6 (10.7)
Tachypnea 5 (17.8) 6 (21.4) 11 (19.6)
Tachycardia 9 (32.1) 9 (32.1) 18 (32.1)
LOC 2 (7.1) 3 (10.7) 5 (8.9)
Fever blister 8 (28.5) 8 (28.5) 16 (28.5)
Rash 5 (17.8) 5 (17.8) 10 (17.8)
Suffusion 11 (39.2) 12 (42.8) 23 (41.0)
Icter 9 (32.1) 12 (42.8) 21 (37.5)
LAP 0 1 (3.5) 1 (1.7)
Rales 4 (14.2) 4 (14.2) 8 (14.2)
Abdominal tenderness 5 (17.8) 6 (21.4) 11 (19.6)
Splenomegaly 2 (7.1) 3 (10.7) 5 (8.9)
Hepatomegaly 0 1 (3.5) 1 (1.7)
Muscular tenderness 10 (35.7) 10 (35.7) 20 (35.7)
Arrhythmia 1 (3.5) 0 1 (1.7)
Oliguria 5 (17.8) 5 (17.8) 10 (17.8)
EKG Changes 2 (7.1) 1 (3.5) 3 (5.35)
CXR Changes 5 (17.8) 7 (25) 12 (21.4)
5. Discussion
There was no significant difference between the two (not in the moderate subgroup). To optimally determine
groups regarding renal, pulmonary or hepatic involve- whether adjunctive steroid use in leptospirosis is ben-
ment, intubation, mortality rate and hospitalization eficial, an adequately powered randomized control trial
duration in ICU. The above situations were not improved with a larger sample size is recommended.
Acknowledgements
with treatment of glucocorticoid. Despite the fact, re-
quired duration for the improvement of thrombocytope-
nia and duration of hospitalization in two groups were We would like to thank nurses of the infection diseases
different significantly. On the other hand, treatment with Ward of Ghaemshahr Razi Hospital to help in data col-
glucocorticoid caused more rapid recovery of thrombo- lection.
cytopenia and shorter hospital stay. Corticosteroids have
an essential role in the treatment of many immune-as- Authors’ Contributions
sociated diseases, such as SLE, rheumatoid arthritis (RA) Study concept and design: Shahriar Alian, Alireza
and ITP. Prednisolone (1 mg/kg/day) is used for the treat- Davoudi, Narges Najafi, Hasan Asghari, Jamshid Yazdani.
ment of mild ITP (Immune or Idiopathic Thrombocyto- Acquisition of data: Shahriar Alian, Hasan Asghari, Ali-
penic Purpura); while, high-dose corticosteroid (steroid reza Davoudi. Analysis and interpretation of data: Hasan
pulse therapy) is used for the severe forms (1, 13). Russell Asghari, Jamshid Yazdani. Drafting of the manuscript:
Villanueva et al. in the Philippines, performed an investi- Alireza Davoudi. Critical revision of the manuscript for
gation on 36 patients with leptospirosis and found no sig- important intellectual content: Narges Najafi. Statistical
nificant reduction in mortality, duration of hospitaliza- analysis: Jamshid Yazdani.
tion and dialysis rates between the control and steroids
Funding/Support
groups (12). Furthermore, a study by Trivedi et al. in India
performed on 602 patients showed that renal and liver
involvements had no effect on mortality (14). Similarly, in This project was supported by a grant received from the
this study, statistical analysis showed that renal, lung or Vice-Chancellor for research of Mazandaran University of
liver involvements and the severity of thrombocytopenia Medical Sciences.
had no effect on mortality. Contrary to our results, a clini-
cal trial on 30 patients by VV Shenoy et al. in India showed References
that corticosteroid therapy within 12 hours of pulmonary 1. Speelman P. leptospirosis. In: Braunwald E, Fauci A, kasper D edi-
involvement due to leptospirosis decreased the mortality tors. Harrison's principles of Internal Medicine. New York: McGraw-
rate (15). Hill; 2012.
2. Levett P. Leptospira species. In: Mandell GL, Bennett JE, Dolin R
Our study showed that corticosteroid therapy decreased editors. principles and practice of infectious disease. 7th ed; 2010.
hospital stay only in severe subgroup thrombocytopenia pp. 3059–65.
3. Mansour-Ghanaei F, Sarshad A, Fallah MS, Pourhabibi A, sis. Expert Opin Pharmacother. 2004;5(4):819–27.
Pourhabibi K, Yousefi-Mashhoor M. Leptospirosis in Guilan, a 10. Vitale G, La Russa C, Galioto A, Chifari N, Mocciaro C, Caruso R,
northern province of Iran: assessment of the clinical presenta- et al. Evaluation of an IgM-ELISA test for the diagnosis of human
tion of 74 cases. Med Sci Monit. 2005;11(5):CR219–23. leptospirosis. New Microbiol. 2004;27(2):149–54.
4. Bharti AR, Nally JE, Ricaldi JN, Matthias MA, Diaz MM, Lovett MA, 11. Yitzhaki S, Barnea A, Keysary A, Zahavy E. New approach for sero-
et al. Leptospirosis: a zoonotic disease of global importance. Lan- logical testing for leptospirosis by using detection of leptospira
cet Infect Dis. 2003;3(12):757–71. agglutination by flow cytometry light scatter analysis. J Clin Mi-
5. Kuo HL, Lin CL, Huang CC. Reversible thick ascending limb dys- crobiol. 2004;42(4):1680–5.
function and aseptic meningitis syndrome: early manifestation 12. Villanueva R, Onoya C, Esmiller F, Francisco M. Use of steroid in
in two leptospirosis patients. Ren Fail. 2003;25(4):639–46. leptospirosis to improve survival: an exploratory study. Philipp J
6. Aliyan S, Babamahmoodi F, Najafi N, Ghasemian R, Teymori S, Microbiol Infectious Dis. 2010;39(1):71–5.
Shahbaznezhad L. Clinical and paraclinical findings of leptospi- 13. Trivedi SV, Vasava AH, Bhatia LC, Patel TC, Patel NK, Patel NT.
rosis in Mazandaran. J Mazandaran Univ Med Sci. 2006;16:78–85. Plasma exchange with immunosuppression in pulmonary
7. Babamahmoodi F, Motamed N, Mahdavi MR, Nikkhah F, Gha- alveolar haemorrhage due to leptospirosis. Indian J Med Res.
vi Bonyeh KH. Seroepdemiological study of leptospirosis in 2010;131:429–33.
GhaemshahrMazandaranprovinc. J Mazandaran Univ Med Sci. 14. Trivedi SV, Vasava AH, Patel TC, Bhatia LC. Cyclophosphamide in
2006;16:51–6. pulmonary alveolar hemorrhage due to leptospirosis. Indian J
8. Boland M, Sayers G, Coleman T, Bergin C, Sheehan N, Creamer E, Crit Care Med. 2009;13(2):79–84.
et al. A cluster of leptospirosis cases in canoeists following a com- 15. Shenoy VV, Nagar VS, Chowdhury AA, Bhalgat PS, Juvale NI. Pul-
petition on the River Liffey. Epidemiol Infect. 2004;132(2):195–200. monary leptospirosis: an excellent response to bolus methyl-
9. Faucher JF, Hoen B, Estavoyer JM. The management of leptospiro- prednisolone. Postgrad Med J. 2006;82(971):602–6.