| Literature DB >> 28587195 |
Maria Cristina Schneider1, Jorge Velasco-Hernandez2, Kyung-Duk Min3, Deise Galan Leonel4, David Baca-Carrasco5, Matthew E Gompper6, Rudy Hartskeerl7, Claudia Munoz-Zanzi8.
Abstract
Record-breaking and devastating rainfall events have occurred in the past decade. Rain and floods are considered the main risk factors for leptospirosis and several outbreaks have been reported following extreme weather events. In such situations, one possible intervention to prevent leptospirosis cases in high-risk groups is the use of chemoprophylaxis. However, not enough evidence of its effect is available. The objectives of this study were to review the literature on the current practices of chemoprophylaxis for leptospirosis and to explore, using a mathematical model, how various chemoprophylaxis scenarios may affect the progression of a leptospirosis outbreak. Twenty-six peer-reviewed publications were selected (10 quantitative studies, two systematic reviews and 14 articles of other types). Oral doxycycline was the most used antibiotic for chemoprophylaxis of leptospirosis. Post-exposure prophylaxis was assessed in four studies following a natural disaster. Although evidence of the effectiveness of post-exposure prophylaxis is inconsistent, the direction of association supported a protective effect for morbidity and mortality. The theoretical model showed how the assumed benefit of chemoprophylaxis was influenced by the time and rate of administration. Future models should consider the heterogeneity of affected communities, improved estimates of the effect of chemoprophylaxis on leptospirosis infection and disease, as well as potential detrimental impacts. Additional research is critical to provide clear evidence-based recommendations for leptospirosis control during an outbreak. The results of this study suggest that chemoprophylaxis may provide some protection in reducing the number of leptospirosis cases after a high-risk exposure; however, the effective benefit may depend on a variety of factors such as the timing and coverage of prophylaxis. The information summarized can be used to support decision-making during a high-risk event.Entities:
Keywords: chemoprophylaxis; extreme weather; leptospirosis; outbreaks
Mesh:
Substances:
Year: 2017 PMID: 28587195 PMCID: PMC5486280 DOI: 10.3390/ijerph14060594
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Number of natural disasters by type and subtype, Central America, 2000–2016.
| Type | Subtype | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007 | 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Drought | Drought | 2 | 4 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | 3 | 0 | 1 | 2 | 1 | 3 | 3 | 0 | 22 |
| Earthquake | Ground movement | 2 | 3 | 0 | 4 | 1 | 1 | 1 | 1 | 0 | 2 | 1 | 2 | 3 | 1 | 4 | 0 | 0 | 26 |
| Epidemic | - | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
| Bacterial disease | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | |
| Viral disease | 1 | 0 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | 4 | 1 | 0 | 0 | 4 | 1 | 1 | 0 | 15 | |
| Extreme temperature | Cold wave | 1 | 1 | 1 | 1 | 1 | 0 | 3 | 0 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 10 |
| Severe winter conditions | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 1 | |
| Flood | - | 3 | 2 | 1 | 1 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 15 |
| Coastal flood | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | |
| Flash flood | 1 | 2 | 1 | 1 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 10 | |
| Riverine flood | 4 | 0 | 9 | 4 | 5 | 9 | 4 | 9 | 12 | 9 | 13 | 12 | 4 | 2 | 5 | 6 | 1 | 108 | |
| Landslide | Landslide | 1 | 0 | 1 | 2 | 1 | 2 | 2 | 1 | 2 | 0 | 3 | 1 | 0 | 0 | 0 | 1 | 1 | 18 |
| Mass movement (dry) | Landslide | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
| Storm | - | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
| Convective storm | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 0 | 5 | |
| Tropical cyclone | 4 | 10 | 6 | 2 | 0 | 16 | 3 | 9 | 6 | 4 | 15 | 6 | 2 | 4 | 7 | 1 | 8 | 103 | |
| Volcanic activity | Ash fall | 2 | 0 | 2 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | 1 | 1 | 0 | 1 | 0 | 9 |
| Wildfire | - | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
| Forest fire | 1 | 0 | 1 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 4 | |
| Land fire | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | |
| Total | 24 | 22 | 29 | 19 | 12 | 30 | 14 | 22 | 22 | 23 | 35 | 25 | 12 | 13 | 21 | 18 | 15 | 356 |
Source: International Disaster Database from the Centre for Research on the Epidemiology of Disasters.
Figure A1Flood in the Department of Leon Nicaragua (photo credit: Gilberto Moreno).
Figure A2Road after a flood in Leon, Nicaragua (photo credit: Gilberto Moreno).
Figure A3Health workers after a flood bringing health care to an affected population in Achuapa, Nicaragua (photo credit: Gilberto Moreno).
Figure 1Conceptual diagram of the potential effect of chemoprophylaxis on the dynamics of a leptospirosis outbreak and its health impact.
Model parameter description and baseline values.
| Parameter | Description | Baseline | References |
|---|---|---|---|
| Per capita contact rate (1/day) | 1.42 | Set parameter (default) | |
| Half-saturation density | 0.5 | Set parameter (default) | |
| Mortality rate by other causes | 0 | Set parameter (default) | |
| Leptospire recruitment rate into environment (1/day) | 0.002 | Set parameter (default) | |
| Leptospire clearance rate in environment (1/day) | 0.2 | [ | |
| Incubation period (days) | 10 | [ | |
| Infectious period (days) | 7 | [ | |
| Probability of severe leptospirosis given infection | 0.2 | Based on Bharti et al. for icteric and other severe forms [ | |
| Probability of mild leptospirosis given infection | 0.3 | Based on Bharti et al. and Faucher et al. 80% of infections are mild or asymptomatic [ | |
| Chemoprophylaxis administration rate (1/day) | 0.2 | Set parameter (default) | |
| Chemoprophylaxis duration (days) | 14 | [ | |
| Probability of developing severe leptospirosis after chemoprophylaxis | 0.1 | Set parameter. 50% lower than before chemoprophylaxis | |
| Probability of developing mild leptospirosis after chemoprophylaxis | 0.15 | Set parameter. 50% lower than before chemoprophylaxis | |
| Probability of not being infected after chemoprophylaxis | 0.3 | Based on Seghal et al. but with a lower protective effect [ |
Figure 2Flow chart for the literature review on chemoprophylaxis use for leptospirosis.
Summary of quantitative studies and systematic reviews on the effectiveness of chemoprophylaxis for leptospirosis.
| Author [Ref] | Year | Country | Antibiotics | Target Population | Situation | Administration | Effectiveness of Treatment |
|---|---|---|---|---|---|---|---|
| Chusri [ | 2014 | Thailand | Doxycycline (200 mg single dose) | Local residents | Flooding | Post exposure | Protective efficacy for leptospiral infection: 92.0% (CI = 81.2%–96.6%) and for leptospirosis: 95.6% (CI = 78.2%–99.3%), among participants with laceration wound. Protective efficacy for leptospiral infection: 89.2% (CI = 63.6%–96.67%), among participants exposed to flood water ≤3 h/day. |
| Shivaraj [ | 2012 | India | Doxycycline (200 mg/week) | Paddy field farmers | Farming | Pre-exposure | Incidence of leptospirosis: nil in the test group and 7.29% in the control group ( |
| Bhardwaj [ | 2010 | India | Doxycycline (200 mg/week) | Local residents | Flooding | Post exposure | Univariate analysis: OR = 0.43 (CI = 0.23–0.78). Multivariate analysis: Adj OR = 0.77 (C.I = 0.35–1.69) |
| Galloway [ | 2009 | N/A * | Doxycycline and azithromycin | N/A | N/A | N/A | Prophylaxis with doxycycline compared to no-prophylaxis strategy. Prophylaxis provided cost savings, decreased severity of illness and mortality, and improved health outcomes. |
| Illangasekera [ | 2008 | Sri Lanka | Penicillin (500 mg/day for a month) | Farmers | Farming | Pre-exposure | Of 5 patients hospitalized with fever, 3 tested positive for leptospirosis, all from the placebo group. |
| Belmaker [ | 2004 | Israel | Doxycycline (200 mg/week) | Dairy workers | Animal husbandry | Post exposure | Either with or without chemoprophylaxis, no dairy workers exposed to herds infected with |
| Sejvar [ | 2003 | Malaysia | Doxycycline (200 mg/week) | Athletes | Race in risk area | Pre-exposure | Taking doxycycline before or during the race was protective (RR = 0.4, 95% CI = 0.2–1.2). |
| Sehgal [ | 2000 | India | Doxycycline (200 mg/week) | Local residents | Endemic area | Pre-exposure | No statistically difference was observed in the infection rates among the doxycycline and the placebo group. A statistically significant difference was observed in the clinical disease attack rates (3.11 vs. 6.82%) between the two groups. |
| Gonsalez [ | 1998 | Brazil | Doxycycline (200 mg single dose) | Local residents | Flooding | Post exposure | A protective association of doxycycline for confirmed leptospirosis cases (RR = 2.3) and seroconversion only (RR = 2.0) was observed, but it was not statistically significant. |
| Takafuji [ | 1984 | Panama | Doxycycline (200 mg/week) | US Army during deployment | Training | Pre-exposure | 95% efficacy. Attack rate of 4.2% in the placebo group compared to an attack rate of 0.2% in the doxycycline group ( |
| Brett-Major [ | 2009 | N/A* | Doxycycline | Varied (Meta-analysis) | Varied (Meta-analysis) | Varied (Meta-analysis) | Three randomized clinical trials met the inclusion criteria. Pre-exposure antibiotic prophylaxis with doxycycline may decrease laboratory identified |
| Guidugli [ | 2000 | N/A* | Doxycycline | Varied (Meta-analysis) | Varied (Meta-analysis) | Varied (Meta-analysis) | Two randomized clinical trials met the inclusion criteria. Doxycycline seems to be an efficient intervention when used in a specific clinical situation, i.e., soldiers who train in endemic areas with high risk of exposure. |
* Not applied (N/A) because was a multi countries study.
Other publications on the effectiveness of chemoprophylaxis for leptospirosis.
| Author | Year | Journal | Type of the Study | Prophylactic Antibiotic | Recommendations/Conclusions |
|---|---|---|---|---|---|
| Devishree [ | 2015 | Review | Doxycycline | Pre-exposure: doxycycline (200 mg/week). Post exposure prophylaxis with doxycycline based on the degree of exposure (low, moderate, high) | |
| Charan [ | 2012 | Review | Doxycycline and penicillin | The role of antibiotics in chemoprophylaxis of leptospirosis is uncertain due to lack of large scale trials. More evidence based studies are required to generate evidence for antibiotics being used as chemoprophylaxis. | |
| Dechet [ | 2012 | Chemoprophylaxis campaign description | Doxycycline | The effectiveness of the massive chemoprophylaxis campaign was inconclusive. | |
| McBride [ | 2010 | Review | Doxycycline | May only act to reduce clinical illness rather than infection. May cause nausea and vomiting | |
| Cruz [ | 2009 | Review | Doxycycline | When high-risk and short-term exposure to leptospira is anticipated, chemoprophylaxis is effective. Doxycycline prophylaxis does not prevent leptospiral infection in endemic areas, but has a protective effect in reducing morbidity and mortality during outbreaks. | |
| Pavli [ | 2008 | Review | Doxycycline | Pre-exposure doxycycline chemoprophylaxis should be considered for adventure travelers, athletes, and military recruits involved in high-risk activities in endemic areas. | |
| Christopher [ | 2005 | Review | Doxycycline | Dr. E.T. Takafuji and colleagues at the Walter Reed Army Institute of Research demonstrated that prophylaxis using doxycycline conferred a 95% risk reduction. | |
| Edwards [ | 2004 | Review | Doxycycline | Short-term chemoprophylaxis with doxycycline in healthy young adults is effective but larger studies are required to demonstrate effectiveness in other ages and resident populations. | |
| Faucher [ | 2004 | Review | Doxycycline | The efficacy of pre-exposure doxycycline has been established by two randomized studies performed in different epidemiological environments. However, the efficacy of doxycycline in post exposure prophylaxis is not firmly established. | |
| Levett [ | 2004 | Review | Doxycycline | Doxycycline may be considered for chemoprophylaxis if high-risk exposures are anticipated. | |
| Bharti [ | 2003 | Review | Doxycycline | Chemoprophylaxis may be impractical to administer in highly endemic areas, but is likely to be useful for adventure travelers and military personnel who visit endemic areas, and also in accidental laboratory infection. | |
| Lo Re III [ | 2003 | Clinical recommendation | Doxycycline | Doxycycline is an effective prophylaxis for travelers to endemic areas who have a high risk of exposure. | |
| Haake [ | 2002 | Case report | Doxycycline | The benefits of doxycycline prophylaxis must be weighed against the potential adverse side effects of prophylaxis. Doxycycline may be used as a chemoprophylaxis strategy against both malaria and leptospirosis for patients who anticipate having a relatively high level of exposure. Clinical trials are needed to validate antibiotics with longer serum half-lives, such as azithromycin. | |
| Gilks [ | 1988 | Case report | Doxycycline and penicillin | Doxycycline, 100 mg twice weekly, over a period of 6 weeks provides a rational regimen for post-exposure prophylaxis, which takes into account the possibility of prolonged incubation. |
Figure 3Effect of chemoprophylaxis on the total number of leptospirosis cases. Prevalence of infection (total cases) without (red line) and with (green line) chemoprophylaxis initiated at day 5 (A) and at day 10 (B) at a rate (1/θ) of 0.2.
Proportion of cases prevented (up to T = 30 days) compared with no chemoprophylaxis as function of chemoprophylaxis rate (θ) and day of start of application (t0).
| Time of Administration (t0, day) | Chemoprophylaxis Rate ( | Proportion of Cases Prevented |
|---|---|---|
| 5 | 0.01 | 0.12 |
| 5 | 0.05 | 0.47 |
| 5 | 0.1 | 0.67 |
| 5 | 0.2 | 0.84 |
| 5 | 0.5 | 0.93 |
| 10 | 0.01 | 0.12 |
| 10 | 0.05 | 0.43 |
| 10 | 0.1 | 0.62 |
| 10 | 0.2 | 0.77 |
| 10 | 0.5 | 0.88 |
Figure 4Impact of chemoprophylaxis initiated at day 5 and at day 10, at varying rates (θ) and durations (∅), on total number of leptospirosis cases.