| Literature DB >> 26158401 |
Víctor-Guillermo Sequera1, Salomé Valencia1, Alberto L García-Basteiro2,3, Andrés Marco4, José M Bayas1,2.
Abstract
From the first day of imprisonment, prisoners are exposed to and expose other prisoners to various communicable diseases, many of which are vaccine-preventable. The risk of acquiring these diseases during the prison sentence exceeds that of the general population. This excess risk may be explained by various causes; some due to the structural and logistical problems of prisons and others to habitual or acquired behaviors during imprisonment. Prison is, for many inmates, an opportunity to access health care, and is therefore an ideal opportunity to update adult vaccination schedules. The traditional idea that prisons are intended to ensure public safety should be complemented by the contribution they can make in improving community health, providing a more comprehensive vision of safety that includes public health.Entities:
Keywords: communicable diseases; disease prevention; health promotion; prisons; vaccination
Mesh:
Year: 2015 PMID: 26158401 PMCID: PMC4685700 DOI: 10.1080/21645515.2015.1051269
Source DB: PubMed Journal: Hum Vaccin Immunother ISSN: 2164-5515 Impact factor: 3.452
Importance of vaccination in prisons
| Access to vulnerable social groups |
|---|
| Groups with little normal access to the health system |
| Prisoners come from disadvantaged social strata (educational and socioeconomic level) |
| Greater history of illicit drug use before entering prison |
| Greater history of alcohol abuse |
| High prevalence of carriers of communicable diseases and other morbidities |
| Overrepresentation of especially-vulnerable groups: LGTB, sex workers, immigrants |
| Progressively greater proportion of elderly adults |
| High risk of acquiring infections in prison |
| Sexual activity, often unprotected, in prisons |
| High rate of starting or returning to illicit drug use (injectable and non-injectable) |
| Tattoos / piercings |
| Physical violence (injuries, rapes) |
| Permanent contact with the community |
| High rotation rates in prison (short sentences, transfers) |
| Visits/ staff/ temporary release |
| High risk of extreme behavior in the first weeks after release (drug abuse) |
| Prison population is known and concentrated in one place |
| Population identified and easily located |
LGBT: gay, lesbian, transgender, bisexual.
Figure 1.Comparison of US estimates of lifetime prevalence (%) of viral hepatitis risk factors and seroprevalence of hepatitis A, B and C virus exposure in inmates vs. the overall population 2009. HBc IgG, IgG antibody to hepatitis B core antigen; HCV Ab, antibody to hepatitis C Total virus. HAV IgG, IgG antibody to hepatitis A. MSM, men who have sex with men. Figure modified from “Viral hepatitis in incarcerated adults: a medical and public health concern;” by Hunt, DR & Saab S.
Figure 2.Transmission of communicable diseases inside and beyond prisons. Figure modified from Guidelines for the Control of Tuberculosis in Prisons, WHO 1998.
Biological Hazards Prison
| Transmisson by serum | |
| HIV | |
| Hepatitis B | |
| Hepatitis C | |
| Respiratory transmission | |
| Tuberculosis | |
| Influenza | |
| Measles | |
| Mumps | |
| Rubella | |
| Meningococcal infection | |
| Pneumococcal infection | |
| Enteric transmission | |
| Hepatitis A | |
| Transmission by contact | |
| Herpes simplex | |
| Varicela Zoster | |
| Scabies | |
| Viral conjuntivitis | |
| HPV | |
| Diphtheria | |
| Tetanus | |
Vaccine available.
Prevalence of Hepatitis B in prison
| Country (reference) | City, State or Region | Survey year | Prisons | Population | Seroprevalence (%) |
|---|---|---|---|---|---|
| Australia (35) | New South Wales, Queensland, Tasmania and Western Australia | 2004, 2007, 2010 | 29 | 1388 914(IDUs) | 2.3% 3.1%(IDUs) |
| Brazil (68) | Goias (State) | 2007–08 | 1 | 150 | 0.7% – 1.3% |
| Brazil (69) | Sao Pablo (State) | 2003 | 1 | 333 | 2.4% – 1.2% |
| Croatia (65) | All country | 2005–2007 | 20 | 3290 | 1.3% |
| England and Wales (66) | Different regions | 1997 – 98 | 8 | 3930 775 (IDUs) | 8% 20%(IDUs) |
| Ghana (70) | Different regions | 2004–05 | 8 | 1366 | 25.5% |
| Hungary (41) | All country | 2007–09 | 20 | 4894 | 1.5% |
| Iran (64) | Isfahan | 2009 | 2 | 970 (IDUs) | 3,3% (IDUs) 13,9% (IDUs) |
| Mexico (67) | West central Mexico | 2007 | 1 | 30 | 20% |
| Nigeria (71) | Nasarawa (State) | 2007 | 4 | 300 | 23% |
| Pakistan (34) | Karachi | 2007–08 | 1 | 357 | 5.9% |
| Spain (31) | All country | 2008 | 18 | 342 | 2.6% |
| USA (42) | Different States | Studies between 1975 and 2005 | 25 | nd / meta-analysis 23 studies | 0,9% – 8% 6,5% – 42% |
EEUU: United States of America. IDUs: prevalence among injecting drug users. HbsAg=hepatitis B surface antigen; HBc IgG=IgG antibody to hepatitis B core antigen.
* = hepatitis B surface antigen (HbsAg).
** = IgG antibody to hepatitis B core antigen (HBc IgG).
*** = HbsAg plus HBc IgG positives. nd = no data.
Research gaps: improving the introduction of prison vaccination programs
| 1 | Cost-effectiveness assessments of integrated vaccine program introduction |
| 2 | Health technology assessment of prison vaccine program introduction |
| Promotion of reports on prison vaccination with a focus on developing countries | |
| 4 | Promotion of studies on the implementation of vaccination in female prisons |
| 5 | Gender studies on vaccination in prisons |
| 6 | Research on elderly prisoners and the impact of vaccines in this group |
| 7 | Research on the impact of vaccines on mentally-ill inmates |
Recommended steps to ensure vaccination schedules in prisons
| Integration of health services with the prison system | 1 | The authority and responsibility for health care in prison lies with the health system |
| 2 | Ensure the integration of prisons with other community health services | |
| Application of a vaccination schedule | 3 | Ensure compliance with the vaccination schedule for healthy adults |
| 4 | Ensure access to vaccination of persons with specific risk factors (HIV, HCV, MSM) | |
| 5 | Establish vaccination priorities for each prison according to identified epidemiological factors and local resources | |
| 6 | Evaluate strategies (coverage, adherence, follow up outside prison) |
Summary of Strategies and Recommended Guidelines
| Vaccine | Recommendations/Strategies | Schedules | Comments |
|---|---|---|---|
| Hepatitis B | All new inmates with negative or unknown serology. | Normal: 0, 1 and 6 months Accelerated: 0, 1, 2 and 12 m Rapidly-accelerated: 0, 7, 21 d and 12 m | Previous serology recommended. |
| New inmates with risk factors: IDUs, chronic disease, MSM, mental illness. | |||
| Hepatitis A | All new inmates with negative or unknown serology. | HA: 0 – 6 months HAV/HAVB: 0, 1, 2 and 12m HAV/HBV: 0, 7, 21 and 12 m | Evaluate age and place of origin. |
| New inmates with risk factors: IDUs (pre-serology not necessary), MSM and hepatic risk factors. | |||
| Tetanus/diphtheria | Prisoners without demonstrated history of vaccination. | 0, 1 and 6–12 months (Td) | Evaluate vaccination if there are lesions. |
| All new inmates with last dose > 10 y ago. | 1 booster dose (Td) | ||
| PCV13 | Prisoners aged more than 65 y | 0 (PCV13) and 6–12 months (PPSV23). If previous PPSV23, PCV13 > = 1 y | Two doses of VP23 recommended in specific risk groups |
| Prisoners aged more than 18 y with baseline pathology included in recommendations | 0 (PCV13), PPSV23 minimum of 8 weeks later | ||
| Seasonal influenza | All new inmates | One annual dose during influenza season. | |
| Risk groups: > 65 years, pregnancy, chronic medical condition or immunosuppression | |||
| Mumps, measles and rubella | All new inmates with negative or unknown serology. | History of childhood vaccination: 1 dose. No history of vaccination: 0, 1 month. | |
| Women of child-bearing age. | |||
| Human papilloma virus | Women with no history of vaccination or incomplete vaccination. | 0, 1–2 and 6 months | Prioritize persons aged less than 26 y Upper limits vary by country |
| Meningococcal C | Inmates aged less than 26 y | 1 doses | |
| Varicella | Prisoners with proven history of vaccination. | 0–4,8 weeks | |
| Prisoners who remember receiving one dose. | One booster dose |
IDUs: injecting drug users. MSM: Men who have sex with men. HAV: Hepatitis A virus. HBV: Hepatitis B virus. PCV13: 13-valent pneumococcal conjugate vaccine. PPSV23: 23-valent pneumococcal polysaccharide vaccine.
CDC 2014 recommendations.
See risk groups: CDC 2012.
WHO 2014: recommends an upper age limit of age of 26 y.