Contents
- 1 Introduction
- 2 List of countries by continental group
- 3 Disease risks and recommendations by continental group and country
- 4 Accidents, injuries and recreational water hazards
- 5 Prevention of travellers' diarrhoea and other food and water-borne diseases
- 6 Prevention of malaria
- 7 Arthropod-borne diseases (other than malaria)
- 8 Immunisation for overseas travel
- 9 Sexually transmitted and blood-borne infections, including HIV and hepatitis B, and overseas travel
- 10 Respiratory diseases and travel
- 11 Environmental hazards: heat, cold and altitude
- 12 Dangerous bites and stings
- 13 Medical considerations for the journey: travel by air, sea or land
- 14 Travellers with pre-existing medical conditions
- 15 Pregnancy and travel
- 16 Travel with children
- 17 The returning travelle
- 18 Bibliography
- Appendix 1 (37KB PDF)
- Appendix 2 (76KB PDF)
- Index of Countries
- Yellow fever endemic zone - South America
- Yellow fever endemic zone - Africa
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8 Immunisation for overseas travel
8.1 Introduction
Immunisation requirements for international travel are often the primary health concern of both prospective travellers and their doctors, usually followed by the choice of malaria tablet.
Immunisation is only one part of health advice for travellers. Attendance for immunisation provides an opportunity to deliver further health protection information on, for example, prevention of accidents and travellers' diarrhoea (Chapters 4 and 5), or specific advice relevant to the individual traveller.
The disease risk for the individual traveller should be assesed, as far as is possible, when choosing travel vaccines. The risk to a business traveller, for example, visiting only the most hygienic, air-conditioned premises for a few days should not be equated with that for someone travelling extensively to rural areas of the same country where not only is the risk to health increased but the facilities for medical treatment are likely to be less developed. The information on which to base such decisions is sometimes inadequate, not least because of limited reporting from some of the geographical areas of greatest risk. Some risks may be seasonal, or limited to certain geographical areas, and many are influenced by personal lifestyle or occupation, eg the risk for hepatitis B and HIV (Chapter 9). The risk of vaccine preventable disease for package holiday travel will depend on the itinerary and on the behaviour of the individuals involved, but will often be low.
Travellers may be informed by travel companies or embassies that "no vaccinations/immunisations are needed" or "nothing is needed" for a certain destination, and may omit to seek further medical advice. Education of travellers should include the information that "nothing needed" may mean no certificates are officially required but that optional immunisations, usually more important for personal health protection, may be advised in addition to other health-related precautions.
8.2 International Certificates of Vaccination
The International Health Regulations adopted by the World Health Organization were devised to help prevent the international spread of diseases and, in the context of international travel, to do so with the minimum of inconvenience to the passenger (WHO, International Travel and Health 2000).
It should be remembered that the Regulations are more a public health measure for the receiving country than for protection of the individual.
8.2.1 Yellow Fever
Yellow fever is now the only disease for which an international vaccination certificate may be required for entry into a country. Many countries (not the UK) require a valid International Certificate of Vaccination from travellers arriving from, or who have been in transit through, yellow fever infected areas or countries with infected areas. The maps inside the back page show the "yellow fever endemic zones" where there is a potential risk of infection. Some countries consider these zones as "infected" areas for the purpose of International Certificate of Vaccination requirements. Other countries require a certificate from all entering travellers. Details of requirements are included in the entries for individual countries (Chapter 3). They are published annually in International Travel and Health, Vaccination Requirements and Health Advice (WHO). Failure to provide a valid certificate to the port health authorities could, in some circumstances, result in a traveller being immunised, denied entry or quarantined.
The International Certificate is valid for ten years beginning ten days after the vaccination date; this should be entered with the month written in letters. It should be signed by the person authorised by the national health administration (a stamp alone is not acceptable) and by the patient (or parent/guardian). (NB. All the partners in a practice which is a Yellow Fever Vaccination Centre are deemed by the Department of Health to be authorised persons). The manufacturer and batch number of the vaccine and the official stamp of the centre must also be included in the correct space provided.
If a physician advises that an individual should not be immunised on medical grounds, including infants under nine months of age, an exemption certificate may be provided (Appendix 1).
Yellow fever vaccination is recommended for travel to all countries in the endemic zones, whether or not an international certificate is required, and especially if rural areas will be visited. (See country by country advice).
8.2.2 Yellow Fever Designated Centres
Yellow fever vaccine may be administered only at centres which are designated by the national health administration and recorded with WHO. This is to ensure that vaccine storage, administration and certification is carried out correctly. (The current UK list of designated centres is available from http://tap.ccta.gov.uk/doh/yellcode.nsf/pages/Home?open, together with information for practices wishing to apply for designation.)
8.2.3 Cholera
In 1973, the International Health Regulations were amended so that no country should require a certificate of vaccination against cholera (WHO, International Travel & Health 1994). This followed acceptance that cholera vaccination does not prevent introduction of the infection into a country. Many countries continued to require proof of cholera immunisation long after 1973, but gradually the present position has been reached where there are no official requirements.
Until recently unofficial demands at a few international air and sea ports resulted in travellers continuing to request immunisation for certification. Reports of such incidents are now extremely rare, and appear to be confined to remote land borders in areas where there have been recent cholera outbreaks.
The conventional parenteral vaccine provided poor protection and is no longer available in the UK. In the rare circumstance where an unofficial demand may be anticipated, confirmation of non-requirement of cholera vaccine may be given on official notepaper signed and stamped by the medical practitioner (Appendix 1). Some new generation cholera vaccines are marketed in certain European countries.
Most travellers are at extremely low risk of contracting cholera. Prevention is by food and water hygiene (see Chapter 5).
8.2.4 Meningococcal vaccination for the pilgrimage to Mecca
Saudi Arabia requires pilgrims to produce proof of immunisation against meningococcal infection issued not more than three years and not less than ten days before arrival in the country. Details are listed in the Saudi Arabia entry (see also important information at 8.4.4).
8.3 Vaccines
| Live vaccines | Inactivated vaccines | ||
|---|---|---|---|
| Measles Mumps Rubella |
} and MMR | Diphtheria toxoid Tetanus toxoid Pertussis |
} and combination vaccines |
| Oral poliomyelitis Oral typhoid BCG (TB) Yellow fever |
Poliomyelitis (injectable) Haemophilus influenza b (Hib) Influenza Pneumococcal |
||
|
Hepatitis A Hepatitis B |
} and combination vaccines | ||
| Typhoid Injectable (and hepatitis A combined vaccine) Meningococcal (A&C) Japanese encephalitis Tick-borne encephalitis Rabies |
|||
8.4 Recommendations
These are contained in the invidual country entries in Chapter 3. They assume that childhood immunisations, including BCG, are up to date.
8.4.1 Routine immunisations
All individuals should have completed primary tetanus, diphtheria and poliomyelitis courses. A full course comprises five doses of each.When over ten years has elapsed since the primary course and travel is to a developing area a tetanus booster should be given; a diptheria booster should also be given if travel is for more than one month. The appropriate combined diptheria/tetanus preparation is now normally used when either of these is due. A polio booster may be advised for travel to certain countries if ten years has elapsed since the primary course (see country by country advice).
8.4.2 Influenza and pneumococcal vaccines
Those who are recommended to have influenza or pneumococcal vaccine as part of UK policy are advised to be immunised before travel.
8.4.3 Hepatitis A
Where hepatitis A protection is recommended for travel, vaccine is the preferred option rather than normal immunoglobulin. There is some evidence of protection even when vaccine is given after exposure, so that if time before departure is short, the vaccine is still considered likely to prevent or at least modify the infection.
8.4.4 Meningococcal vaccine
Conjugate meningococcal C vaccine (MenC) has recently been introduced into the routine UK childhood immunisation programme. This vaccine protects only against group C meningococcal infection, while much meningococcal infection abroad is caused by Group A. The currently used vaccine for travel is therefore meningococcal A&C polysaccharide vaccine.
A quadravalent vaccine, also containing Y and W135 strains, is now more widely available and is the recommended vaccine for all pilgrims to Saudi Arabia.
Some mild urticarial reactions have been reported in children given A&C vaccine shortly after MenC vaccine. It is not known whether this rate is higher than could be expected with A&C alone, but an interval of two weeks is recommended if A&C vaccine is required following MenC. Until further evidence emerges it is also currently recommended that where MenC vaccine is due following A&C vaccine, the MenC vaccine is delayed until six months after A&C vaccine. In high risk situations, however, MenC vaccine should not be delayed. The local Consultant in Communicable Disease Control or Immunisation Co-ordinator should be consulted.
8.4.5 Combination vaccines
Combination travel vaccines are now available containing more than one vaccine in one preparation, such as adult diphtheria and tetanus. Vaccines recommended should be appropriate for the individual.Where a recipient requires protection against both diseases, at least for the early doses, a combination preparation can be useful.
However, where the two components of a combination (eg hepatitis A with hepatitis B or hepatitis A with typhoid) are not both indicated for the individual traveller, the combined vaccine should not replace the individual vaccines.Where the individual components differ in duration of immunity or number of doses required to complete the course, combined vaccines can also complicate scheduling. Single antigen vaccines may be required for boosters.
Modern vaccines and sharp needles produce little discomfort when skilfully administered and many recipients are unable to report the exact number of injections received.
8.4.6 Infants and small children travelling
Routine infant immunisations may be advised earlier than normally scheduled when children are travelling to high-risk countries for prolonged periods and may have close contact with the indigenous population (for example staying with relatives abroad). In particular, earlier immunisation may be advised if travel is so prolonged that routine childhood immunisations would be delayed.
Hepatitis B vaccine and BCG can be given from birth where indicated. Polio can, if necessary, be commenced from birth, but an extra dose is then advised later on; DTP-Hib can be administered from six weeks of age. Children over six months of age who have not yet received their first dose of MMR, travelling to visit relatives in a measles endemic area, should be offered MMR. However two further doses of MMR are then recommended: one as soon as practicable after the first birthday and the normal pre school booster.
Hepatitis A is usually a mild disease in young children, and infection results in lifelong immunity. Vaccine is therefore often considered unnecessary in this age group (although opinions differ). It is more likely to be considered for those travelling to visit friends and relatives for longer periods in areas of high endemicity. There is an argument that the children should be immunised to prevent secondary infection in non-immune adult contacts of the children, eg play group leaders, on their return.
The addition of conjugate meningococcal group C vaccine (MenC) to the routine schedule may result in a small child travelling to, for example, Africa requiring the A&C vaccine close to the new vaccine (see 8.4.4).
The table of immunisations (pages 94-104) provides the lower age limit for travel vaccines where these are specified and the varying ages at which the paediatric dose changes to the adult dose.
8.5 Schedules
Wherever possible, the recommended intervals between doses and between vaccines should be followed and time allowed for antibody to be produced, courses completed and any reaction to have dissipated before the date of travel.
In theory each travel vaccine should be given at least ten days (and preferably three weeks) from another in order to identify the source of any reaction. In practice, time constraints, travel dates and sheer practicality have resulted in many vaccines being given simultaneously without apparent adverse effects.
8.5.1 Live Vaccines
Live vaccines should be administered at least three weeks apart or on the same day. However, the two oral vaccines, typhoid and polio, are usually separated (by at least two weeks) on the theoretical grounds of possible interference in the gut. There is no evidence to preclude oral typhoid being given with yellow fever or human normal immunoglobulin (HNIG).
Live virus vaccines may suppress the tuberculin test and so should be delayed until after the test has been read.
8.5.2 Inactivated Vaccines
Inactivated vaccines can be given simultaneously with any other vaccine, but at a different site, the number given taking into account the comfort of the patient. Concurrent administration of vaccines can make it difficult to elucidate adverse reactions. An exception to the simultaneous administration rule concerns meningococcal A&C and the recently introduced conjugate meningococcal C vaccine (see Meningococcal vaccine 8.4.4).
8.5.3 Human Normal Immunoglobulin (see 8.4.3)
The antibody response to MMR (or measles,mumps or rubella given separately) could be inhibited by HNIG which should be delayed until three weeks after the vaccine. If HNIG has already been given, three months should elapse before giving MMR.
HNIG has not been shown to inhibit yellow fever, oral typhoid or BCG and any effect it has on OPV is unlikely to be significant where the OPV is a booster.
HNIG is anyway usually given after the vaccines and closer to the departure date because of its rapid efficacy and shorter duration of action.
8.5.4 Timing
Courses of most travel vaccines, plus the single dose vaccines, can be administered over a four week period. The final doses should ideally be completed a little ahead of the departure date to allow immunity to develop. It can take up to four weeks, for instance, for full immunity to develop following Japanese encephalitis vaccine. (This vaccine is anyway recommended to be completed at least ten, and preferably 14, days prior to travel because of the possibility of a delayed allergic reaction.)
More time will be required if a primary course of tetanus, polio or diphtheria is necessary. If the full course cannot be completed before departure, it is usually worth giving the maximum number of doses that the travel departure date allows, completing the course on return.
Travellers should be encouraged to plan to start immunisations well in advance of travel.
| Vaccine and age given | Primary course | Interval between doses | Reinforcing doses | Comments |
|---|---|---|---|---|
| BCG | ||||
| Celltech Medeva From birth |
Single dose, 0.1ml id (0.05ml <3/12 of age) after Heaf testing (except for neonates) | N/A | None | Given only if no BCG scar and skin test negative |
| Diphtheria Adsorbed diphtheria vaccine, child - Celltech Medeva |
||||
| <10 years | 3 doses (usually as DTP), 0.5ml sc or im | 4 weeks | At school entry or 3 years after last dose | |
| Adult low dose diphtheria vaccine - Distributed by Farillon (as part of the National Childhood Immunisation Programme) | ||||
| >10 years | 3 doses, 0.5ml sc or im | 4 weeks | At school leaving (as Td) or 10 years after primary course | see 8.4.1 |
| Diphtheria and Tetanus vaccine for adults and adolescents (Td) | ||||
| Diftavax
Aventis Pasteur MSD > 10 years |
3 doses, 0.5 ml deep sc or im | 4 weeks | After 10 years | see 8.4.1 | Hepatitis A - vaccine |
| Avaxim
Aventis Pasteur MSD 16 years and over |
Single dose, 0.5ml im | Booster at 6-12 months predicted to provide antibodies which persist for at least 10 years | ||
| Havrix Monodose
Glaxo Smith Kline 16 years and over |
Single dose, 1ml im | Booster after 6-12 months to provide long- term antibody titres (5-10 years) | ||
| Havrix Junior Monodose
Glaxo Smith Kline 1-15 years |
Single dose, 0.5ml im | Booster after 6-12 months provides immunity for up to 10 years | see 8.4.6 | |
| Vaqta Adult
Aventis Pasteur MSD 18 years and over |
Single dose, 1ml im | Booster after 6-12 months: `long-term duration of serum antibodies to hepatitis A virus unknown' | ||
| Vaqta Paediatric
Aventis Pasteur MSD 2 years up to and including 17years |
Single dose, 0.5ml im | Booster at 6-18 months: 'long term duration of serum antibody to hepatitis A virus unknown' | see 8.4.6 | |
| Hepatitis A - Immunoglobulin (see 8.3) | ||||
| Gammabulin Baxter Hyland Immuno Kabiglobulin (when available) Pharmacia and Upjohn | ||||
| <10 Years | Single injection 125mg for 2 months protection; 250mg for 3-5 months protection | For single short trips | ||
| <10 Years | 250mg for 2 months protection; 500mg for 3-5 months protection | For single short trips | ||
| Hepatitis A + Hepatitis B combined | ||||
| Twinrix Adult
Smith Kline Glaxo 16 years and older |
3 doses, 1ml im | 0, 1 and 6 months | Booster with combined vaccine recommended 5 years after initiation of primary course. If monovalent vaccines used as booster: hepatitis A - administer after 10 years; hepatitis B administer after 5 years | |
| Twinrix Paediatric
Glaxo Smith Kline 1 year up to and including 15 years |
3 doses, 0.5ml im | 0,1 and 6 months | As for Twinrix Adult | |
| Hepatitis A + Typhoid combined | ||||
| Hepatyrix
Glaxo Smith Kline 15 years and over |
Single dose, 1ml im | Booster of hepatitis A at 6-12 months. Single dose of Vi polysaccharide vaccine every 3 years. | ||
| Hepatitis B | ||||
| Engerix B Glaxo Smith Kline | 3 doses, adults and chidren over 15 years, 1ml (20mg) im; neonates and children 15 years and under, 0.5ml (10mg) im | 0, 1 and 6 months | 'Not known whether responders will need booster doses' | For more rapid immunisation
the third dose may be given at
2 months and a booster at
12 months. Accelerated schedule for Engerix B in those 18 years and over: 0, 7 and 21 days with a reinforcing dose at 12 months |
| HB Vax II
Aventis Pasteur MSD
16 years and over |
3 doses, 1ml im | 0, 1 and 6 months or 0, 1, 2 and 12 months | 'Need for booster not yet defined' | Accelerated schedule (0, 1, 2 and 12 months) may induce protective antibody levels earlier |
| HB Vax II Paediatric
Aventis Pasteur MSD Birth through to and including 15 years |
3 doses, 0.5ml | 0, 1 and 6 months or 0, 1, 2 and 12 months | As for HB Vax II | As for HB Vax II |
| Influenza | ||||
| Various manufacturers Check individual manufacturers' current data sheet |
Dose will vary according to age | For risk groups: annual immunisation with vaccine containing the most recent strains | Influenza vaccine is prepared annually from strains recommended for that year by the World Health Organization | |
| Japanese encephalitis NB: Two dose schedules are included in the data sheet; however in non-immune travellers, 3 doses are usually advised for optimum protection. Complete course at least 10-14 days pre-travel. |
||||
| Biken, manufactured in Japan and distributed by Aventis Pasteur MSD | ||||
| < 3 years (but no data < 1 year) | 3 doses, 0.5 ml sc | 0, 7 and 30 days | Booster after 2-4 years | Unlicensed vaccine. Where 3 doses impossible, 2dose regimen provides immunity for 3 months in 80% of recipients. Manufacturer states that 0, 7, 14 days schedule may be used where urgent. |
| or 2 doses, 0.5 ml sc |
0, 7 days | Booster after 3 months | ||
| > 3 years | 3 doses, 1.0 ml sc | 0, 7 and 30 days | Booster after 2-4 years | |
| or 2 doses, 1.0 ml sc |
0, 7 days | Booster after 3 months | ||
| Green Cross, manufactured in Korea and distributed by MASTA | 2 doses | 0, 7-14 days | Booster after 1 year and then 3 years (annually if at high risk) | Unlicensed vaccine. See note above |
| Meningococcal | ||||
| ACWY Vax
GlaxoSmithKline >2 years |
Single dose, 0.5ml deep sc | Children aged 2 months to 2 years may get short lived response to the A, W135 and Y antigens | ||
| AC Vax
GlaxoSmithKline >2 months |
Single dose, 0.5ml deep sc or im | In adults and children > 5 years, immunity will persist for up to 5 years. In younger children, particularly those < 2 years, immunity against group C meningitis is unlikely to persist for more than 1 or 2 years | 8.4.4 | |
| Mengivac A+C
Aventis Pasteur MSD >18 months |
Single dose, 0.5ml deep sc or im | Post vaccination immunity lasts at least 3 years | 8.4.4 | |
| Pneumococcal | ||||
| Pneumovax II
Aventis Pasteur MSD 2 years and above |
Single dose, 0.5ml sc or im | Re-vaccination is not usually recommended, except for individuals in whom antibody levels are likely to have declined more rapidly (see 10.3) | ||
| Poliomyelitis | ||||
| OPV Distributed by Farrillon as part of the National Childhood Immunisation Programme | 3 doses | 4 weeks | Children at entry and
before leaving school Adults 10 yearly if at continuing risk |
Faecal excretion of vaccine virus up to 6 weeks. May be longer if immuno suppressed. |
| IPV Distributed by Farillon | 3 doses, 0.5ml sc or im | 4 weeks | As above | Unlicensed vaccine; named patients only |
| Rabies Pre-exposure | ||||
| Aventis Pasteur MSD (human diploid cell vaccine) No lower age stated |
3 doses, 1.0ml sc or im or 0.1 ml id | 0, 7 and 28 days | 2-3 years if at continued exposure | Id route is unlicensed |
| 2 doses, 1.0ml sc or im or 0.1 ml id | 0 and 28 days | Booster at 6-12 months then 2-3 years | Most, but not all,individuals
seroconvert after 2 doses. May be acceptable for travellers who are not animal handlers |
|
| Rabipur (purified chick embryo cell vaccine) Chiron distributed by MASTA | 3 doses, 1.0ml im | 0.7 and 21 or 28 days | Generally every 2-5 years (see manufacturer's information) | |
| Tetanus | ||||
| Celltech Medeva | ||||
| <10 years (usual childhood course) | 3 doses usually as DTP, 0.5ml sc or im | 4 weeks | At school entry or 3 years after last dose | |
| >10 years | 3 doses adsorbed vaccine or as Td 0.5ml sc or im | 4 weeks | At school leaving (as Td) or 10 years after primary course; further booster 10 years later | |
| Tick-borne encephalitis - vaccine | ||||
| Ticovac
Baxter Hyland Immuno >36 months |
3 doses, 0.5ml im (the first dose should be 0.25ml for children 36 months to 15 years) | 0, 21 days-3 months, then 9-12 months | Booster after 3 years | Vaccine licensed Spring 2000 Protection after 2 doses lasts 12 months. |
| or 2 doses, 0.5 ml im (the first dose should be 0.25ml for children 36 months to 15 years) | 0 and 14 days, then 1 year | |||
| FSME-Immuno
Baxter Hyland Immuno No lower age limit given |
3 doses 0.5 ml sc or im | 0, 4-12 weeks then, 9-12 months | Booster after 3 years | Unlicensed vaccine named patients only |
| or 2 doses, 0.5 ml sc or im | 0 and 14 days | 2 dose regimen gives immunity for one year | ||
| Encepur
Chiron (distributed by
MASTA) 12 years and over |
3 doses, 0.5ml im | 0, 4 weeks then 9-12 months | Booster after 3 years | Unlicensed vaccine - for named patients only |
| or, 0, 7, 21 days then 12-18 months | ||||
| Tick-borne encephalitis - immunoglobulin | ||||
| FSME-BULIN Baxter Hyland Immuno | Single dose, dependent on body weight | Unlicensed. Rarely considered for pre-exposure, may be considered for post-exposure (see 7.4) | ||
| Typhoid | ||||
| Typherix
GlaxoSmithKline > 2 years |
Single dose, 0.5 ml im | Single dose every 3 years | ||
| Typhim Vi
Aventis Pasteur MSD > 18 months |
Single dose, 0.5ml deep sc or im | Single dose every 3 years | ||
| Typhoid | ||||
| Vivotif Live, oral
Strain Ty21a (distributed
by MASTA) > 6 years |
3 doses of one capsule | Alternate days | Full 3 dose course annually | Remind recipient of appropriate storage (in fridge) |
| Hepatyrix (combined hepatitis A + typhoid) - see under Hepatitis A vaccine | ||||
| Yellow fever | ||||
| Celltech Medeva > 9 months |
Single dose, 0.5 ml sc | 10 yearly | Given at designated centres only | |
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