Hepatitis B vaccination in the Royal Australian Navy

In   Issue Volume 2 No. 2 Doi No https://doi-ds.org/doilink/03.2023-12585117/JMVH Vol 2 No 2

Surgeon Lieutenant-Commander A.G Robertson RAN

The Naval Health Services are responsible for the health care of all RAN personnel. The Naval Health Services1 mandate includes the provision of preventive as well as curative health services with a primary aim of ensuring that a high percentage of Naval personnel are fit for operational duties, especially for seagoing duties.

Australia, apart from some high risk groups, has a low incidence of hepatitis B infection. The prevalence of HBV markers is 3 to 6 percent in the Australian population1. Naval ships, however, operate constantly throughout South East Asia and the South West Pacific where the prevalence of HBV markers may be over 80 percent in some populations2 and there is a high prevalence of carriers. Additionally, other countries’ military personnel have been shown to have an increased prevalence of hepatitis B markers. Although this increased prevalence has not been shown in Pavli’s study of serological markers in RAN personnel1, naval personnel have been involved in tattooing, accidents and unsafe sex in these areas, despite educational campaigns, with a consequential increase in risk.

History

Given these factors, the RAN has been developing policy in this area for nearly 20 years. Navy first issued policy in 1975 when routine screening of personnel was not recommended3.

In April 1983, hepatitis B vaccine was released in Australia. Navy issued policy in August 1983 stating that the vaccine was not to be given without specific approval from Navy Office. Following the National Health and Medical Research Council recommendations on screening and immunization of high risk groups in August 1983 and 1984, the RAN policy was reconsidered. In June 1985, a Naval Health Circular4 was issued requiring the screening of dental and laboratory personnel for hepatitis B and the offer of H-B-Vax to these personnel.

In November 1987, the NH and MRC recommended that Australians residing in endemic areas should be vaccinated against hepatitis B5. The Surgeon General, Australian Defence Force (SGADF) recommended that all Defence Department Personnel with postings of three months or more in endemic areas be immunised.

With the introduction of Engerix B vaccine by Smith, Kline and Beecham in late 1987, SGADF introduced a Technical Policy Directive6 requiring:
– HBsAg testing of all entrants
– HBsAg testing of at risk populations, including medical staff
– immunization of at-risk populations.

By August 1998, the Director General, Naval Health Services (DGNHS) had questioned the rationale, on cost-effective grounds, of testing entrants and RAN policy throughout 1988 and 1989 was not to test entrants but to carry out the other requirements of the Directive. In addition, by May 1989, there were increasing operational requests from ships and patrol boats for the vaccination of their crews. The ensuing discussions considering operational demand, cost-effectiveness (based on Pavli et al’s paper1), the requirement to maintain the integrity of the ‘floating’ blood bank, and the decreasing cost of the vaccine, led to a review. On 30 January 1990, SGADF notified his intention of introducing phased vaccination for all personnel, starting with entrants and health service personnel7.

A Navy Health Circular was issued in March 1990 requiring the screening and vaccination of all new entrants and the vaccination of at risk groups. This was followed in August 1990 by the issue of an SGADF Technical Policy Directive8 requiring:
– the screening for HBsAg of entrants and those personnel clinically suspected of having or carrying hepatitis B
– the immunization of entrants
– the continued screening of HBsAg with routine HIV screening
– immunization of the remainder of the Defence Forces progressively, without either pre- or post-vaccination screening.

The use of condoms and infection control procedures was also reinforced.

In 1991, a census was carried out to identify the effectiveness of the programme. Ships and establishments were directed again to have all vaccinations complete by 1 March. The SGADF policy was updated and refined9 and in January 1993, the RAN carried out a further census of the vaccination programme.

Censuses

The census in 1991 showed different pictures between the fleet and establishments.

In fleet, three quarters were vaccinated or in the progress of being vaccinated (Figure 1). This was still of considerable concern because of fleet operations in South East Asia and the South West Pacific.

[See Figure 1 in download]

The establishments, however, were of more concern, with 45 percent not yet commenced on the vaccination programme (Figure 2).

[See Figure 2 in download]

The picture at the census in February 1993 was considerably different (Figure 3). Ninety-two point five percent of Fleet was now vaccinated with only 0.5 percent not yet started.

[See Figure 3 in download]

Similarly, the majority of personnel at the establishments were now vaccinated (Figure 4).

[See Figure 4 in download]

The remaining high number of incompletely vaccinated personnel were primarily entrants undergoing their hepatitis B course. This percentage is unlikely to change markedly as new groups enter the RAN. Vaccinations are continuing, with the majority of personnel expected to be fully vaccinated by the end of 1993.

Discussion

Is the ADF doing the right thing? There is good evidence to support current policy.

Firstly, ADF methods. The ADF has elected to immunize all of its personnel, commencing with high risk groups. This is supported by Atler et al10 who have found the percentage of hepatitis B due to heterosexual transfer is increasing and targeting only high risk groups may not be effective. Indeed, the rising incidence of hepatitis B has forced the US to reconsider its position and to broaden recommendations to include those with occupational and lifestyle risks11.

The ADF also does not routinely do pre- or post-vaccination testing. Although advocated by some parties12, such testing is not advocated by either Australian13 or overseas authors, including the Immunisation Practices Advisory Committee (ACIP) of the Centre for Disease Control14. The ADF does, however, recommend the serological testing of those at high risk, a practice which is generally supported14,15.

Secondly, we need to look at results. Pavli et al1 estimated an attack rate in RAN personnel of less than one percent, which is similar in scale to the US military rate of 0.5 percent. Is vaccinating a population with such a low attack rate cost effective? Numerous studies have examined this question. Given the three to ten percent of adults who subsequently become carriers, and the reduced cost of vaccines, now only $21 for a Naval course, the literature would support this view. Indeed, Mauskopf et al16 asserts that the vaccine programme would only have to avoid one or more cases per 6,517 low risk workers to be cost-effective.

Additional analysis, utilizing vaccine at $7 a dose and strike rates of 0.35% to 2%, suggest that such a regime is both cost-effective and cost beneficial17,18,19. Even Pavli et al1, who felt immunization was not cost-effective in 1988, noted that it was likely to become cost effective as vaccine costs fell. With vaccine costs at one-third of their 1988 values, vaccination of populations with attack rates of less than one percent, using the Mulley model20, is cost effective.

Effectiveness can be measured by calculating the effect of the programme on the incidence of new disease and of carriers. As between three and ten percent develop chronic carrier states, with the potential for chronic active hepatitis and hepatic cancer in the future, any regime ideally should prevent carrier states. Whittle et al21 have found hepatitis B vaccination 97 percent effective in preventing chronic infections. The RAN’s programme has already identified a number of chronic carriers and enabled their closer monitoring. Review in five years is anticipated to show a drop in carrier rates with associated long term benefits. Operationally, the integrity of the ‘floating blood poo’, now screened for hepatitis B, hepatitis C and HIV, will remain at a high standard.

Conclusion

Where to now? Research is continuing into the effectiveness of various immunization strategies, and a combined hepatitis A – hepatitis B vaccination study has commenced at the Australian Defence Force Academy this year. Research into non-responders and the timing of booster shots is also planned.

Navy has implemented an effective hepatitis B immunization programme that will stand it in good stead in the future. Mass programmes of this type can be useful in groups with occupational risks of HBV and should be considered as part of any overall vaccination strategy.

 

 

References

  1. Pavil P et al, 1989. The prevalence of serological markers for hepatitis B virus infection in Australian Naval personnel. Med J Aust 151:71-75 2. Maher CP et al, 1991. Seroepidemiology of hepatitis B infection in children in Vanuatu. Med J Aust 154:249-253 3. RAN Medical Technical Instruction 27, 1975 4. Naval Health Circular – Policy 22/85 5. National Health and Medical Research Council letter 87/29567 dated January 1988. 6. SGADF Technical Policy Directive 213/88 dated 10 July 1988 7. SGADF minute 73/1990 dated 20 January 1990 8. SGADF Technical Policy Directive 213/90 9. SGADF Health Policy Directive 214 10. Atler MJ et al, 1990. The changing epidemiology of hepatitis B in the United States. JAMA 263(9):1218-1222 11. Stoeckle MY, Douglas RG, 1992. Infectious diseases. JAMA 268(3):366-368 12. Coassart YE, 1991. Cost-effectiveness of hepatitis B vaccine in Greece. Int J Tech Assess in Health Care7(3):256-262 13. Whitby M, 1991. Testing for immunity after hepatitis B vaccination. MJA 154(6):638 14. Immunisation Practices Advisory Committee, 1991. Hepatitis B virus. A comprehensive strategy for eliminating transmission in the United States through universal childhood vaccination. MMWR 40(RR-10):1-25 15. Waldrom HA, 1990/ Antibody response to hepatitis B vaccination. BJIM 47:354-355 16. Mauskopf JA et al, 1991. Benefit cost analysis of hepatitis B vaccine programmes of occupationally exposed workers. JOM 33(6):691-698 17. Hatziandreu EJ et al, 1991. Cost-effectiveness of hepatitis B vaccine in Greece. Int J Tech Assess in Health Care 7(3):379-402 19. Lahaye D et al, 1987. Cost benefit analysis of hepatitis B vaccination. Lancet 441-443 20. Mulley AG et al, 1982. Indications for use of hepatitis B vaccine, based on cost effectiveness analysis. NEJM 307:644-652 21. Whittle HL, et al; 1991. Vaccination against hepatitis B and protection against chronic viral carriage in the Gambia. Lancet 337(8744):747-750

Acknowledgements

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