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Eurosurveillance, Volume 18, Issue 45, 07 November 2013
Perspectives
Ethics of mandatory vaccination for healthcare workers
  1. Department of Paediatrics and Joint Graduate Programme in Bioethics, University of Crete, Heraklion, Greece
  2. European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden

Citation style for this article: Galanakis E, Jansen A, Lopalco PL, Giesecke J. Ethics of mandatory vaccination for healthcare workers. Euro Surveill. 2013;18(45):pii=20627. Article DOI: http://dx.doi.org/10.2807/1560-7917.ES2013.18.45.20627
Date of submission: 03 February 2013

Healthcare workers (HCWs) are at increased risk of contracting infections at work and further transmitting them to colleagues and patients. Immune HCWs would be protected themselves and act as a barrier against the spread of infections and maintain healthcare delivery during outbreaks, but vaccine uptake rates in HCWs have often been low. In order to achieve adequate immunisation rates in HCWs, mandatory vaccination policies are occasionally implemented by healthcare authorities, but such policies have raised considerable controversy. Here we review the background of this debate, analyse arguments for and against mandatory vaccination policies, and consider the principles and virtues of clinical, professional, institutional and public health ethics. We conclude that there is a moral imperative for HCWs to be immune and for healthcare institutions to ensure HCW vaccination, in particular for those working in settings with high-risk groups of patients. If voluntary uptake of vaccination by HCWs is not optimal, patients’ welfare, public health and also the HCW’s own health interests should outweigh concerns about individual autonomy: fair mandatory vaccination policies for HCWs might be acceptable. Differences in diseases, patient and HCW groups at risk and available vaccines should be taken into consideration when adopting the optimal policy.


Background

Healthcare workers (HCWs) – all persons employed in acute or long-term healthcare facilities having direct contact with patients or patient’s’ specimens, regardless of their employment status – are at increased risk of contracting infections and further transmitting them to colleagues and patients. Immunisation against vaccine-preventable diseases would protect HCWs themselves, act as a barrier against the spread of infections and maintain healthcare delivery during outbreaks. However, immunisation rates among HCWs have often been very low, even for highly transmissible infections such as influenza, measles, pertussis and hepatitis B [1-3]. Barriers to vaccination include not only concerns about vaccine effectiveness and safety, medical contraindications, religious beliefs and conscientious objection, but also inconvenience, underestimation of the person’s susceptibility to the infection and of the potential to spread it further, and belief that the disease may be mild, useful or acquired from the vaccine [4-7].

The gap between the desired level of vaccination and the reality raises the question whether voluntary uptake should be replaced by mandatory vaccination. This debate also emerges in outbreaks and pandemics, when control measures should be adopted rapidly, at a time when there is some scientific uncertainty regarding the vaccine. It should also be noted that no consensus exists on the desired vaccine uptake levels, say for influenza [6]. Mandatory policies are being increasingly adopted by healthcare institutions and public health authorities – in particular in the United States – but have generated vigorous opposition [8]. Legislation on mandatory smallpox vaccination dates from 1809 in the United States and from 1840 in Britain; in 1898, the concept of ‘conscientious objector’ was introduced into British law for parents objecting to smallpox vaccination for their children and in 1905 the United States Supreme Court ruled that the state could not require vaccination to protect an individual, but could do so to protect the public [9].

The ethical dimensions of mandatory vaccination have been analysed adequately for seasonal influenza, less so for pandemic influenza and even less for other highly transmissible diseases (e.g. measles, pertussis, hepatitis B) or the vaccine-preventable diseases as a whole. Here we review the involvement of HCWs in the transmission of vaccine-preventable diseases and the evidence on whether HCW vaccination contributes to patients’ health. It should be stressed that this evidence used in this article comes mainly from influenza studies. We also evaluate whether voluntary vaccination has failed and whether mandatory policies can achieve higher uptake rates and at what cost, present the practical and ethical arguments for and against mandatory policies, and try to draw some conclusions on the ethical rationale for implementing mandatory vaccination for HCWs. Given that this article is a perspective, we have cited only a small proportion of the numerous relevant studies.

For which vaccine-preventable diseases is HCW vaccination worth considering?

Most vaccine-preventable diseases are transmissible to a greater or lesser extent and have a basic immunisation schedule in childhood. These infections differ regarding the severity of infection, risk to patients or specific HCW groups and effectiveness of the vaccine. HCWs should be expected to be immune by the time they are employed. However, for some diseases, waning immunity may call for booster doses, e.g. for pertussis. Seasonal influenza requires annual vaccination and outbreaks or pandemics may require additional administration of existing or new vaccines.

Despite the long existence of effective vaccines, vaccine-preventable diseases remain a major health threat worldwide. In the United States, mortality rates of seasonal influenza are equal to that of breast cancer and three times that of human immunodeficiency/acquired immunodeficiency syndrome (HIV/AIDS) [8,10]. Measles is on the rise in Europe [3] and pertussis is also increasing in many countries worldwide [1]. Antimicrobial agents may be ineffective (e.g. for influenza where there is an issue of resistance or for pertussis) or do not exist (e.g. for measles). Hence, prevention including vaccination is of paramount importance.

Vaccine-preventable diseases may be transmitted before symptoms develop and are often subclinical, thus permitting HCWs to keep working and spreading the pathogens. Transmission involving HCWs has been reported for a variety of healthcare facilities and diseases, including seasonal and pandemic influenza, measles, mumps, rubella, varicella, pertussis, hepatitis A, hepatitis B and meningococcal invasive disease: this nosocomial transmission has led to outbreaks and deaths, and the burden for HCWs themselves has been considerable in terms of morbidity and mortality [2,3,11-13].

Are the effectiveness, safety and cost-effectiveness of HCW vaccination documented?

Vaccines are in general highly effective, in particular when the recipients are healthy adults, as HCWs often are. Most vaccines currently in use have been given to millions of individuals and have been shown to be safe. Long debate has cleared hepatitis B and measles-mumps-rubella vaccines from alleged side effects [14,15]. Guillain-Barré syndrome following influenza vaccination seems to be extremely rare; narcolepsy has recently been related to the pandemic influenza A(H1N1)pdm09 vaccine, but this vaccine has in general been shown to be safe [16]. HCW influenza vaccination has been reported to be cost-effective [17]: this might also be true for other vaccines, through prevention of illness, absenteeism and disruption of healthcare delivery.

Do patients benefit as a result of HCW vaccination?

Influenza-like illness and all-cause mortality were shown to decrease in residents of long-term care facilities when HCWs were vaccinated against influenza in several studies, including four randomised controlled trials [18-21]. Vaccination of five and eight HCWs was estimated to prevent one case of influenza-like illness and death of one resident, respectively [20]. However, a recent systematic review did not provide reasonable evidence that HCW influenza vaccination affects the outcome of elderly residents (aged 60 years or older) [22]. HCW influenza vaccination has been shown to protect hospitalised patients, including bone marrow transplant recipients [11,12]. The impact of HCW vaccination in acute care settings is more difficult to study, as patients may have been exposed to other, non-nosocomial contacts before and after hospitalisation.

Further well-designed studies seem to be required for firm conclusions to be drawn on whether vaccinating HCWs protects patients or residents of care facilities, on the numbers of HCWs to be vaccinated in order to prevent one nosocomial infection, and on risk assessment for different groups and settings. However, further randomised, placebo-controlled studies might not be ethical, given the existing evidence and the known protection by vaccines for HCWs and patients [23,24]. Not much is known about protecting patients through vaccinating HCWs for infections other than influenza and this lack of solid evidence should be taken into consideration when deciding on voluntary versus mandatory vaccination policies.

Have voluntary vaccination policies for HCWs failed?

Annual vaccination: seasonal influenza
Voluntary vaccination programmes for HCWs seem to have been fruitless for decades, despite consistent recommendations, dedicated efforts, vaccine availability free of charge, publicity (including posters and flyers), education, posters and flyers, incentives and rewards, buttons for vaccinated individuals to wear, and mobile vaccination teams [10,24,25]. Despite recommendations by the United States Centers for Disease Control and Prevention (CDC) on influenza vaccination for all HCWs since the early 1980s, uptake rates in the United States have stagnated around 40–50% [4,7], only reaching up to 60–70% after intense promotion and sustained campaigns [4,6,11]. In Europe, despite recommendations since at least 2000, uptake rates are commonly less than 35% and often less than 25% [6,17,26].

Basic vaccination: measles and pertussis
Immunity against measles and pertussis may be the result of both vaccination and natural infection, and it would seem reasonable to expect HCWs to be highly immune. However, susceptibility rates of HCWs to measles in Europe have been found to range from 3% to 17% [27]. Low vaccination rates have been reported for the booster dose of pertussis among HCWs in France (33%) [1] and Australia (13–23%) [28].

Pandemic influenza vaccination
HCWs were declared by the World Health Organization (WHO), CDC and the European Union (EU) Health Security Committee as apriority group to receive the pandemic influenza A(H1N1)pdm09 vaccine [29]. However, vaccine uptake rates by HCWs were not always high, ranging from 13% to 83% [2,5], compatible with the 2–82% shown for seasonal influenza in a 2005 review [6]. As with seasonal influenza, rates varied among different groups of HCWs [2].

Have mandatory vaccination policies for HCWs performed well?

Healthcare institutions often require, as a condition of employment, confirmed immunity to infections such as measles, rubella, mumps, varicella and hepatitis B and tuberculosis screening, and this policy has been well accepted [4,10,13,24].The first institution to make influenza vaccination a ‘fitness-for-duty’ condition for all HCWs seems to have been Virginia Mason Medical Center, Seattle, Washington, United States, effective from 2005, achieving rates of 98% [30]. Subsequent mandatory programmes in the United States have increased influenza coverage rates from 71% in 2007 to 98% in 2008 [24] and from 69% in 2009 to 96% in 2010 [25]. These policies have occasionally met intense resistance by individual HCWs and their associations in the United States [6,7,24,25,31,32] and the promising results may not be easy to replicate in all settings or in all European countries.

Enforcement of mandatory vaccination
Enforced mandatory policies are meant to be policies with well-defined consequences for HCWs who decline, such as firing, fines, reallocation to other positions, imposing a mask or prophylactic regimens during patient care and providing different badges to non-vaccinated HCWs [8,9,12,24,25,33]. Firing or resignation of the HCW have been reported in the United States, with rates of 0.02% to 0.15% [24,26,30], but not in Europe [33]. Even in European countries with mandatory policies, such policies may not be fully implemented in practice [33] and it is uncertain whether HCWs have ever paid fines for non-compliance.

Exemptions and declination policies
In mandatory vaccination programmes in the United States, HCWs have retained the right to apply for exemption, usually for medical (0.2–1.9% of all HCWs) or religious (0.1–2.4% of all HCWs) reasons [24,25,30,34]; however, little is known about this in Europe. Issues arise on how to distinguish between legitimate and illegitimate reasons and between conscientious objectors and ‘free riders’ (i.e. individuals relying on the immunity of others) and on how to achieve the desired vaccine uptake if objectors form a considerable proportion of HCWs. Furthermore, overuse of exemptions on non-documented medical, religious and conscience grounds might suggest that vaccination is not really important. Disease outbreaks have occurred in areas where too many HCWs opted out [9].

Several institutions have adopted declination policies, i.e. signed statements by HCWs who object to vaccination for hepatitis B or influenza [7,23]. Declination statements were provided by 10.7% of the HCWs in an influenza programme in the United States National Institutes of Health Clinical Center, in 2008–09 [34].

When asked, 25–75% of HCWs in Hong Kong, United Kingdom and Singapore would agree with mandatory vaccination for pandemic influenza [5] and 59% of nurses would agree with mandatory vaccination for seasonal influenza provided that declination would be allowed [35]. HCWs might be more likely to accept policies targeting specific groups of HCWs, such as those caring for infants or immunocompromised patients, and this seems to be a promising research field.

Is mandatory vaccination needed for HCWs?

An overview of arguments of a rather practical nature (Table 1) may elucidate important aspects of the voluntary versus mandatory vaccination debate.

Table 1. Practical arguments for and against mandatory vaccination for healthcare workers as a means to protect patients’ health


 
Improvement of voluntary uptake
Vaccine uptake is known to be affected by modifiable factors (such as education and ease of access to vaccination) and the potential of voluntary programmes may not have been exhausted [6,7,26]. Voluntary vaccination policies have often had little support and multifaceted programmes have not been widely implemented [6]. Making clear to HCWs that they serve as vectors for disease transmission to their own patients seems to be a key motivation [6,23,32]. Sustaining declination policies and requiring institutions to report HCW vaccination rates for a series of vaccine-preventable diseases as a measure of quality of care could facilitate vaccine uptake [19,23,33]. However, the definition of a HCW is sometimes  vague and high-risk groups should better be targeted, such as those caring for infants, elderly people and immunocompromised patients. Finally, voluntary policies respect civil liberties and the principles of subsidiarity and of least infringement [26].

Is mandatory vaccination of HCWs ethically justified?

Discussion to date has often focused on the principles of clinical ethics; however, ethical arguments for and against mandatory policies are also related to professional, institutional and public health ethics [31,36]. In public health ethics, the approach often differs from that of clinical ethics. For example, autonomy is a key principle in clinical ethics, but not in public health ethics. We present how principles and virtues have been used in vaccination issues, without weighing them against each other (Table 2).

Table 2. Ethical arguments for and against mandatory vaccination for healthcare workers as a means to protect patients’ health

Professional ethics: addressing professional obligations
Healthcare professional societies have a responsibility to guide their members on decorum and the virtues of healing professions and also to meet the public’s expectations. Public trust will be damaged if HCWs appear to suggest vaccines for others but avoid them for themselves [10,26]. Vaccination is consistent with a collective professional obligation, and being immune is a part of the responsibility of being a healer [7,9,31]. In general, HCWs have freely chosen their profession, and this assumes adopting professional virtues and accepting some level of personal risk in providing care. It could also be further argued that non-immune HCWs should accept being reallocated to positions without patient contact or leave the profession [8,31,32,36].

Institutional ethics: the duty to protect employees and patients and keep working
In addition to protecting their employees, healthcare institutions have an obligation to reduce risks to patients and residents and costs from nosocomial transmission, and to remain effective during disease outbreaks. Hence, there is an imperative for institutions to achieve adequate vaccination rates among HCWs by adopting the most appropriate policy (Figure) [26].

Figure. Proposed stepwise implementation of vaccination policies for healthcare workers upon employment and in controlling vaccine-preventable diseases

Public health ethics: control of disease and limits on liberty
Controlling the spread of infection is a top priority in public health [36]. Hence, when the choice is to be made between safety and liberty, limits on liberty may be justified, as the right of the community to protection seem to outweigh the right of HCWs to free decisions. Even spending resources on unsuccessful voluntary vaccination campaigns seems not to be justified, as such resources could better be used elsewhere [36].

Conclusions

It is morally justified to summon HCWs in particular to be voluntarily vaccinated, along with adherence to all other preventive measures for disease control. If voluntary vaccine uptake has failed to achieve the desired rates, mandatory policies should be considered, provided that benefits outweigh harm for HCWs, patients’ welfare is enhanced, and fair rules and exemptions are defined. Decisions should be balanced, taking into consideration differences in diseases, vaccines, specific healthcare settings and HCW groups at high risk, as well as special conditions such as epidemics. For supporters of mandatory vaccination, all scientific, ethical, legal, and financial conditions have been met. Vaccination should thus be routine for HCWs as are standard precautions and hand washing. For the opponents of mandatory policies, it is preferable for higher uptake rates to be achieved through consensus rather than coercion, as coercive policies would bear the cost of conflict and mistrust, devalue HCWs and thus alienate important allies and have long-term detrimental effects.

Healthcare institutions have a duty to protect patients, avoid nosocomial spread of infection, keep working efficiently during outbreaks and meet the public’s trust. The higher the immunity rates among HCWs, the better it is for themselves, their patients and the public. Hence there is a moral imperative for healthcare authorities to secure vaccination rates among HCWs that are as high as possible, by adopting the optimal policy. Recommendations for HCW vaccination issued in different countries are quite similar; in contrast, however, considerable differences are observed in the endorsement of mandatory policies, and policies that seem to work in the United States may not work in Europe and vice versa. It should be stressed that data on mandatory policies come mainly from the United States, thus conclusions may not be applicable to the rest of the world. What the optimal policy is may thus vary among countries and facilities: a ‘one-fits-all’ strategy seems not to exist.


Acknowledgements
Emmanouil Galanakis was at the ECDC on Sabbatical from the University of Crete, Greece.

Conflict of interest
None declared.

Authors’ contributions
Emmanouil Galanakis contributed to the design and the discussion, and drafted and revised the manuscript. Andreas Jansen contributed to the design and the discussion and revised the manuscript. Pietro Luigi Lopalco contributed to the design and the discussion and revised the manuscript. Johan Giesecke contributed to the design and the discussion and revised the manuscript.


 

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