Summary
Invasive meningococcal disease (IMD) is a severe disease caused by various Neisseria meningitidis serogroups that represents a serious public health problem worldwide. In Italy, serogroups B and C are the major causes of IMD. On 14 January 2013, the European Medicines Agency authorized the use of the first vaccine available to protect against meningococcal serogroup B (4CMenB).
The aim of this study was to assess the IMD epidemiology knowledge and 4CMenB vaccine attitudes of healthcare workers (HCWs) with regard to recommending this vaccine for use, vaccine practices and infectious disease control in the Campania region in Italy. A cross-sectional study was conducted among 293 HCWs (49.5% physicians and 46.4% nurses)interviewed using a self-administered questionnaire.
The majority of the HCWs had sufficient knowledge about the disease incidence and lethality, but they were less informed about the higher risk age categories and the serogroups most frequently involved. Additionally, their knowledge about the vaccine was poor with regard to the targeted categories and side effects. Approximately30.0% of the HCWs reported incidences of fever and pain and swelling at the injection site. Moreover,32.8% of the HCWs knew that the risk of developing adverse reactions increases when the 4CMenB vaccine is co-administered with other vaccines.
Overall, all of the HCWs were convinced that vaccinations are an important instrument for preventing infectious diseases, and they were aware of their central role in promoting the 4CmenB vaccination and their need to be better informed.
Keywords: Healthcare workers, Vaccination strategy, Invasive meningococcal disease, Multicomponent meningococcal serogroup B vaccine, 4CMenB
Introduction
An invasive meningococcal disease (IMD)is a severe and a life-threatening disease caused by various Neisseria meningitidis serogroups, and it represents a serious public health problem worldwide, with an annual number of cases estimated to be at least 1.2 million [1-3]. In Europe, the USA and other industrialized regions, serogroups B and C are the major causes of IMDs [4, 5]. Approximately one in ten cases are fatal, and among those who survive, long-term sequelae, such as hearing loss, neurological defects or amputation, can occur [6, 7]. Vaccination practices (MenC and ACWY135 vaccines) have significantly changed the epidemiology of this disease, so that serogroup B is currently the predominant cause of IMDs in Europe, Latin America and North America [5, 8, 9]. In Italy, the IMD incidence is higher in children 0 to 4 years old than in the other age categories, particularly in infants less than 1 year old (IMD incidence = 4.01/100,000 in 2013) [10, 11]. The serogroup mainly involved in infants less than 1 year old is type B (IMD incidence = 3.44/100,000 in 2013), with the highest incidence among children younger than 24 months, peaking at 4-8 months [10, 12]. Between 2014 and 2016, the IMD incidence among individuals 15-24 years old increased, from 0.30/100,000 in 2014 to 0.90/100,000 in 2016, and decreased in adults older than 25 years during the same time period [10].
In Italy, the IMD surveillance system based on laboratory-confirmed cases (almost 70%) revealed that between 2011 and 2017, serogroup B was the most common IMD-causing type [10], except between 2015 and 2016 when a hyper virulent meningococcal C strain was responsible for an unexpected increased IMD incidence in the Tuscany region. Following this episode, the Italian Health Authorities implemented immunization campaigns and enhanced IMD surveillance. On 14 January 2013, the European Medicines Agency authorized the use of the first vaccine available to protect against meningococcal serogroup B (Bexsero; GSK, Philadelphia, PA, USA) [13-16]. It is a multicomponent vaccine (4CMenB) composed of three purified recombinant antigenic proteins from Neisseria meningitides serogroup B and the outer membrane vesicles of the bacterium. The 4CMenB vaccination schedule for infants consists of three doses: the first dose is given at three months old, the second dose is given between 1 and 2 months after the first dose, and the third “booster” dose is given at 13 months old. As with other vaccinations, the most common adverse reactions from the4CMenB vaccination consist of fever, pain and swelling at the injection site, abnormal crying and irritability, eating disorders and gastrointestinal symptoms, sleepiness and a cutaneous rash. The uncommon adverse reactions consist of febrile or non-febrile convulsions and pallor, while the rarest adverse reactions are urticaria and Kawasaki syndrome [17].
The 4CMenB vaccination strategy differs across the European countries; for example, in Italy, the vaccination strategies are set out by different regions through the Regional Health Plan. This plan must respect the guidelines defined by the National Health Plan and the National Vaccine Prevention Plan (Piano Nazionale Prevenzione Vaccinale, PNPV) [18]. The latter defines the best vaccination policy to be carried out in each region in accordance with the best scientific evidence available. Each region can issue their own vaccination strategy in terms of the target population and costs that might being incurred by the citizens. This can lead to differences in the vaccine administration across Italian regions, resulting in heterogeneous vaccine coverage. The decreasing immunization adherence trend in Italy over recent years further compromises homogeneous and efficacious vaccine coverage, and this includes an unjustified fear of adverse reactions, scarce awareness regarding severe outcomes when not vaccinated, and the media’s role in spreading incorrect information about vaccines. Many people’s attitudes toward vaccinations may have been affected after an unverified association between the measles, mumps and rubella vaccine and autism was reported by the media, as well as after the Fluad case. The latter followed the withdrawal of the Novartis vaccine against influenza by the Italian Medicines Agency known as “Agenzia Italiana del Farmaco” after the occurrence of 3 deaths in 48 hours. Although there was prompt readmission of the Novartis vaccine, the media event had already affected people’s attitudes towards vaccinations. These events have increased both citizens and healthcare workers’ (HCWs) loss of faith in Italian institutions.
Previous studies have documented the strong influence that HCWs have on a patient’s decision making process regarding whether or not to undergo vaccination [19-22]. However, some HCWs feel poorly informed and poorly trained on how to answer patient questions, and they often struggle when dealing with those who distrust the efficacy and safety of vaccines [23, 24]. Therefore, the aim of our study was to assess the knowledge and attitudes of HCWs involved in vaccination programs and infectious disease control with regard to recommending the 4CMenB vaccine in the Campania region of Italy.
Methods
PARTICIPANTS AND SETTING
Within each Local Health Service (Aziende Sanitarie Locali, ASL) that manages public healthcare, the communicable disease prevention is run by two departments, the Maternal Childhood Health Protection Department, which delivers vaccines to children through its Maternal Childhood Operative Unit (Unità Operativa Materno Infantile, UOMI), and the Public Health Department, which looks at infectious disease surveillance and control through the Epidemiology Service (Servizio di Epidemiologia e Prevenzione) and Public Hygiene Service (Servizio di Igiene e Sanità Pubblica) and administers vaccines to adults and travellers through the Collective Prevention Operative Unit (Unità Operativa Prevenzione Collettiva).
A cross-sectional study was conducted from 1 January 2017 through 30 June 2017 at the ASLs in the metropolitan areas of Naples, Caserta and Salerno in the Campania region among the HCWs involved in the surveillance and control of infectious diseases or vaccine administration (the total number of HCWs at these ASLs was around 750). In each unit, a healthcare operator was identified as a reference contact, and they collaborated to explain the study objectives and raise awareness among the HCWs. In addition, this individual distributed the questionnaires and collected them immediately after they were completed anonymously by the participants. The questionnaires focused on the HCWs’ knowledge about IMD epidemiology and preventability and their attitudes towards 4CMenB vaccine use. It consisted of 45 items gathered into 3 main topics described as follows:
Socio-demographic information (sex, age, marital status, how many children, any children < 5 years old, education, degree type and medical specialty) and professional characteristics (ASL, workplace, occupational category, type of activity and seniority).
Knowledge about serogroup B meningococcal disease and the 4CMenB vaccine (epidemiology of meningococcal meningitis in Italy and its lethality and mortality rate, knowledge about the 4CMenB vaccination and its side effects).
Attitudes toward vaccination practices, specifically toward the 4CMenB vaccination (opinions about the 4CMenB vaccine, its efficacy and safety, the opportunity to recommend it and make it mandatory; opinions about the reasons why parents do or do not vaccinate their children), and updating resources (self-evaluation of their own level of knowledge about the 4CMenB vaccine and updating resources used).
SAMPLE SIZE
The number of HCWs needed was determined on the assumption that 75% of the HCWs had appropriate knowledge regarding IMDs and the 4CmenB vaccine, a confidence interval of 95% and a ratio unexp/exp 1:2. The results showed that a total number of 365 HCWs needed to be enrolled in the study.
DATA ANALYSIS
The data was analysed using Stata: Data Analysis and Statistical Software version 10.1 (Stata Corp LLC, College Station, TX, USA). Following the descriptive analysis, a univariate analysis was performed using a chi-squared test to identify the associations between each independent variable and the outcomes of interest. Then, only those variables with a p value < 0.25 in the univariate analysis were included in the final multivariate logistic regression models. The p values were assessed using two-sided tests, with the statistical significance for p defined at a value of ≤ 0.05.
The independent variables were the sex, age, number of children, education, occupational category, department type and activity type. The dependent variables were the knowledge about meningococcal meningitis (incidence, most common serogroup in Italy, lethality and mortality rate) and knowledge about the 4CMenB vaccine (vaccine recommended age groups, vaccinations schedule, inclusion or exclusion among recommended vaccinations by the PNPV in Italy and by the Regional Vaccine Prevention Plan in Campania, and risk for adverse reactions when the 4CMenB vaccine is co-administered with another vaccine).
ETHICAL CONSIDERATIONS
All of the participants were informed that the data was collected anonymously and stored in a confidential manner. None of the participants could be identified based on the material submitted, and no incentives were offered to the HCWs for their participation in this study.
Results
A total of 293 HCWs completed the survey, with a response rate of 80.3%. As shown in Table I, 63.8% were women, 65.9% were between 41 and 59 years old, 79.2% were married, 83.6% had at least one child, 6.1% had a child less than 5 years old, 55.6% had graduated, and 7.4% and 88.9% had graduated from nursing and medicine, respectively. Among those who were physicians, the majority were specialists in hygiene and preventive medicine (35.2%), 21.4% were in paediatrics and just a few of them were specialists in infectious diseases (4.8%). Moreover, 50.8% of the HCWs worked in ASLs in Naples, 51.9% worked in UOMIs, the majority were physicians (49.5%), 46.4% were nurses and only 4.1% were other types of HCWs, like medical assistants, biologists and professional educators. Additionally, 51.9% of the participants were directly involved in vaccination programs, 17.1% were in infectious disease surveillance and control, and 23.2% were involved in both activities.
Tab. I.
Sociodemographic and professional characteristics of the healthcare workers (HCWs) (n = 293).
| n | % | ||
|---|---|---|---|
| Sex | 98 | 33.5 | 98 |
| 187 | 63.8 | 187 | |
| 8 | 2.7 | 8 | |
| 293 | 100.0 | 293 | |
| Age | ≤ 40 | 8 | 2.7 |
| 41–59 | 193 | 65.9 | |
| ≥ 60 | 84 | 28.7 | |
| No response | 8 | 2.7 | |
| Total | 293 | 100.0 | |
| Marital status | Married | 232 | 79.2 |
| Unmarried | 23 | 7.9 | |
| Widow/Widower | 4 | 1.4 | |
| Separate/Divorced | 11 | 3.7 | |
| No response | 23 | 7.8 | |
| Total | 293 | 100.0 | |
| Have children | Yes | 245 | 83.6 |
| No | 32 | 10.9 | |
| No response | 16 | 5.5 | |
| Total | 293 | 100.0 | |
| Children less than 5 years old a | Yes | 15 | 6.1 |
| No | 230 | 93.9 | |
| Total | 245 | 100.0 | |
| Type of degree b | Medicine | 145 | 88.9 |
| Nursing | 12 | 7.4 | |
| Other | 6 | 3.7 | |
| Total | 163 | 100.0 | |
| Medical specialty c | Hygiene and preventive medicine | 51 | 35.2 |
| Paediatrics | 31 | 21.4 | |
| Infectious disease | 7 | 4.8 | |
| Other | 17 | 11.7 | |
| Not specialized | 39 | 26.9 | |
| Total | 145 | 100.0 |
UOPC: Collective Prevention Operative Unit; UOMI: Maternal Childhood Operative Unit; SEP: Epidemiology Service ; SISP :Public Hygiene Service;
a Calculated only for the HCWs who reported at least one child (n = 245);
b Calculated only for the HCWs who graduated (n = 163);
c Calculated only for the physicians (n = 145).
Table II shows the results of the IMD knowledge among the physicians and nurses with relative confidence intervals; 24.1% of the physicians and 17.7% of the nurses reported that the meningococcal meningitis incidence in Italy was not high, while 50.3% of the physicians and only 38.2% of the nurses identified serogroup B as the most common. Regarding the age groups at a higher risk of contracting meningococcal meningitis, 27.3% of the HCWs indicated < 1 year old, 30.6% indicated from 1-4 years old and 27.3% indicated from 15-24 years old; however, only 7.6% of the physicians and 4.4% of the nurses indicated all three age groups that were at a higher risk (data not shown). Moreover, 80.4% of the HCWs indicated that the meningococcal meningitis lethality rate was high, while 48.3% and 36.0%,respectively, indicated that the mortality rate was very low.
Tab. II.
Healthcare workers’ (HCWs) knowledge about the meningococcal meningitis epidemiology (n = 281).
| Physicians | Nurses | Total | |||||
|---|---|---|---|---|---|---|---|
| % | (95% CI) | % | (95% CI) | n | % | ||
| In Italy the incidence of meningococcal meningitis is high, do you agree? | Strongly agree | 3.4 | (1.3-5.4) | 4.4 | (2.0-6.7) | 11 | 3.9 |
| Somewhat agree | 16.6 | (12.3-20.8) | 21.3 | (16.6-25.9) | 53 | 18.9 | |
| Somewhat disagree* | 53.8 | (48.0-59.5) | 45.6 | (39.9-51.3) | 140 | 49.8 | |
| Disagree* | 24.1 | (19.2-29.0) | 17.7 | (13.3-22.0) | 59 | 21.0 | |
| Don’t know/No response | 2.1 | (0.4-3.7) | 11.0 | (7.4-14.5) | 18 | 6.4 | |
| Total | 100.0 | 100.0 | 281 | 100 | |||
| Which are the most common meningococcus serogroups in Italy? | Serogroup A | 0.0 | 0.0 | 0 | 0.0 | ||
| Serogroup B* | 26.2 | (21.1-31.2) | 19.1 | (14.6-23.6) | 64 | 22.8 | |
| Serogroup B and C* | 24.1 | (19.2-29.0) | 19.1 | (14.6-23.6) | 61 | 21.7 | |
| Serogroup C | 47.6 | (41.8-53.3) | 59.6 | (53.9-65.2) | 150 | 53.4 | |
| Serogroup Y or serogroup W135 | 0.0 | 0.7 | (-0.2-1.6) | 1 | 0.3 | ||
| Don’t know/No response | 2.1 | (0.46-3.74) | 1.5 | (0.1-2.8) | 5 | 1.8 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Which are the age categories at higher risk in Italy? (more than one answer allowed)a | < 1 year* | 29.2 | (23.9-34.4) | 25.4 | (20.4-30.3) | 114 | 27.3 |
| 1-4 years* | 33.0 | (27.6-38.3) | 28.2 | (23.0-33.3) | 128 | 30.6 | |
| 5-14 years | 10.5 | (6.9-14.0) | 8.1 | (4.9-11.2) | 39 | 9.3 | |
| 15-24 years* | 22.0 | (17.2-26.7) | 32.6 | (27.2-37.9) | 114 | 27.3 | |
| > 25 years | 4.3 | (1.9-6.6) | 4.3 | (1.9-6.6) | 18 | 4.3 | |
| Don’t know/No response | 1.0 | (-0.1-2.1) | 1.4 | (0.0-2.7) | 5 | 1.2 | |
| Total | 100.0 | 100.0 | 418 | 100.0 | |||
| Is meningococcal type B meningitis a lethal disease? | Yes* | 82.1 | (77.7-86.4) | 78.7 | (74.0-83.3) | 226 | 80.4 |
| No | 10.3 | (6.8-13.7) | 12.5 | (8.7-16.2) | 32 | 11.4 | |
| Don’t know/No response | 7.6 | (4.5-10.6) | 8.8 | (5.5-12.0) | 23 | 8.2 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| How high is the meningococcal type B meningitis mortality rate in Italy? | Very high | 2.1 | (0.4-3.7) | 5.1 | (2.5-7.6) | 10 | 3.6 |
| High | 30.3 | (25.0-35.5) | 28.0 | (22.8-33.1) | 82 | 29.2 | |
| Low* | 11.0 | (7.4-14.5) | 14.7 | (10.6-18.7) | 36 | 12.8 | |
| Very low* | 48.3 | (42.5-54.0) | 36.0 | (30.5-41.5) | 119 | 42.3 | |
| Don’t know/No response | 8.3 | (5.1-11.4) | 16.2 | (11.9-20.4) | 34 | 12.1 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
CI: confidence interval;
*Correct answer; a Calculated based on the total number of answers given by the HCWs (n = 418).
The results from the HCWs’ knowledge about the 4CmenB vaccine are described in Table III. Most of the participants (69.0%) had at least sufficient knowledge about the 4CMenB vaccine, and 79.4% had sufficient knowledge about its vaccination schedule. However, only 34.1% of the HCWs indicated < 1 year old as the targeted group for the 4CMenB vaccination, while 18.2% and 20.5% indicated 1-4 years old and immune-suppressed individuals, respectively. Only 2.7% of the physicians and 2.9% of the nurses correctly identified all three targeted groups (results not shown). In order to assess their knowledge about the vaccination schedule, the HCWs were asked about the number of doses, timing and whether a booster shot was needed. Only 31.0% of the physicians and 21.3% of the nurses knew the 4CMenB vaccination schedule for all of the age groups.
Tab. III.
Knowledge about the meningococcal serogroup B multicomponent (4CMenB) vaccine (n = 281).
| Physicians | Nurses | Total | |||||
|---|---|---|---|---|---|---|---|
| % | (95% CI) | % | (95% CI) | n | % | ||
| What do you consider your overall knowledge about the 4CMenB vaccine to be? | Scarce | 8.3 | (5.1–11.4) | 14.7 | (10.6–18.7) | 32 | 11.4 |
| Not sufficient | 19.3 | (14.7–23.8) | 19.9 | (15.3–24.4) | 55 | 19.6 | |
| Sufficient | 36.6 | (31.0–42.1) | 30.1 | (24.8–35.3) | 94 | 33.5 | |
| Good | 30.3 | (25.0–35.5) | 35.3 | (29.8–40.7) | 92 | 32.7 | |
| Excellent | 5.5 | (2.8–8.1) | 0.0 | 8 | 2.8 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Are you familiar with the4CMenB vaccination schedule? | Yes | 82.0 | (77.6–86.4) | 76.5 | (71.6–81.3) | 223 | 79.4 |
| No | 18.0 | (13.6–22.4) | 23.5 | (18.6–28.3) | 58 | 20.6 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Which age groups are recommended to receive the 4CMenB vaccination? (more than one answer allowed)a | < 1 year* | 34.9 | (29.4–40.3) | 33.2 | (27.8–38.5) | 199 | 34.1 |
| 1-4 years* | 20.5 | (15.8–25.1) | 15.5 | (11.3–19.6) | 106 | 18.2 | |
| 5-14 years | 8.1 | (4.9–11.2) | 6.1 | (3.3–8.8) | 42 | 7.2 | |
| 15-24 years | 14.7 | (10.6–18.7) | 16.3 | (12.0–20.5) | 90 | 15.4 | |
| > 25 years | 1.3 | (0.0–2.6) | 3.6 | (1.4–5.7) | 14 | 2.4 | |
| Immunosuppressed* | 19.5 | (14.9–24.0) | 21.7 | (16.9–26.4) | 120 | 20.5 | |
| Don’t know/No response | 1.0 | (-0.1–2.1) | 3.6 | (1.4–5.7) | 13 | 2.2 | |
| Total | 100.0 | 100.0 | 584 | 100.0 | |||
| Infants | |||||||
| Assessment of the HCWs’ knowledge about the 4CMenB vaccination schedule for each of the following age groups: | Correct | 47.6 | (41.8–53.3) | 36.8 | (31.2–42.3) | 119 | 42.3 |
| Incorrect | 52.4 | (46.6–58.1) | 63.2 | (57.6–68.7) | 162 | 57.7 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Children | |||||||
| Correct | 42.8 | (37.1–48.4) | 39.7 | (34.1–45.3) | 116 | 41.3 | |
| Incorrect | 57.2 | (51.5–62.8) | 60.3 | (54.7–65.9) | 165 | 58.7 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Teenagers | |||||||
| Correct | 45.5 | (39.8–51.2) | 34.6 | (29.1–40.0) | 113 | 40.2 | |
| Incorrect | 54.5 | (48.8–60.2) | 65.4 | (59.9–70.8) | 168 | 59.8 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| All ages | |||||||
| Correct | 31.0 | (25.7–36.3) | 21.3 | (16.6–25.9) | 74 | 26.3 | |
| Incorrect | 69.0 | (63.7–74.3) | 78.7 | (74.0–83.3) | 207 | 73.7 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Has the 4CMenB vaccination been included among those recommended by the National Vaccine Prevention Plan in Italy? | Yes* | 64.2 | (58.7–69.6) | 61.0 | (55.4–66.5) | 176 | 62.6 |
| No | 18.6 | (14.1–23.0) | 22.8 | (18.0–27.6) | 58 | 20.7 | |
| Don’t know | 17.2 | (12.8–21.5) | 16.2 | (11.9–20.4) | 47 | 16.7 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Has the 4CMenB vaccination been included in the Regional Campania Vaccine Prevention Plan in Campania? | Yes | 40.7 | (35.0–46.3) | 33.8 | (28.3–39.2) | 105 | 37.4 |
| No* | 27.6 | (22.4–32.7) | 33.8 | (28.3–39.2) | 86 | 30.6 | |
| Don’t know | 31.7 | (26.3–37.0) | 32.4 | (27.0–37.7) | 90 | 32.0 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
CI: confidence interval, HCWs: healthcare workers;
* Correct answer;
a Calculated based on the total number of answers given by the HCWs (n = 584).
Of the HCWs, 62.6% knew that the PNPV recommends the 4CMenB vaccine, while only 30.6% knew that the Regional Campania Vaccine Prevention Plan has not implemented the 4CMenB vaccine.
When assessed with regard to the 4CMenB-related adverse reactions (Tab. IV), 32.0% of the HCWs reported fever and 31.0% reported pain and swelling at the injection site. A few of the HCWs identified gastrointestinal disorders, headaches, somnolence, asthenia, convulsions, pallor, Kawasaki syndrome, malaise and arthralgia among the possible adverse reactions to the vaccine (data not shown). Only 32.8% of the HCWs knew that the risk of developing adverse reactions increases when the 4CMenB vaccine is co-administered with other vaccines. In addition, 40.0% of the physicians and 52.2% of the nurses knew that the 4CMenB vaccine must be administered several days after the other recommended vaccinations, while 36.2% of the physicians and only 15.5% of the nurses knew that the main reason for this was the increased risk for adverse reactions. Most of the physicians (81.4%) and nurses (72.8%) disagreed with the idea that the inclusion of the 4CMenB vaccine in the vaccination schedule would reduce adherence to the other vaccinations.
Tab. IV.
Knowledge about the risks related to the meningococcal serogroup B multicomponent (4CMenB) vaccine (n = 281).
| Physicians | Nurses | Total | ||||||
|---|---|---|---|---|---|---|---|---|
| % | (95% CI) | % | (95% CI) | n | % | |||
| How frequently occurring are the following 4CMenB vaccine side effects? | Fever | Correct | 34.5 | (29.0-39.9) | 29.4 | (24.1-34.6) | 90 | 32.0 |
| Incorrect | 65.5 | (60.0-70.9) | 70.6 | (65.3-75.8) | 191 | 68.0 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| Pain and swelling at the injection site | Correct | 32.4 | (27.0-37.7) | 29.4 | (24.1-34.6) | 87 | 31.0 | |
| Incorrect | 67.6 | (62.2-72.9) | 70.6 | (65.3-75.8) | 194 | 69.0 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| Irritability | Correct | 26.2 | (21.1-31.2) | 21.3 | (16.6-25.9) | 67 | 23.8 | |
| Incorrect | 73.8 | (68.7-78.8) | 78.7 | (74.0-83.3) | 214 | 76.2 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| Cutaneous rash | Correct | 6.9 | (4.0-9.8) | 8.1 | (4.9-11.2) | 21 | 7.5 | |
| Incorrect | 93.1 | (90.2-96.0) | 91.9 | (88.7-95.0) | 260 | 92.5 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| Does the risk of developing an adverse reaction increase when the 4CMenB vaccine is co-administered with another vaccine? | Yes* | 34.5 | (29.0-39.9) | 30.9 | (25.6-36.1) | 92 | 32.8 | |
| No | 46.2 | (40.4-51.9) | 48.5 | (42.7-54.2) | 133 | 47.3 | ||
| Don’t know | 19.3 | (14.7-23.8) | 20.6 | (15.9-25.2) | 56 | 19.9 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| Must the 4CMenB vaccine be administered several days after any other vaccination? | Yes* | 40.0 | (34.3-45.6) | 52.2 | (46.4-57.9) | 129 | 45.9 | |
| No | 28.3 | (23.1-33.4) | 22.8 | (18.0-27.6) | 72 | 25.6 | ||
| It makes no difference | 20.7 | (16.0-25.3) | 10.3 | (6.8-13.7) | 44 | 15.7 | ||
| Don’t know | 11.0 | (7.4-14.5) | 14.7 | (10.6-18.7) | 36 | 12.8 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| Why must the 4CMenB vaccine be administered several days after any other vaccination? (more than one answer allowed) a | To avoid an increased risk for adverse reactions* | 36.2 | (30.7-41.7) | 15.5 | (11.3-19.6) | 32 | 24.8 | |
| Vaccination schedule is too busy | 15.5 | (11.3-19.6) | 22.5 | (17.7-27.2) | 25 | 19.4 | ||
| To better asses adverse reactions | 10.4 | (6.9-13.9) | 4.3 | (1.9-6.6) | 9 | 7.0 | ||
| To improve patient compliance | 6.9 | (4.0-9.8) | 5.6 | (2.9-8.2) | 8 | 6.9 | ||
| To avoid hyperstimulation of immune system | 6.9 | (4.0-9.8) | 1.4 | (0.0-2.7) | 5 | 3.9 | ||
| To reduce parents’ anxiety | 0.0 | 2.8 | (0.9-4.6) | 2 | 1.4 | |||
| No response | 24.1 | (19.2-29.0) | 47.9 | (42.1-53.6) | 46 | 35.6 | ||
| Total | 100.0 | 100.0 | 129 | 100.0 | ||||
| In your opinion, would any other vaccination be refused if the 4CMenB vaccination was added to the vaccination schedule? | Yes | 2.1 | (0.4-3.7) | 7.4 | (4.4-10.4) | 13 | 4.6 | |
| No | 81.4 | (76.9-85.8) | 72.8 | (67.7-77.9) | 217 | 77.2 | ||
| Don’t know | 16.5 | (12.2-20.7) | 19.8 | (15.2-24.3) | 51 | 18.2 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | ||||
| If yes, which of the following vaccinations would be refused? (more than one answer allowed) b | Trivalent vaccine | 16.7 | (12.4-20.9) | 43.8 | (38.1-49.4) | 8 | 36.4 | |
| Pneumococcus | 33.3 | (27.9-38.7) | 25.0 | (20.0-29.9) | 6 | 27.3 | ||
| Hexavalent vaccine | 16.7 | (12.4-20.9) | 25.0 | (20.0-29.9) | 5 | 22.7 | ||
| Meningococcal C | 33.3 | (27.9-38.7) | 6.2 | (3.4-8.9) | 3 | 13.6 | ||
| Total | 100.0 | 100.0 | 22 | 100.0 | ||||
CI: confidence interval;
* Correct answer;
a Calculated based on the total number of answers given by the healthcare workers (n = 129);
b Calculated based on the total number of answers given by the healthcare workers who answered yes to the previous question (n = 22).
As shown in Table V, 56.6% of the HCWs stated that the 4CMenB vaccine was extremely efficacious, and 65.5% stated that the vaccine was safe. Additionally, 90.4% of the HCWs stated that encouraging people to allow their children to receive the 4CMenB vaccine was their professional duty, and 53.4% would make it mandatory. The fear of the disease and its complications was the reason most often given by the HCWs (61.9%) to address why the parents chose to vaccinate their children, while the fear of severe adverse reactions (31.6%), disinformation (24.0%) and a poor perception of the disease severity (20.5%) were the most common reasons why the parents chose not to vaccinate their children. Almost all of the HCWs(91.5%) believed that the distrust that the parents had with regard to vaccinating their children had no scientific basis.
Tab. V.
Healthcare workers’ (HCWs) attitudes toward the meningococcal serogroup B multicomponent (4CMenB) vaccine use and updating sources (n = 281).
| Physicians | Nurses | Total | |||||
|---|---|---|---|---|---|---|---|
| % | (95% CI) | % | (95% CI) | n | % | ||
| Is the 4CMenB vaccine efficacious in preventing bacterial meningitis? | Extremely efficacious | 55.9 | (50.2-61.5) | 57.4 | (51.7-63.0) | 159 | 56.6 |
| Efficacious | 40.0 | (34.3-45.6) | 39.7 | (34.1-45.3) | 112 | 39.9 | |
| Scarcely efficacious | 4.1 | (1.8-6.3) | 2.9 | (0.9-4.8) | 10 | 3.5 | |
| Inefficacious | 0.0 | 0.0 | 0 | 0.0 | |||
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Is the 4CMenB vaccine safe? | Extremely safe | 28.3 | (23.1-33.4) | 30.9 | (25.6-36.1) | 83 | 29.6 |
| Safe | 66.2 | (60.7-71.6) | 64.7 | (59.2-70.1) | 184 | 65.5 | |
| Scarcely safe | 5.5 | (2.8-8.1) | 1.5 | (0.1-2.8) | 10 | 3.5 | |
| Not safe | 0.0 | 2.9 | (0.9-4.8) | 4 | 1.4 | ||
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Do you consider encouraging people to get the 4CMenB vaccination to be an HCWs’ professional duty? | Yes | 91.7 | (88.5-94.8) | 89.0 | (85.4-92.5) | 254 | 90.4 |
| No | 2.1 | (0.4-3.7) | 2.9 | (0.9-4.8) | 7 | 2.5 | |
| Don’t know | 6.2 | (3.4-8.9) | 8.1 | (4.9-11.2) | 20 | 7.1 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Would you agree to make the 4CMenB vaccination mandatory? | Yes | 56.5 | (50.8-62.1) | 50.0 | (44.2-55.7) | 150 | 53.4 |
| No | 26.9 | (21.8-31.9) | 27.9 | (22.7-33.0) | 77 | 27.4 | |
| Don’t know | 16.6 | (12.3-20.8) | 22.1 | (17.3-26.8) | 54 | 19.2 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Why do people decide to vaccinate their children? (more than one answer allowed)a | Fear of the disease and its complications | 60.7 | (55.1-66.2) | 63.3 | (57.7-68.8) | 245 | 61.9 |
| Vaccination is mandatory | 25.6 | (20.6-30.6) | 24.9 | (19.9-29.8) | 100 | 25.3 | |
| Vaccine is safe | 10.4 | (6.9-13.9) | 9.7 | (6.3-13.0) | 40 | 10.1 | |
| Correct information provided by HCWs | 1.4 | (0.0-2.7) | 0.5 | (-0.3-1.3) | 4 | 1.0 | |
| Trust the source that recommends the vaccination | 0.5 | (-0.3-1.3) | 0.5 | (-0.3-1.3) | 2 | 0.4 | |
| Increased number of new cases within the community | 0.5 | (-0.3-1.3) | 0.0 | 1 | 0.3 | ||
| Don’t know | 0.9 | (-0.1-1.9) | 1.1 | (0.0-2.2) | 4 | 1.0 | |
| Total | 100.0 | 100.0 | 396 | 100.0 | |||
| Why do people decide not to vaccinate their children? (more than one answer allowed)b | Fear of adverse reactions | 31.8 | (26.4-37.1) | 31.3 | (25.9-36.6) | 208 | 31.6 |
| Disinformation | 21.3 | (16.6-25.9) | 26.9 | (21.8-31.9) | 158 | 24.0 | |
| Poor perception of disease severity | 22.4 | (17.6-27.1) | 18.4 | (13.9-22.8) | 135 | 20.5 | |
| Vaccine is not mandatory | 11.1 | (7.5-14.7) | 10.4 | (6.9-13.9) | 71 | 10.8 | |
| Fear of unknown long-term effects | 8.2 | (5.0-11.3) | 8.9 | (5.6-12.1) | 56 | 8.5 | |
| Vaccination schedule is too busy | 4.0 | (1.7-6.2) | 3.2 | (1.1-5.2) | 24 | 3.6 | |
| Costs | 0.3 | (-0.3-0.9) | 0.6 | (-0.2-1.4) | 3 | 0.4 | |
| Advertisement campaigns on websites | 0.6 | (-0.2-1.4) | 0.0 | 2 | 0.3 | ||
| Don’t know | 0.3 | (-0.3-0.9) | 0.3 | (-0.3-0.9) | 2 | 0.3 | |
| Total | 100.0 | 100.0 | 659 | 100.0 | |||
| Do you consider the parents’ choice not to vaccinate their children to be scientifically based? | Yes | 1.4 | (0.0-2.7) | 1.5 | (0.1-2.8) | 4 | 1.4 |
| No | 93.8 | (91.0-96.5) | 89.0 | (85.4-92.5) | 257 | 91.5 | |
| Don’t know | 4.8 | (2.3-7.2) | 9.5 | (6.1-12.8) | 20 | 7.1 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Must HCWs be constantly updated on vaccination-related scientific evidence? | Yes | 99.3 | (98.3-100.2) | 98.5 | (97.1-99.8) | 278 | 98.9 |
| No | 0.0 | 0.0 | 0 | 0.0 | |||
| Don’t know | 0.7 | (-0.2-1.6) | 1.5 | (0.1-2.8) | 3 | 1.1 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| Do you need to be better informed about the 4CMenB vaccine? | Yes | 82.1 | (77.7-86.4) | 89.7 | (86.2-93.1) | 241 | 85.8 |
| No | 13.1 | (9.2-16.9) | 7.3 | (4.3-10.2) | 29 | 10.3 | |
| Don’t know | 4.8 | (2.3-7.2) | 3.0 | (1.0-4.9) | 11 | 3.9 | |
| Total | 100.0 | 100.0 | 281 | 100.0 | |||
| How did you get informed about the 4CMenB vaccine? (more than one answer allowed) c | Updating courses/congresses | 7.6 | (4.5–10.6) | 11.4 | (7.7–15.0) | 46 | 9.3 |
| Internet | 9.7 | (6.3–13.0) | 5.0 | (2.5–7.5) | 38 | 7.7 | |
| National journals | 1.5 | (0.1–2.8) | 7.8 | (4.7–10.8) | 21 | 4.2 | |
| Pharmaceutical promoters | 0.7 | (-0.2–1.6) | 3.2 | (1.1–5.2) | 9 | 1.8 | |
| International journals | 0.0 | 3.6 | (1.4–5.7) | 8 | 1.6 | ||
| Television | 0.4 | (-0.3–1.1) | 0.5 | (-0.3–1.3) | 2 | 0.4 | |
| Vaccine information leaflets | 2.2 | (0.5–3.8) | 3.6 | (1.4–5.7) | 14 | 2.8 | |
| Colleagues | 1.1 | (0.0–2.2) | 1.4 | (0.0–2.7) | 6 | 1.2 | |
| National health plan | 100.0 | 100.0 | 496 | 100.0 | |||
| No source of updating | 7.6 | (4.5–10.6) | 11.4 | (7.7–15.0) | 46 | 9.3 | |
| No response | 9.7 | (6.3–13.0) | 5.0 | (2.5–7.5) | 38 | 7.7 | |
| Total | 1.5 | (0.1–2.8) | 7.8 | (4.7–10.8) | 21 | 4.2 | |
CI: confidence interval;
a Calculated based on the total number of answers given by the HCWs (n = 396);
b Calculated based on the total number of answers given by the HCWs (n = 659);
c Calculated based on the total number of answers given by the HCWs (n = 496).
Of the participants, 98.9% stated that HCWs must constantly be updated on vaccination-related scientific evidence, and 85.8% stated that they needed better information. In addition, the HCWs reported courses and conferences (30.5%) and the internet (26.2%) as their major sources of information about the 4CMenB vaccine.
Table VI shows the results of the multivariate models for which significant associations were identified between the variables and the outcomes of interest. The knowledge about the most common serogroup was lower among those HCWs who were < 50 years old [odds ratio (OR) = 2.02, 95% confidence interval (CI) = 1.1-3.6, p = 0.022)]. Moreover, the HCWs who worked in the Public Health Department and those who were involved in the surveillance and control of the disease (OR = 0.29, 95% CI = 0.1–0.5, p = 0.000 and OR = 0.35, 95% CI = 0.1-0.8, p = 0.015, respectively) were more likely to have this knowledge. Being male and being involved in the surveillance and control of the disease (OR = 0.51, 95% CI = 0.2-0.9, p = 0.034 and OR = 0.34, 95% CI = 0.1-0.8, p = 0.014, respectively) were associated with greater knowledge about the meningococcal B meningitides mortality rate.
Tab. VI.
Knowledge about the meningococcal meningitis epidemiology and meningococcal serogroup B multicomponent (4CMenB) vaccine.
| Univariate | Multivariate | |||
|---|---|---|---|---|
| OR (95% CI) | p | OR (95% CI) | p | |
| HCWs’ knowledge about the most common meningococcal serogroup in Italy | ||||
| Sex (Male vs. Female*) | 0.76 (0.4-1.2) | 0.284 | n.v. | |
| Age (< 50 vs. ≥ 50*) | 1.74 (1.0-2.9) | 0.037 | 2.02 (1.1-3.6) | 0.022 |
| Children (No vs. Yes*) | 1.28 (0.6-2.7) | 0.513 | n.v. | |
| Degree (No vs. Yes*) | 1.90 (1.1-3.1) | 0.010 | 1.68 (0.4-6.3) | 0.440 |
| Profession (Doctor vs. Nurse*) | 0.58 (0.3-0.9) | 0.023 | 1.62 (0.4-6.0) | 0.474 |
| Department (Public health vs. Maternal childhood*) | 0.17 (0.1-0.2) | 0.000 | 0.29 (0.1-0.5) | 0.000 |
| Activity (Surveillance and control vs. Vaccination program*) | 0.18 (0.0-0.3) | 0.000 | 0.35 (0.1-0.8) | 0.015 |
| HCWs’ knowledge about the meningococcal meningitis mortality rate | ||||
| Sex (Male vs. Female*) | 0.47 (0.2-0.8) | 0.005 | 0.51 (0.2-0.9) | 0.034 |
| Age (< 50 vs.≥ 50*) | 1.54 (0.9-2.6) | 0.108 | 1.15 (0.6-2.0) | 0.645 |
| Children (No vs. Yes*) | 1.09 (0.5-2.3) | 0.811 | n.v. | |
| Degree (No vs. Yes*) | 1.43 (0.8-2.3) | 0.145 | 1.28 (0.3-4.5) | 0.704 |
| Profession (Doctor vs. Nurse*) | 0.71 (0.4-1.1) | 0.149 | 1.59 (0.4-5.8) | 0.481 |
| Department (Public health vs. Maternal childhood*) | 0.54 (0.3-0.8) | 0.013 | 0.80 (0.4-1.4) | 0.464 |
| Activity (Surveillance and control vs. Vaccination program*) | 0.36 (0.1-0.7) | 0.005 | 0.34 (0.1-0.8) | 0.014 |
| HCWs’ knowledge about the 4CMenB vaccination schedule | ||||
| Sex (Male vs. Female*) | 0.98 (0.5-1.7) | 0.932 | n.v. | |
| Age (< 50 vs.≥ 50*) | 0.77 (0.4-1.4) | 0.389 | n.v. | |
| Children (No vs. Yes*) | 0.69 (0.3-1.5) | 0.358 | n.v. | |
| Degree (No vs. Yes*) | 1.53 (0.8-2.6) | 0.133 | 0.90 (0.1-4.6) | 0.901 |
| Profession (Doctor vs. Nurse*) | 0.60 (0.3-1.0) | 0.066 | 0.32 (0.0-1.6) | 0.174 |
| Department (Public health vs. Maternal childhood*) | 2.95 (1.6-5.2) | 0.000 | 3.31 (1.6-6.7) | 0.001 |
| Activity (Surveillance and control vs. Vaccination program*) | 2.04 (0.9-4.6) | 0.087 | 1.40 (0.5-3.6) | 0.487 |
| HCWs’ knowledge about the 4CMenB vaccination being included among those recommended by the National Vaccine Prevention Plan | ||||
| Sex (Male vs. Female*) | 1.78 (1.0-2.9) | 0.026 | 1.52 (0.8-2.6) | 0.138 |
| Age (< 50 vs.≥ 50*) | 0.99 (0.5-1.6) | 0.983 | n.v. | |
| Children (No vs. Yes*) | 0.51 (0.2-1.1) | 0.118 | 0.46 (0.1-1.1) | 0.086 |
| Degree (No vs. Yes*) | 1.18 (0.7-1.9) | 0.515 | n.v. | |
| Profession (Doctor vs. Nurse*) | 0.88 (0.5-1.4) | 0.590 | n.v. | |
| Department (Public health vs. Maternal childhood*) | 3.04 (1.8-5.0) | 0.000 | 3.22 (1.8-5.5) | 0.000 |
| Activity (Surveillance and control vs. Vaccination program*) | 1.07 (0.5-2.0) | 0.842 | n.v. | |
| HCWs’ knowledge about the 4CMenB vaccination not being included among those implemented by the Regional Vaccine Prevention Plan in Campania | ||||
| Sex (Male vs. Female*) | 0.81 (0.4-1.3) | 0.446 | n.v. | |
| Age (< 50 vs.≥ 50*) | 0.93 (0.5-1.6) | 0.811 | n.v. | |
| Children (No vs. Yes*) | 1.42 (0.6-3.3) | 0.413 | n.v. | |
| Degree (No vs. Yes*) | 0.85 (0.5-1.4) | 0.536 | n.v. | |
| Profession (Doctor vs. Nurse*) | 1.34 (0.8-2.2) | 0.257 | n.v. | |
| Department (Public health vs. Maternal childhood*) | 0.50 (0.3-0.8) | 0.010 | 0.36 (0.2-0.6) | 0.001 |
| Activity (Surveillance and control vs. Vaccination program*) | 1.56 (0.7-3.2) | 0.238 | 2.83 (1.2-6.3) | 0.012 |
| HCWs’ knowledge about the increased risk for adverse reactions when the 4CMenB vaccine is co-administered with another vaccine | ||||
| Sex (Male vs. Female*) | 1.02 (0.6-1.7) | 0.931 | n.v. | |
| Age (< 50 vs.≥ 50*) | 0.97 (0.5-1.6) | 0.919 | n.v. | |
| Children (No vs. Yes*) | 0.44 (0.2-0.9) | 0.030 | 0.41 (0.1-0.8) | 0.020 |
| Degree (No vs. Yes*) | 1.03 (0.6-1.7) | 0.923 | n.v. | |
| Profession (Doctor vs. Nurse*) | 0.85 (0.5-1.4) | 0.521 | n.v. | |
| Department (Public health vs. Maternal childhood*) | 1.78 (1.0-2.9) | 0.025 | 1.76 (1.0-2.9) | 0.037 |
| Activity (Surveillance and control vs. Vaccination program*) | 1.38 (0.6-2.7) | 0.368 | n.v. | |
OR: odds ratio; CI: confidence interval; HCWs: healthcare workers; n.v.: not valuated (p > 0.250 in the univariate analysis);
* Reference category
Working in the Public Health Department (OR = 3.31, 95% CI = 1.6-6.7, p = 0.001) was the only variable associated with knowledge about the 4CMenB vaccination schedule. Additionally, knowledge about the National Health Plan was lower among those who worked in the Public Health Department (OR = 3.22, 95% CI = 1.8-5.5, p = 0.000). Being involved in the surveillance and control of the disease(OR = 2.83, 95% CI = 1.2-6.3, p = 0.012) was associated with lesser knowledge about the Regional Health Plan, while this knowledge was higher among the HCWs who worked in the Public Health Department (OR = 0.36, 95% CI = 0.2-0.6, p = 0.001). Not having children and working in the Public Health Department (OR = 0.41, 95% CI = 0.1-0.8, p = 0.020 and OR = 1.76, 95% CI = 1.0-2.9, p = 0.037, respectively) were associated with knowledge about the increased risk for adverse reactions when the 4CMenB vaccine was co-administered with another vaccine.
Discussion
This study was conducted after the 4CMenB vaccine was placed on the market. This vaccine specifically prevents serogroup B meningitis, which is the serogroup most frequently involved in this disease, and against which no traditionally made vaccines were previously available. Since its approval for use, many concerns about the most appropriate vaccination strategy have been raised within the international and national scientific communities [17]. In fact, in the years following the 4CMenB vaccine being placed on the market, the scientists and public health advisors in charge of health policies have had different opinions on how to provide the 4CMenB vaccine to the general population [14]. Therefore, the aim of the present study was to assess HCWs’ knowledge about the 4CMenB vaccine and its vaccination strategy, while considering the role HCWs play in implementing vaccination coverage (whatever their position) within operative or decision-making units.
The present analysis determined that the majority of HCWs have sufficient knowledge about the lethality of the disease, but they are less informed about the incidence, higher risk age categories and most frequent serogroups involved. Many of them are confused about what is meant by mortality and lethality, and they mistakenly consider this disease to have a high mortality rate in the general population. The majority of the HCWs considered their knowledge about the vaccine and its vaccination schedule to be good, but only a few identified all of the targeted categories. This is particularly evident when considering immunosuppressed individuals, who are considered by the scientific community to be the group at highest risk and the most appropriate to receive the vaccine; however, they were identified as a target category by few of the HCWs. Moreover, some of the HCWs’ answers were not consistent. For instance, one-third of the nurses believed that administering the 4CMenB vaccine with another vaccine enhanced the risk for adverse reactions, but only 15.0% indicated that the 4CMenB vaccine must be administered several days after another vaccine in order to reduce the risk for adverse reactions. Interestingly, those HCWs involved in surveillance and control activities had more knowledge about the epidemiological characteristics of the disease when compared with those working in the UOMI, where the HCWs are mainly involved in administering the vaccine to children. However, the HCWs working in the UOMI had better knowledge about the 4CmenB vaccination strategy and adverse reactions.
It was unexpected that only a few of the HCWs knew about the PNPV (60.0% of the HCWs) and Campania Vaccine Prevention Plan (30.0% of the HCWs) indications about 4CmenB vaccine use, considering that both of these documents represent reference tools for HCWs.
One limitation of this study was that the questionnaire was self-administered; therefore, we cannot be sure that the participants responded without having first been informed about the topics of interest. However, the results from the present analysis did show that the HCWs’ knowledge was often partial and incorrect.
Overall, it must be noted that all of the HCWs were still convinced that vaccinations are important instruments for infectious disease prevention, and they were aware of the key role that they play in promoting 4CmenB vaccinations, as well as other vaccines, and their need to be better informed.
Conclusions
This study highlights the importance of and need to implement professional training courses for HCWs with interactive teaching methods. These should be suitable for an audience of experienced HCWs, as focus group, specific to the epidemiological aspects of meningococcal disease and the 4CmenB vaccine. These interventions would be useful for ensuring that HCWs are able to correctly answer patients’ questions about the vaccine risks and benefits, because they represent the interface between public institutions and citizens [23].
Figures and tables
Acknowledgements
Rosanna Ortolani: Epidemiology Service ASL Naples 1. Gennaro Volpe: Primary Cure Department ASL Naples 1. Ugo Vairo: Maternal Childhood Department ASL Naples 1. Maria Rosaria Granata: Epidemiology Service ASL Naples 2. Francesco Giugliano: Public Health Department ASL Naples 3. Massimo Matarese: Public Health Department ASL Naples 3. Maria Grazia Panico: Epidemiology Service ASL Salerno. Gelsomina Lamberti: Public Health Department ASL Salerno. Marialuigia Trabucco: Epidemiology Service ASL Caserta. Giovanna Capone: Maternal Childhood Department ASL Caserta.
Funding sources: this research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Footnotes
Conflict of interest statement
None declared.
Authors’ contributions
EA conceived the study and revised it critically for important intellectual content; DP participated in its design and coordination, in interpretation data and wrote the manuscript; MGC revised the manuscript and contributed to data interpretation; AD has been involved in acquisition data and performed data entry and statistical analysis and contributed to data interpretation.
References
- [1].McIntyre PB, O’Brien KL, Greenwood B, Van de Beek D. Effect of vaccines on bacterial meningitis worldwide. Lancet 2012;380:1703-11. doi: 10.1016/S0140-6736(12)61187-8. [DOI] [PubMed] [Google Scholar]
- [2].Jafri RZ, Ali A, Messonnier NE, Tevi-Benissan C, Durrheim D, Eskola J, Fermon F, Klugman KP, Ramsay M, Sow S, Zhujun S, Bhutta ZA, Abramson J. Global epidemiology of invasive meningococcal disease. Popul Health Metrics 2013;11-7. doi: 10.1186/1478-7954-11-17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [3].Rouphael NG, Stephens DS. Neisseria meningitidis: biology, microbiology, and epidemiology. Methods Mol Biol 2012;799:1-20. doi: 10.1007/978-1-61779-346-2_1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [4].Working group European Centre for Disease Prevention and Control (ECDC). Surveillance of invasive bacterial diseases in Europe. 2012. Available athttps://ecdc.europa.eu/sites/portal/files/media/en/publications/Publications/Surveillance%20of%20IBD%20in%20Europe%202012.pdf (Accessed 18/05/2018).
- [5].Stefanelli P, Fazio C, Neri A, Boros S, Renna G, Pompa MG. Changing epidemiology of infant meningococcal disease after the introduction of meningococcal serogroup C vaccine in Italy, 2006-2014. Vaccine 2015;33:3678-81. doi: 10.1016/j.vaccine.2015.06.032 [DOI] [PubMed] [Google Scholar]
- [6].Brigham KS, Sandora TJ. Neisseria meningitidis: epidemiology, treatment and prevention in adolescents. Curr Opin Pediatr 2009;21:437-43. doi: 10.1097/MOP.0b013e32832c9668. [DOI] [PubMed] [Google Scholar]
- [7].Stein-Zamir C, Shoob H, Sokolov I, Kunbar A, Abramson N, Zimmerman D. The clinical features and long-term sequelae of invasive meningococcal disease in children. Pediatr Infect Dis J 2014;33:777-9. doi: 10.1097/INF.0000000000000282. [DOI] [PubMed] [Google Scholar]
- [8].Stefanelli P, Rezza G. Impact of vaccination on meningococcal epidemiology. Hum Vacc Immunother 2016;12:1051-5. doi: 10.1080/21645515.2015.1108502. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [9].Pace D. Novel quadrivalent meningococcal A, C, W-135 and Y glycoconjugate vaccine for the broader protection of adolescents and adults. Future Microbiol 2010;5:1629-40. doi: 10.2217/fmb.10.137. [DOI] [PubMed] [Google Scholar]
- [10].Stefanelli P, Pantosti A, Cerquetti M, Riccardo F. Dati di sorveglianza delle malattie batteriche invasive - Istituto Superiore della Sanità (ISS). 2017. Available athttp://old.iss.it/binary/mabi/cont/Report_MBI_20170403_finale.pdf(Accessed 18/05/2018).
- [11].Signorelli C, Chiesa V, Odone A. Meningococcal serogroup B vaccine in Italy: state-of-art, organizational aspects and perspectives J Prev Med Hyg 2015;56:125-32. [PMC free article] [PubMed] [Google Scholar]
- [12].Azzari C, Canessa C, Lippi F, Moriondo M, Indolfi G, Nieddu F, Martini M, De Martino M, Castiglia P, Baldo V, Resti M. Distribution of invasive meningococcal B disease in Italian pediatric population: implications for vaccination timing. Vaccine 2014;32:1187-91. doi: 10.1016/j.vaccine.2013.09.055. [DOI] [PubMed] [Google Scholar]
- [13].Alfonsi V, D’Ancona F, Giambi C, Nacca G, Rota MC. Regional coordinators for infectious diseases and vaccinations. Current immunization policies for pneumococcal, meningococcal C, varicella and rotavirus vaccinations in Italy. Health Policy 2011;103:176-83. doi: 10.1016/j.healthpol.2011.10.002. [DOI] [PubMed] [Google Scholar]
- [14].Rizzo C, Bonanni P, Carsetti R, Ciofi degli Atti M, Esposito S, Lippi F, et al. Il nuovo vaccino antimeningococco B: implicazioni e prospettive di prevenzione vaccinale. Rivista di Immunologia e Allergologia Pediatrica 2014;28(04):2-8. [Google Scholar]
- [15].Martin NG, Snape MD. A multicomponent serogroup B meningococcal vaccine is licensed for use in Europe: what do we know and what are we yet to learn? Expert Rev Vaccines 2013;12:837-58. doi: 10.1586/14760584.2013.814862. [DOI] [PubMed] [Google Scholar]
- [16].Findlow J, Bai X, Findlow H, Newton E, Kaczmarski E, Miller E, Borrow R. Safety and immunogenicity of a four-component meningococcal group B vaccine (4CMenB) and a quadrivalent meningococcal group ACWY conjugate vaccine administered concomitantly in healthy laboratory workers. Vaccine 2015;33:3322-30. doi:10.1016/j.vaccine.2015.05.027. [DOI] [PubMed] [Google Scholar]
- [17].Working group National Center for Epidemiology, Surveillance and Health Promotion (CNESPS). Vaccinazione anti-meningococco B: dati ed evidenze disponibili per l’introduzione in nuovi nati e adolescenti - Istituto Superiore di Sanità (ISS). 2014(Anti-meningococcalvaccination B: data and evidence available for introduction into newborns and adolescents). Available at http://www.epicentro.iss.it/temi/vaccinazioni/pdf/Istruttoria%20MENINGOCOCCO%20B.pdf(Accessed 18/05/2018).
- [18].Piano Nazionale Prevenzione Vaccinale 2014-2018 (National Health Plan). Approved with agreement state-regions on 13th November 2014. Available at http://www.salute.gov.it/imgs/C_17_pubblicazioni_2285_allegato.pdf (Accessed 18/05/2018).
- [19].Wiley KE, Massey PD, Cooper SC, Wood N, Quinn HE, Leask J. Pregnant women’s intention to take up a post-partum pertussis vaccine, and their willingness to take up the vaccine while pregnant: a cross sectional survey. Vaccine 2013;31:3972-8. doi: 10.1016/j.vaccine.2013.06.015. [DOI] [PubMed] [Google Scholar]
- [20].Vishram B, Letley L, Jan Van Hoek A, Silverton L, Donovan H, Adams C, Green D, Edwards A, Yarwood J, Bedford H, Amirthalingam G, Campbell H. Vaccination in pregnancy: attitudes of nurses, midwives and health visitors in England. Hum Vaccin Immunother 2018;14:179-88. doi: 10.1080/21645515.2017.1382789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [21].Kennedy C, Gray Brunton C, Hogg R. ‘Just that little bit of doubt’: Scottish parents’, teenage girls’ and health professionals’ views of the MMR, H1N1 and HPV vaccines. Int J Behav Med. 2014;21:3-10. doi: 10.1007/s12529-013-9356-4. [DOI] [PubMed] [Google Scholar]
- [22].Ellingson M, Chamberlain AT. Beyond the verbal: pregnant women’s preferences for receiving influenza and Tdap vaccine information from their obstetric care providers. Hum Vaccin Immunother 2018;14:767-71. doi: 10.1080/21645515.2018.1425114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [23].Paterson P, Meurice F, Stanberry LR, Glismann S, Rosenthal SL, Larson HJ. Vaccine hesitancy and healthcare providers. Vaccine 2016;34:6700-6. doi: 10.1016/j.vaccine.2016.10.042. [DOI] [PubMed] [Google Scholar]
- [24].Ammon A, Prats Monnè XP. Vaccines, trust and European public health. Euro Surveill 2018;23:18 doi: 10.2807/1560-7917. [DOI] [PMC free article] [PubMed] [Google Scholar]
