The Scientific World Journal
Volume 2019 (2019), Article ID 9482607, 11 pages
https://doi.org/10.1155/2019/9482607

Research Article

Hepatitis B and C Viral Infection: Prevalence, Knowledge, Attitude, Practice, and Occupational Exposure among Healthcare Workers of Jimma University Medical Center, Southwest Ethiopia

Habtemu J. Hebo,¹ Desta H. Gemeda,¹ and Kedir A. Abdusemed²

¹Department of Epidemiology, Public Health Faculty, Institute of Health, Jimma University, P.O. Box 378, Jimma, Ethiopia
²Department of Medical Laboratory Sciences and Pathology, Health Sciences Faculty, Institute of Health, Jimma University, P.O. Box 378, Jimma, Ethiopia

Correspondence should be addressed to Habtemu J. Hebo; hjarso@rocketmail.com

Received 14 October 2018; Accepted 27 December 2018; Published 3 February 2019

Academic Editor: Antonella d'Arminio Monforte

Copyright © 2019 Habtemu J. Hebo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. Blood-borne infections have been recognized as an occupational hazard for nearly 50 years. Current treatment for hepatitis B virus (HBV) is very expensive for individuals in developing countries and cannot clear infection after it progresses to the chronic stage. Thus, early screenings of people who are at higher risk like healthcare workers and vaccination and awareness creation on standard precautions (SP) to prevent transmission are mandatory. This study determined seroprevalence of HBV and hepatitis C virus (HCV) among healthcare workers of Jimma University Medical Center (JUMC). Methods. An institution based cross-sectional study was conducted from Nov 2015 to Jan 2016. The lottery method was used to select 240 healthcare workers. Data were collected by a self-administered questionnaire. Five to ten milliliters of whole venous blood was collected from each participant. The blood samples were analyzed (tested) for hepatitis B surface antigen (HBsAg) and anti-HCV antibody using automated Enzyme-Linked Immunosorbent Assay (ELISA). Data were entered into EpiData 3.1 and analyzed by SPSS 23. Results. The positivity of HBsAg was 2.5% (6/240; 95% CI: 0.52-4.48%) and that of anti-HCV antibody was 0.42% (1/240; 95% CI: 0.0-1.23%). Most participants had good knowledge of HBV (73.9%), HCV (60.9%), and SP (82.2%) and positive attitude towards SP (88.7%), but only 42.6% had a good practice of SP. More than half (60%) and nearly half (43%) had a history of ever exposure and exposure in the last one year before the survey, respectively. Females were at lower risk of both having ever exposure (95% CI: (0.241, 0.777)) and exposure in the last one year before the survey (95% CI: (0.297, 0.933)) compared to males. Conclusion. The prevalence of HBV was intermediate according to the endemicity classification by WHO. The practice of SP was poor in most participants and, thus, occupational exposure was high. Therefore, regular screening and vaccination of healthcare workers, regular provision of basic or refresher training and availing logistics, and regular motivation of healthcare workers on the practice of standard precautions are recommended.

1. Background

In their occupational environment, healthcare workers (HCWs) are exposed to hazardous blood-borne pathogens such as hepatitis B virus (HBV) and hepatitis C virus (HCV). HBV and HCV are common causes of occupational diseases transmitted from patients to HCWs and vice versa and also to HCWs’ families. HBV and HCV infections are serious public health problems that can have consequences in terms of psychological and occupational diseases [1]. HBV is contagious and can easily be transmitted from one infected individual to another by blood contact, from mother to child, by unprotected sexual intercourse, or by sharing of eating utensils and other barber shop and beauty salon equipment. The main transmission routes include prenatal infection, skin and mucous membrane infections caused by contaminated blood or body fluid, sexual contact, and injection drug abuse. In addition, tattooing, ear piercing, acupuncture, dialysis, and even use of a syringe can be the source of infection [2].

Hepatitis B is a very important public health problem affecting almost 10% of the world population. According to the 2009 WHO report, about 2 billion people are affected with HBV worldwide, more than 350 million suffered from chronic, lifelong infection, and more than one million individuals died because of cirrhosis and liver cancer every year [2–4]. It is also estimated that 170 million are chronically infected with HCV [5]. The burden of HBV infection is highest in the developing world, particularly in Asia and sub-Saharan Africa. WHO estimated that the prevalence of HBV infection in Africa is on average more than 10%. However, a study conducted in Addis Ababa, Ethiopia, showed that the mean prevalence of HBsAg was 6.1% [4].

The Centers for Disease Control (CDC) reported that 3.9 million individuals (1.8%) are infected with HCV, and 2.7 million of these infections will become chronic [1]. The prevalence of anti-HB virus antibody among volunteer blood donors ranged from 5 to 10%. But the prevalence is higher in persons from lower socioeconomic statuses, people of older age groups, and those persons exposed to blood products [2]. It has been estimated that 14.4% and 1.4% of hospital workers are infected with HBV and HCV, respectively [1]. Healthcare personnel, including support staff, who work in healthcare settings, represent a high-risk population for serious, potentially life-threatening infections such as HIV and HBV. Direct contact with blood and other body fluids is the most common or frequent risk healthcare workers encounter while caring for patients [3]. Studies in the United States have shown that the risk of acquiring HBV after being stuck with a needle from an HBV+ client ranged from 27 to 37%. In addition, the risk of acquiring HCV after being stuck with a needle from an infected person ranged from 3 to 10%. The efficiency for transmission of hepatitis B is high. For example, an accidental splash in the eye of as little as 10⁻⁸ ml of infected blood can transmit HBV to a susceptible host [6].

A safe and effective vaccine against HBV has been available for 20 years and is effective in preventing infection and the serious consequences of hepatitis, including liver cancer and cirrhosis, when given before or after exposure [2] but there is currently no vaccine for HCV [5]. Hepatitis B vaccine is recommended for pre- and/or postexposure prophylaxis of all persons at risk of contact with blood, blood products, or bodily secretions. Ideally, immunization against hepatitis B should be completed prior to health professional training because the risk of infection is thought to be higher at this time. Immunizing HCWs against hepatitis B prevents nosocomial transmission of the virus from HCWs to patients and from patients to HCWs as it gives long-term protection from hepatitis B infection, possibly lifelong [2, 7]. Since 1990 new hepatitis B infections among children and adolescents have dropped by more than 95% and by 75% in other age groups. However, in Ethiopia, the hepatitis B vaccine for children was introduced into the expanded program for immunization (EPI) program in 2007 [2]. There is not yet routine vaccination of HBV for all adults except for what is being done by some hospitals for their health professionals. There is not also yet postexposure prophylaxis (PEP) for HBV in Ethiopia. The current treatment for hepatitis B virus infection is very expensive for individuals in developing countries like Ethiopia and cannot clear infection after it progresses to a chronic stage [4]. Thus, early screenings of people who are at risk, such as healthcare workers, and the implementation of effective interventions such as vaccination and awareness creation for standard precautions to prevent transmission are mandatory.

Up to date, very few studies have been conducted to determine the seroprevalence of HBV and HCV in different population groups such as blood donors, medical waste handlers, VCT clients, commercial sex workers, and antenatal attendees in Ethiopia. Thus, the aim of this study was to determine the seroprevalence of HBV and HCV among healthcare workers in a specific study area. The study also aimed to assess the knowledge, attitude, practice, and occupational exposure of healthcare workers to guide interventions rendered at prevention and control of HBV and HCV infections in the health facilities.

2. Methods and Materials

2.1. Study Area, Period, and Design

An institution based cross-sectional study was conducted from 11 Nov 2015 to 09 Jan 2016 at Jimma University Medical Center, 350 Kms southwest of Addis Ababa. There were a total of 810 healthcare workers (HCWs) (physicians, dentists, health officers, anesthetists, nurses, midwives, and laboratory personnel/technicians).

2.2. Population

2.2.1. Source Population

The source population included all health workers (physicians, dentists, health officers, anesthetists, nurses, midwives, and laboratory technicians) at Jimma University Medical Center who had direct patient care or specimen contact during the study period.

2.2.2. Study Population

The study population included all health workers as described under the source population and those who had direct patient care or specimen contact at least for the last 1 year.

2.3. Sample Size and Sampling Technique

2.3.1. Sample Size

The sample size was calculated using a single population proportion formula assuming 8.7% prevalence (P) of HBV among healthcare workers [8], 5% level of significance (α), 3% margin of error (d), and 15% nonresponse rate.

When corrected using the finite population correction factor (because the size of the source population (N=606) was less than 10,000), the final sample size became 251.

2.3.2. Sampling Technique

The sample size was proportionally allocated to each unit (wards, outpatient departments, and operation rooms). Then, the required number of study participants was selected by the lottery technique from each unit.

2.4. Variables

(i)Dependent variables

(a)Seroprevalence of HBV(b)Seroprevalence of HCV

(ii)Independent variables

(a)Sociodemographic characteristics

(1)Age, sex, religion, ethnicity, marital status, profession, and work experience

(b)History of occupational exposure(c)Knowledge of HBV and HCV transmission and prevention(d)Knowledge of standard precautions(e)Attitude towards standard precautions(f)Level of the practice of standard precautions

2.5. Measurements

Knowledge of hepatitis B and C virus was assessed by questions focusing on risk groups and procedures, transmission, treatment, and prevention of hepatitis B and C infection. There were 7 knowledge items for each virus and the total scores ranged from 0 (smallest) to 21 (largest). Knowledge, attitude, and practice of standard precautions were assessed by a set of questions and statements focusing on standard precautions. There were 8 knowledge items and the total scores ranged from 0 (smallest) to 27 (largest). There were 11 attitude statements whose responses were scored on the basis of a Likert scale. The scores ranged from 23 (strongly disagree) to 115 (strongly agree). There were 4 Likert scale questions to assess the frequency of compliance (practice) to standard precautions and the scores ranged from 0 (smallest) to 16 (largest).

Five to ten milliliters of whole venous blood was collected from each participant using a syringe, needle, and organ function test tube. The sample was transported to the JUMC Laboratory by a laboratory professional daily using a cold chain. Serum was separated from cells within an hour of arrival and serum samples were stored at -20 degrees Celsius. The HBsAg and anti-HCV-IgG antibody Enzyme-Linked Immunosorbent Assay (ELISA) was performed according to the manufacturer’s instructions. Samples found positive at initial screening were analyzed again for the second time. Fortunately, all the samples found positive initially were found positive on repeated analysis.

2.6. Data Collection Plan

A self-administered structured English version questionnaire was used to collect data on sociodemographic characteristics, history of occupational exposure, knowledge of hepatitis B or C virus infections, and knowledge, attitude, and practice (KAP) of standard precautions. Data collection from HCWs was facilitated by two staff members (one healthcare worker who was not included in the study and a laboratory professional for blood collection) at each unit.

2.7. Data Analysis

Data were edited, entered into EpiData 3.1, exported to SPSS 20, and cleaned to check for completeness and extreme and missing values. Univariate analyses were performed and presented in tables, charts, and graphs. We could not conduct logistic regression because cases were limited (6 for HBV and 1 for HCV infection) for this purpose.

2.8. Data Quality Assurance

Before starting data collection, the research team thoroughly reviewed the questionnaire. One day orientation was given for facilitators and blood sample collectors to ensure a common understanding of the tool and methods of data collection. The questionnaire was pretested on 10% of the study participants who were not included in the actual study. The validity of the questionnaire was tested by an expert and peer review and the reliability (internal consistency) was checked by Cronbach’s alpha coefficient. During the actual study, collected data were sorted and checked for errors and completeness on site daily. Overall data collection activities were supervised by the principal investigator. The participants anonymously responded to the items on the questionnaire. For laboratory data, specimen quality was checked for hemolysis, transportation conditions (temperature, tubes), and amount. HBsAg and anti-HCV-IgG antibody positive and negative controls were used for ELISA tests.

2.9. Ethical Considerations

The ethical clearance was secured from the College of Health Sciences Institutional Review Board (IRB), Jimma University. A letter of permission was submitted to the Jimma University Medical Center administration body and the administration bodies of each hospital’s unit. The objective of the study was explained to each study participant. The participants were informed that there are interviews and blood sample collection for HBV and HCV screening. Written informed consent for participation was obtained from each study participant. The participation in the study was on a voluntary basis and the participants could withdraw from the study during the interview.

Participants were ensured that all collected data will be used only for the research purpose. Test results were kept confidential by using unique codes given to each study participant. Laboratory personnel had access only to the unique codes written on a sample containing test tubes. The research team members had access to both the unique codes and participants’ identifiers (name and phone number) written in a separate format. All participants were informed of the result and those with a positive result were counseled and linked to care.

2.10. Plan for Data Dissemination

The finding of the study was reported to the Research Coordinating Office of Jimma University. A summary report was also submitted to Jimma University Medical Center.

2.11. Terms and Operational Definitions

(i)Good knowledge or good practice was scored as greater than or equal to 70%(ii)Positive attitude was scored as greater than 69 and negative attitude was scored as less than 69. A score equal to 69 was considered neutral(iii)Good practice was scored as greater than or equal to 60%

3. Result

3.1. Sociodemographic/Economic Characteristics

A total of 240 participants gave a sample and tested for both HBV and HCV, though 10 participants did not return the questionnaire. However, 11 (4.4%) healthcare workers refused to participate in the study. Most of the refusals (8) were from operation room healthcare workers and the remaining were from the ophthalmology, pediatrics, and psychiatry wards. The majority of participants (120 (52.2%)) were in the age group 25-29 years. The median age of participants was 25 (IQR=24-27) years. The proportion of males and females who participated in the study was almost the same. The leading proportion (102 (44.3%)) of participants was Orthodox Christian and most (137 (59.6%)) were Oromo. The majority of participants (134 (58.3%)) were single and the leading proportion (99 (43%)) was clinical nurses. The majority of participants (121 (52.6%)) had diploma level academic qualification and 148 (64.3%) had work experience of 1-3 years. The median work experience of participants was 3 years (IQR=2-5). A higher percentage (78 (33.9%)) had a monthly salary of 1601-3142 ETB and the mean (SD) of monthly salary was 2598.4 (1119.9) ETB (Table 1).

Table 1: Distribution of sociodemographic/economic characteristics of healthcare workers of JUMC, 11 Nov 2015 to 09 Jan 2016.

Sociodemographic
Number
Percent
Sociodemographic
Number
Percent

characteristics
characteristics

Age (years)

Profession

    20-24
82
35.7
    Clinical nurse
99
43.0

    25-29
120
52.2
    Midwifery nurse
30
13.0

    30+
28
12.2
    Professional nurse
77
33.5

Sex

    Others
24
10.4

    Male
116
50.4
Academic qualification

    Female
114
49.6
    Diploma
121
52.6

Religion

    BSc
101
43.9

    Muslim
55
23.9
    MSc/MPH
5
2.2

    Orthodox
102
44.3
    Specialist MD
3
1.3

    Protestant
67
29.1
Work experience (years)

    Others (Catholic & Wakefeta)
6
2.6
    1-3 years
148
64.3

Ethnicity

    4-6 years
49
21.3

    Oromo
137
59.6
    6+ years
33
14.3

    Amhara
53
23.0
Monthly salary

    Others
40
17.4
    < 1301
21
9.1

Marital status

    1301-1600
31
13.5

    Single
134
58.3
    1601-3142
78
33.9

    Currently married
91
39.6
    3143-3901
67
29.1

    Separated/divorced
2
0.9
    >3901
33
14.3

    Widowed
3
1.3

n =230 (denominator used to calculate the percentages), BSc = Bachelor of Science, MSc = Master of Science, MPH = Master of Public Health, and MD = Medical Doctor.

3.2. Risky Behavior and Medical Procedures

Most participants did not have risky behaviors and medical procedures, except for the injection of drugs where a considerable percentage (89 (38.7%)) of participants had it (Table 2).

Table 2: Distribution of risky behaviors and medical procedures among healthcare workers of JUMC, 11 Nov 2015 to 09 Jan 2016.

Risky behaviors and medical procedures
Number
Percent

Alcohol drinking
Yes
27
11.7

Cigarette smoking
Yes
12
5.2

Khat chewing
Yes
30
13.0

Shisha smoking
Yes
6
2.6

Multiple sexual partner/s
Yes
14
6.1

Practicing tattoos
Yes
10
4.3

IV drug use
Yes
6
2.6

Blood transfusion
Yes
9
3.9

Injection of any drug
Yes
89
38.7

Any incision/surgery
Yes
26
11.3

Any dental procedure
Yes
54
23.5

3.3. Knowledge of Hepatitis B and C Viruses

3.3.1. Knowledge of Hepatitis B Virus

The reliability (internal consistency) of knowledge items was good (Cronbach’s alpha = 0.712). Most respondents (170 (73.9%)) had good overall knowledge about hepatitis B virus. However, only near to one-third (74 (32.2%)) of the respondents knew that it is not transmitted by contaminated water/food prepared by a person suffering from this infection. Similarly, only less than half (112 (48.7%)) of the respondents knew that HBV infection is treatable and only less than two-thirds (139 (60.5%)) knew that it has postexposure prophylaxis. The details of the responses to each question are indicated (Table 3).

Table 3: Knowledge of healthcare workers of JUMC about hepatitis B virus, 11 Nov 2015 to 09 Jan 2016.

Items
Number
Percent

(1) Who are vulnerable groups to Hepatitis B virus (HBV) infection?

    Healthcare workers
Yes
209
90.9

    Commercial sex workers
Yes
157
68.3

    IV drug users
Yes
108
47.0

    Students on clinical practice
Yes
134
58.3

(2) Which of the following procedures may expose to the Hepatitis B virus (HBV) infection?

    Injections
Yes
209
90.9

    Blood sampling
Yes
192
83.5

    Incisions/surgery
Yes
195
84.8

    Tattooing
Yes
148
64.3

(3) Hepatitis B virus (HBV) can be transmitted through:

    Contaminated blood transfusion
Yes
228
99.1

    Unsafe sexual contact/practice
Yes
212
92.2

    Contaminated water/food prepared by a person suffering from this infection?
No
74
32.2

    Sharing needles or other equipment used for injecting illegal drugs
Yes
218
94.8

    Accidental stuck with a used needle or other sharp instruments that has an infected person's blood on it
Yes
222
96.5

    Blood or body fluid splashes onto an exposed surface (eyes, mouth, or cut in the skin)
Yes
221
96.1

    Birth canal during childbirth (mother to newborn)
Yes
204
88.7

    Breastfeeding
Yes
190
82.6

    Sharing grooming items such as razors or toothbrushes
Yes
208
90.4

(4) Is HBV infection treatable?
Yes
112
48.7

(5) Is HBV infection curable?
No
154
67.0

(6) Can we prevent HBV transmission?
Yes
208
90.4

(7) Does HBV have post-exposure prophylaxis?
Yes
139
60.4

3.3.2. Knowledge of Hepatitis C Virus

The reliability (internal consistency) of knowledge items was good (Cronbach’s alpha = 0.786). A majority of the respondents (140 (60.9%)) had good overall knowledge about hepatitis C virus. However, only a bit greater than one-fifth (52 (22.6%)) and less than one-fifth (34 (14.8%)) of the respondents knew that it is not transmitted by contaminated water/food prepared by a person suffering from this infection and breastfeeding, respectively. Similarly, only a bit greater than one-third (82 (35.7%)) knew that HBV infection is curable and only a bit greater than one-fourth (60 (26.1%)) knew that it has no postexposure prophylaxis. The details of the responses to each question are indicated (Table 4).

Table 4: Knowledge of healthcare workers of JUMC about hepatitis C virus, 11 Nov 2015 to 09 Jan 2016.

Items
Number
Percent

(1) Who are vulnerable groups to Hepatitis C virus (HCV) infection?

    Healthcare workers
Yes
174
75.7

    Commercial sex workers
Yes
131
57.0

    IV drug users
Yes
94
40.9

    Students on clinical practice
Yes
116
50.4

(2) Which of the following procedures may expose to the Hepatitis C virus (HCV) infection?

    Injections
Yes
191
83.0

    Blood sampling
Yes
177
77.0

    Incisions/surgery
Yes
178
77.4

    Tattooing
Yes
135
58.7

(3) Hepatitis C virus (HCV) can be transmitted through:

    Contaminated blood transfusion
Yes
210
91.3

    Unsafe sexual contact/practice
Yes
196
85.2

    Contaminated water/food prepared by a person suffering from this infection?
No
52
22.6

    Sharing needles or other equipment used for injecting illegal drugs
Yes
200
87.0

    Accidental stuck with a used needle or other sharp instruments that has an infected person's blood on it
Yes
208
90.4

    Blood or body fluid splashes onto an exposed surface (eyes, mouth, or cut in the skin)
Yes
205
89.1

    Birth canal during childbirth (mother to newborn)
Yes
187
81.3

    Breastfeeding
No
34
14.8

    Sharing grooming items such as razors or toothbrushes
Yes
192
83.5

(4) Is HCV infection treatable?
Yes
141
61.3

(5) Is HCV infection curable?
Yes
82
35.7

(6) Can we prevent HCV transmission?
Yes
207
90.0

(7) Does HCV have post-exposure prophylaxis?
No
60
26.1

3.4. Knowledge, Attitude, and Practice of Standard Precautions

3.4.1. Knowledge of Standard Precautions

The reliability (internal consistency) of knowledge items was good (Cronbach’s alpha = 0.728). Most respondents (189 (82.2%)) had good overall knowledge about standard precautions. However, the level of knowledge in some components of standard precautions was not sufficient. For instance, only near to two-thirds (152 (66.1%)) of the respondents knew that standard precautions apply to blood, all body fluids, secretions, and excretions (except sweat), nonintact skin, or mucous membranes. Similarly, only less than half (103 (44.8%)) knew that standard precautions are intended not only for patients who have signs and symptoms of disease (s). Again, only a bit more than half (134 (58.3%)) of the respondents knew that needles should not be disposed mixed with other wastes/rubbish. The details of the responses to each question are indicated (Table 5).

Table 5: Knowledge of healthcare workers of JUMC about standard precautions, 11 Nov 2015 to 09 Jan 2016.

Items
Number
Percent

(1) Standard precautions:

    Are first level precautions designed for use in caring for all people – both clients and
Yes
166
72.2

    patients attending healthcare facilities

    Apply to blood, all body fluids, secretions and excretions (except sweat), non-intact
Yes
152
66.1

    skin or mucous membranes.

    Are second level precautions intended for use in patients known or highly suspected
No
72
31.3

    of being infected or colonized with pathogens transmitted by air, droplet or contact

    Are intended only for patients who have signs and symptoms of disease (s)
No
103
44.8

(2) Hand hygiene (hand washing with soap and water or use of an antiseptic hand rub) is mandatory:

    After touching blood, body fluids, secretions, excretions, and contaminated items
Yes
205
89.1

    Immediately after removing gloves
Yes
194
84.3

    Between patient contacts
Yes
177
77.0

(3) Gloves are used:

    For contact with blood, body fluids, secretions/excretions or contaminated items
Yes
215
93.5

    For contact with mucous membranes or non-intact skin
Yes
207
90.0

    For any contact with patients
Yes
190
82.6

(4) Gown/Apron is used to:

    Protect skin from blood or body fluid contact
Yes
213
92.6

    Prevent soiling of clothing during procedures that may involve contact with blood
Yes
207
90.0

    or any body fluids (secretions/excretions)

    For any contact with patients
No
55
23.9

(5) Mask, goggles or face shield are used to protect
Yes
206
89.6

     mucous membranes of eyes, nose or mouth when

     contact with blood or body fluids is likely

(6) Which of the following is Safe Injection Practices?

    Avoid recapping, bending, breaking, or hand manipulating used needles
Yes
191
83.0

    If recapping is required, use a one-handed scoop technique only
Yes
176
76.5

    Avoid removing used needles from disposable syringes
Yes
184
80.0

    Place used needles in a puncture-resistant container at the point of use
Yes
184
80.0

(7) Where/how should needles be disposed?

    Open pail
No
123
53.5

    In sharp and liquid proof container without removing the syringe
Yes
165
71.7

    In sharp and liquid proof container after separating the needle from the syringe
No
99
43.0

    Mixed with other wastes/rubbish
No
134
58.3

(8) Which of the following is a component of Standard Precautions to prevent

     occupationally transmitted Blood Borne Infections?

    Hand hygiene
Yes
215
93.5

    Using Gloves
Yes
223
97.0

    Using Aprons
Yes
218
94.8

    Safe disposal of sharp
Yes
219
95.2

    Safe disposal of needles
Yes
218
94.8

3.4.2. Attitude towards Standard Precautions

Attitude towards standard precautions was assessed by 23 items. The reliability (internal consistency) of items was good (Cronbach’s alpha = 0.777). Respondents with a score greater than 69 (233) were considered as having a positive attitude and those less than 69 were considered as having a negative attitude. Most of the respondents (88.7%) had a positive attitude towards standard precautions and only 8 (3.5%) were neutral. Positive attitude towards some components of standard precautions was not adequate. To mention just an example, only a bit greater than one-third (82, 35.7%) of the respondents disagree or strongly disagree that contaminated needles should be recapped immediately after use. The details of the responses to each statement are indicated (Table 6).

Table 6: The attitude of healthcare workers of JUMC towards standard precautions, 11 Nov 2015 to 09 Jan 2016.

Items
Strongly disagree
Disagree
Neutral
Agree
Strongly agree

Since no one really knows what organism’s clients or patients may have, it is essential that standard precautions be used all the time.
0
9
17
61
143

In the absence of compliance to standard precautions, healthcare facilities can be the source of infection and epidemic diseases
7
10
19
59
135

The glove should be used by all patient care contacts as a useful strategy for reducing the risk of transmission of organisms
1
6
15
55
153

Physical barriers (protective goggles, face masks or aprons) should be used if splashes or spills of any body fluids (secretions or excretions) are likely.
3
14
13
43
157

Strongly agree
Agree
Neutral
Disagree
Strongly disagree

It is safe to use syringe between patients if the needle is changed
63
40
16
28
83

To prevent accidental injury, contaminated needles should be recapped immediately after use
95
32
21
31
51

Hand washing:

Hand washing between every patient encounter is unnecessary
41
31
9
52
97

Hand washing does not affect clinical outcome
33
28
9
60
100

Hand washing is unnecessary when gloves are worn
27
30
16
61
96

Routine or frequent hand washing is unnecessary
29
22
13
66
100

Frequent hand washing interrupts efficient patient care
31
33
15
63
88

Frequent hand washing damages skin and causes cracking, dryness, irritation, and dermatitis
32
46
24
57
71

Hand washing damages nails and nail polish
21
25
18
75
91

Hand washing is inconvenient
35
37
28
67
63

Hand washing takes too much time
34
32
17
76
71

Strongly disagree
Disagree
Neutral
Agree
Strongly agree

Wearing gloves do not replace the need for hand hygiene
30
48
20
60
72

A separate pair of gloves must be used for each client.
18
34
12
55
111

A separate pair of gloves must be used when moving from one site to another site on the same patient (i.e., from respiratory care to a dressing change)
32
49
17
47
85

Sharps container should be:

Put as close to the point of use as possible, ideally within arm’s reach.
21
22
15
79
93

Attached to walls or other surfaces if at all possible.
13
27
31
79
80

Marked clearly so that people will not unknowingly use them for discarding other items.
16
15
27
69
103

Marked the fill line at the three-quarters full level.
8
26
27
63
106

Not be shaken to settle its contents and make room for more sharps.
16
20
26
73
95

3.4.3. Practice of Standard Precautions

Only less than half (98 (42.6%)) of the respondents had a good overall practice of standard precautions. Only less than half (94 (40.9%)) of the respondents usually or always practiced standard blood or body fluid precautions in their workplace. Similarly, only less than half (95 (41.3%)) of the respondents usually or always wore personal protective equipment (PPE) when needed. Details of the responses to each item are indicated (Table 7).

Table 7: The practice of standard precautions by healthcare workers of JUMC, 11 Nov 2015 to 09 Jan 2016.

Items
Never
Rarely
Sometimes
Usually
Always

How frequently do you practice standard blood or body fluid precautions at your workplace?
41
27
68
22
72

How frequently do you wash your hands before examining a patient?
33
26
101
16
54

How frequently do you wear PPE when needed?
56
16
63
28
67

How frequently do you remove all finger rings, watches and bracelets during surgical hand scrub?
78
14
40
14
84

3.5. Occupational Exposure

More than half (60%) of the participants reported having ever exposure and 43% reported exposure in the last one year before the survey to blood or body fluid through splashing into the eyes and/or mouth or sharps or needlestick injury. A significant proportion (43%) of the respondents had a history of needlestick injury and the majority (56.6%) of this occurred within one year before the survey. More than one-third (38.3%) of the respondents had a history of sharp injury other than needlestick and the majority (57.95%) of this happened within one year before the survey. Nearly one-third (32.2%) of the respondents had a history of blood or body fluid splash into the eyes and/or mouth and nearly three-fourths (74.3%) of this occurred within one year before the survey (Table 8).

Table 8: Occupational exposure of healthcare workers of JUMC, 11 Nov 2015 to 09 Jan 2016.

Type of exposure
Number
Percent

Have you ever had a needle stick injury?
Yes
99
43

No
126
56.1

Don’t remember
5
2.2

Have you faced a needle stick injury within the last one year?
Yes
56
24.3

No
169
73.5

Don’t remember
5
2.2

Have you ever had sharp injury other than needle stick?
Yes
88
38.3

No
130
56.5

Don’t remember
12
5.2

Have you faced a sharp injury within the last one year?
Yes
51
22.2

No
162
70.4

Don’t remember
17
7.4

Have you ever had blood or body fluid splash into your eye and/or mouth?
Yes
74
32.2

No
150
65.2

Don’t remember
6
2.6

Have you had blood or body fluid splash into your eye and/or mouth within the last one year?
Yes
55
23.9

No
161
70.0

Don’t remember
14
6.1

NB: those who did not remember their exposure were considered as not exposed.

Among sociodemographic characteristics, only sex was associated with occupational exposure of the participants to blood or body fluid through splashing into the eyes and/or mouth or sharps or needlestick injury. Females were more than almost 57% lower at the risk of having ever exposure (AOR = 0.432; 95% CI: (0.241, 0.777)) and more than 42% lower at the risk of being exposed in the last one year before the survey (AOR = 0.527; 95% CI: (0.297, 0.933)) compared to males.

3.6. Prevalence of HBV and HCV Infection

Out of a total of 240 participants, 6 (2.5%; 95% CI: 0.52 to 4.48%) were positive for HBsAg whereas only 1 (0.42%; 95% CI: 0.0 to 1.23%) participant was positive for anti-HCV antibody. There was not any coinfection of HBV and HCV found among the participants. Five of those who were positive for HBsAg were in the age group 20-24 years and one was 48 years old. Five were males; 4 were single and 2 were currently married. Five of them were professional nurses and one was a psychiatry nurse. Five of them were BSc nurses and one was a diploma nurse. Five of them had work experience of 0-2 years and one had work experience of 32 years. All had an adequate overall knowledge of HBV and standard precautions whereas five had adequate knowledge of HCV. Five had a positive attitude towards standard precautions and one was neutral. Four of them had a good practice of standard precautions. Four had a history of ever needlestick injury; two had a history of sharp injury other than needlestick. Two had also a history of blood or body fluid splash into the eyes and/or mouth.

The only positive participant for HCV was a 25-year-old female. She had adequate knowledge of HBV, HCV, and standard precautions. She also had a positive attitude and good practice of standard precautions. She had no history of ever needlestick injury and did not remember the history of blood or body fluid splash into the eyes and/or mouth.

4. Discussion

Studies conducted at different areas and on different populations regarding seroprevalence of hepatitis B and C viruses and their associated risk factors have reported different findings. Physicians, dentists, nurses, laboratory staff, and dialysis center personnel are at high risk of acquiring the infection. This study determined the prevalence of HBV and HCV infections among healthcare workers of a tertiary level public hospital.

The prevalence of HBV infection among healthcare workers was 2.5% indicating intermediate endemicity (2-7%) of the problem according to the WHO classification of the prevalence of HBV infection [9, 10] despite high (60%) prevalence of having ever been exposed to blood or body fluid through splashing into the eyes and/or mouth or sharps or needlestick injury. This could be because of lower prevalence of HBV infection in the general community and/or because most healthcare workers had a good overall knowledge of HBV and HCV and standard precautions and positive attitude towards standard precautions contrary to the report of FMOH, Ethiopia [6].

The prevalence of HBV infection determined in this study was comparable to the prevalence of 4.4% reported among healthcare workers in Khartoum, Sudan [11], and the prevalence of 2.9% reported among healthcare workers of a tertiary hospital in Rwanda [12] and the 4.2% prevalence reported among medicine and health science students of Wollo University, Northeast Ethiopia [13]. However, it was lower than the prevalence of 7.3% reported among healthcare workers of Bule Hora Woreda, Southern Ethiopia [14], the prevalence of 8.7% reported among healthcare workers of the Najran region, Southwestern Saudi Arabia [8], the prevalence of 8.1% reported among healthcare workers of a tertiary hospital in Uganda [15], and the prevalence of 7.0% reported among healthcare workers of a tertiary hospital in Tanzania [16]. On the other hand, it was higher than the 1.0% and 0.4% prevalence reported among healthcare workers of a tertiary care hospital in India [17, 18]. This could be because of differences in the level of knowledge of HBV and standard precautions and attitude and practice of standard precautions and occupational exposure.

The prevalence of HCV infection in this study (0.42%) was similar to the 0% prevalence report among healthcare workers of the Najran region, Southwestern Saudi Arabia [8], the prevalence of 1.3% among healthcare workers of a tertiary hospital in Rwanda [12], and the prevalence of 0.7% among medicine and health science students of Wollo University, Northeast Ethiopia [13]. This could be because students and healthcare workers might have a similar level of knowledge and practice of standard precautions and, thus, might have similar exposure and infection.

Limitations. This study might underestimate the true prevalence of both HBV and HCV infections as eight healthcare workers working in the operation room refused to participate in the study suspecting that they were already infected and did not want to know their status. The study might also have been underpowered for detecting cases of HCV as the sample size calculated for HBV was used because of resource scarcity. HBsAg positivity indicates either acute (active) or chronic infections. HBsAg negativity also indicates either the true absence of infection (susceptibility) or immunity due to vaccination or immunity due to resolved infection. These statuses can be differentiated by performing HBsAb, HBcAb, and HBcAb IgM tests. However, we did not perform these tests because of resource limitation. We might have also overestimated the practice of standard precautions as it was self-reported (social desirability bias) by the respondents and no attempt was made to directly observe actual practice. The same was true for the history of occupational exposure which was also self-reported (recall bias) by the respondents and no attempt was made to revise their health records.

5. Conclusion

This study has determined the prevalence of HBV and HCV infections among healthcare workers and found intermediate endemicity of HBV infection and nonnegligible prevalence of HCV. The practice of standard precautions was also poor in most participants and, thus, occupational exposure was high. Thus, we recommended that JUMC regularly screen healthcare workers and avail vaccine which was started soon after completion of this study and interrupted later. We also recommend that JUMC and other interested stakeholders regularly provide basic or refresher training for healthcare workers on blood-borne infections and their effective prevention methods (standard precautions). JUMC should also avail logistics and regularly motivate healthcare workers on the practice of standard precautions.

Abbreviations

AOR: | Adjusted odds ratio
CI: | Confidence interval
ELISA: | Enzyme-Linked Immunosorbent Assay
ETB: | Ethiopian Birr
FMOH: | Federal Ministry of Health
HBsAg: | Hepatitis B surface antigen
HBV: | Hepatitis B virus
HCWs: | Healthcare workers
HCV: | Hepatitis B virus
HIV: | Human Immunodeficiency Virus
JUMC: | Jimma University Medical Center
KAP: | Knowledge, attitude, and practice
Kms: | Kilometers
SP: | Standard precautions
VCT: | Voluntary counseling and testing.

Data Availability

All relevant data are within the manuscript.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Authors’ Contributions

Habtemu J. Hebo, Desta H. Gemeda, and Kedir A. Abdusemed conceptualized the study. Habtemu J. Hebo, Desta H. Gemeda, and Kedir A. Abdusemed designed the methods. Habtemu J. Hebo, Desta H. Gemeda, and Kedir A. Abdusemed acquired the funding. Habtemu J. Hebo and Kedir A. Abdusemed curated the data. Habtemu J. Hebo conducted formal analysis. Habtemu J. Hebo and Desta H. Gemeda wrote the report. Habtemu J. Hebo prepared the draft manuscript.

Acknowledgments

This research was funded by the Institute of Health, Jimma University, as part of the academic staff mega project research. We would like to extend our gratitude to Jimma University for funding this study. We are also grateful to the participants of this study and the data collectors including laboratory personnel.

References

M. Askarian, M. Yadollahi, F. Kouchak, M. Danaei, V. Vakili, and M. Momeni, “Precautions for health care workers to avoid hepatitis b and c virus infection,” International Journal of Occupational Medicine and Environmental Health, vol. 2, no. 4, pp. 191–198, 2011.

Y. M. Mesfin, K. T. Kibret, and O. Schildgen, “Assessment of Knowledge and Practice towards Hepatitis B among Medical and Health Science Students in Haramaya University, Ethiopia,” PLoS ONE, vol. 8, no. 11, p. e79642, 2014.

S. Chouhan, “Hepatitis B prophylaxis practice among medical students : An overview,” Hepatitis B Annual, vol. 5, no. 1, p. 102, 2008.

B. Anagaw, Y. Shiferaw, Y. Belyhun et al., “Seroprevalence of Hepatitis B and C Viruses among Medical Waste Handlers at Gondar Town Health Institutions, Northwest Ethiopia,” BMC Research Notes, vol. 5, no. 55, 2012.

WHO, Guidance on Prevention of Viral Hepatitis B and C among People Who Inject Drugs, Switzerland, Geneva, 2012.

FMOH, Infection Prevention and Patient Safety: Reference Manual for Service Providers and Managers in Healthcare Facilities of Ethiopia, Addis Ababa, Ethiopia, June 2010.

APIC, Text of Infection Control and Epidemiology, The Association for Professionals in Infection Control and Epidemiology, New York, NY, USA, 2nd edition, 2005.

J. M. Alqahtani, S. A. Abu-Eshy, A. A. Mahfouz, A. A. El-Mekki, and A. M. Asaad, “Seroprevalence of hepatitis B and C virus infections among health students and health care workers in the Najran region, southwestern Saudi Arabia: The need for national guidelines for health students,” BMC Public Health, vol. 14, no. 1, p. 577, 2014.

European Centre for Disease Prevention and Control, “Hepatitis B and C surveillance in Europe,” ECDC, Stockholm, 2012.

R. Zampino, A. Boemio, C. Sagnelli et al., “Hepatitis B virus burden in developing countries,” World Journal of Gastroenterology, vol. 21, no. 42, pp. 11941–11953, 2015.

M. Abdalwhab and M. Nafi, “Sero-frequency of Hepatitis B Infection among Health Care Workers in Khartoum,” American Journal of Research Communication, vol. 2, p. 12, 2014.

F. Kateera, T. D. Walker, L. Mutesa et al., “Hepatitis B and C seroprevalence among health care workers in a tertiary hospital in Rwanda,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 109, no. 3, pp. 203–208, 2015.

W. Demsiss, A. Seid, T. Fiseha, and I. Chemin, “Hepatitis B and C: Seroprevalence, knowledge, practice and associated factors among medicine and health science students in Northeast Ethiopia,” PLoS ONE, vol. 13, no. 5, p. e0196539, 2018.

A. Geberemicheal, A. Gelaw, F. Moges, and M. Dagnaw, “Seroprevalence of hepatitis B virus infections among health care workers at the Bulle Hora Woreda Governmental Health Institutions, Southern Oromia, Ethiopia,” Journal of Environmental and Occupational Science, vol. 2, no. 1, p. 9, 2013.

A. K. Ziraba, J. Bwogi, A. Namale, C. W. Wainaina, and H. Mayanja-Kizza, “Sero-prevalence and risk factors for hepatitis B virus infection among health care workers in a tertiary hospital in Uganda,” BMC Infectious Diseases, vol. 10, no. 1, p. 191, 2010.

A. Mueller, L. Stoetter, S. Kalluvya et al., “Prevalence of hepatitis B virus infection among health care workers in a tertiary hospital in Tanzania,” BMC Infectious Diseases, vol. 15, no. 1, article no. 386, 2015.

T Pazhaniaandi, K Subhashraj, and K Chakravarthy, “Hepatitis-B infection: Awareness among medical, dental interns in India,” Annals of Tropical Medicine and Public Health, vol. 2, no. 2, pp. 33–36, 2009.

V. Singhal, D. Bora, and S. Singh, “Prevalence of Hepatitis B Virus infection in Healthcare Workers of a Tertiary care centre in India and their vaccination status,” Journal of Vaccines and Vaccination, vol. 2, no. 2, 2011.