Seroprevalence, risk associations, and testing cost of screening for HCV, HBV, and HIV infections among a group of pre-operative Egyptian patients

Cover Page


Cite item

Full Text

Abstract

Background. Routine pre-operative testing for Human Immunodeficiency Virus (HIV) and other blood-borne viruses, Hepatitis B Virus, Hepatitis C Virus (HBV, HCV) has been stated as a strategy to reduce the risk of healthcare workers’ infection by preventing and reducing their infection. However, the argument that screening is essential or not is strong. This study aims to determine the incidence of HBV, HCV, and HIV infections identified during pre-operative screening in a cohort of Egyptian individuals, along with the associated risk factors and the subsequent testing costs. Materials and methods. This study comprised 138 patients, with 92 (66.7%) males and 46 (33.3%) females. All patients scheduled for surgical procedures underwent testing for HCV Ab, HBsAg, and HIV Ag/Ab by chemiluminescent microparticle immunoassay conducted with the “ARCHITECT i2000SR Immunoassay” (Abbot Japan CO., Ltd, Tokyo, Japan). Among the participants, 23 out of 138 (16.7%) tested positive for HCV, while 5 out of 138 (3.3%) showed equivocal results for HCV, and 110 out of 138 (79.7%) tested negative for HCV. Additionally, 2 out of 138 (1.4%) were positive for HBsAg, while 136 out of 138 (98.6%) tested negative for HBsAg. Furthermore, 1 out of 138 (0.7%) was found to be HIV-positive, while 137 out of 138 (99.3%) tested negative for HIV. Results. The prevalence of each infection detected through pre-operative testing of HCV, HBV and HIV and a questionnaire was compared. Furthermore, we calculated the screening cost per confirmed infection by assessing the incidence of infections linked to different risk factors, ages, genders, and levels of HBV vaccination. Conclusions Age markedly impacted HCV and HBV rates. There was no link between viral infections and gender. The expenses associated with each affirmative result were 1763 LE for HCV, 5520 LE for HBV, and 22 080 LE for HIV. While self-assessment through questionnaires can be partially efficacious, it lacks sufficient screening accuracy.

Full Text

Introduction

In recent years, Egypt has been estimated to be one of the countries with the highest HCV incidence globally. Anti-HCV testing revealed that 6% of individuals aged 1–59 years had a positive result, and 4% were determined to be suffering from an active infection with higher prevalence in males among most age groups except in children [1, 13]. In past years, Egypt was considered one of the highest countries in HCV prevalence but starting 2018/2019, Egypt started applying screening, diagnosis and treating HCV patients to achieve HCV control and eliminating infection by 2030 [1, 26]. HBV infection in Egypt is a significant public health issue [8]. According to research, the estimated national prevalence was 3.67% [95% CI: 3: 4.39). With a history of HBV immunization during infancy, children under 20 had the lowest prevalence (0.69%). Pregnant women, blood donors, and healthcare professionals had combined prevalence rates of HBV infection of 2.95%, 1.8%, and 1.1%, respectively. The largest prevalence was seen in patients with hemolytic anemia and hemodialysis, cancer patients, patients with HCC, and patients with chronic liver disease (6.34%, 25.5%, 18.6%, and 34%, respectively). Research comparing the prevalence of HBV in urban and rural areas found that the rates were similar, at 2.43% and 2.15%, respectively [8].

HIV prevalence rates in Egypt are estimated to be 0.1 percent in the general population. Nevertheless, United Nations agencies such as UNAIDS and UNICEF, along with stakeholders within the Egyptian National AIDS Program (NAP), express concerns regarding a potentially significant increase [10]. HIV-positive individuals have been identified in an increasing number of studies conducted globally [12, 33]. The prevalence of HIV among the general population remains low in Egypt. That is supported by data from HIV testing services (HTS) provided to pregnant women. However, Egypt continued to witness an increasing trend of HIV new infection and incidence rate, which is reflecting a rapidly evolving disease spread. The incidence rate has increased by five folds between 2010 and 2019. In 2019, men (mainly young men aged between 15 and 24 years) had the highest HIV new infections compared to women. There was a rapid increase in the estimated number of adults and children living with HIV in the country during the period 2015 and 2020. UNAIDS Estimated around 24 000 People Living with HIV by end of 2020 in Egypt. Programmatic data on HIV testing and surveillance continue to indicate that specific population groups are increasing risks of new HIV infections. People who inject drugs (PWID) and other men who engage in sex with men (MSM) are at higher risk of HIV infection than other population groups. Despite the focus on PWIDs and MSM, data from HIV testing and assessments indicate the significance of other population groups at risk of HIV infection due to specific risk factors [6].

From the previous data, preventing and limiting viral infection spread and transmission is crucial, especially among medical health workers (HCW) and staff. According to estimates from the World Health Organization (WHO), over 3 million healthcare workers sustain injuries annually from contaminated edges with at least one form of HIV (~170 000 exposures), hepatitis B (~2 000 000 exposures), or hepatitis C (~900 000 exposures). The only available method of prevention for HCV currently is the use of normal precautions along with rigorous attention to post-exposure prophylactic measures. This is because there is currently no immunization against HCV [24].

As for HBV infection, HCW are at increased risk of hepatitis B virus (HBV) infection because of their frequent exposure to blood and other body fluids. Once infected, HCW may transmit HBV to their patients [14, 19, 28].

Globally, Europe (0.6–1.2%) and several Asian nations (India, Iran, Turkey, and the United Arab Emirates, for example) were reported to have low rates of hepatitis B infection among HCW [3, 15, 21, 27]. Nonetheless, some Asian nations (up to 9.85%) and African nations (2.3–11.8%) had significantly greater prevalence [16, 20]. Vietnam had the highest incidence in Asia.

In HCW in Cameroon, Mauritania, Sierra Leone, and Tanzania, an alarmingly high incidence rate of > 8.7% of HBsAg has been recorded.

In Egypt, a study showed that 0.4% of HCW were positive for HBsAg and 15.6 for anti-HBc [17].

As for HCV infection, HCV infection prevalence among Egyptian HCW was estimated to be around 8% [7, 25], another study reported that, out of 1000 studied HCWs, 90 cases (9%) were positive for hepatitis C antibody (HCV Ab) and 53.70% of all HCW exposed to needle sticks injury (NSI) [6].

As for HIV, prevalence rates in Egypt are estimated to be 0.1 percent in the general population.

Pre-operative monitoring for HIV and the hepatitis virus is now pervasive in medical facilities. A significant concern for the economy’s well-being and clinical management is the administration of non-essential and irregular pre-operative blood tests before elective surgery.

However, the argument that screening is essential or not is strong. Routine pre-operative HIV and other blood-borne viruses (HCV and HBV) checking is defined as an approach to reduce the risk of healthcare workers’ infection by preventing and reducing their infection. Moreover, after a sharp injury, the surgeon and healthcare workers would know whether to begin post-exposure prophylaxis immediately. Furthermore, it is critical to determine whether or not to increase the use of personal protective equipment (PPE) as an additional precaution throughout operations. Additionally, it assists surgeons in organizing their surgery schedule and prioritizing patients in the correct order. However, this aids surgeons in determining the necessary environmental sterilization and apparatus to be utilized after each procedure [17].

Regarding patients, it has been proposed that regular pre-operative testing for HIV, HBV, and HCV could be advantageous by enabling the identification of undetected cases and the timely management of those cases before manifesting liver cancer, cirrhosis, or AIDS [12, 29, 32].

Research has indicated that a significant portion of the concerns surrounding the spread of infections could be mitigated by implementing universal precautions instead of universal screening; this represents the primary critique of the universal screening approach. However, the maximum significance of universal precautions is preventing blood contact through barrier protection. However, the risk of gaining infection is higher with needle stick injury (NSI), where barrier precautions are unavailing [2].

Despite specific precautions to prevent infection as wearing protective gloves, googles and cloth, providing sinks for hands washing, providing appropriate treatment and prophylactic IVIgG and raising the awareness of HCW on how to deal after exposure, still the risk of gaining infection is higher with needle stick injury (NSI) and exposure to injury with sharp objects.

This research investigates the impact of pre-operative screening on HIV, HCV, and HBV infection rates in Egyptian individuals, evaluating risk correlations and checking costs, self-reported positivity rates, and hepatitis incidence by gender and age.

Materials and methods

The Faculty of Medicine Ethics Committee at Cairo University has approved the research (#N-280-2023). The study corresponded with the principles of the Declaration of Helsinki. All participants provided informed consent before enrollment.

The study was conducted on 138 patients undergoing elective operation in King Fahd Unit Al-Kasr Al-ainy Hospitals, Cairo University. Immunocompromised patients and patients under corticosteroids or immunosuppressant medications were excluded.

Patients were subjected to a questionnaire discussing their entire history, kind of upcoming elective operation, job, HBV vaccination state, risk factors including previous operation, drugs, blood transfusion, organ transplantation, previous endoscopy or catheter, tooth manipulation, professional risk, and sharing personal tools. Clinicians in the King Fahd unit in Cairo University hospitals performed clinical examinations of patients, data of the patients are discussed in Table 1 in [29].

 

Table 1. Demographic characteristics of the patients

 

Frequency (N)

Percent (%)

Gender

male

92

66.7

female

46

33.3

HB vaccine

no

116

84.1

yes

22

15.9

Job

no or housewife

45

32.6

employee

14

10.1

skillful worker

17

12.3

worker

20

14.5

retired

22

15.9

student

10

7.2

farmer

8

5.8

health care worker

2

1.4

Total

138

100.0

Upcoming operation

stones

36

26.1

endoscopy

68

49.3

stint

6

4.3

biopsy

1

.7

open surgery

26

18.8

renal donation

1

.7

Total

138

100.0

Risk factors for infection

Drugs

no

113

81.9

smoking

21

15.2

cannabinoids

2

1.4

tramadol

1

.7

past history

1

.7

Previous operation

yes

107

77.5

Blood transfusion

yes

24

17.4

Organ transplantation

no

138

100.0

Previous endoscopy catheter

yes

59

42.8

Tooth manipulation

yes

106

76.8

Professional risk

yes

106

76.8

Sharing personal tools

yes

10

7.2

Total

138

100.0

 

A peripheral venous blood sample was collected to detect HCV antibodies, HBsAg and HIV antigen/antibody using a chemiluminescent microparticle immunoassay conducted with the “ARCHITECT i2000SR Immunoassay” (Abbott Japan CO., Ltd, Tokyo, Japan), kits used for HCV ab are ARCHITECT, Lot (57289BE00), for HBsAg Lot (59411FZ00) and for HIV antigen/antibody Lot (60457BE00).

All patients whose findings for HIV Ag/Ab > 1.0 S/CO, HBsAg > 1.0 S/CO) was reported as positive for HIV and HBV, respectively.

For HCV Ab, patients whose findings were < 1.0 S/CO was reported as negative and from 1 to 5 S/CO was reported equivocal and positive > 5 S/CO.

Statistical methods. Data analysis was conducted using SPSS version 21. Qualitative data were presented using numbers and percentages, while quantitative data were presented using means and standard deviations. Significance testing included parametric and non-parametric tests: chi-square with Fisher’s exact test for qualitative data, Student’s t-test and ANOVA for parametric normally distributed data, and the Bonferroni test for post hoc analysis. The significance level was set at a p-value ≤ 0.05.

Cost analysis. In the context of testing cost analysis, the cost associated with identifying patients with cleared or active viral loads was determined by multiplying the test cost by the number of patients and then dividing the result by the number of positive cases. This process enabled the computation of the testing expense.

Results

A total of 138 patients participated in this study, comprising 92 (66.7%) males and 46 (33.3%) females. The mean age was 50.20, with a standard deviation of 17.05 (with 10 years old minimum age and 87 years old maximum age). Data regarding previous HBV vaccinations, upcoming operations, occupations, and infection risk factors are presented in Table 1.

Viral screening test counts and positivity rates. All patients scheduled for upcoming surgical procedures underwent testing for HCV, HBV, and HIV. Among the 138 patients, 23 (16.7%) tested positive for HCV, while 5 (3.3%) showed equivocal results for HCV, and 110 (79.7%) tested negative for HCV. Additionally, 2 (1.4%) tested positive for HBsAg, while 136 (98.6%) tested negative. Furthermore, 1 (0.7%) patient was found to be HIV-positive, while 137 (99.3%) were negative for HIV. These findings are summarized in Table 2.

 

Table 2. HCV Ab, HBsAg and HIV Ag/Ab results

 

HCV Ab (n = 138)

HBsAg (n = 138)

HIV Ag/Ab (n = 138)

Positive

23

16.7

2

1.4

1

0.7

Negative

110

79.7

136

98.6

137

99.3

Equivocal

5

3.3

 

Investigating self-reported positivity rate of patients. All HCV cases known to be infected tested seropositive, whereas 12.9% of cases known not to be infected tested seropositive and 3.7% tested equivocal, with a significance level of p-value < 0.001, as shown in Table 3.

 

Table 3. Investigating self-reported positivity rate of patients (HCV)

 

HCV Ab result

Total

P value

Negative

Positive

Equivocal

Known HCV

no

Count

110

17

5

132

0.001

% within HCV Ab

83.3%

12.9%

3.7%

100.0%

yes

Count

0

6

0

6

% within HCV Ab

0.0%

100.0%

0.0%

100.0%

Total

Count

110

23

5

138

% within HCV Ab

79.7%

16.7%

3.6%

100.0%

 

Regarding HBV infection, 75% of known infections tested negative for HBsAg, while 0.7% of cases known not to be infected tested positive for HBsAg, with a significance level of p-value < 0.001, as illustrated in Table 4.

 

Table 4. Investigating self-reported positivity rate of patients (HBV)

 

HBsAg results

Total

P value

Negative

Positive

Known HBV

no

Count

133

1

134

0.001

% within HBsAg

99.3%

0.7%

100.0%

yes

Count

3

1

4

% within HBsAg

75.0%

25.0%

100.0%

Total

Count

136

2

138

% within HBsAg

98.6%

1.4%

100.0%

 

As for HIV infection, no statistically significant difference was detected (Table 5).

 

Table 5. Investigating self-reported positivity rate of patients (HIV)

 

HIV Ag/Ab result

Total

P value

Negative

Positive

Known HIV

no

Count

137

1

138

Cannot be calculated

% within HIVAg/Ab

100.0%

100.0%

100.0%

Total

Count

137

1

138

% within HIVAg/Ab

100.0%

100.0%

100.0%

Note. Odds ratio and p value can’t be calculated.

 

Association between age, gender, HBV vaccination state, and different risk factors for HCV infection. A statistically significant difference was observed regarding HCV infection status and age, with a higher prevalence noted in older age groups (p-value = 0.018), as indicated in Table 6.

 

Table 6. Association between age and HCV infection state

 

N

Mean

Std. Deviation

Std. Error

95% Confidence Interval for Mean

Minimum

Maximum

P value

Lower Bound

Upper Bound

Negative

110

48.109

16.2827

1.5525

45.032

51.186

10.0

87.0

0.015

Positive

23

58.783

17.7839

3.7082

51.092

66.473

19.0

80.0

 

Equivocal

5

56.800

19.8671

8.8848

32.132

81.468

22.0

70.0

 

Total

138

50.203

17.0504

1.4514

47.333

53.073

10.0

87.0

 

 

Statistically significant difference between positive cases in young age and negative cases in older age by P value 0.035. No statistically significant difference between age and HIV infection.

A statistically significant difference was observed between HCV-positive cases vaccinated with the HBV vaccine (36.4%) compared to those not vaccinated (12.9%), with a p-value of 0.008. However, no statistically significant differences were detected between gender, occupation, various risk factors, and HCV infection.

Association between age, gender, HBV vaccination state, and different risk factors with HBV infection. A statistically significant difference was found regarding HBV infection status and age, with a higher prevalence observed in younger age groups (p-value = 0.035). Additionally, a statistically significant difference was detected between positive HBsAg cases and previous blood transfusions (p-value = 0.026). However, no other statistically significant differences were observed between gender, occupation, HBV vaccination status, or any other listed risk factors, as shown in Table 7.

 

Table 7. Association between age and both HBV and HIV infection state

HBsAg result

N

Mean

Std. Deviation

P value

Positive

2

25.000

8.4853

0.035

Negative

136

50.574

16.8802

 

HIV Ag/Ab result

N

Mean

Std. Deviation

P value

Positive

1

59.000

 

0.606

Negative

137

50.139

17.0963

 

 

Association between age, gender, HBV vaccination state, and different risk factors for HIV infection. No statistically significant differences were detected between HIV infection state and age, gender, job, HBV vaccination state, and other risk factors.

Cost analysis. All screening tests for HBV, HCV and HIV cost: 56 442 LE, as for HBV cost was 16 560 LE; HCV cost was17 802 LE and HIV cost was 22 080 LE. A total of 138 patients were screened, cases with positive results for all viral infections cost was: 4132 LE. HBV positive cases cost 360 LE; HCV positive cases cost 2967 and 645 LE for equivocal while For HIV positive cases the cost was 160 LE.

Cost analysis for all screening test was 56 442/ 27 positive cases =2090.4 LE (with equivocal HCV results = 56 442/32 = 1763 LE) for HBV = 16 560/3 positive cases =5520 LE/positive case. For HCV= 17 802/23 positive cases = 774 LE/ positive cases (HCV with equivocal 17 802/28 = 635.8 LE per non-negative case) and for HIV = 22 080/1 = 22 080 LE per positive case. So, HCV is the most efficient screening among all, followed by HBV.

Discussion

In this study, the prevalence of HBV, HCV, and HIV in a group of Egyptian patients scheduled to undergo operations at King Fahd Unit Cairo University was investigated. The respective prevalence rates for HCV, HBV, and HIV were 16.7%, 1.4%, and 0.7%. Age was a crucial determinant influencing HCV and HBV exclusively; gender had no discernible effect on HCV, HBV, or HIV. The self-reported positivity rates of HCV are 100%, as all known infections are seropositive, but 12.9% of those known not to be infected are seropositive, and 3.7% are equivocal. In the case of HBV, 75% of individuals known to be infected are HBsAg negative. For patients with a history of infection, HBsAg negative cases should undergo investigation for HB core total and HBsAb to assess their HBV infection status. However, for screening purposes, a positive history is sufficient to warrant precautions. 0.7% of known not to be HBV-infected cases are HBsAg positive, and for HIV, the only positive case did not know about the presence of infection. Despite the small number of HIV-positive cases, it is essential to know the patient’s condition before entering the operation to protect the surgeons and medical staff from the danger of virus transmission because of the threat it poses to their lives and the future of medical staff.

The corresponding prevalence rates for HCV, HBV, and HIV were 16.7%, 1.4%, and 0.7%. Ahmed A Dahab et al. [11] reported concordant rates for HCV, HBV (12.4%) (0.2%), respectively with higher HCV rates. As for HIV, Amgad Ali et al. [5] reported a rate of (0.15%), these results support higher HCV rate of infection compared to HBV rate of infection and lower HIV rates in Egypt. Takata et al. reported lower rates of HCV infections (5.8%) and higher HBV rates (2.1%) in Japan compared to the current study [22]. Another study by Shintaro Sukegawa et al. [30] in Japan demonstrated lower rates for HCV (0.76%), HBV (0.39%), and HIV (0.07%) compared to the current findings. Another study in India by Manjul Mohan et al. [23] reported rates of HBV infections (2.09%), Hepatitis C virus infection rate (1.77%) with higher HBV rates compared to our results, HIV sero-positivity was found to be (0.25%) which is concordant with our study. Moreover, Akhtar Khan and Taranum Siddiqui [18] reported in Pakistan 1.8% subjects were found to be Hepatitis B positive, 1.2% subjects were found to be Hepatitis C positive with higher HBV rates compared to our results.

The outcomes of this work exhibit that gender does not have a significant impact on HBV, HCV, or HIV. However, these results contradict Amgad Ali et al. [5] reporting a higher HIV prevalence among males in Egypt. Moreover, Shintaro Sukegawa et al. [30], Tanaka et al. [31] and Manjul Mohan et al. [23] demonstrated that gender and age do have a significant influence on hepatitis, with younger men being more susceptible, these results contradict the current study results. These researchers attributed this to the higher prevalence of sexual activity among youth compared to older adults. Akhtar Khan and Taranum Siddiqui reported that Hepatitis B positive cases 61.5% were males and 38.4% were females with higher male rates contradicting our study while 1.2% subjects were found to be Hepatitis C positive, out of these 50% were males and 50% were females, this result agree with the current study result [18].

In the current work, a statistically substantial difference was detected regarding the HBV state of infection and age being higher in younger ages with a p-value of 0.035. This finding aligns with the results of Shintaro Sukegawa et al. [30], Tanaka et al. and Manjul Mohan et al. [12, 23].

For HCV, a statistically significant difference was detected regarding the state of infection and age being higher in older age with a p-value of 0.018. However, this result contrasts with Shintaro Sukegawa et al. and Tanaka et al. [12], as infection was more prevalent at a younger age. This difference may be related to the Egyptian government’s effort and plan to eliminate the transmission of the virus, and this plan started years ago. As for HIV, there is no statistically significant difference between age and infection rate, these results contradict Amgad Ali et al. who reported high HIV prevalence among young persons and males, with high HIV prevalence among unemployed persons, manual workers and single persons [5].

This study detected a relationship between HBsAg-positive cases and previous blood transfusions, which are major risk factors for transmission. However, this agrees with the survey conducted by Candotti and Pierre [4].

Binkaa et al. [9] mentioned intravenous drug addiction as a significant risk factor for HBV, HCV, and HIV infection, but in the current study, there were no statistically significant differences between drug addiction and infections. However, this is due to the restriction of the type of addiction to oral tramadol and cannabinoids.

All screening tests incurred a cost of 56 442 LE. Specifically, HBV screening costs 16 560 LE, HCV screening costs 17 802 LE, and HIV screening costs 22 080 LE.

In this study, the cost analysis showed that out of 138 screened patients, the total cost for cases with positive results for all viral infections was 4132 LE.

HBV-positive cases cost 360 LE; HCV-positive cases cost 2967 LE and 645 LE for equivocal, while for HIV-positive cases, the cost was 160 LE. Cost analysis for all screening tests was 56 442/27 positive cases = 2090.4 LE (with equivocal HCV results = 56 442/32 = 1763 LE) for HBV = 16 560/3 positive cases = 5520 LE/positive case. HCV = 17 802/23 positive cases = 774 LE/ positive case (HCV with equivocal 17 802/28 = 635.8 LE per non-negative case), HIV = 22 080/1 = 22 080 LE per positive case. However, this data indicates that HCV is the most efficient screening, followed by HBV.

Sukegawa et al [30] determined that the aggregate expenditure for HCV, HBV, and HIV screening amounted to 16 630 950 yen ($138 591.3), 13 904 960 yen ($116 174.7), and 14 274 400 yen ($118 953.3), correspondingly. Screenings were conducted on 15 839, 15 842, and 12 745 cases, respectively, with HCV, HBV, and HIV infections. The cost per positive outcome for HBV (total HBV testing expense: 13 940 960 yen/62 positive cases), HCV (total HCV testing expense: 16 630 950 yen/153 positive cases), and HIV (HIV screening total expense: 14 274 400 yen/10 positive cases) was 224 854.2 yen ($1873.8), 108 699.0 yen ($905.8), and 1 427 440 yen ($11 895.3), respectively. This result is in substantial agreement with the current findings, as it suggests that while the expense per positive outcome was beneficial for hepatitis, it was comparatively less effective for HIV.

Conclusion

In conclusion, our study investigated the prevalence of HBV, HCV, and HIV in patients scheduled for surgical operation in King Fahd unit Al-Kasr Al-ainy hospital Cairo University. The prevalence of HBV, HCV, and HIV was 1.4, 16.7, and 0.7%, respectively. Patients-assessment using questionnaires may be effective to some extent, but the screening accuracy was inadequate. Age was a significant factor affecting HBV and HCV, while gender does not affect infection state. The cost per positive result was useful for hepatitis, but less useful for HIV.

The current study should be expanded to include a larger sample size. Additionally, it is advisable to compare the cost per test with the cost of universal precautions. However, the current study did not include this comparison due to challenges in collecting data and determining the exact cost of these precautions.

×

About the authors

Hany William Z. Hanna

Cairo University

Author for correspondence.
Email: Hanywilliam@kasralainy.edu.eg

MD of Clinical and Chemical Pathology, Lecturer of Clinical and Chemical Pathology, Kasr Al Ainy, Faculty of Medicine

Египет, Cairo

R.M.H. Shahin

Cairo University

Email: Hanywilliam@kasralainy.edu.eg

MD and Professor of Clinical and Chemical Pathology, Kasr Al Ainy, Faculty of Medicine

Египет, Cairo

L.A. Samy

Cairo University

Email: Hanywilliam@kasralainy.edu.eg

MD and Lecturer of Clinical and Chemical Pathology, Kasr Al Ainy, Faculty of Medicine

Египет, Cairo

References

  1. Abdel-Gawad M., Nour M., El-Raey F., Nagdy H., Almansoury Y., El-Kassas M. Gender differences in prevalence of hepatitis C virus infection in Egypt: a systematic review and meta-analysis. Sci. Rep., 2023, vol. 13, no. 1: 2499. doi: 10.1038/s41598-023-29262-z
  2. Ahmed R., Bhattacharya S. Universal screening versus universal precautions in the context of preoperative screening for HIV, HBV, HCV in India. Indian J. Med. Microbiol., 2013, vol. 31, no. 3, pp. 219–225. doi: 10.4103/0255-0857.115623
  3. Al-Amad S.H. Prevalence of hepatitis B, C, and HIV among patients attending a teaching dental hospital. A 7-year retrospective study from the United Arab Emirates. Saudi Med J., 2018, vol. 39, no. 5, pp. 500–505. doi: 10.15537/smj.2018.5.22116
  4. Allain J.P., Candotti D. Diagnostic algorithm for HBV safe transfusion. Blood Transfus., 2009, vol. 7, no. 3, pp. 174–182. doi: 10.2450/2008.0062-08
  5. Alzahaby A.A., Ghazy A.M., Abdelrazik O.M., Salem G.M. The prevalence of HIV infection among blood donors and patients undergoing surgical procedures in Alhussien university hospital. Al-Azhar Int. Med. J., 2023, vol. 4, no. 7: 41.
  6. Ameen S.G., Rageh I.M., Essa E., Mohammed Farid El Zamek E. Prevalence of hepatitis C antibodies among health care workers at Benha Hospitals. Egypt. Benha Med. J., 2020, vol. 37, no. 3, pp. 477–487. doi: 10.21608/bmfj.2020.103528
  7. Anwar W.A., El Gaafary M., Girgis S.A., Rafik M., Hussein W.M., Sos D., Mossad I.M., Fontanet A., Temime L. Hepatitis C virus infection and risk factors among patients and health-care workers of Ain Shams University hospitals, Cairo, Egypt. PLoS One, 2021, vol. 16, no. 2: e0246836. doi: 10.1371/journal.pone.0246836
  8. Azzam A., Khaled H., Elbohy O.A., Mohamed S.A., Mohamed S.M.H., Abdelkader A.H., Ezzat A.A., Elmowafy A.O.I., El-Emam O.A., Awadalla M., Refaey N., Rizk S.M.A. Seroprevalence of hepatitis B virus surface antigen (HBsAg) in Egypt (2000–2022): a systematic review with meta-analysis. BMC Infect. Dis., 2023, vol. 23, no. 1: 151. doi: 10.1186/s12879-023-08110-5
  9. Binka M., Butt Z.A., McKee G., Darvishian M., Cook D., Wong S., Yu A., Alvarez M., Samji H., Wong J., Krajden M., Janjua N.Z. Differences in risk factors for hepatitis B, hepatitis C, and human immunodeficiency virus infection by ethnicity: a large population-based cohort study in British Columbia, Canada. Int. J. Infect. Dis., 2021, vol. 106, pp. 246–253. doi: 10.1016/j.ijid.2021.03.061
  10. Boutros S., Skordis J. HIV/AIDS surveillance in Egypt: current status and future challenges. East Mediterr Health J., 2010, vol. 16, no. 3, pp. 251–258.
  11. Dahab A.A., Youssef M.M., Eid H.M., Elsadi K.W. Reporting the undiagnosed cases of hepatitis B and hepatitis C viruses among patients undergoing elective eye surgery in a specialized eye hospital in Egypt. J. Ophthalmol., 2019, no. 2019: 3985865. doi: 10.1155/2019/3985865
  12. Gerberding J.L. Does knowledge of human immunodeficiency virus infection decrease the frequency of occupational exposure to blood? Am. J. Med., 1991, vol. 91, no. 3B, pp. 308S–311S. doi: 10.1016/0002-9343(91)90387-d
  13. Hassan E.E., Eltomy E.M., Abuzeid Khalefa M. The Impact of contraceptive use on women health: a study of rural area, Minia, Egypt. Medico-legal Update, 2021, vol. 21, no. 3.
  14. Hebo H.J., Gemeda D.H., Abdusemed K.A. Hepatitis B and C viral infection: prevalence, knowledge, attitude, practice, and occupational exposure among healthcare workers of Jimma University Medical Center, Southwest Ethiopia. Scientific World Journal, 2019, no. 2019: 9482607. doi: 10.1155/2019/9482607
  15. Hiva S., Negar K., Mohammad-Reza P., Gholam-Reza G., Mohsen A., Ali-Asghar N.G., Mohammed-Jafar S. High level of vaccination and protection against hepatitis B with low rate of HCV infection markers among hospital health care personnel in north of Iran: a cross-sectional study. BMC Public Health, 2020, vol. 20, no. 1: 920. doi: 10.1186/s12889-020-09032-6
  16. Ijoma U.N., Meka I.A., Omotowo B., Nwagha T.U., Obienu O., Onodugo O.D., Onyekonwu C.L., Okoli E.V., Ndu A.C., Ugwu E.O. Sero-prevalence of Hepatitis B virus infection: a cross-sectional study of a large population of health care workers in Nigeria. Niger J. Clin. Pract., 2021, vol. 24, no. 1, pp. 38–44. doi: 10.4103/njcp.njcp_671_19
  17. Karim H.M.R., Mıstry T. Influence of workplace, location and experience on preoperative routine viral screening tests: a post-hoc observation from an online survey. The Ulutas Med. J., 2020, vol. 6, no. 2, pp. 74–79. doi: 10.5455/umj.20200311082916
  18. Khan A.J., Siddiqui T.R. Prevalence and Importance of hepatitis B & C screening in cases undergoing elective eye surgery. Pakistan J. Ophthalmol., 2007, vol. 23, no. 01.
  19. Mabunda N., Vieira L., Chelene I., Maueia C., Zicai A.F., Duajá A., Chale F., Chambal L., Vubil A., Augusto O. Prevalence of hepatitis B virus and immunity status among healthcare workers in Beira City, Mozambique. PLoS One, 2022, vol. 17, no. 10: e0276283. doi: 10.1371/journal.pone.0276283
  20. Machange R.E., Mosha D., Pyuza J.J., Nyombi B.B., Shao E.R. Seroprevalence and knowledge of hepatitis B virus infection among laboratoryworkers at Kilimanjaro Christian Medical Centre in Moshi, Tanzania. East Afr. Health Res. J. 2017, vol. 1, no. 2, pp. 80–85. doi: 10.24248/EAHRJ-D-16-00362
  21. Mercan Başpınar M. Screening of hepatitis A and B seropositivity among turkish healthcare providers admitted to occupational health services. Int. J. Clin. Pract., 2022, no. 2022: 6065335. doi: 10.1155/2022/6065335
  22. Ministry of health and population. Egypt health issues survey 2015. El-Zanaty and Associates Cairo, Egypt The DHS Program ICF International Rockville, Maryland, USA.
  23. Mohan M., Sharma M., Pandey C.P., Agarwal A. Preoperative Screening of HIV, HBV, HCV essential for surgical team and patients both — a research study in department of surgery, tertiary care institute of north india, rohilkhand medical college and hospital, Bareilly (U.P.) India. Int. J. Contemp. Med. Res., 2018. doi: 10.21276/ijcmr.2018.5.7.22
  24. Monif G.R., Sebastian F., Baker D.A. Infectious diseases in obstetrics and gynecology. CRC Press, 2008. doi: 10.3109/9781439801994
  25. Munier A., Marzouk D., Abravanel F., El-Daly M., Taylor S., Mamdouh R., Eldin W.S., El-Arab H.E., Sos D.G., Momen M., Okasha O., Le Fouler L., El-Hosini M., Izopet J., Rafik M., Albert M., Abdel-Hamid M., Mohamed M.K., Delarocque-Astagneau E., Fontanet A. Frequent transient hepatitis C viremia without seroconversion among healthcare workers in Cairo, Egypt. PLoS One. 2013, vol. 8, no. 2: e57835. doi: 10.1371/journal.pone.0057835
  26. Naguib G.G., Farid A., Hassan M., Elshafie A., Shazly Y.E., Shaker M.K., Ezzat H., Safwat E., Ahmed O.A., Dabbous H., Sherief A.F., Hassany M., Elserafy M., Elsayed M.H. Direct-acting antiviral regimens in Egyptian patients with chronic hepatitis C virus infection: a real-world single-center experience. Arab J. Gastroenterol., 2021, vol. 22, no. 4, pp. 285–291. doi: 10.1016/j.ajg.2021.06.001
  27. Nayyar C., Saksena R., Manchanda V. Prevalence of transfusion-transmitted viral pathogens among health-care workers and risk mitigation programme in a paediatric tertiary care hospital. Indian J. Med. Microbiol., 2017, vol. 35, no. 2, pp. 296–298. doi: 10.4103/ijmm.IJMM_15_133
  28. Nikolopoulou G.B., Tzoutzas I., Tsakris A., Maltezou H.C. Hepatitis B in healthcare personnel: an update on the global landscape. Viruses, 2023, vol. 15, no. 12: 2454. doi: 10.3390/v15122454
  29. Scully C., Greenspan J.S. Human immunodeficiency virus (HIV) transmission in dentistry. J. Dent. Res., 2006, vol. 85, no. 9, pp. 794–800. doi: 10.1177/154405910608500903
  30. Sukegawa S., Sukegawa Y., Hasegawa K., Ono S., Nakamura T., Fujimura A., Fujisawa A., Nakano K., Takabatake K., Kawai H., Mukainaka Y., Nagatsuka H., Furuki Y. The effectiveness of pre-operative screening tests in determining viral infections in patients undergoing oral and maxillofacial surgery. Healthcare (Basel), 2022, vol. 10, no. 7: 1348. doi: 10.3390/healthcare10071348
  31. Tanaka E., Alter H.J., Nakatsuji Y., Shih J.W., Kim J.P., Matsumoto A., Kobayashi M., Kiyosawa K. Effect of hepatitis G virus infection on chronic hepatitis C. Ann. Intern. Med., 1996, vol. 125, no. 9, pp. 740–743. doi: 10.7326/0003-4819-125-9-199611010-00007
  32. Tarantola A., Abiteboul D., Rachline A. Infection risks following accidental exposure to blood or body fluids in health care workers: a review of pathogens transmitted in published cases. Am. J. Infect. Control, 2006, vol. 34, no. 6, pp. 367–375. doi: 10.1016/j.ajic.2004.11.011
  33. Tatar M., Keeshin S.W., Mailliard M., Wilson F.A. Cost-effectiveness of universal and targeted hepatitis C virus screening in the United States. JAMA Netw Open, 2020, vol. 3, no. 9: e2015756. doi: 10.1001/jamanetworkopen.2020.15756

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2025 Hanna H.W., Shahin R., Samy L.

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ПИ № ФС 77 - 64788 от 02.02.2016.


This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies