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Review

Factors Correlating to the Development of Hepatitis C Virus Infection in Hemodialysis Patients—Findings Mainly from Asiatic Populations: A Systematic Review and Meta-Analysis

by
Gaofeng Cai
1,
Hongjie Zheng
2,
Lan Luo
2,
Zhengting Wang
1,
Zhenggang Jiang
1,
Shuangfei Xu
1,
Huakun Lv
1,3,
Yongdi Chen
1,*,†,
Biao Zhou
1,† and
Chonggao Hu
1,†
1
Zhejiang Provincial Center for Disease Control and Prevention, 3399 Binsheng Road, Hangzhou 310051, China
2
College of Medical and Technology, Zhejiang Chinese Medical University, Hangzhou 310051, China
3
Zhejiang provincial key laboratory of infectious disease vaccine and prevention and control, 3399 Binsheng Road, Hangzhou 310051, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to the work.
Int. J. Environ. Res. Public Health 2019, 16(8), 1453; https://doi.org/10.3390/ijerph16081453
Submission received: 19 March 2019 / Revised: 17 April 2019 / Accepted: 18 April 2019 / Published: 24 April 2019
(This article belongs to the Section Infectious Disease Epidemiology)
Browse Figures
Review Reports Versions Notes

Abstract

:
Hemodialysis is an effective replacement therapy for chronic renal failure patients. In recent decades, the number of hemodialysis patients has grown rapidly and some measures for preventing blood-borne diseases have been implemented, but hepatitis C virus (HCV) infection remains a significant problem. The meta-analysis published in 2009 on HCV infection-related factors was based on localized study objects, and some additional studies have been published since 2009; however, the contribution of these factors remains under dispute. Our study pooled the odds ratios (ORs) or mean standard deviations (MDs) with 95% confidence intervals (CIs) and analyzed sensitivity using Review Manager 5.1 software (5.1 version Copenhagen: The Nordic Cochrane Centre; 2011) by searching data in the PubMed, Elsevier, Springer, Wiley, and EBSCO databases. Spearman correlation analysis was performed using the SPSS package. In our meta-analysis, 1715 HCV-infected hemodialysis patients and 7093 non-HCV-infected hemodialysis patients from 44 studies were analyzed. The pooled ORs with 95% CIs were: histories of blood transfusion, 4.30 (3.11, 5.96); weekly hemodialysis times > 2, 6.00 (3.25, 11.06); kidney transplantation, 5.80 (3.95, 8.52); hemodialysis units > 2, 6.90 (2.42, 19.68); shared hemodialysis devices, 5.00 (2.35, 10.65); and drug addiction, 4.73 (1.54, 14.47). The pooled MDs with 95% CIs were duration of hemodialysis (months) 27.48 (21.67, 33.30). There was a positive correlation between duration of hemodialysis and the HCV infection rate (p < 0.01). Hemodialysis patients, especially from Asia, with shared hemodialysis devices, hemodialysis units > 2, blood transfusion, kidney transplantation, and drug addiction were at increased risk of HCV infection. The HCV infection rate increased with the duration of hemodialysis. High-risk hemodialysis patients should be monitored and receive timely screening.

1. Introduction

Hemodialysis is an effective replacement therapy for chronic renal failure patients that can increase survival times [1]. In recent decades, the number of patients administered hemodialysis has grown rapidly. In 2012, a study showed that an estimated 2.1 million patients needed hemodialysis therapy and that this number would increase by 7% annually on a global scale [2].
Hemodialysis patients are at high risk of blood-borne diseases, especially infectious hepatitis C virus (HCV) and hepatitis B virus (HBV) [3,4,5]. The infection rate of HBV and HCV in hemodialysis patients is dramatically different in different regions of the world; for example, the infection rate in the UK was reported to be 1%, compared with more than 90% in Eastern Europe [6]. In China, a multi-center study by Zhuang (2000) showed that the HCV infection rate was 16.3%–32.1% among hemodialysis patients [7], and another multi-center meta-analysis by Sun et al. (2009) showed a median rate of HCV infection of 41.10% for Chinese hemodialysis patients [8].
However, the rate and number of HBV infections have declined greatly since the World Health Organization recommended that HBV vaccination be included in national immunization programs in 1992, and subsequently mass vaccination for hepatitis B has been implemented on a population-wide scale [9,10,11,12].
By contrast, an effective vaccine is lacking for HCV, and hemodialysis patients who require regular invasive treatment and are at high risk of HCV infection [13]. A study by Abdulkarim et al. showed that the main cause of liver disease among hemodialysis patients was HCV infection [14]. In a large-scale clinical study by Tanaka et al., HCV-infected hemodialysis patients had a higher mortality rate compared with hemodialysis patients without HCV infection [15]. Furthermore, a study by Alter et al. showed that HCV-infected hemodialysis patients had a lower quality of life [16] and another study by Za et al. reported that the HCV-infected population had a higher incidence of liver fibrosis and liver cancer [17].
Over the past 10 years, most countries have published standard operating procedures for blood purification including measures such as using a dialyzer only once [18], dialyzing HCV-infected patients in a designated area [19,20], as well as introducing more stringent disinfection procedures and improving screening methods for donors [21].
However, although the rate of HCV infection among patients has declined, HCV infection among hemodialysis patients remains a significant problem [4,20,22].
Previous studies have shown that many factors influence the development of HCV infection, such as blood transfusion, duration on hemodialysis, weekly hemodialysis times, and a history of kidney transplantation [23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40]. In 2009, Sun et al. performed meta-analyses on Chinese hemodialysis patients, along with a limited subgroup analysis [8]. Some additional studies on risk factors of HCV infection in hemodialysis patients have also been published since 2009 [41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63]. However, the contribution of each of these factors is under dispute.
In this study, we used hemodialysis patients as research objects and extended the analysis of risk factors for HCV infection by performing a meta-analysis.

2. Materials and Methods

2.1. Literature Search Strategy

Searches were performed for each of the specified databases on the Bo Ku data service platform. We used the search terms “Hepatitis C”, “HCV”, and “Hemodialysis” in the search field “Title/Abstract”, and the electronic databases searched included the following six international databases: PubMed, Elsevier, Springer, Wiley, OVID, and EBSCO. We also used the search terms “Hepatitis C”, “HCV”, and “Hemodialysis” in the search field “Abstract” and searched two Chinese electronic databases: Chinese Medical Journal Database and Chinese National Knowledge Infrastructure. The searches were completed in the first week of September, 2018. We also searched the references listed at the end of the included articles.

2.2. Inclusion and Exclusion Criteria

In this study, the eligibility criteria for the inclusion of literature in the meta-analysis were as follows: (1) the literature is the original research; (2) the literature was an observational study with specific temporal and geographic characteristics; (3) the literature was published with the full text available; (4) all cases and controls were hemodialysis patents and the source of samples was clearly stated; (5) hepatitis C was diagnosed according to the national diagnostic criteria that existed at that time [64] and possible risk factors were reported; and (6) the literature was published in Chinese or English.
Literature was excluded from the meta-analysis when (1) the data reported could not be used to calculate the odds ratio (OR) or mean standard deviation (MD) with 95% confidence interval (CI) for the main variable; (2) the literature duplicated the same research; (3) the literature used the same research objects; and (4) the literature was deemed to be of poor quality literature (based on Ebrahim et al.’s declaration, the number of items satisfied in the corresponding research type declaration was less than half of total items) [65,66].

2.3. Data Extraction

We used a pre-made form for data extraction, and then two trained reviewers assessed the literature one by one and completed the form. The following data were extracted from the qualified studies: first author, year of the study, location, the number of hemodialysis patients in the HCV-infected group and the non-HCV-infected group, sample size, male to female ratio, and age distribution for HCV infection development among hemodialysis patents.
Discrepancies between the assessment results obtained by the two reviewers were resolved by discussion and checking the original documents.

2.4. Sensitivity Analysis

The studies with the widest 95% CI for the OR or MD were omitted from the subgroup analysis for this factor, and the remaining studies were pooled and pooled MDCI or pooled ORCI values with 95% CIs were obtained for this study factor, and then this pooled MDCI or pooled ORCI was compared with the total pooled OR or pooled MD before omitting this study factor. The studies with the maximum weight were omitted from the subgroup analysis, and then pooled, and the pooled MDweight or ORweight values with 95% CI for this study factor were obtained and then this pooled MDweight or pooled ORweight was compared with the total pooled MD or pooled OR before omitting this study factor.
In this meta-analysis, subgroup analyses were used to determine the associations between different study factors and HCV infection, a sensitivity analysis was used to examine the reliability of the associations, and a funnel plot was used to examine publication bias. According to the manufacturer’s instructions, the normal ranges of values for serum alanine aminotransferase (ALT) are about 5–40 units per liter of serum. Based on the standard procedure reported in the instructions, HCV infection was confirmed when a serum sample tested positive for HCV antibodies.

2.5. Statistical Analysis

The OR or MD with 95% CI were taken as the main indicators in this meta-analysis. Review Manager 5.1 software (5.1 version Copenhagen: The Nordic Cochrane Centre; 2011) was used to analyze the fixed-effect model without heterogeneity or the random-effect model with heterogeneity, after the heterogeneity test. The heterogeneity among different studies for study factors was evaluated by Cochran’s chi-square test with a significance level α = 0.1 and I2 statistics. The OR or MD was not pooled when its number for the study factor was less than 4. In the meta-analysis, I2 statistics, ranging from 0% to 100%, were used to assess the levels of heterogeneity; values of 0%, 25%, 50%, 75%, and 100% were taken as no, low, medium, high, and significant heterogeneity, respectively [67]. In this meta-analysis, I2 ≤ 50% was accepted. Correlation analysis was performed using SPSS version 16 software (SPSS Inc., Chicago, IL, USA). Spearman correlation was used for ranked data, with α = 0.05 considered to indicate statistical significance.

3. Results

3.1. Literature Search

In this meta-analysis, a total of 44 research articles were included, and a flow chart of the literature selection process is shown in Figure 1.
Of the literature selected, 44 studies included 1715 HCV-infected hemodialysis patients and 7093 non-HCV-infected hemodialysis patients. The study characteristics, region, study type, number of HCV-infected hemodialysis patients and non-HCV-infected hemodialysis patients, study factors, sample size, male/female ratio, and mean participant age (years) are shown in Table 1.
The 11 study factors used to pool OR or MD with 95% CI were as follows: gender (15 studies, 867 cases, 3874 controls), age (16 studies, 953 cases, 4770 controls); a history of blood transfusion (28 studies, 820 cases, 3663 controls); weekly hemodialysis times > 2 (5 studies, 103 cases, 344 controls); a history of kidney transplantation (8 studies, 234 cases, 1507 controls); hemodialysis units > 2 (6 studies, 127 cases, 389 controls); shared hemodialysis devices (6 studies, 275 cases, 1358 controls); serum alanine aminotransferase (ALT) levels (abnormal) (6 studies, 280 cases, 1344 controls); drug addiction (4 studies, 86 cases, 639 controls); a history of surgery (7 studies, 161 cases, 1123 controls); and duration of hemodialysis (months) (28 studies, 940 cases, 4044 controls).

3.2. Results of Pooled ORs or MDs

In this meta-analysis, the pooled ORs and their 95% CIs for study factors were as follows: histories of blood transfusion, 4.30 (3.11, 5.96); weekly hemodialysis times > 2, 6.00 (3.25, 11.06); a history of kidney transplantation, 5.80 (3.95, 8.52); hemodialysis units > 2, 6.90 (2.42, 19.68); shared hemodialysis devices, 5.00 (2.35, 10.65); serum ALT levels (abnormal), 5.62 (2.35, 13.40); drug addiction, 4.73 (1.54, 14.47); a history of surgery, 1.98 (1.37, 2.85); and gender (male), 0.98 (0.83, 1.15).
In this meta-analysis, the pooled MDs and their 95% CIs for study factors were as follows: duration of hemodialysis (months), 27.48 (21.67, 33.30); and age (years), −0.3 (−2.29, 1.69).
The pooled ORs with their 95% CIs for study factors including histories of blood transfusion, weekly hemodialysis times > 2, kidney transplantation, serum ALT levels (abnormal), drug addiction, a history of surgery, hemodialysis units > 2, and shared hemodialysis devices are detailed in Figure 2, Figure 3, Figure 4 and Figure 5.

3.3. Results of Rank Correlation Analysis

In terms of the duration of hemodialysis, groups of patients that underwent hemodialysis for 1–2 years, 2–3 years, 3–5 years, 5–10 years, and >10 years had HCV infection rates of 8.57%, 17.99%, 23.68%, 56.76%, and 60.47%, respectively, and pooled ORs with 95% CIs of 0.09 (0.06, 0.13), 0.57 (0.34, 0.97), 1.50 (0.86, 2.61), 6.07 (4.45, 8.28), and 5.76 (2.89, 11.46), respectively. There was a positive correlation between the duration of hemodialysis and the HCV infection rate (rspearman = 0.990, p < 0.01) and between the duration of hemodialysis and the pooled OR (rspearman = 0.900, p = 0.037).

3.4. Results of Heterogeneity Evaluation

A heterogeneity test for pooled ORs with 95% CIs showed that variations among ORs for study factors including histories of blood transfusion, hemodialysis units > 2, shared hemodialysis devices, and serum ALT levels were statistically significant (p < 0.10). The effects of these factors were then pooled using the random-effect model, whereas weekly hemodialysis times, kidney transplantation, drug addiction, a history of surgery, and gender were pooled using the fixed-effect model (p > 0.10). A heterogeneity test for pooled MDs with 95% CIs showed that the variation among studies for the duration of hemodialysis (months) was statistically significant (p < 0.10). The effects were then pooled using the random-effect model. These results are detailed in Figure 2, Figure 3, Figure 4 and Figure 5.

3.5. Publication Bias

In the meta-analysis, a funnel plot of the articles including the duration of hemodialysis was symmetrical, with the axis of symmetry (MD = 0) being to the right of center, as detailed in Figure 6.

3.6. Sensitivity Analysis

In view of the reliability of the pooled ORs or MDs using the random-effect model for terms including histories of blood transfusion, shared hemodialysis devices, hemodialysis units > 2, serum ALT levels, and duration of hemodialysis (months), we omitted studies with the widest 95% CIs for the ORs and MD values, respectively, and pooled and acquired ORCI and MDCI values with the 95% CIs, and these pooled values were close to the respective pooled OR and MD values with 95% CIs, as detailed in Table 2.
In view of the reliability of pooled ORs using the random-effect model for terms including histories of blood transfusion, shared hemodialysis devices, hemodialysis units > 2, serum ALT levels, and duration of hemodialysis (months), we omitted studies with the highest weights, and pooled and acquired ORweight or MDweight values with 95% CIs, and these pooled values were close to the respective pooled OR or MD values with 95% CIs, as detailed in Table 2.

4. Discussion

This study showed that, for hemodialysis patients, the rate of HCV infection increased with the duration of hemodialysis treatment. This meta-analysis also found that hemodialysis patients with a duration of hemodialysis treatment >5 years and/or histories of blood transfusion and/or shared hemodialysis devices and/or hemodialysis units >2 and/or weekly hemodialysis times >2 and/or kidney transplantation and/or histories of surgery and/or drug addiction were at increased risk of developing HCV infection, whereas the age and gender of hemodialysis patients did not affect the risk of developing HCV infection.
Our study analyzed the rate of HCV infection among groups of patients with a duration of hemodialysis treatment of 1–2 years, 2–3 years, 3–5 years, 5–10 years, and >10 years, and the study found that the longer the duration of hemodialysis treatment, the higher the rate of HCV infection; this result was consistent with the results reported in the meta-analysis by Sun et al. in 2009 [8].
More specifically, our study showed that patients with a duration of hemodialysis treatment >5 years were at increased risk of developing HCV infection, whereas patients with a duration of hemodialysis treatment <5 years did not have an increased risk of developing HCV infection. This result was not consistent with the findings of the 2009 meta-analysis, which reported that patients with a duration of hemodialysis treatment >1 year were at increased risk of developing HCV infection [8]. These differences may reflect the implementation of effective management measures imposed by relevant healthcare organizations in recent years.
In our meta-analysis, the result of a quantitative analysis (Figure 4) also showed that the duration of hemodialysis for HCV-infected patients was 27.48 months longer than the duration of hemodialysis for non-HCV-infected patients. This finding was longer than the 15.41 months reported in the 2009 meta-analysis by Sun et al. [8], and this difference may also reflect the implementation of the above-mentioned effective management measures in recent years. Moreover, this result of the quantitative analysis was also consistent with those of qualitative analysis in this study (i.e., patients with a duration of hemodialysis treatment >5 years did show an increased risk of developing HCV infection, whereas patients with a duration of hemodialysis treatment < 5 years were not at higher risk).
In general, exposure to HCV-contaminated medical equipment or goods can increase the risk of HCV infection, and during the process of hemodialysis, patients have many possible opportunities for exposure to HCV-contaminated equipment or goods [68,69].
The findings of this meta-analysis showed that hemodialysis patients with a history of shared hemodialysis devices and/or hemodialysis units >2 and/or weekly hemodialysis times >2 and/or a duration of hemodialysis >5 years were at increased risk of HCV infection, and this may be related to the fact that these hemodialysis patients had more opportunities to be exposed to HCV- contaminated medical equipment, HCV-contaminated goods, or the HCV-contaminated hands of medical personnel, potentially leading to nosocomial infection.
A study by Alfurayh et al. confirmed the existence of nosocomial transmission in hemodialysis centers by sequence analysis [70]. Moreover, the findings of this meta-analysis showed that hemodialysis patients with a history of drug addiction were at increased risk of HCV infection and this may be related to the fact that these hemodialysis patients had shared HCV-contaminated needles and syringes, leading to cross infection. From what has been discussed above, we suggest that disposable goods, such as disposable dialysis dialyzers, disposable dialysis pipes, and so on, should be used to cut off cross infection during hemodialysis.
The findings of this meta-analysis also showed that kidney transplantation hemodialysis patients were at increased risk of HCV infection, and this may be related to the fact that these hemodialysis patients had taken immunosuppressants, which may have resulted in low lymphocyte activation following HCV infection [71]. Moreover, the findings of this meta-analysis also showed that hemodialysis patients with abnormal serum ALT levels were at increased risk of HCV infection, and this may be related to the chronological order of the development of abnormal elevated serum ALT levels, which could not be identified in the observational studies included, or the fact that these hemodialysis patients had disrupted normal liver structure and function, which may have resulted in low lymphocyte activation following HCV infection.
In general, ELISA was the routine method for screening blood donors for HCV infection, but molecular-based tests such as PCR are more sensitive diagnostic assays, and thus it is possible that some blood donors screened by traditional ELISA methods may have been HCV infectors [72,73,74]. This may explain our finding that hemodialysis patients with histories of blood transfusion were at higher risk of developing HCV infection. Thus, we suggest that blood donors and hemodialysis patient populations should be tested regularly with more sensitive PCR diagnostic assays.
Our meta-analysis also found that the age and gender of hemodialysis patients did not affect the risk of developing HCV infection, and this result was consistent with the findings of the 2009 meta-analysis [8].
The sensitivity analysis performed as part of our meta-analysis found that, after omitting studies with the widest 95% CIs for OR or MD values and studies with the maximum weight in subgroup analyses for the duration of hemodialysis treatment (months), histories of blood transfusion, shared hemodialysis devices, hemodialysis units >2, and abnormal serum ALT levels, the two overall effects were not reversed and the pooled OR or MD values were similar to those observed before omitting the studies. This revealed that the pooled ORs or MDs for these study factors were reliable and stable.
The limitations of this study were that only articles published in English or Chinese were included in the meta-analysis. In addition, even though the ORs or MDs of the six factors were pooled using a random-effect method, study heterogeneity may have influenced the findings to some extent. Furthermore, some study factors, for example, the degree of deterioration and the socioeconomic status of patients, were not available to be pooled. Lastly, studies included were carried out in the following countries: Iran, Australia, Egypt, and China, and this aspect limits the generalizability of conclusions.

5. Conclusions

It can be concluded that, for hemodialysis patients, the rate of HCV infection increases with the duration of hemodialysis treatment, and that hemodialysis patients, especially from Asia, with histories of blood transfusion and/or weekly hemodialysis times >2 and/or shared hemodialysis devices and/or hemodialysis units >2 and/or kidney transplantation and/or drug addiction were at increased risk of developing HCV infection. High-risk hemodialysis patients should be closely monitored and receive timely screening and therapeutic intervention to reduce the risk of HCV nosocomial infection.

Author Contributions

Study design: G.C., Y.C., B.Z., C.H.; Statistical analysis and interpretation: H.L., Y.C.; Manuscript preparation: G.C., H.L., Z.J., S.X., B.Z., Z.J., L.L., Z.W.; Critical review of manuscript: B.Z., Y.C., C.H. All authors read and approved the final manuscript.

Conflicts of Interest

The authors declare that they have no conflict of interests.

List of Abbreviations

The following abbreviations are used in this manuscript:
HBVhepatitis B virus
HCVhepatitis C virus
CIconfidence interval
MDmean difference
ORodds ratio
ALTalanine aminotransferase

References

  1. Fleming, G.M. Renal replacement review: Past, present and future. Organogenesis 2011, 7, 2–12. [Google Scholar] [CrossRef] [PubMed]
  2. Fresenius Medical Care. ESRD Patients in 2012: A Global Perspective; Fresenius Medical Care AG & Co. KGaA, Hof a.d. Saale: Bad Homburg, Germany, 2012. [Google Scholar]
  3. Santos, M.G.; Danguilan, R.A.; Que, E.T.; Balmaceda, R.P.; Padilla, B.S. Prevalence of hepatitis B and hepatitis C in hemodialysis patients. Nephrology 1998, 4, 101–104. [Google Scholar] [CrossRef]
  4. Zahedi, M.J.; Moghaddam, S.D.; Alavian, S.M.; Dalili, M. Seroprevalence of Hepatitis Viruses B, C, D and HIV Infection Among Hemodialysis Patients in Kerman Province, SouthEast Iran. Hepat. Mon. 2012, 12, 339. [Google Scholar] [CrossRef] [PubMed]
  5. Al-Jamal, M.; Al-Qudah, A.; Al-Shishi, K.F.; Al-Sarayreh, A.; Al-Quraan, L. Hepatitis C virus (HCV) infection in hemodialysis patients in the south of Jordan. Saudi J. Kidney Dis. Transpl. 2009, 20, 488. [Google Scholar] [PubMed]
  6. Hinrichsen, H.; Leimenstoll, G.; Stegen, G.; Schrader, H.; Fölsch, U.R.; Schmidt, W.E. Prevalence and risk factors of hepatitis C virus infection in haemodialysis patients: A multicentre study in 2796 patients. Gut 2002, 52, 429–433. [Google Scholar] [CrossRef]
  7. Zhuang, H. Current situation and objective of hepatitis b prevention and treatment in China. Chin. J. Pract. Med. 2008, 47, 793–795. [Google Scholar]
  8. Sun, J.; Yu, R.; Zhu, B.; Wu, J.; Larsen, S.; Zhao, W. Hepatitis C infection and related factors in hemodialysis patients in China: Systematic review and meta-analysis. Ren. Fail 2009, 31, 610–620. [Google Scholar] [CrossRef] [PubMed]
  9. World Health Organization, Expanded Programme on Immunization, Global Advisory Group. Meeting (14th: 1991: Antalya, Turkey) & WHO Expanded Programme on Immunization. (1992). Expanded Programme on Immunization: Report of the 14th Global Advisory Group, 14–18 October 1991, Antalya, Turkey. Available online: http://apps.who.int/iris/handle/10665/61561 (accessed on 16 May 2018).
  10. Zanetti, A.R.; Mariano, A.; Romanò, L.; D’Amelio, R.; Chironna, M.; Coppola, R.C.; Cuccia, M.; Mangione, R.; Marrone, F.; Negrone, F.S.; et al. Long-term immunogenicity of hepatitis B vaccination and policy for booster: An Italian multicentre study. Lancet 2005, 366, 1379–1384. [Google Scholar] [CrossRef]
  11. Liang, X.; Bi, S.; Yang, W.; Wang, L.; Cui, G.; Cui, F.; Zhang, Y.; Liu, J.; Gong, X.; Chen, Y.; et al. Epidemiological serosurvey of hepatitis B in China declining HBV prevalence due to hepatitis B vaccination. Vaccine 2009, 27, 6550–6557. [Google Scholar] [CrossRef] [PubMed]
  12. Liang, X.; Bi, S.; Yang, W.; Wang, L.; Cui, G.; Cui, F.; Zhang, Y.; Liu, J.; Gong, X.; Chen, Y.; et al. Evaluation of the impact of hepatitis B vaccination among children born during 1992–2005 in China. J. Infect. Dis. 2009, 200, 39–47. [Google Scholar] [CrossRef]
  13. Kumagai, J.; Komiya, Y.; Tanaka, J.; Katayama, K.; Tatsukawa, Y.; Yorioka, N.; Miyakawa, Y.; Yoshizawa, H. Hepatitis C virus infection in 2744 hemodialysis patients followed regularly at nine centers in Hiroshima during November 1999 through February 2003. J. Med. Virol. 2005, 76, 498–502. [Google Scholar] [CrossRef]
  14. Abdulkarim, A.S.; Zein, N.N.; Germer, J.J.; Kolbert, C.P.; Kabbani, L.O.; Krajnik, K.L.; Hola, A.L.; Agha, M.N.; Tourogman, M.O.; Persing, D.H. Hepatitis C virus genotypes and hepatitis G virus in hemodialysis patients from Syria: Identification of two novel hepatitis C virus subtypes. Am. J. Trop. Med. Hyg. 1998, 59, 571–576. [Google Scholar] [CrossRef]
  15. Tanaka, J.; Katayama, K.; Matsuo, J.; Akita, T.; Asao, T.; Ohisa, M.; Tsuchiya, S.; Yorioka, N. The Association of Hepatitis C Virus Infection with the Prognosis of Chronic Hemodialysis Patients: A Retrospective Study of 3064 Patients Between 1999 and 2010. J. Med. Virol. 2015, 87, 1558–1564. [Google Scholar] [CrossRef]
  16. Alter, M.J.; Favero, M.S.; Maynard, J.E. Impact of infection control strategics on the incidence of dialysis associated hepatitis in the United States. J. Infect. Dis. 1998, 153, 1149–1151. [Google Scholar] [CrossRef]
  17. Improving Global Outcomes (KDIGO) Transplant Work Group. KDIGO Clinical practice guideline for the care of kidney transplant recipients. Am. J. Transpl. 2009, 9, 155–158. [Google Scholar]
  18. Wang, N.S.; Zhu, Y.G.; Zhou, S.S.; Tang, L.Q.; Liao, L.T. Logisic Analysis of Risk Factors of Hepatitis C Virus in Patients with Maintenance Hemodialysis. Chin. J. Hosp. Infect. 2002, 12, 169–171. [Google Scholar]
  19. Zhang, Y.Z.; Shang, Y.Q.; Su, W.; Zhao, X.Y. Clinical analysis of HCV infection in hemodialysis patients. Jilin Med. 2012, 33, 476–479. [Google Scholar]
  20. Chen, X.J.; He, Y.C.; Wan, Q.J. The risk factors of hepatitis C virus infection in maintenance hemodialysis patients. Chin. J. Blood Purif. 2013, 12, 617–4620. [Google Scholar]
  21. Edey, M.; Barraclough, K.; Johnson, D.W. Review article: Hepatitis B and dialysis. Nephrology 2010, 15, 9. [Google Scholar] [CrossRef] [PubMed]
  22. Kheirabad, A.K.; Kargar, F.B.; Ghasemzadeh, I. Hepatitis C and G Virus Infection Prevalence Among Hemodialysis Patients and Associated Risk Factors in the Hormozgan Province of Southern Iran. Hepat. Mon. 2016, 16, e40375. [Google Scholar] [CrossRef]
  23. Zhang, X.L.; Fu, W.L. Evaluation of the prevalence HCV infection in hemodialysis patients and its infective risk factors. Chin. J. Nosocomiol. 1999, 9, 77–79. [Google Scholar]
  24. Cao, Y.L.; Wang, S.X.; Guo, P.; Liu, H. Hepatitis C virus infection in maintenance hemodialysis patients. Chin. J. Blood Purif. 2006, 5, 430–432. [Google Scholar]
  25. Chen, L.; Xuewang, L.I.; Peng, L. Hepatitis B and C virus infection in uremia patients on chronic hemodialysis. Chin. J. Pract. Med. 2002, 22, 407–409. [Google Scholar]
  26. Liu, G.; Fu, B.Y.; Wei, J.R.; Sun, B.; Zhang, Q.S. Study on HCV infection in hemodialysis patients. Chin. J. Metall. Ind. Med. 1996, 13, 77–79. [Google Scholar]
  27. Liu, H.L.; Li, G.G.; Duan, X.F.; Cai, Q. Clinical Characteristics of hepatitis B and C viral infection in hemodialysis patients. Chin. J. Intern. Med. 1998, 37, 758–4761. [Google Scholar]
  28. Liu, J.M. Clinical study on 120 patients with maintenance hemodialysis complicated with viral hepatitis. J. Nongken Med. 2005, 27, 194–196. [Google Scholar]
  29. Wang, L.; Hu, C.Y.; Li, X.Y. Clinical investigation of the maintenance hemodialysis patients complicated with viral hepatitis. Chin. J. Blood Purif. 2003, 2, 24–26. [Google Scholar]
  30. Wang, Z.H.; Chen, N.; Zhu, P.; Qing, Y.; Shen, P.Y.; Wang, G.Y. Prevalence of hepatitis B and C viral infection in uremia patients treated by chronic hemodialysis. J. Diagn. Concepts Pr. 2004, 3, 9–11. [Google Scholar]
  31. Xiao, G.Q.; Ji, D.X.; Chen, C.H.; Huan, H.D.; Xie, H.L.; Liu, Y.; Liu, Z.H.; Li, L.S. Study on HCV infection in hemodialysis patients and dialysis center staff. J. Nephrol. Dialy Transpl. 1997, 6, 525–530. [Google Scholar]
  32. Zhao, H.; Chang, M.; Xing, S.Q. Analysis of hepatitis virus infection in hemodialysis patients. Chin. J. Blood Purif. 2008, 7, 207–209. [Google Scholar]
  33. Lin, Y.Y.; Yu, Y.; Sun, S.Q.; Hong, J.P.; Chen, J. Analysis of hepatitis virus infection in hemodialysis patients. J. Clin. Nephrol. 2008, 8, 60–62. [Google Scholar]
  34. Qin, F.Q.; Li, P. A comprehensive analysis of 135 hemodialysis patients with viral hepatitis b and c infection. Chin. J. Blood Purif. 2003, 2, 267–268. [Google Scholar]
  35. Tong, Q.; Wu, B.B.; Zhang, L.M. Hepatitis virus infection in maintenance hemodialysis patients. Shanghai Med. 2006, 29, 838–840. [Google Scholar]
  36. Liu, G.L.; Xu, W.L.; Wei, J.F.; Wang, X.L. Investigation of HBV infection in hemodialysis patients. Prev. Med. Lit. Inf. 2001, 7, 1–3. [Google Scholar]
  37. Niu, A.N.; Yang, L.M. Analysis of infection status and related factors of HBV- HCV in hemodialysis patients. Shenzhen Med. 1999, 12, 17–18. [Google Scholar]
  38. Yin, L.F.; Huang, D.S. Observation of hepatitis virus infection in hemodialysis patients. Railw. Med. 1994, 22, 27–28. [Google Scholar]
  39. Xie, M.X.; Chen, Y.F. Comparison of positivity rates of anti-HCV in patients under dialysis. China Trop. Med. 2007, 7, 548–550. [Google Scholar]
  40. Li, Z.H.; Wu, Q.Z.; Wang, Z.H. Analysis of hepatitis B, C infection in maintenance hemodialysis patients. Int. Med. Health Guid. News 2007, 13, 37–38. [Google Scholar]
  41. Liu, J.C. Detection and analysis of hepatitis virus infection in hemodialysis patients. Chin. Folk Med. 2010, 16, 89–90. [Google Scholar]
  42. Liu, Q.; Yao, L.; Liu, X.D.; Liu, X.D.; Zhu, X.W.; Geng, Y.; Fen, M.L.; Wang, L.N. Analysis of viral hepatitis infection in hemodialysis patients. Chin. Blood Purif. 2012, 8, 417–420. [Google Scholar]
  43. Mao, W.J.; Li, X.Q.; Zhen, T.T. Investigation and analysis of HCV infection in hemodialysis patients. Chin. J. Hosp. Infect. 2013, 5, 1002–1003. [Google Scholar]
  44. Wang, H. Analysis of HCV infection related factors in maintenance hemodialysis patients in a primary hospital. Chin. J. Infect. Control 2012, 5, 376–378. [Google Scholar]
  45. Ling, L.; Wang, S.F.; Qian, Y.M. Analysis of HCV infection in hemodialysis patients and its influencing factors. Anhui Med. 2014, 8, 1045–1048. [Google Scholar]
  46. Wang, Q.; Pang, Y.S.; Li, L. Analysis of hepatitis c infection and influencing factors in 120 dialysis patients with type 2 diabetes mellitus and renal failure. Pract. Prev. Med. 2018, 1, 96–98. [Google Scholar]
  47. Wang, L.F.; Ma, L.B. Analysis of related factors of hemodialysis hepatitis b and hepatitis c infection and discussion of preventive measures. Pract. Prev. Med. 2014, 5, 598–599. [Google Scholar]
  48. Xu, X.Y.; Liu, F.J.Z. Clinical study of viral hepatitis in 150 patients with maintenance hemodialysis. Contemp. Med 2010, 20, 21–22. [Google Scholar]
  49. Yan, S.P.; Pan, H.Q.; Li, L.C.; Li, X.L.; Li, M.L.; Zhou, M. Risk factors of HCV infection in hemodialysis patients in a hospital in Changsha. Chin. J. Infect. Control 2012, 2, 112–114. [Google Scholar]
  50. Yang, M.; Wang, J.S.; Zhu, J.T.; Zhang, X.L.; Zhu, B. A multicenter clinical study of HCV infection in hemodialysis patients. J. Nanjing Med. Univ. 2012, 6, 852–854. [Google Scholar]
  51. Zeng, S.Y.; Xue, S.Q.; Lou, G.P. Risk factors and prevention of HCV nosocomial infection in hemodialysis patients. Chin. J. Integr. Nephrop. 2011, 4, 318–320. [Google Scholar]
  52. Zhang, W.C.; Li, H.; Yu, L.; Wang, S.X. Serological changes and risk factors of HCV infection in hemodialysis patients: Follow-up data for three years attached. Chin. J. Clin. 2013, 1, 125–127. [Google Scholar]
  53. Zhang, T.; Sun, X.F.; Chen, X.M.; Wang, Y.D. The occurrence and cause of hepatitis virus infection in hemodialysis patients. Chin. Blood Purif. 2010, 10, 577–579. [Google Scholar]
  54. Zhu, B.; Wang, Y.F.; Zhou, Y.F.; Bao, Z.Y.; Zhao, W.H. Clinical study on HCV infection in hemodialysis patients in changshu district. Chin. Blood Purif. 2015, 4, 213–215. [Google Scholar]
  55. Zhang, H.L. Analysis of the correlation between hemodialysis and hepatitis c virus infection in patients with type 2 diabetic renal failure. Med. Clin. Res. 2018, 35, 377–378. [Google Scholar]
  56. Chen, B.L.; Yao, P.; Tan, Q.L.; Zhang, H.; Yao, M.C. Analysis of related factors of hemodialysis hepatitis c virus infection in patients with type 2 diabetic renal failure. Chin. J. Hosp. Infect. 2015, 25, 171–173. [Google Scholar]
  57. Zhang, X.L.; Zhu, B.; Yu, R.B.; Zhao, W.H. A multicenter clinical study of HCV infection in hemodialysis patients. Chin. Blood Purif. 2011, 10, 429–432. [Google Scholar]
  58. Zhao, B.; Yang, W.; Ni, X.Y.; Zhang, L.G. Investigation of hepatitis c infection in hospital maintenance hemodialysis patients (2008–2009). J. Pract. Med. 2010, 27, 555–556. [Google Scholar]
  59. Duong, C.M.; Olszyna, D.P.; McLaws, M.L. Hepatitis B and C virus infections among patients with end stage renal disease in a low-resourced hemodialysis center in Vietnam: A cross-sectional study. BMC Public Health 2015, 15, 192–199. [Google Scholar] [CrossRef]
  60. Somi, M.H.; Etemadi, J.; Ghojazadeh, M.; Farhang, S.; Faramarzi, M.; Foroutan, S.; Soleimanpour, M. Risk factors of HCV seroconversion in hemodialysis patients in Tabriz, Iran. Hepat. Mon. 2014, 14, e17417. [Google Scholar] [CrossRef]
  61. Kalantari, H.; Ebadi, S.; Yaran, M.; Maracy, M.; Shahshahan, Z. Prevalence and risk factors of hepatitis B and C viruses among hemodialysis patients in Isfahan, Iran. Adv. Biomed. Res. 2014, 3, 73. [Google Scholar] [PubMed]
  62. Chang, J.M.; Huang, C.F.; Chen, S.C.; Dai, C.Y.; Yeh, M.L.; Huang, J.F.; Kuo, H.T.; Chuang, W.L.; Yu, M.L.; Hwang, S.J.; et al. Discrepancy between serological and virological analysis of viral hepatitis in hemodialysis patients. Int. J. Med. Sci. 2014, 11, 436. [Google Scholar] [CrossRef]
  63. Soliman, A.R.; MomtazAbdElaziz, M.; ElLawindi, M.I. Evaluation of an isolation program of hepatitis C virus infected hemodialysis patients in some hemodialysis centers in Egypt. Nephrology 2013, 2013, 395467. [Google Scholar] [CrossRef]
  64. National Health and Family Planning Commission of The People’s Republic of China. WS 213-018 Diagnosis for hepatitis C. J. Clin. Hepatol. 2018, 34, 3–5. [Google Scholar]
  65. Ebrahim, S.; Clarke, M. STROBE: New standards for reporting observational epidemiology, a chance to improve. Internat. J. Epidemiol. 2007, 36, 946–948. [Google Scholar] [CrossRef] [PubMed]
  66. Strobe Statement: Strengthening the Reporting of Observational Studies in Epidemiology [EB /OL]. Available online: http: //www.strobe-statement.org /index.php? id = strobe-translations (accessed on 1 May 2013).
  67. Ades, A.E.; Lu, G.; Higgins, J.P. The interpretation of random-effects meta-analysis in decision models. Med. Decis. Mak. 2005, 25, 646–654. [Google Scholar] [CrossRef]
  68. Schaefer, M.; Mauss, S. Hepatitis C treatment in patients with drug addiction: Clinical management of interferon-alpha-associated psychiatric side effects. Curr. Drug Abus. Rev. 2008, 1, 177–187. [Google Scholar] [CrossRef]
  69. Dolan, K.A.; Shearer, J.; White, B.; Zhou, J.; Kaldor, J.; Wodak, A.D. Four-year follow-up of imprisoned male heroin users and methadone treatment:mortality, re-incarceration and hepatitis C infection. Addiction 2005, 100, 820–828. [Google Scholar] [CrossRef] [PubMed]
  70. Alfurayh, O.; Sabeel, A.; Al Ahdal, M.N.; Almeshari, K.; Kessie, G.; Hamid, M.; Cruz, D.D. Hand contamination with hepatitis C virus in staff looking after hepatitis C-positive hemodialysis patients. Am. J. Nephrol. 2000, 20, 103–106. [Google Scholar] [CrossRef] [PubMed]
  71. Girndt, M.; Kohler, H.; Schiedhelm-Weick, E. T-cell activation defect in HD patients: Evidence for a role of tlle B7/CD28 pathway. Kidney Int. 1933, 44, 359–365. [Google Scholar] [CrossRef]
  72. Huraib, S.O. Hepatitis C in dialysis patients. Saudi J. Kidney Dis. Transpl. 2003, 14, 442–450. [Google Scholar]
  73. Zeldis, J.B.; Depner, T.A.; Kuramoto, I.K.; Gish, R.G.; Holland, P.V. The prevalence of hepatitis C virus antibodies among hemodialysis patients. Ann. Intern. Med. 1990, 112, 958–960. [Google Scholar] [CrossRef]
  74. Marinaki, S.; Boletis, J.N.; Sakellariou, S.; Delladetsima, I.K. Hepatitis C in hemodialysis patients. World J. Hepatol. 2015, 7, 548–558. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. A flow chart of the literature selection process [68].
Figure 1. A flow chart of the literature selection process [68].
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Figure 2. Effects of pooled odds ratios (ORs) for factors correlating to the development of hepatitis C virus infection in hemodialysis patients ((A) shared hemodialysis devices; (B) kidney transplantation; (C): serum alanine aminotransferase levels (abnormal)).
Figure 2. Effects of pooled odds ratios (ORs) for factors correlating to the development of hepatitis C virus infection in hemodialysis patients ((A) shared hemodialysis devices; (B) kidney transplantation; (C): serum alanine aminotransferase levels (abnormal)).
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Figure 3. Effects of pooled ORs for factors correlating to the development of hepatitis C virus infection in hemodialysis patients ((D) hemodialysis units > 2; (E) weekly hemodialysis times > 2; (F) a history of surgery; (G) drug addiction).
Figure 3. Effects of pooled ORs for factors correlating to the development of hepatitis C virus infection in hemodialysis patients ((D) hemodialysis units > 2; (E) weekly hemodialysis times > 2; (F) a history of surgery; (G) drug addiction).
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Figure 4. Effects of pooled mean standard deviations (MDs) for duration of hemodialysis (months) correlating to the development of hepatitis C virus infection in hemodialysis patients.
Figure 4. Effects of pooled mean standard deviations (MDs) for duration of hemodialysis (months) correlating to the development of hepatitis C virus infection in hemodialysis patients.
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Figure 5. Effects of pooled OR for histories of blood transfusion correlating to the development of hepatitis C virus infection in hemodialysis patients.
Figure 5. Effects of pooled OR for histories of blood transfusion correlating to the development of hepatitis C virus infection in hemodialysis patients.
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Figure 6. A funnel plot of the articles including the duration of hemodialysis.
Figure 6. A funnel plot of the articles including the duration of hemodialysis.
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Table
Table 1. Characteristics of the studies.
Table 1. Characteristics of the studies.
Reference NumberAuthor and Year of PublicationRegionsStudy TypeParticipants Category (Case/Control)Sample Size (Case/Control)Male/FemaleAge (Years) *
4Zahedi 2012Iran, Kermanobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients16/2224/1451 ± 9
20Chen 2013Guangdong, Shenzhenobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients19/164117/6647.14 ± 15.196
22Kargar 2016Iran, Hormozgan observational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients5/14492/5756.23 ± 12.35
23Zhang 1999China, Chongqingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients17/3130/1850.5 ± 13.5
59Duong 2015Australia, Sydneyobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients8/10559/5453 ± 16
60Somi 2014Iran, Tabriz observational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients37/418275/18055.98 ± 15.6
61Kalantari 2014Iran, Isfahan observational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients26/473303/19652.3 ± 12.8
62Chang 2014Taiwan, Kaohsiung observational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients290/1391824/85762.2 ± 12.9
63Soliman 2013Egypt, Cairoobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients28/5547/3652.29 ± 12.10;
49.47 ± 15.5
24Cao 2006China, Beijingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients10/7842/8852.33 ± 12.55;
57.45 ± 12.16
25Chen 2002China, Beijingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients28/7157/4258.1 ± 13.2;
57.7 ± 12.9 1)
26Liu 1996China, Shenyangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients17/2833/1223–62
27Liu 1998China, Beijingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients34/1521/2853.1 ± 11.2
28Liu 2005Xinjiang, Shiheobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients48/7280/4019–81
29Wang 2003Anhui, Benyangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients22/3140/1146.68 ± 10.18;
47.50 ± 13.44
30Wang 2004China, Shanahaiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients51/9757/9151 ± 14
31Xiao 1997Jiangsu, Nanjiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients121/33110/4446.0 ± 12.8
32Zhao 2008China, Dalinobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients124/583_60.25 ± 13.95;
63.51 ± 17.52
33Li 2008Fujian, Fuzhouobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients29/120101/4813–82
34Qin 2003China, Dalinobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients59/13577/11749.7 ± 16.4
35Tang 2006China, Shanahaiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients32/7859/5149.2 ± 14.3
36Liu 2001Shandong, Liaochengobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients20/2836/1217–76
37Niu 1999Guangdong, Shenzhenobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients12/3827/2348.5 + 12.8;
49.4 + 16.8
38Yin 1994Jiangsu, Nanjiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients14/1317/1021–69
39Xie 2007Haikou, Hainanobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients15/3936/1848.4
40Li 2007Guangdong, Zhanjiangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients8/7846/4049.3 (25–71)
41Liu 2010Jilin, Songyuanobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients16/3632/2048.7 ± 2.1
42Liu 2012Liaoning, Shenyangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients7/8942/5452.8 ± 15.4
43Mao 2013Zhejiang, Taizhouobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients4/9657/4350.8 (25–72)
44Wang 2012Hunan, Zhuzhouobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients22/3235/1951.88 ± 13.10
45Wang, S.F. 2014Anhui, Hefeiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients19/1301.33/152.6 ± 11.3
46Wang 2018China, Chongqingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients15/10569/5157.86 ± 7.85
47Wang, L.F. 2014Zhejiang, Qunanobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients59/409249/21921–78
48Xu 2010Guangdong, Zhanjiangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients64/8680/7017–84
49Yan 2012Hunan, Changshaobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients23/5147/2747.72 ± 18.93
50Yang 2012Jiangsu, Yangzhouobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients39/264194/10948.49 ± 11.45;
50.08 ± 12.95
51Zeng 2011Guangdong, Qingyuanobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients47/165116/9616–76
52Zhang 2013China, Beijingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients20/16497/8755.0 ± 15.6
53Zhang 2010China, Beijingobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients14/131__
54Zhu 2015Jiangsu, Changzhouobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients15/214134/9556.25 ± 13.38;
51.04 ± 13.20
55Zhang 2018Hebei, Shijiazhuangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients39/6074/2554.58 ± 11.88
56Chen 2015Hubei, Enshiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients31/4543/3353.21 ± 10.61
57Zhang 2011Jiangsu, Nanjiobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients176/620492/30453 ± 12;
52 ± 14
58Zhao 2010Shandong, Weifangobservational studyHCV-infected hemodialysis patients/non-HCV-infected hemodialysis patients15/3627/24l9–78
Note: HCV: hepatitis C virus; *: mean ± standard deviation; mean (minimum–maximum); minimum–maximum; mean.
Table
Table 2. The subgroup characteristics of study factors associated with HCV infection in hemodialysis patients after omitting the studies with maximum value of weight or widest interval of 95% CI for OR or MD values in subgroup analysis.
Table 2. The subgroup characteristics of study factors associated with HCV infection in hemodialysis patients after omitting the studies with maximum value of weight or widest interval of 95% CI for OR or MD values in subgroup analysis.
Subgroup Analyses by Study FactorsOR or MD(95% CI) before Reference OmittedOR or MD (95% CI) after Reference OmittedReversal of OR or MD (95% CI) after Reference Omitted Compared with that before Reference OmittedReference Omitted
The studies with wide interval of 95% CI for OR values
Histories of blood transfusion4.30 (3.11–5.96)5.13 (3.43–7.68)No42
Shared hemodialysis devices5.00 (2.35–10.65)4.10 (1.66–10.16)No50
Hemodialysis units > 26.90 (2.42–19.68)6.35 (2.01–20.08)No43
Serum alanine aminotransferase levels5.62 (2.35–13.40)4.17 (1.89–9.23)No50
The studies with wide interval of 95% CI for MD values
Duration of hemodialysis (months)28.96 (22.11–35.80)23.38 (18.17–28.59)No59
The studies with maximum value of weight (OR)
Histories of blood transfusion4.30 (3.11–5.96)4.45 (3.26–6.09)No57
Shared hemodialysis devices5.00 (2.35–10.65)3.97 (1.89–8.32)No57
Hemodialysis units > 26.90 (2.42–19.68)10.16 (4.95–20.85)No44
Serum alanine aminotransferase levels5.62 (2.35–13.40)5.06 (1.60–15.98)No57
The studies with maximum value of weight (MD)
Duration of hemodialysis (months)28.96 (22.11–35.80)26.36 (19.53–33.19)No61,47

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Cai, G.; Zheng, H.; Luo, L.; Wang, Z.; Jiang, Z.; Xu, S.; Lv, H.; Chen, Y.; Zhou, B.; Hu, C. Factors Correlating to the Development of Hepatitis C Virus Infection in Hemodialysis Patients—Findings Mainly from Asiatic Populations: A Systematic Review and Meta-Analysis. Int. J. Environ. Res. Public Health 2019, 16, 1453. https://doi.org/10.3390/ijerph16081453

AMA Style

Cai G, Zheng H, Luo L, Wang Z, Jiang Z, Xu S, Lv H, Chen Y, Zhou B, Hu C. Factors Correlating to the Development of Hepatitis C Virus Infection in Hemodialysis Patients—Findings Mainly from Asiatic Populations: A Systematic Review and Meta-Analysis. International Journal of Environmental Research and Public Health. 2019; 16(8):1453. https://doi.org/10.3390/ijerph16081453

Chicago/Turabian Style

Cai, Gaofeng, Hongjie Zheng, Lan Luo, Zhengting Wang, Zhenggang Jiang, Shuangfei Xu, Huakun Lv, Yongdi Chen, Biao Zhou, and Chonggao Hu. 2019. "Factors Correlating to the Development of Hepatitis C Virus Infection in Hemodialysis Patients—Findings Mainly from Asiatic Populations: A Systematic Review and Meta-Analysis" International Journal of Environmental Research and Public Health 16, no. 8: 1453. https://doi.org/10.3390/ijerph16081453

APA Style

Cai, G., Zheng, H., Luo, L., Wang, Z., Jiang, Z., Xu, S., Lv, H., Chen, Y., Zhou, B., & Hu, C. (2019). Factors Correlating to the Development of Hepatitis C Virus Infection in Hemodialysis Patients—Findings Mainly from Asiatic Populations: A Systematic Review and Meta-Analysis. International Journal of Environmental Research and Public Health, 16(8), 1453. https://doi.org/10.3390/ijerph16081453

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