|
RENAL DATA FROM THE ARAB WORLD |
|
|
|
Year : 2010 | Volume
: 21
| Issue : 3 | Page : 548-554 |
|
Prevention of hepatitis C virus in hemodialysis patients: Five years experience from a single center |
|
Waleed Z Mohamed
Nephrology Division, Medical Department, Dawmat Aljandal General Hospital, Aljouf, Saudi Arabia
Click here for correspondence address and email
Date of Web Publication | 26-Apr-2010 |
|
|
 |
|
Abstract | | |
Hepatitis C virus (HCV) has been a significant problem in hemodialysis (HD) patients. In general, it carries significant morbidity including liver cirrhosis, liver cell failure and hepatoma. The study was conducted on 36 seronegative HD patients. All patients were managed with strict application of infection control guidelines as well as isolation of HCV-positive patients. None of the patients received any blood transfusions and were managed with iron and erythropoietin. After five years of follow-up, we found that the incidence of HCV seroconversion was zero. Our study further suggests that following infection control guidelines, isolation of seropositive patients and minimizing blood transfusions can help in prevention of HCV transmission among HD patients.
How to cite this article: Mohamed WZ. Prevention of hepatitis C virus in hemodialysis patients: Five years experience from a single center. Saudi J Kidney Dis Transpl 2010;21:548-54 |
How to cite this URL: Mohamed WZ. Prevention of hepatitis C virus in hemodialysis patients: Five years experience from a single center. Saudi J Kidney Dis Transpl [serial online] 2010 [cited 2022 Aug 10];21:548-54. Available from: https://www.sjkdt.org/text.asp?2010/21/3/548/62724 |
Introduction | |  |
Hepatitis C virus (HCV) infection is a major public health problem, with an estimated global prevalence of 3% occurring in about 170 million persons worldwide. [1] Patients with renal disease are at an increased risk of acquiring HCV because of prolonged vascular access and the potential for exposure to infected patients and contaminated equipment. [2] An estimated 5-20% of HCV-infected patients have, or will develop cirrhosis, 1-4% of whom will annually develop hepatocellular carcinoma. [2]
Hepatitis C is the most common cause of liver disease in patients on HD, while liver disease itself is a significant cause of morbidity and mortality in patients with end-stage renal disease (ESRD) treated by dialysis or transplantation. [3]
We implemented and followed a protocol for prevention and control of HCV in our HD unit with follow-up for five years and are herewith reporting our findings.
Patients and Methods | |  |
In November 2003, an outbreak occurred in our unit during which, five HCV-negative patients out of 13 got seroconverted to HCVpositive status and investigations revealed that the outbreak was caused by a breach in application of standard infection control precautions in daily HD practice. Thus, from December 2003, we ensured that infection control guidelines are strictly followed in our HD unit, which catered to 16 patients at that time. During the period of five years, 36 patients who were HCVnegative underwent HD at our unit. Seropositive patients were dialyzed in a separate hall consisting of five machines and HD session was performed by two nurses for 3-4 hours, three times per week. Seronegative patients underwent dialysis in an adjacent hall that contained seven HD machines and were managed by four to five nurses. In general, the patient/ nurse ratio was 2:1. We established a training program for implementing infection control guidelines in dialysis units, with special concern to the standard precautions (hand washing/ alcohol-based hand rub, wearing personal protective equipment, proper waste and sharp disposal, environmental cleaning, disinfection of common equipment shared by patients and applying a protocol for use of multi-dose vials along with direct strict observation and reporting.
However, the construction of our HD unit is not ideal regarding the area and availability of hand washing facilities as recommended; it consists of two halls which are continuous with each other.
All patients were interviewed for risk factors to HCV infection including general risk factors like acupuncture, tattooing, illicit drug abuse, sexually transmitted diseases, any blood contact e.g. dental clinic, multiple partners and risk factors related to HD like minimizing blood transfusions, management of anemia using iron and erythropoietin, standard precautions and treatment in multiple units.
A standardized form was used to collect data on age, sex and blood transfusions between 2004 and 2008 (mandatory screening for antiHCV in blood banks). A protocol for any new patients or a visitor-patient to the unit was applied so that the patient had to be screened for HCV Ab, HBsAg and HIV Ab irrespective of his/her previous results, and to do proper disinfection of the area including machine as per infection control protocol and manufacture instructions.
A protocol for patients who traveled to another area for dialysis, regarding monthly screening for HCVAb, HBsAg and HIVAb, in addition to monthly regular evaluation of liver function tests, bilirubin (total and direct) and liver enzymes, was followed strictly. Additionally, we also started application of the K-DOQI guidelines in management of anemia by restricting blood transfusions which was restricted for only emergency use.
The HD machines (Fresenius AG, Homburg, Germany), were disinfected with chemical (Puristeril; 340, Fresenius AG, Homburg, Germany) after each session and, at the end of each day, with heat and chemical as per instructions of the manufacturers.
Seronegative patients were screened regularly for HCV-antibody at the Dawmat Aljandal General Hospital laboratory using ELISA technique second generation, every three months.
Standard descriptive statistical tests were performed as indicated using SPSS (Statistics Program for Social Sciences) version 16.0, SPSS Inc., Chicago, IL, USA
Results | |  |
During the period of five years, 36 patients who were HCV-negative [16 female (44.4%) and 21 male (55.6%)] with mean age of 56.36 ?21.38 years (range 16-89 years) underwent HD at our center. Of them, 11 (30.6%) patients expired, three (8.3%) underwent renal transplantation, one patient (2.8%) converted to CAPD and 21 patients (58.3%) continue to be on HD in December 2008.
We found that the incidence of HCV seroconversion during this period (1 st December 2004 - 31st December 2008) in these 36 patients was zero, while the prevalence showed a decline with each passing year; thus, it decreased from 50% in November 2003 to 23% in December 2008 [Figure 1].
The duration on dialysis of the study patients is shown in [Figure 2]. By the end of the study period, ten patients (27.8%) were on HD for less than one year, 12 (33.3%) were on HD for 1 - 3 years, 12 others (33.3%) for 3 - 5 years while two patients (5.6%) were on HD for more than five years. During their dialysis period, a mean of 5 ?2.97 transfusions were administered to the study patients [Figure 3].
Discussion | |  |
The prevalence of HCV infection varies greatly among patients on HD from different geographic regions. In a review of data published in 1999, Wreghitt [4] described a range from 4% in the UK to 71% in Kuwait for HCV prevalence among the HD population. Since 1999, the reported anti-HCV seropositivity has ranged from 1.9% in the Slovenian 2001 annual report, [5] to 84.6% in Saudi Arabia. [6]
HCV infection still remains a major problem among patients on maintenance HD. The immune suppression seen in this patient population, resulting in an absence of clinical and biochemical evidence of liver disease, is believed to accelerate further dissemination of the virus. [7] The importance of prevention of HCV infection and control is due to its well documented progression to hepatic cirrhosis, liver malignancies and liver failure. [8] HCV infection is considered to be of particular relevance in this group of patients and can result in disastrous sequelae after kidney transplantation due the immunosuppressive therapy used. [9]
This study showed that successful prevention and control of HCV transmission is multifactorial including un-modifiable factors like duration of the patients on dialysis and modifiable factors including:
- implementation of infection control guidelines including standard precautions,
- isolation if feasible and,
- minimizing blood transfusions.
Almost all recent surveys have congruently suggested the length of time on HD as a risk factor for HCV seropositivity. [10],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20],[21] A relatively large study in Brazil demonstrated that patients on HD for more than three years had a 13.6fold greater risk of HCV-positivity compared to subjects with less than one year HD treat?ment. [20]
Several recent studies [22],[23],[24],[25],[26] have reported nosocomial patient-to-patient transmission of HCV infection among HD patients. Some investigators have suggested that the decline in HCV prevalence among HD patients in recent years is mostly attributable to strict adherence to standard precautions. [27],[28],[29],[30],[31],[32],[33] Thus, lack of strict adherence to standard precautions by the staff and sharing of articles such as instruments or multi-dose drugs might be the main mode of nosocomial spread of HCV among HD patients. [34],[35],[36] In addition, Piazza et al showed that HCV RNA was resistant to drying at room temperature for at least 48 hours. [37] Also, recently Froio et al suggested the importance of environmental contamination of surfaces for HCV transmission. [38]
As a result, the CDC recommends that special precautions should be observed in dialysis units, including wearing and changing of gloves and water-proof gowns between patients, systematic decontamination of the equipment circuit and surfaces after each patient treatment, and no sharing of instruments (e.g., tourniquets, stethoscope, blood pressure cuff) or medications (e.g., multiuse vials of heparin) among patients. [39]
Although some studies found that nosocomial spread of HCV declined when HCV-infected patients were treated in dedicated HD units, [28],[30] other investigators could control nosocomial spread of HCV by strict application of hygienic precautions without isolation of HCV-infected subjects or machine segregation. [40],[41]
In this study, none of the transfused patients developed HCV seroconversion. Historically, the number of blood transfusions received has been consistently reported in the literature to be associated with an increased prevalence of HCV-positive dialysis patients. [4] However, several recent reports could not recognize blood transfusion as an independent risk factor in HCV spread among HD subjects. [15],[17],[18],[19],[23],[42],[43],[44],[45],[46],
Indeed, the wide use of erythropoietin from the late 1980s reduced the need for blood transfusions among HD patients. Furthermore, the introduction of nucleic acid amplification testing for the screening of blood donors has markedly reduced the risk of HCV transmission through blood product transfusion. The current risk of transfusion-associated hepatitis C is approximately one in every two million people. [47]
A history of organ transplantation, [10],[17],[44],[45] older age, [46],[48] younger age, [49] dialysis in multiple centers, [20],[44],[50],[51] associated hepatitis B infection, [21] human immunodeficiency virus infection, and diabetes mellitus, [52] are other factors that have been suggested to be associated with HCVpositivity.
Nakayama et al, found that Anti-HCV seropositivity was an independent risk factor for death.
In conclusion, isolation and proper application of infection control guidelines in HD units is recommended to avoid burden of virus transmission and morbidity.
Acknowledgment | |  |
The author would like to thank the hospital administration and nursing team at the AKU in Dawmat Aljandal General Hospital.
References | |  |
1. | Global surveillance and control of hepatitis. Report of a WHO Consultation organized in collaboration with the Viral Hepatitis Prevention board Antwerp, Belgium. J Viral Hepat 1999;6:35-47. |
2. | Yen T, Keeffe EB, Ahmed A. The epidemiology of hepatitis C virus infection. J Clin Gastroenterol 2003;36 : 47-53. [PUBMED] [FULLTEXT] |
3. | Fabrizi F, Poordad FF, Martin P. Hepatitis C infection and the patient with end-stage renal disease. Hepatology 2002;36:3-10. [PUBMED] [FULLTEXT] |
4. | Wreghitt TG. Blood-borne virus infections in dialysis units: A review. Rev Med Virol 1999; 9:101-9. [PUBMED] [FULLTEXT] |
5. | Buturovic-Ponikvar J. Expert Group for Dialysis in Slovenia at the Ministry of Health, Republic of Slovenia. Renal replacement therapy in Slovenia: annual report 2001. Nephrol Dial Transplant 2003;18(suppl 5):v53-5. |
6. | Omar MN, Tashkandy MA. Liver enzyme and protein electrophoretic pattern in hemodialysis patients with antibodies against the hepatitis C virus. Saudi Med J 2003;2:S122. |
7. | Carneiro MA, Teles SA, Dias MA, et al. Decline of hepatitis C infection in hemodialysis patients in Central Brazil: A ten years of surveillance. Mem Inst Oswaldo Cruz 2005;100 (4):345-9. |
8. | Bukh J, Wantzin P, Krogsgaard K, et al. High prevalence of hepatitis C virus (HCV) RNA in dialysis patients: Failure of commercially available antibody tests to identify a significant number of patients with HCV infection. J Infect Dis 1993;168:1343-8. [PUBMED] |
9. | Seeff LB. Natural history of hepatitis C. Hepatology 1997;26:21S-8S. [PUBMED] [FULLTEXT] |
10. | Amiri ZM, Shakib AJ, Toorchi M. Seroprevalence of hepatitis C and risk factors in haemodialysis patients in Guilan, Islamic Republic of Iran. East Mediterr Health J 2005;11:372-6. [PUBMED] |
11. | Alavian SM, Einollahi B, Hajarizadeh B, Bakhtiari S, Nafar M, Ahrabi S. Prevalence of hepatitis C virus infection and related risk factors among Iranian haemodialysis patients. Nephrology (Carlton) 2003;8:256-60. [PUBMED] [FULLTEXT] |
12. | Ansar MM, Kooloobandi A. Prevalence of hepatitis C virus infection in thalassemia and haemodialysis patients in north Iran-Rasht. J Viral Hepat 2002;9:390-2. [PUBMED] [FULLTEXT] |
13. | Bdour S: Hepatitis C virus infection in Jordanian haemodialysis units: serological diagnosis and genotyping. J Med Microbiol 2002;51: 700-70. |
14. | Hussein MM, Mooij JM, Hegazy MS, Bamaga MS. The impact of polymerase chain reaction assays for the detection of hepatitis C virus infection in a hemodialysis unit. Saudi J Kidney Dis Transpl 2007;18:107-13. [PUBMED] |
15. | Al-Shohaib SS, Abd-Elaal MA, Zawawi TH, Abbas FM, Shaheen FA, Amoah E. The prevalence of hepatitis C virus antibodies among hemodialysis patients in Jeddah area, Saudi Arabia. Saudi Med J 2003;2:S125. |
16. | Ahmetagic S, Muminhodzic K, Cickusic E, Stojic V, Petrovic J, Tihic N. Hepatitis C infection in risk groups. Bosn J Basic Med Sci 2006;6:13-7. |
17. | Salama G, Rostaing L, Sandres K, Izopet J. Hepatitis C virus infection in French hemodialysis units: a multicenter study. J Med Virol 2000;61:44-51. [PUBMED] [FULLTEXT] |
18. | Hinrichsen H, Leimenstoll G, Stegen G, Schrader H, Folsch UR, Schmidt WE, Prevalence and risk factors of hepatitis C virus infection in haemodialysis patients: a multicentre study in 2796 patients. Gut 2002;51:429-33. |
19. | Ben Othman S, Bouzgarrou N, Achour A, Bourlet T, Pozzetto B, Trabelsi A. High prevalence and incidence of hepatitis C virus infections among dialysis patients in the East-Centre of Tunisia. Pathol Biol (Paris) 2004;52:323-7. [PUBMED] [FULLTEXT] |
20. | Carneiro MA, Martins RM, Teles SA, et al. Hepatitis C prevalence and risk factors in hemodialysis patients in Central Brazil: A survey by polymerase chain reaction and serological methods. Mem Inst Oswaldo Cruz 2001;96: 765-9. [PUBMED] [FULLTEXT] |
21. | Fissell RB, Bragg-Gresham JL, Woods JD, et al. Patterns of hepatitis C prevalence and seroconversion in hemodialysis units from three continents: the DOPPS. Kidney Int 2004;65: 2335-42. [PUBMED] [FULLTEXT] |
22. | Iwasaki Y, Esumi M, Hosokawa N, Yanai M, Kawano K. Occasional infection of hepatitis C virus occurring in haemodialysis units identified by serial monitoring of the virus infection. J Hosp Infect 2000;45:54-6. [PUBMED] [FULLTEXT] |
23. | Schneeberger PM, Keur I, van Loon AM, et al. The prevalence and incidence of hepatitis C virus infections among dialysis patients in the Netherlands: a nationwide prospective study. J Infect Dis 2000;182:1291-9. [PUBMED] [FULLTEXT] |
24. | Almroth G, Ekermo B, Mansson AS, Svensson G, Widell A. Detection and prevention of hepatitis C in dialysis patients and renal transplant recipients. A long-term follow up (1989-January 1997). J Intern Med 2002;251:119-28. |
25. | Kondili LA, Genovese D, Argentini C, et al. Nosocomial transmission in simultaneous outbreaks of hepatitis C and B virus infections in a hemodialysis center. Eur J Clin Microbiol Infect Dis 2006;25:527-31. [PUBMED] [FULLTEXT] |
26. | Halfon P, Roubicek C, Gerolami V, et al. Use of phylogenetic analysis of hepatitis C virus (HCV) hypervariable region 1 sequences to trace an outbreak of HCV in an autodialysis unit. J Clin Microbiol 2002;40:1541-5. [PUBMED] [FULLTEXT] |
27. | Jadoul M, Poignet JL, Geddes C, et al. The changing epidemiology of hepatitis C virus (HCV) infection in haemodialysis: European multicentre study. Nephrol Dial Transplant 2004;19:904-9. [PUBMED] [FULLTEXT] |
28. | Gallego E, Lopez A, Perez J, et al. Effect of isolation measures on the incidence and prevalence of hepatitis C virus infection in hemodialysis. Nephron Clin Pract 2006;104:c1-6. |
29. | Carneiro MA, Teles SA, Dias MA, et al. Decline of hepatitis C infection in hemodialysis patients in Central Brazil: ten years of surveillance. Mem Inst Oswaldo Cruz 2005;100:345?9. [PUBMED] [FULLTEXT] |
30. | Yang CS, Chang HH, Chou CC, Peng SJ. Isolation effectively prevents the transmission of hepatitis C virus in the hemodialysis unit. J Formos Med Assoc 2003;102:79-85. [PUBMED] |
31. | Barril G, Traver JA. Decrease in the hepatitis C virus (HCV) prevalence in hemodialysis patients in Spain: effect of time, initiating HCV prevalence studies and adoption of isolation measures. Antiviral Res 2003;60:129-34. |
32. | Shamshirsaz AA, Kamgar M, Bekheirnia MR, et al. The role of hemodialysis machines dedication in reducing hepatitis C transmission in the dialysis setting in Iran: A multicenter prospective interventional study. BMC Nephrol 2004; 5:13. [PUBMED] [FULLTEXT] |
33. | Saxena AK, Panhotra BR, Sundaram DS, et al. Impact of dedicated space, dialysis equipment, and nursing staff on the transmission of hepatitis C virus in a hemodialysis unit of the middle east. Am J Infect Control 2003;31:26-33. [PUBMED] [FULLTEXT] |
34. | Jadoul M, Cornu C, van Ypersele de Strihou C. Universal precautions prevent hepatitis C virus transmission: a 54 month follow-up of the Belgian Multicenter Study. The Universitaires Cliniques St-Luc (UCL) Collaborative Group. Kidney Int 1998;53:1022-5. [PUBMED] [FULLTEXT] |
35. | Saxena AK, Panhotra BR. The impact of nurse understaffing on the transmission of hepatitis C virus in a hospital-based hemodialysis unit. Med Princ Pract 2004;13:129-35. [PUBMED] [FULLTEXT] |
36. | Alfurayh O, Sabeel A, Al Ahdal MN, et al. Hand contamination with hepatitis C virus in staff looking after hepatitis C-positive hemodialysis patients. Am J Nephrol 2000;20:103-6. [PUBMED] [FULLTEXT] |
37. | Piazza M, Borgia G, Picciotto L, Cicciarello S, Nappa S. HCV-RNA survival as detected by PCR in the environment. Boll Soc Ital Biol Sper 1994;70:167-70. [PUBMED] |
38. | Froio N, Nicastri E, Comandini UV, et al. Contamination by hepatitis B and C viruses in the dialysis setting. Am J Kidney Dis 2003;42: 546-50. [PUBMED] [FULLTEXT] |
39. | Centers for Disease Control and Prevention. Recommendations for preventing transmission of infections among chronic hemodialysis patients. MMWR Recomm Rep 2001;50:1-43. |
40. | Gilli P, Soffritti S, De Paoli Vitali E, Bedani PL. Prevention of hepatitis C virus in dialysis units. Nephron 1995;70:301-6. [PUBMED] |
41. | Shaheen FA, Huraib SO, Al-Rashed R, et al. Prevalence of hepatitis C antibodies among hemodialysis patients in Jeddah area, Saudi Arabia. Saudi Med J 2003;2:S125-6. |
42. | Othman B, Monem F. Prevalence of antibodies to hepatitis C virus among hemodialysis patients in Damascus, Syria. Infection 2001;29: 262-5. [PUBMED] [FULLTEXT] |
43. | Sypsa V, Psichogiou M, Katsoulidou A, et al. Incidence and patterns of hepatitis C virus seroconversion in a cohort of hemodialysis patients. Am J Kidney Dis 2005;45:334-43. |
44. | Sivapalasingam S, Malak SF, Sullivan JF, Lorch J, Sepkowitz KA. High prevalence of hepatitis C infection among patients receiving hemodialysis at an urban dialysis center. Infect Control Hosp Epidemiol 2002;23:319-24. [PUBMED] [FULLTEXT] |
45. | El-Amin HH, Osman EM, Mekki MO, et al. Hepatitis C virus infection in hemodialysis patients in Sudan: two centers' report. Saudi J Kidney Dis Transpl 2007;18(1):101-6. |
46. | Stramer SL. Current risks of transfusion transmitted agents: a review. Arch Pathol Lab Med 2007;131:702-7. [PUBMED] [FULLTEXT] |
47. | Saxena AK, Panhotra BR. The vulnerability of middle-aged and elderly patients to hepatitis C virus infection in a high-prevalence hospital?based hemodialysis setting. J Am Geriatr Soc 2004;52:242-6. [PUBMED] [FULLTEXT] |
48. | Kalantar-Zadeh K, Kilpatrick RD, McAllister CJ, et al. Hepatitis C virus and death risk in hemodialysis patients. J Am Soc Nephrol 2007; 18:1584-93. [PUBMED] [FULLTEXT] |
49. | Hosseini-Moghaddam SM, Keyvani H, Kasiri H, et al. Distribution of hepatitis C virus genotypes among hemodialysis patients in Tehran: A multicenter study. J Med Virol 2006;78:569?3. [PUBMED] [FULLTEXT] |
50. | Petrosillo N, Gilli P, Serraino D, et al. Prevalence of infected patients and understaffing have a role in hepatitis C virus transmission in dialysis. Am J Kidney Dis 2001;37:1004-10. [PUBMED] [FULLTEXT] |
51. | Ocak S, Duran N, Kaya H, Emir I. Seroprevalence of hepatitis C in patients with type 2 diabetes mellitus and non-diabetic on haemodialysis. Int J Clin Pract 2006;60(6):670-4. |
52. | Nakayama E, Akiba T, Marumo F, Sato C. Prognosis of anti-hepatitis C virus antibodypositive patients on regular hemodialysis therapy. J Am Soc Nephrol 2000;11:1896-902. [PUBMED] [FULLTEXT] |

Correspondence Address: Waleed Z Mohamed Nephrology Division, Medical Department, Dawmat Aljandal General Hospital, Dawmat Aljandal, Aljouf Saudi Arabia
 Source of Support: None, Conflict of Interest: None  | Check |
PMID: 20427892  
[Figure 1], [Figure 2], [Figure 3] |
|
This article has been cited by | 1 |
Epidemiology of viral hepatitis in Saudi Arabia: Are we off the hook |
|
| Abdo, A.A. and Sanai, F.M. and Al-Faleh, F.Z. | | Saudi Journal of Gastroenterology. 2012; 18(6): 349-357 | | [Pubmed] | | 2 |
Hepatitis B and C infection in haemodialysis patients in Libya: prevalence, incidence and risk factors |
|
| Alashek, W.A. and McIntyre, C.W. and Taal, M.W. | | BMC Infectious Diseases. 2012; 12(265) | | [Pubmed] | | 3 |
De novo HBV infection in a Mayo Clinic hemodialysis population: Economic impact of reduced HBV testing and a call for changes in current US CDC guidelines on HBV testing protocols |
|
| Onuigbo, M.A.C. and Onuigbo, N.T.C. | | Hemodialysis International. 2012; 16(SUPPL. 1): S32-S38 | | [Pubmed] | | 4 |
SASLT practice guidelines: Management of hepatitis C virus infection |
|
| Alfaleh, F.Z. and Alghamdi, A.S. and Alghamdi, H. and Alqutub, A. and Alswat, K. and Altraif, I. and Sanai, F. and Ismail, M. and Shah, H. | | Saudi Journal of Gastroenterology. 2012; 18(SUPPL. 1): S1-S32 | | [Pubmed] | | 5 |
A prospective study of hepatitis c virus infection in hemodialysis patients in Jeddah, Saudi Arabia |
|
| Azhar, E.I. and Jamjoom, G.A. and Al-Ghamdi, A.K. and Chaudhary, A.G. and Al-Ghamdi, S.M. and El-Kafrawy, S.A. and Shaheen, F.A. | | International Journal of Tropical Medicine. 2011; 6(6): 124-128 | | [Pubmed] | | 6 |
Rising burden of Hepatitis C Virus in hemodialysis patients |
|
| Khan, S. and Attaullah, S. and Ali, I. and Ayaz, S. and Naseemullah and Khan, S. and Siraj, S. and Khan, J. | | Virology Journal. 2011; 8(438) | | [Pubmed] | | 7 |
Hemodialysis of patients with HCV infection: Isolation has a definite role |
|
| Agarwal, S.K. | | Nephron - Clinical Practice. 2011; 117(4): c328-c332 | | [Pubmed] | |
|
|
 |
 |
|
|
|
|
|
|
Article Access Statistics | | Viewed | 4545 | | Printed | 133 | | Emailed | 0 | | PDF Downloaded | 803 | | Comments | [Add] | | Cited by others | 7 | |
|

|