Subido por Roque Garcia

A prospective study of hepatitis C virus

Anuncio
zyxw
zyxw
zyxwvutsrqponm
zyx
Copyright 0 Munkszuurd 1996
Liver 1996: 16: 331-334
Printed in Denmark . AN rights reserved
LIVER
ISSN 0106-9543
A prospective study of hepatitis C virus
infection after needlestick accidents
Arai Y, Noda K, Enomoto N, Arai K, Yamada Y, Suzuki K, Yoshihara H.
A prospective study of hepatitis C virus infection after needlestick accidents.
Liver 1996: 16: 331-334. 0 Munksgaard, 1996
I
Abstract: There have been few prospective studies of hepatitis C virus
(HCV) infection after needlestick accidents in hospital employees. In the
present study, the prevalence and features of HCV infection after needlestick accidents were evaluated prospectively measuring serum HCV-RNA.
Subjects were 56 employees who had HCV needlestick accidents.
To monitor the development of hepatitis, the serum ALT levels and HCVrelated seromarkers, such as first generation anti-HCV (RIA), second
generation anti-HCV (PHA) and HCV-RNA (RT-PCR) were measured
every month for at least 12 months after the accidents. Three of 56 (5.4%)
recipients developed HCV infection. HCV-RNA was detected in all three
recipients within 4 months after the exposure, and second-generation
HCV antibody was detected in two of three recipients. The detection of
HCV-RNA was earlier than that of HCV antibody. Two of three HCVinfected recipients developed type C acute hepatitis and one of two received interferon therapy; however, the other case received no medication. The detection of HCV-related seromarkers and the elevation of
ALT levels were transient in these three recipients; thus, none developed
chronic hepatitis. In conclusion, HCV infection developed in 5.4% of recipients within 4 months after HCV accidents. All of these HCV-infected
recipients showed fair prognosis. HCV-RNA was a beneficial parameter
for early detection of HCV infection.
Vumi Arai, Katsuhisa Noda,
Norihiro Enomoto, Keiichi Arai,
Vukinori Vamada, Kunio Suzuki and
Harumasa Voshihara
Department of Gastroenterology, Osaka Rosai
Hospital, Osaka, Japan
zyxwvutsr
Transmission of viral hepatitis via blood or
blood products is a problem for health care
workers. Hepatitis B virus (HBV) infection is
now controllable by both passive and active immunization (1-2). There have been a few reports
concerning transmission of non-A, non-B
(NANB) hepatitis infection in hospital employees
through accidental exposure to patients’ blood
(3-14). To our knowledge, there has been only
one prospective study using assays for HCVRNA and antibodies to hepatitis C virus (HCV)
which suggested that the risk of transmission of
HCV is not so high as that of hepatitis B after
needlestick injury (13). However, the prevalence
and features of HCV infection after needlestick
accidents have not been well-established. Therefore, in the present study, we evaluated prospectively the prevalence and features of HCV infection after needlestick accidents by measuring
serum HCV-RNA chronologically.
Key words: HCV-antibody - HCV-RNA - hepatitis
C virus - interferon therapy - needlestick’
accidents
Harumasa Yoshihara, M.D., Department of
Gastroenterology, Osaka Rosai Hospital,
1179-3 Nagasone-cho, Sakai-city, Osaka 591,
Japan
Received 29 May 1995, accepted for publication
4 June 1996
Material and methods
Patients
The accidental exposure of a hospital employee to
a patient’s blood through medical procedures was
defined as a “needlestick accident”, such as percutaneous injury with noticeable bleeding by medical
instruments contaminated with a patient’s blood,
and splash of a patient’s blood into the eye. All
needlestick accidents were reported to the Hepatitis Prevention Committee in our hospital by the
injured employees. Subjects were 56 employees
who had HCV needlestick accidents from January
1991 to August 1993 in our hospital.
Measurements of liver function test and hepatitis virus
seromarkers
We measured second-generation anti-HCV (HCV
2nd) by passive hemagglutination (PHA, Abbott
331
Arai et al.
zyxwvutsrq
zyxwvu
Laboratories) (15) and HBs antigen (HBsAg) by
commercially available enzyme linked immunosorbent assay(EL1SA tests, Abbott Laboratories)
in all donors routinely on admission before the accident. To monitor the development of hepatitis
after needlestick accidents in recipients, the serum
levels of alanine aminotransferase (ALT; normal
range, 0-30 IUA) as well as HCV-related seromarkers were measured every month for at least 12
months (length of follow-up, 18.926.6 months).
As HBV-related seromarkers, HBsAg and HBs
antibody (HBsAb) were also measured just after
the accident. As HCV-related seromarkers, we
measured first-generation anti-HCV (HCV 1st) by
radioimmunoassay (RIA, Ortho kit), second-generation anti-HCV (HCV 2nd) by PHA (Abbott
Laboratories), and HCV genomic RNA (HCVRNA) detected by a reverse transcription polymerase chain reaction (RT-PCR) assay using
primers from the highly conserved 5' non-coding
region (16) in all HCV-needlestick recipients. The
infection of HCV was diagnosed by the positiveness of serum HCV-RNA in association with
the positiveness of HCV antibody or an increase
in serum ALT level. Additionally, in one case of
acute hepatitis after the accident, serum HCVRNA levels and genotype were also analyzed by
competitive RT-PCR (17) and RT-PCR (18), respectively. All recipients were confirmed to be
negative for HBsAg, HCV Ist, HCV 2nd and
HCV-RNA just after the needlestick accidents. All
donors were confirmed to be negative for HBsAg
and positive for HCV 2nd.
Results
(-)
HCV2nd
*
HCV-RNA
7
(+)
(-)
zyx
zyxwvut
zy
OJ
'91'
5 6
"
\\-\I-
"
' '92" "
9 10 11 12 1 2 3 4 5
"
7 8
'I4
month
zyxwvuts
zyxwvut
zyxwvut
As to the mode of exposure of health care workers
to patient's blood, needlesticks were observed in 49
(87.5%), which was the most frequent accident in
all 56 cases. The other modes of accidents were
cuts with sharp objects in 4 (7.1%), splash into eye
in 2 (3.6%) and blood contamination of a wound
in 1 (1.8%). HCV infection developed in 3 of 56
(5.4%) recipients after anti-HCV positive needlestick accidents. All three donors were negative for
HBsAg and positive for HCV 2nd, associated with
chronic liver disease. Recipients who turned positive for anti-HCV lst, anti-HCV 2nd and HCVRNA were 1 of 56 (1.8%), 2 of 56 (3.6%) and 3 of
56 (5.4%), respectively. None of the three recipients
had a history of hepatitis and drug abuse or heavy
drinking of alcohol. These three recipients had
normal liver function test and negative HBV- and
HCV-related seromarkers (anti-HCV 1st, antiHCV 2nd, HCV-RNA) at the time of needlestick
accidents and were negative for HBV-, EpsteinBarr virus- and cytomegalo virus-related serum
332
HCVlst
Fig. 1. A clinical course following needlestick accident in case
1 . The recipient was a 21-year-old nurse. A11 HCV related
markers were measured every month. The normal range of ALT
level and negative serum HCV-related markers persisted for
more than one year after normalization of ALT.
3
\
2
30.
20
E
2
8
04
'92 '
1112
"93
1
'
2
'
'
3
4
'
5
7
'94'
'
'
'
6
8
9
2
month
Fig. 2. A clinical course following needlestick accident in case
2. The recipient was a 29-year-old nurse. All HCV-related
markers were measured every month.
markers at the time of developing hepatitis. Of the
three HCV-infected recipients, two cases showed
no elevation or slight elevation of serum ALT level
(below 60 IUA) during their clinical course after
the accidents and received no medications (Figs. 1
and 2). One case showed typical acute hepatitis,
associated with an elevation of serum ALT level up
to 1375 IUA, and positiveness of anti-HCV lst,
anti-HCV 2nd and HCV-RNA, and received interferon (IFN) therapy. In the donor, serum HCVRNA level was lo6 copy/ml and genotype was type
11, while, in the recipient, the peak level of HCVRNA was lo8 copy/ml and genotype was type I1
(Fig. 3). In the three HCV-infected recipients, the
detection of HCV-RNA was earlier than that of
HCV antibody or abnormal serum ALT levels. In
addition, one HCV-infected recipient showed positive HCV-RNA in the absence of any positive-
zy
zyxwvutsrqpo
HCV infection after needlestick accidents
zyxwvutsrqpon
zyxwvutsrq
1.4 2.5 5.9 10
- +‘
HCV2nd + +
-
HCV 1st
9.5
2.3
1.5
’+
’+
4
HCV-RNA1 mi)
(COPY
+
+
-‘
b r
<lo4
108 <1$*
Liver
5 1000
U
zyxwvuts
zyxwvutsrqponm
f 500j
w
zee-infection units for HBeAg-positive sera (21).
Thus, the most probable explanation for the low
rate of infection after anti-HCV-positive needlestick accidents is that the amount of contaminated
blood is very little and that the titer of HCV in
human sera is orders of magnitude lower than the
titer of HBV in HBeAg-positive human sera. In
the present study, HCV-RNA was detected within
4 months after the exposure. HCV-RNA was detected earlier than the other HCV-related seromarkers or an elevation of serum ALT level, indicating
that HCV-RNA is a beneficial parameter for early
detection of HCV infection. Kato et al. (22) also
reported that, in acute non-A, non-B hepatitis,
HCV-RNA was detected 9 2 1 1 weeks before the
detection of anti-Cl00-3.
Omata et al. (23) reported the effectiveness of
IFN therapy for acute NANB hepatitis, and for
the prevention of chronic hepatitis. In the present
study, one case was administered IFN to avoid developing chronic hepatitis. However, there is also a
possibility that IFN therapy affected, to a minimal
extent, the natural course of acute hepatitis C,
since her serum ALT level returned to the normal
level before IFN therapy. The number of reports is
extremely limited as to the long-term prognosis of
acute hepatitis after HCV-needlestick accidents.
Sodeyama et al. (13) reported two recipients of
HCV-needlestick accidents who developed acute
hepatitis, followed by chronic hepatitis in the presence of serum HCV-RNA. By contrast, our study
showed fair prognosis of three HCV-infected recipients, without developing chronic hepatitis, giving an evident difference from Sodeyama’s report.
The type C post-transfusion hepatitis is well
known to be associated with following chronic
hepatitis in 40 to 50% of cases (24). The present
finding cannot be evidence for the different prognosis between type C post-transfusion hepatitis
and HCV-needlestick accidents since the number
of HCV-infected recipients was too small. Thus, in
order to clarify the long-term prognosis of HCVinfected recipients after needlestick accidents,
further studies are required.
o
(
::
‘94
3
month
Fig. 3. A clinical course following needlestick accident in case
3. The recipient was a 22-yedr-old nurse. Each number on the
arrow of anti-HCV 1st indicates the titer. The interferon (IFN)
was administered daily for 2 weeks, thereafter intermittently for
10 weeks. The histology of liver biopsy was compatible with
that of recovery stage in acute hepatitis.
’93
4
8
10
12
HCV antibodies. The elevation of serum ALT
levels and the detection of HCV-seromarkers were
transient resulting in a normalization of ALT
levels and disappearance of HCV-RNA during the
observation period. Thus, all these HCV-infected
recipients showed fair prognosis.
Discussion
There have been a few retrospective studies concerning transmission of NANB hepatitis (3-14) or
type C hepatitis (9) in hospital employees through
accidental exposure to patients’ blood. However,
to our knowledge, there has been only one prospective study concerning the risk of transmission
of HCV after needlestick injury; i.e., Sodeyama et
al. (13) reported that acute hepatitis C developed
in 2 of 62 (3.20/0)recipients when donors were positive for anti-C100-3, and in 2 of 88 (2.3%) when
donors were positive for anti-HCV 2nd. However,
in his study, HCV-transmission was not confirmed
by the detection of HCV-RNA in all recipients.
The infection rate (5.4%) of HCV needlestick accidents in the present study seems to be a little bit
higher than Sodeyama’s report (2-3%), which
might be attributed to the measurement of HCVRNA in all recipients of our study. The rate of
HCV infection after HCV-needlestick accidents is
low compared with the rate of 67% found in
HBeAg-positive needlestick accidents (19). The infectivity titer of human non-A, non-B hepatitis
sera is generally less than 1O2 chimpanzee-infection
units, as shown in chimpanzee transmission studies
(20), which is extremely lower than lo8 chimpan-
References
zyxw
1. SEEFFL B, WRIGHTE C, ZIMMERMAN
H J, et al. Type B
hepatitis after needlestick exposure: prevention with hepatitis B immune globulin: final report of the Veterans Administration cooperative study. Ann Intern Med 1978: 88:
285-293.
.
2. SEEFTL B, HOOFNAGLE
J H. Immunoprophylaxis of viral
hepatitis. Gastroenterol 1979: 77: 161-182.
3. KIYOSAWA
K, GIBOG, SODEYAMA
T, et al. Possible infectious causes in 651 patients with acute viral hepatitis during
a 10-year period (1976-1985). Liver 1987: 7: 165-168.
4. ALTERM J, GERETYR J, SMALLWOOD
L A, et al. Sporadic
333
zyxwvutsrq
zyxwvutsrqp
zyxwvutsrqpo
zyxwvutsr
Arai et al.
non-A, non-B hepatitis: frequency and epidemiology in an
urban US population. J Infect Dis 1982: 145:886-893.
5. GERBERDING
J L.Current epidemiologic evidence and case
reports of occupationally acquired HIV and other blood
borne disease. Infect Control Hosp Epidemioll990:11: 558-
560.
6.AHTONEJ, FRANCIS
D, BRADLEY
D, MAYNARD
J. Non-A,
non-B hepatitis in a nurse after percutaneous needle exposure. Lancet 1980: 1: 1142.
W, PETERSON
E, TAYLOR
J W. Non-A, non-B hepa7. HERRON
titis infection transmitted via a needle. M M W R 1978: 28:
157-158.
8. MAYO-SMJTH
M F. Type non-A, non-B and type B hepatitis
transmitted by a single needlestick. A m J Infect Control
1987: 15: 266-261.
9. VAGLIA
A, NICOLIN
R, PUROV, IPPOLITO
G, BETTJNI
C, DELALLA
H. Needlestick hepatitis C virus seroconversion in a
surgeon. Lancet 1990:36: 1315-1316.
U. ROCGENDORF
M, CHOLMAKOW
K, WJSE
10. SCHLJPKOTER
A, DEINHARDT
F. Transmission of hepatitis C virus (HCV)
from a haemodialysis patient to a medical staff member.
Scrrnd J Infect Dis 1990: 22:757-758.
11. KIYOSAWA
K, SODEYAMA
T, TANAKA
E, et al. Hepatitis C in
hospital employees with needlestick injuries. Ann Intern
Med 1991: 115: 367-369.
12. CARIANI
E,ZONARO
A, PRJMID, et al. Detection of HCVi
RNA and antibodies to HCV after needlestick injury. Lancet 1991:337: 850.
13.SODEYAMA
T, KIYOSAWA
K, URUSHIHARA
A, et al. Detection
of hepatitis C virus markers and hepatitis C virus genomicRNA after needlestick accidents. Arch Intern Med 1993:
153: 1565-1572.
14. FUKUI
T, NODAH, HINAMIF, et al. Blood contamination
for medical staff and positive rate of HCV antibody in inpatients. Jpn J Traumatol Occup Med 1992:40:603-607.
15. OSADAK, SAMESHIMA
Y, FUJIIH, SHIMIZU
M, WATANABE
J, NISHIOKA
K. Effect of donor blood screening for antiHCV antibody by the second-generation passive hemagglutination test on the incidence of post-transfusion
hepatitis. In: Nishioka, ed. Viral hepatitis and liver disease. Hong Kong: Springer-Verlag Tokyo Publishing,
1994: 562-564.
16. ULRICHP P, ROMEOJ M, LANEP K, KELLYI, DANIEL
W,
VYASG N. Detection, semiquantitation, and genetic vari-
ation in hepatitis C virus sequence amplified from the
plasma of blood donors with elevated alanine aminotransferase. J Clin Invest 1990:86: 1609-1614.
17. GILLILAND
G, PERRIN
S, BLANCHARD
K, BUNNH F. Analysis of cytokine mRNA and DNA: detection and quantitation by competitive polymerase chain reaction. Proc Natl
Acad Sci USA 1990:87: 2725-2729.
18. OKAMOTO
H, SUGIYAMA
Y, OKADA
S, et al. Typing hepatitis
C virus by polymerase chain reaction with type-specific
primers: application to clinical surveys and tracing infectious sources. J Gen Virol 1992: 73: 673-679.
19.US. National Heart and Lung Institute Collaborative
Study Group and Phoenix Laboratories Division, Bureau
of Epidemiology, Center for Disease Control. Relation of e
antigen to infectivity of HBsAg-positive inoculations
among medical personnel. Lancet 1976:2: 492.
20. YOSHIZAWA
H. ITOH Y, IWASAKI
S, et al. Non-A, non-B
(type 1) hepatitis agent capable of inducing tubular structures in the hepatocyte cytoplasm of chimpanzees: inactivation by formalin and heat. Gastroenterol 1982: 82: 502-
zyxwvutsrq
zyxwvutsrq
334
506.
21. SHIKATA
T, KARASAWA
T, ABEK, et al. Hepatitis B e antigen and infectivity of hepatitis B virus. J Iffect Dis 1977:
136: 571-576.
22. KATON,YOKOSUKA
0, HOSODA
K, ITOY, OHTAM, OMATA
M. Detection of hepatitis C virus in acute non-A, non-B
hepatitis as an early diagnostic tool. Biochem Siophys Res
Comm 1993: 192:800-807.
23. OMATAM, YOKOSUKA
0, TAKANO
S, et al. Resolution of
acute hepatitis C after therapy with natural beta interferon.
Lancet 1991:338: 914-915.
24. KORETZR L, STONE0,GITNJCK
G L. The long-term course
of non-A, non-B post-transfusion hepatitis. Gastroenterol
1980:79:893-898.
Descargar