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COMPLIANCE INFO_1991-2019
Environmental Health - Public
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EHD Program Facility Records by Street Name
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C
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COMMERCE
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65
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4500 - Medical Waste Program
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PR0450112
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COMPLIANCE INFO_1991-2019
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Last modified
6/12/2024 2:22:36 PM
Creation date
7/3/2020 10:20:23 AM
Metadata
Fields
Template:
EHD - Public
ProgramCode
4500 - Medical Waste Program
File Section
COMPLIANCE INFO
FileName_PostFix
1991-2019
RECORD_ID
PR0450112
PE
4530
FACILITY_ID
FA0002435
FACILITY_NAME
ARC STOCKTON COMMERCE ST
STREET_NUMBER
65
Direction
N
STREET_NAME
COMMERCE
STREET_TYPE
ST
City
STOCKTON
Zip
95202
APN
13728012
CURRENT_STATUS
01
SITE_LOCATION
65 N COMMERCE ST
P_LOCATION
01
P_DISTRICT
001
QC Status
Approved
Scanner
SJGOV\cfield
Supplemental fields
FilePath
\MIGRATIONS\MW\MW_4530_PR0450112_65 N COMMERCE_.tif
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EHD - Public
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Hepatitis B envelope antigen (HBeAg) also appears in <br />serum at the time that HBsAg is first detected. It persists <br />for less time than HBsAg in the majority of patients. HBeAg <br />is a reliable and sensitive marker for the presence of high <br />levels of virus, and therefore a high degree of infectivity. <br />HBsAg -positive individuals who are HBeAg positive are highly <br />infectious; they have a higher absolute number of infectious <br />viral particles in their serum. <br />As HBeAg disappears from the serum, antibody to it <br />(anti -HBe) develops. This seroconversion generally occurs <br />at the peak of clinical symptoms and suggests that the dis- <br />ease is on the wane. Persons who progress to the chronic <br />HBsAg carrier state do not seroconvert from HBeAg to anti - <br />HBe during this phase of acute infection. The persistence <br />of HBeAg by radioimmunoassay for more than 10 weeks is asso- <br />ciated with the carrier state and with chronic -persistent or <br />chronic -active hepatitis. <br />In addition to HBsAg and HBeAg, there is HBcAg, or core <br />antigen, the 27 -nanometer nucleocapsid core found in the <br />nuclei of liver cells infected with HBV. Under normal <br />conditions, it is not found free in serum. However, anti - <br />HBc is found in serum, appearing 2 4 weeks after HBsAg is <br />first detected. <br />The final serologic marker of HBV infection is anti - <br />HBs. It does not arise until the convalescent period. In <br />all but a few cases, anti -HBs is not detectable in serum <br />until HBsAg has disappeared and recovery is complete. <br />Therefore, anti -HBs is a marker of recovery and immunity. <br />Hepatitis B infection is commonly spread by the <br />parenteral route or by intimate sexual contact. Serologic <br />markers of prior hepatitis B infection are common among <br />drug addicts, medical personnel and dialysis patients. Only <br />about 50% of persons with acute type B hepatitis give a <br />history of known parenteral exposure, even after close and <br />thorough questioning. In these cases, inapparent parenteral <br />spread may have occurred, such that the virus entered the <br />body through a tiny insignificant break in the skin or <br />mucous membrane.-- HBV does not seem capable of crossing the <br />intact skin. Experimental studies have shown that the virus <br />has extremely low infectivity by oral, nasal or respiratory <br />routes. <br />Health care professionals who handle open containers of <br />blood frequently are at an increased risk of contracting <br />hepatitis B compared to the general population. Several <br />surveys have confirmed this increased risk. In one, 26% of <br />blood bank workers demonstrated serologic markers indicative <br />of previous HBV infection. In contrast, only 14% of den- <br />tists, 10% of intensive care nurses, and 4% of hospital wor- <br />kers with no patient contact have evidence of prior hepati- <br />tis B. Before surrogate testing began, 5% of all volunteer <br />blood donors had HBV markers indicating prior exposure to <br />HBV. <br />BIOSAFETY - INFAGT - 0491 - PAGE 2 <br />
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