Rubella laboratory tests: Difference between revisions
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==Overview== | ==Overview== | ||
Rubella virus specific [[IgM]] antibodies are present in people recently infected by Rubella virus but these antibodies can persist for over a year and a positive test result needs to be interpreted with caution.<ref name="pmid17337363">{{cite journal | Rubella virus specific [[IgM]] antibodies are present in people recently infected by Rubella virus but these antibodies can persist for over a year and a positive test result needs to be interpreted with caution.<ref name="pmid17337363">{{cite journal | ||
|author=Best JM | |author=Best JM | ||
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==Laboratory Findings== | |||
Many [[rash]] illnesses can mimic rubella infection, and as many as 50% of rubella [[infections]] may be subclinical. The only reliable evidence of acute rubella infection is a positive [[viral culture]] for rubella or detection of rubella virus by [[polymerase chain reaction]], the presence of rubella-specific IgM [[antibody]], or demonstration of a significant rise in IgG antibody from paired acute-and convalescent-phase sera. | |||
Rubella virus can be isolated from [[nasal]], [[blood]], [[throat]], [[urine]] and [[cerebrospinal fluid]] specimens from rubella and CRS patients. Virus may be isolated from the [[pharynx]] 1 week before and until 2 weeks after rash onset. Although isolation of the virus is diagnostic of rubella infection, viral cultures are labor intensive, and therefore not done in many laboratories; they are generally not used for routine diagnosis of rubella. Viral isolation is an extremely valuable epidemiologic tool and should be attempted for all suspected cases of rubella or CRS. | |||
[[Serology]] is the most common method of confirming the diagnosis of rubella. Acute rubella infection can be serologically confirmed by a significant rise in rubella antibody titer in acute-and convalescent-phase [[serum]] specimens or by the presence of serum rubella IgM. Serum should be collected as early as possible (within 7–10 days) after onset of illness, and again 14–21 days (minimum of 7) days later. | |||
False-positive serum rubella IgM tests have occurred in persons with [[parvovirus]] infections, with a positive [[heterophile]] test for infectious [[mononucleosis]], or with a positive [[rheumatoid factor]]. | |||
The serologic tests available for laboratory confirmation of rubella infections vary among laboratories. The state health department can provide guidance on available laboratory services and preferred tests. | |||
Enzyme-linked immunosorbent assay (ELISA). ELISA is sensitive, widely available, and relatively easy to perform. It can also be modified to measure IgM antibodies. Most of the diagnostic testing done for rubella antibodies uses some variation of ELISA. | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
{{WH}} | |||
{{WS}} | |||
[[Category:Teratogens]] | |||
[[Category:Viral diseases]] | |||
[[Category:Pediatrics]] | |||
[[Category:Togaviruses]] | |||
[[Category:Emergency medicine]] |
Latest revision as of 00:04, 30 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Rubella virus specific IgM antibodies are present in people recently infected by Rubella virus but these antibodies can persist for over a year and a positive test result needs to be interpreted with caution.[1] The presence of these antibodies along with, or a short time after, the characteristic rash confirms the diagnosis.[2]
Laboratory Findings
Many rash illnesses can mimic rubella infection, and as many as 50% of rubella infections may be subclinical. The only reliable evidence of acute rubella infection is a positive viral culture for rubella or detection of rubella virus by polymerase chain reaction, the presence of rubella-specific IgM antibody, or demonstration of a significant rise in IgG antibody from paired acute-and convalescent-phase sera.
Rubella virus can be isolated from nasal, blood, throat, urine and cerebrospinal fluid specimens from rubella and CRS patients. Virus may be isolated from the pharynx 1 week before and until 2 weeks after rash onset. Although isolation of the virus is diagnostic of rubella infection, viral cultures are labor intensive, and therefore not done in many laboratories; they are generally not used for routine diagnosis of rubella. Viral isolation is an extremely valuable epidemiologic tool and should be attempted for all suspected cases of rubella or CRS.
Serology is the most common method of confirming the diagnosis of rubella. Acute rubella infection can be serologically confirmed by a significant rise in rubella antibody titer in acute-and convalescent-phase serum specimens or by the presence of serum rubella IgM. Serum should be collected as early as possible (within 7–10 days) after onset of illness, and again 14–21 days (minimum of 7) days later.
False-positive serum rubella IgM tests have occurred in persons with parvovirus infections, with a positive heterophile test for infectious mononucleosis, or with a positive rheumatoid factor.
The serologic tests available for laboratory confirmation of rubella infections vary among laboratories. The state health department can provide guidance on available laboratory services and preferred tests.
Enzyme-linked immunosorbent assay (ELISA). ELISA is sensitive, widely available, and relatively easy to perform. It can also be modified to measure IgM antibodies. Most of the diagnostic testing done for rubella antibodies uses some variation of ELISA.
References
- ↑ Best JM (2007). "Rubella". Semin Fetal Neonatal Med. 12 (3): 182–92. doi:10.1016/j.siny.2007.01.017. PMID 17337363.
- ↑ Stegmann BJ, Carey JC (2002). "TORCH Infections. Toxoplasmosis, Other (syphilis, varicella-zoster, parvovirus B19), Rubella, Cytomegalovirus (CMV), and Herpes infections". Curr Womens Health Rep. 2 (4): 253–8. PMID 12150751.