51842-3
Plasmodium falciparum IgM Ab [Titer] in Serum by Immunofluorescence
Active
Part Descriptions
LP14839-2 Plasmodium falciparum
Four species of the Plasmodium protozoa are considered true parasites of humans as they use humans almost exclusively as a natural intermediate host: P. falciparum, P. vivax, P. ovale and P. malariae. Malaria today is usually restricted to tropical and subtropical areas and altitudes below 1,500 m., although in the past malaria was endemic in much of North America, Europe and even parts of northern Asia, and today is still present on the Korean peninsula. However, this present distribution could be affected by climatic changes and population movements. P. falciparum is the most prevalent species and responsible for the most morbidity and mortality worldwide. Early detect is of paramount importance due to the incidence of cerebral malaria and drug resistance. Malarial infections caused by P. falciparum are the most likely to progress to severe, potentially fatal forms with central nervous system involvement (cerebral malaria), acute renal failure, severe anemia, or acute respiratory distress syndrome.[CDC]
Source: Regenstrief LOINC, CDC
LP20149-8 Plasmodium
Malaria is a parasitic disease that is passed from one human to another by the bite of an infected Anopheles mosquito with one of four protozoan parasites: Plasmodium falciparum, vivax, malariae or ovale. The parasites enter the bloodstream and infect red blood cells where they multiply and infect more red blood cells. Symptoms usually occur 10 days to 4 weeks after infection and include anemia, high fevers, shaking chills, muscle pain, and nausea. Antimalarial agents used to treat malaria include Quinine, Quinidine, Mefloquine, Chloroquine, and Hydroxychloroquine. The effectiveness of the agents depends on which phase or phases of the Plasmodium life cycle is interrupted. In most cases, treatment outcome is expected to be good except in cases of a p. falciparum infection. Adverse effects from antimalaria medications include vomiting, diarrhea, headaches, cardiac arrhythmias, EKG abnormalities, deafness, damage to liver and kidney and muscle weakness.
Source: NMS labs
Fully-Specified Name
- Component
- Plasmodium falciparum Ab.IgM
- Property
- Titr
- Time
- Pt
- System
- Ser
- Scale
- SemiQn
- Method
- IF
Additional Names
- Short Name
- P falciparum IgM Titr Ser IF
- Display Name
- P. falciparum IgM IF (S) [Titer]
- Consumer Name Alpha Get Info
- Plasmodium falciparum IgM antibody, Blood
Basic Attributes
- Class
- MICRO
- Type
- Laboratory
- First Released
- Version 2.24
- Last Updated
- Version 2.75
- Order vs. Observation
- Both
Member of these Groups Get Info
LOINC Group | Group Name |
---|---|
LG41640-0 | Plasmodium |
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
de-DE | German (Germany) | Plasmodium falciparum Ak.IgM: |
es-ES | Spanish (Spain) | Plasmodium falciparum IgM: Synonyms: Semicuantitativo |
es-MX | Spanish (Mexico) | Plasmodium falciparum Ab.IgM: |
fr-CA | French (Canada) | Plasmodium falciparum, IgM: |
fr-FR | French (France) | Plasmodium falciparum Ac IgM: |
it-IT | Italian (Italy) | Plasmodium falciparum Ab.IgM: Synonyms: Anticorpi IgM anticorpo Immunofluorescenza (IF) Microbiologia Punto nel tempo (episodio) Siero Titolo |
nl-NL | Dutch (Netherlands) | Plasmodium falciparum As.IgM: Synonyms: antistof; |
pl-PL | Polish (Poland) | Plasmodium falciparum Ab.IgM: Synonyms: IgM Plasmodium falciparum Przeciwciała do Plasmodium falciparum Przeciwciała IgM do Plasmodium falciparum |
pt-BR | Portuguese (Brazil) | Plasmodium falciparum Ac.IgM: Synonyms: ; |
zh-CN | Chinese (China) | 恶性疟原虫 抗体.IgM: Synonyms: Ab.IgM; |
Example Units
Unit | Source |
---|---|
{titer} | Example UCUM Units |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=51842-3
LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright