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Medical test

From Wikipedia, the free encyclopedia
(Redirected fromDiagnostic agent)
Medical procedure

For sociological tests, seeLaboratory studies. For laboratory test, seeBlood test.
"Medical investigation" redirects here. For the television series, seeMedical Investigation.
Medical intervention
Medical test
X-ray of a hand. X-rays are a common medical test.
MeSHD019937

Amedical test is amedical procedure performed todetect,diagnose, ormonitor diseases, disease processes, susceptibility, or to determine a course of treatment. Medical tests such as, physical and visual exams,diagnostic imaging, genetic testing, chemical and cellular analysis, relating toclinical chemistry andmolecular diagnostics, are typically performed in amedical setting.

Types of tests

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By purpose

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Medical tests can be classified by their purposes, including diagnosis, screening or monitoring.

Diagnostic

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Lungscintigraphy evaluating lung cancer

A diagnostic test is a procedure performed to confirm or determine the presence of disease in an individual suspected of having a disease, usually following the report of symptoms, or based on other medical test results.[1][2] This includesposthumous diagnosis. Examples of such tests are:

Screening

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Main article:Screening (medicine)

Screening refers to a medical test or series of tests used to detect or predict the presence of disease in at-risk individuals within a defined group such as a population, family, or workforce.[4][5] Screenings may be performed to monitor disease prevalence, manage epidemiology, aid in prevention, or strictly for statistical purposes.[6]

Examples of screenings include measuring the level ofTSH in theblood of a newborninfant as part ofnewborn screening forcongenital hypothyroidism,[7] checking forLung cancer in non-smoking individuals who are exposed tosecond-hand smoke in an unregulated working environment, andPap smear screening for prevention or early detection ofcervical cancer.[citation needed]

Monitoring

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Main article:Monitoring (medicine)

Some medical tests are used tomonitor the progress of, or response tomedical treatment.

By method

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Most test methods can be classified into one of the following broad groups:

By sample location

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In vitro tests can be classified according to the location of the sample being tested, including:

Accuracy and precision

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Main article:Accuracy and precision
  • Accuracy of a laboratory test is its correspondence with the true value. Accuracy is maximized by calibrating laboratory equipment with reference material and by participating in external quality control programs.
  • Precision of a test is its reproducibility when it is repeated on the same sample. An imprecise test yields widely varying results on repeated measurement. Precision is monitored in laboratory by using control material.

Detection and quantification

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Tests performed in aphysical examination are usually aimed at detecting asymptom orsign, and in these cases, a test that detects a symptom or sign is designated apositive test, and a test that indicated absence of a symptom or sign is designated a negative test, as further detailed in a separate section below.A quantification of a target substance, a cell type or another specific entity is a common output of, for example, mostblood tests. This is not only answeringif a target entity is present or absent, but alsohow much is present. In blood tests, the quantification is relatively well specified, such as given inmass concentration, while most other tests may be quantifications as well although less specified, such as a sign of being "verypale" rather than "slightly pale". Similarly, radiologic images are technically quantifications of radiologic opacity of tissues.[citation needed]

Especially in the taking of amedical history, there is no clear limit between a detecting or quantifying test versus ratherdescriptive information of an individual. For example, questions regarding the occupation or social life of an individual may be regarded as tests that can be regarded as positive or negative for the presence of various risk factors, or they may be regarded as "merely" descriptive, although the latter may be at least as clinically important.[citation needed]

Positive or negative

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Further information:Positive and negative predictive values andFalse positives and false negatives

The result of a test aimed at detection of an entity may bepositive ornegative: this has nothing to do with a badprognosis, but rather means that the test worked or not, and a certain parameter that was evaluated was present or not. For example, a negativescreening test forbreast cancer means that no sign of breast cancer could be found (which is in fact very positive for the patient).[citation needed]

The classification of tests into either positive or negative results in abinary classification, allowing for the application ofbayesian probability and the calculation ofdiagnostic test accuracy measures, such assensitivity, specificity,likelihood ratios, and thediagnostic odds ratio.[14][15] These metrics are commonly used insystematic review of diagnostic test accuracy andmeta-analyses ofdiagnostic accuracy studies.[16]

Continuous values

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Tests whose results are of continuous values, such as mostblood values, can be interpreted as they are, or they can beconverted to a binary ones by defining acutoff value, with test results being designated as positive or negative depending on whether the resultant value is higher or lower than the cutoff.

Interpretation

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Further information:Pre- and post-test probability

In the finding of apathognomonic sign or symptom it is almost certain that the target condition is present, and in the absence of finding asine qua non sign or symptom it is almost certain that the target condition is absent. In reality, however, the subjective probability of the presence of a condition is never exactly 100% or 0%, so tests are rather aimed at estimating apost-test probability of a condition or other entity.

Most diagnostic tests basically use areference group to establish performance data such aspredictive values,likelihood ratios andrelative risks, which are then used to interpret the post-test probability for an individual.

In monitoring tests of an individual, the test results from previous tests on that individual may be used as a reference to interpret subsequent tests.

Risks

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Some medical testing procedures have associated health risks, and even requiregeneral anesthesia, such as themediastinoscopy.[17] Other tests, such as theblood test orpap smear have little to no direct risks.[18] Medical tests may also haveindirect risks, such as the stress of testing, and riskier tests may be required as follow-up for a (potentially)false positive test result. Consult the health care provider (includingphysicians,physician assistants, andnurse practitioners) prescribing any test for further information.

Indications

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Each test has its ownindications and contraindications. Anindication is a valid medical reason to perform the test. Acontraindication is a valid medical reason not to perform the test. For example, a basiccholesterol test may beindicated (medically appropriate) for a middle-aged person. However, if the same test was performed on that person very recently, then the existence of the previous test is a contraindication for the test (a medically valid reason to not perform it).

Information bias is thecognitive bias that causes healthcare providers to order tests that produce information that they do not realistically expect or intend to use for the purpose of making a medical decision. Medical tests are indicated when the information they produce will be used. For example, a screening mammogram is not indicated (not medically appropriate) for a woman who is dying, because even if breast cancer is found, she will die before any cancer treatment could begin.

In a simplified fashion, how much a test is indicated for an individual depends largely on itsnet benefit for that individual. Tests are chosen when the expected benefit is greater than the expected harm. The net benefit may roughly be estimated by:[19]

bn=Δp×ri×(bihi)ht{\displaystyle b_{n}=\Delta p\times r_{i}\times (b_{i}-h_{i})-h_{t}}

, where:

  • bn is the net benefit of performing a test
  • Λp is the absolute difference betweenpre- and posttest probability of conditions (such as diseases) that the test is expected to achieve. A major factor for such an absolute difference is the power of the test itself, such as can be described in terms of, for example,sensitivity and specificity orlikelihood ratio. Another factor is the pre-test probability, with a lower pre-test probability resulting in a lower absolute difference, with the consequence that even very powerful tests achieve a low absolute difference for very unlikely conditions in an individual (such asrare diseases in the absence of any other indicating sign), but on the other hand, that even tests with low power can make a great difference for highly suspected conditions. The probabilities in this sense may also need to be considered in context of conditions that are not primary targets of the test, such asprofile-relative probabilities in a differential diagnostic procedure.
  • ri is the rate of how muchprobability differences are expected to result inchanges in interventions (such as a change from "no treatment" to "administration of low-dose medical treatment"). For example, if the only expected effect of a medical test is to make one disease more likely compared to another, but the two diseases have the same treatment (or neither can be treated), then, this factor is very low and the test is probably without value for the individual in this aspect.
  • bi is the benefit ofchanges in interventions for the individual
  • hi is the harm ofchanges in interventions for the individual, such asside effects of medical treatment
  • ht is the harm caused by the test itself.

Some additional factors that influence a decision whether a medical test should be performed or not included: cost of the test, availability of additional tests, potential interference with subsequent test (such as anabdominal palpation potentially inducing intestinal activity whose sounds interfere with a subsequentabdominal auscultation), time taken for the test or other practical or administrative aspects. The possible benefits of a diagnostic test may also be weighed against the costs of unnecessary tests and resulting unnecessary follow-up and possibly even unnecessary treatment of incidental findings.[20]

In some cases, tests being performed are expected to have no benefit for the individual being tested. Instead, the results may be useful for the establishment of statistics in order to improve health care for other individuals. Patients may giveinformed consent to undergo medical tests that will benefit other people.

Patient expectations

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In addition to considerations of the nature of medical testing noted above, other realities can lead to misconceptions and unjustified expectations among patients. These include: Different labs have different normal reference ranges; slightly different values will result from repeating a test; "normal" is defined by a spectrum along a bell curve resulting from the testing of a population, not by "rational, science-based, physiological principles"; sometimes tests are used in the hope of turning something up to give the doctor a clue as to the nature of a given condition; and imaging tests are subject to fallible human interpretation and can show"incidentalomas", most of which "are benign, will never cause symptoms, and do not require further evaluation," although clinicians are developing guidelines for deciding when to pursue diagnoses of incidentalomas.[21]

Standard for the reporting and assessment

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The QUADAS-2 revision is available.[22]

List of medical tests

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Main article:list of medical tests

See also

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References

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  1. ^abAl-Gwaiz LA, Babay HH (2007)."The diagnostic value of absolute neutrophil count, band count and morphological changes of neutrophils in predicting bacterial infections".Med Princ Pract.16 (5):344–347.doi:10.1159/000104806.PMID 17709921.
  2. ^Harvard.eduArchived 2014-12-23 at theWayback Machine
    Guide to Diagnostic Tests from Harvard Health
  3. ^"Harvard.edu". Archived fromthe original on 2017-06-18. Retrieved2016-11-07.
  4. ^Ratcliffe JM, Halperin WE, Frazier TM, Sundin DS, Delaney L, Hornung RW (1986)."The prevalence of screening: a report from the National Institute of Occupational Safety and the Health National Occupational Hazard Survey".Journal of Occupational Medicine.28 (10):906–912.doi:10.1097/00043764-198610000-00003.PMID 3021937.Archived from the original on 2021-10-20. Retrieved2019-09-16.
  5. ^Osha.govArchived 2020-08-10 at theWayback Machine
    US Dept. of Labor – Occupational Safety and Health Admin.
  6. ^Murthy LI, Halperin WE (1995)."Medical Screening and Biological Monitoring: A guide to the literature for physicians".Journal of Occupational and Environmental Medicine.37 (2):170–184.doi:10.1097/00043764-199502000-00016.PMID 7655958.S2CID 24916505.Archived from the original on 2021-10-20. Retrieved2020-09-08.
  7. ^Moltz KC, Postellon DC (1994). "Congenital hypothyroidism and mental development".Comprehensive Therapy.20 (6):342–346.PMID 8062543.
  8. ^OSA | Design of a high-sensor count fibre optic manometry catheter for in-vivo colonic diagnostics
  9. ^"Directive 98/79/CE on in vitro diagnostic medical devices".Archived from the original on 2021-10-21. Retrieved2013-10-10.
  10. ^"In Vitro Diagnostic (IVD) tests".European Diagnostic Manufacturers Association. Archived fromthe original on 23 April 2009.
  11. ^"Glucose Tests".Lab Tests Online UK. 14 November 2019.Archived from the original on 11 December 2011. Retrieved10 October 2013.
  12. ^ab"Liver Function Tests".Lab Tests Online UK. 10 January 2020.Archived from the original on 5 December 2011. Retrieved10 October 2013.
  13. ^"Electrolytes and Anion Gap".Lab Tests Online UK. 9 October 2019.Archived from the original on 27 November 2011. Retrieved10 October 2013.
  14. ^Altman DG, Bland JM. Diagnostic tests 1: sensitivity and specificity. BMJ. 1994;308(6943):1552.
  15. ^Deeks JJ, Altman DG. Diagnostic tests 4: likelihood ratios. BMJ. 2004;329:168.
  16. ^"Handbook for DTA Reviews". Cochrane. Retrieved6 April 2025.
  17. ^"Mediastinoscopy".Harvard Health. Harvard.edu. October 2016. Archived fromthe original on 6 October 2014.
  18. ^Diagnostic Tests > Pap Smear,Harvard University, archived fromthe original on June 8, 2007
  19. ^Mikael Häggström, M.D."Clinical pathology".Patholines.org. Retrieved2024-02-15.
  20. ^Jarvik J, Hollingworth W, Martin B, Emerson S, Gray D, Overman S, Robinson D, Staiger T, Wessbecher F, Sullivan S, Kreuter W, Deyo R (2003). "Rapid magnetic resonance imaging vs radiographs for patients with low back pain: a randomized controlled trial".JAMA.289 (21):2810–8.doi:10.1001/jama.289.21.2810.PMID 12783911.S2CID 22897506.
  21. ^Hall H (2019). "Too Many Medical Tests".Skeptical Inquirer.43 (3):25–27.
  22. ^Whiting PF, Rutjes AW, Westwood ME, Mallett S, Deeks JJ, Reitsma JB, Leeflang MM, Sterne JA, Bossuyt PM, et al. (QUADAS-2 Group) (October 2011). "QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies".Annals of Internal Medicine.155 (8):529–36.doi:10.7326/0003-4819-155-8-201110180-00009.PMID 22007046.

Further reading

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X-ray/
radiography
2D
CT scan
Techniques
Targets
Other
MRI
Ultrasound
Radionuclide
2D/scintigraphy
Full body
3D/ECT
SPECT (gamma ray)
PET (positron)
Optical/Laser
Thermography
Target conditions
Components and results ofurine tests
Components
Chemical properties
Abnormal findings
Red blood cells
White blood cells
Proteinuria
Small molecules
Other
Clinical biochemistryblood tests
Electrolytes
Acid-base
Iron tests
Hormones
Metabolism
Cardiovascular
Liver function tests
Pancreas
Small molecules
Blood sugar level
Nitrogenous
Proteins
LFT
Other
Complete blood count
Other tests ofred blood cells
Coagulation
Other
Medical tests onCerebrospinal fluid (CPT 82000-84999)
Albumin
Glucose
Other
Medical tests used inimmunology (CPT 86000–86849)
Immunoprecipitation
Immunoassay
Agglutination
Other
Blood products
General concepts
Methods
Tests
Transfusion reactions
and adverse effects
Blood group systems
Bacterial infection
Viral infection
Protozoan infection
Bloodstream infections
General
Principles of pathology
Anatomical pathology
Clinical pathology
Heart
Central nervous system
Peripheral nervous system
Ears
Eyes
Digestive system
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