Cystic fibrosis diagnostic study of choice: Difference between revisions
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=== Study of choice: === | === Study of choice: === | ||
* | * The sweat chloride test is the gold standard test for the diagnosis of cystic fibrosis.<ref name="pmid28538779">{{cite journal |vauthors=Servidoni MF, Gomez CCS, Marson FAL, Toro AADC, Ribeiro MÂGO, Ribeiro JD, Ribeiro AF |title=Sweat test and cystic fibrosis: overview of test performance at public and private centers in the state of São Paulo, Brazil |journal=J Bras Pneumol |volume=43 |issue=2 |pages=121–128 |date= 2017 |pmid=28538779 |pmc=5474375 |doi=10.1590/S1806-37562016000000076 |url=}}</ref> | ||
* The sweat chloride test should be performed when:<ref name="pmid28129811">{{cite journal |vauthors=Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, Howenstine M, McColley SA, Rock M, Rosenfeld M, Sermet-Gaudelus I, Southern KW, Marshall BC, Sosnay PR |title=Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation |journal=J. Pediatr. |volume=181S |issue= |pages=S4–S15.e1 |date=February 2017 |pmid=28129811 |doi=10.1016/j.jpeds.2016.09.064 |url=}}</ref> | * The sweat chloride test should be performed when:<ref name="pmid28129811">{{cite journal |vauthors=Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, Howenstine M, McColley SA, Rock M, Rosenfeld M, Sermet-Gaudelus I, Southern KW, Marshall BC, Sosnay PR |title=Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation |journal=J. Pediatr. |volume=181S |issue= |pages=S4–S15.e1 |date=February 2017 |pmid=28129811 |doi=10.1016/j.jpeds.2016.09.064 |url=}}</ref> | ||
** Positive newborn screening | ** Positive newborn screening | ||
** Signs and/or symptoms of cystic fibrosis | ** Signs and/or symptoms of cystic fibrosis | ||
** Positive family history | ** Positive family history | ||
===== Diagnostic results ===== | ===== Diagnostic results ===== | ||
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The [name of investigation] should be performed when: | The [name of investigation] should be performed when: | ||
* The patient presented with symptoms/signs 1, 2, and 3 as the first step of diagnosis. | * The patient presented with symptoms/signs 1, 2, and 3 as the first step of diagnosis. | ||
* A positive [test] is detected in the patient, to confirm the diagnosis. | * A positive [test] is detected in the patient, to confirm the diagnosis.<br> | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} |
Revision as of 15:12, 23 February 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]
Overview
Diagnostic Study of Choice
Template statements
Study of choice:
- The sweat chloride test is the gold standard test for the diagnosis of cystic fibrosis.[1]
- The sweat chloride test should be performed when:[2]
- Positive newborn screening
- Signs and/or symptoms of cystic fibrosis
- Positive family history
Diagnostic results
The following result of [investigation name] is confirmatory of [disease name]:
- Result 1
- Result 2
Sequence of Diagnostic Studies
The [name of investigation] should be performed when:
- The patient presented with symptoms/signs 1, 2, and 3 as the first step of diagnosis.
- A positive [test] is detected in the patient, to confirm the diagnosis.
References
- ↑ Servidoni MF, Gomez C, Marson F, Toro A, Ribeiro M, Ribeiro JD, Ribeiro AF (2017). "Sweat test and cystic fibrosis: overview of test performance at public and private centers in the state of São Paulo, Brazil". J Bras Pneumol. 43 (2): 121–128. doi:10.1590/S1806-37562016000000076. PMC 5474375. PMID 28538779. Vancouver style error: initials (help)
- ↑ Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, Howenstine M, McColley SA, Rock M, Rosenfeld M, Sermet-Gaudelus I, Southern KW, Marshall BC, Sosnay PR (February 2017). "Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation". J. Pediatr. 181S: S4–S15.e1. doi:10.1016/j.jpeds.2016.09.064. PMID 28129811.