Primary ciliary dyskinesia screening: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
 
(4 intermediate revisions by 2 users not shown)
Line 5: Line 5:
==Overview==
==Overview==


There is insufficient evidence to recommend routine screening for [disease/malignancy].  
There is insufficient [[evidence]] to recommend routine [[screening]] for primary ciliary dyskinesia, however patients with persistent [[sinusitis]], [[rhinitis]], and no known [[etiology]] should be screened by [[Nitric oxide|nasal nitric oxide test]], low levels of nasal [[nitric oxide]] is diagnostic of primary ciliary dyskinesia and should prompt further testing with [[biopsy]] and ciliary beat pattern(CBP).


OR
According to the [guideline name], screening for [disease name] is not recommended.
OR
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3].
==Screening==
==Screening==
There is insufficient evidence to recommend routine screening for [disease/malignancy].
There is insufficient evidence to recommend routine [[screening]] for [[primary ciliary dyskinesia]], however patients with persistent [[sinusitis]], [[rhinitis]], and no known [[etiology]] should be screened by nasal [[nitric oxide]] test, low levels of nasal [[nitric oxide]] is [[diagnostic]] of primary ciliary dyskinesia and should prompt further testing with [[biopsy]] and ciliary beat pattern(CBP).  


OR
*Nasal nitric oxide test is more reliable in children above 5 years old and in adults because of difficult techniques and interpretation.
 
*Saccharine test is performed to assess transport in the nose and [[mucociliary clearance]].<ref name="pmid/10.1080/01913120590951220">{{cite journal| author=Schmoldt A, Benthe HF, Haberland G| title=Digitoxin metabolism by rat liver microsomes. | journal=Biochem Pharmacol | year= 1975 | volume= 24 | issue= 17 | pages= 1639-41 | pmid=/10.1080/01913120590951220 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10  }} </ref>
According to the [guideline name], screening for [disease name] is not recommended.
 
OR
 
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with:
*[Condition 1]
*[Condition 2]
*[Condition 3]


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


[[Category:Genetic disorders]]
[[Category:Genetic disorders]]

Latest revision as of 12:48, 23 September 2021

Primary ciliary dyskinesia Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Primary ciliary dyskinesia from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Interventions

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Primary ciliary dyskinesia screening On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Primary ciliary dyskinesia screening

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Primary ciliary dyskinesia screening

CDC on Primary ciliary dyskinesia screening

Primary ciliary dyskinesia screening in the news

Blogs on Primary ciliary dyskinesia screening

Directions to Hospitals Treating Primary ciliary dyskinesia

Risk calculators and risk factors for Primary ciliary dyskinesia screening

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Hafsa Ghaffar, M.B.B.S[2]

Overview

There is insufficient evidence to recommend routine screening for primary ciliary dyskinesia, however patients with persistent sinusitis, rhinitis, and no known etiology should be screened by nasal nitric oxide test, low levels of nasal nitric oxide is diagnostic of primary ciliary dyskinesia and should prompt further testing with biopsy and ciliary beat pattern(CBP).

Screening

There is insufficient evidence to recommend routine screening for primary ciliary dyskinesia, however patients with persistent sinusitis, rhinitis, and no known etiology should be screened by nasal nitric oxide test, low levels of nasal nitric oxide is diagnostic of primary ciliary dyskinesia and should prompt further testing with biopsy and ciliary beat pattern(CBP).

  • Nasal nitric oxide test is more reliable in children above 5 years old and in adults because of difficult techniques and interpretation.
  • Saccharine test is performed to assess transport in the nose and mucociliary clearance.[1]

References

  1. Schmoldt A, Benthe HF, Haberland G (1975). "Digitoxin metabolism by rat liver microsomes". Biochem Pharmacol. 24 (17): 1639–41. PMID /10.1080/01913120590951220 Check |pmid= value (help).


Template:WH Template:WS