Eisenmenger’s syndrome diagnostic study of choice: Difference between revisions
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{{ | {{Template:Eisenmenger's syndrome}} | ||
{{CMG}}; {{ | {{CMG}}'''; Associate Editor(s)-In-Chief:''' {{AIA}}, [[Priyamvada Singh|Priyamavada Singh, MBBS]] [mailto:psingh13579@gmail.com], [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
== | ==Overview== | ||
=== | ==2018 ACC/AHA Guidelines for the Management of Adults With Congenital Heart Disease (DO NOT EDIT)<ref name="pmid30586767">Stout KK, Daniels CJ, Aboulhosn JA, Bozkurt B, Broberg CS, Colman JM et al. (2019) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=30586767 2018 AHA/ACC Guideline for the Management of Adults With Congenital Heart Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.] ''Circulation'' 139 (14):e698-e800. [http://dx.doi.org/10.1161/CIR.0000000000000603 DOI:10.1161/CIR.0000000000000603] PMID: [https://pubmed.gov/30586767 30586767]</ref>== | ||
[ | {| class="wikitable" | ||
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| colspan="1" style="text-align:center; background:LightGreen"|[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''1.''' Care of adult patients with [[CHD]]-related PAH should be performed in centers that have shared expertise and training in both ACHD and [[PAH]]. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''2.''' The evaluation of all ACHD patients with suspected PAH should include [[noninvasive]] assessment of [[cardiovascular]] [[anatomy]] and potential [[shunting]], as detailed below:<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''a.''' [[Pulse oximetry]], with and without administration of supplemental oxygen, as appropriate. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''b.''' [[Chest x-ray]]. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''c.''' [[ECG]]. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''d.''' Diagnostic cardiovascular imaging via [[TTE]], [[TEE]], [[MRI]], or [[CT]] as appropriate. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
[ | |- | ||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''e.''' [[Complete blood count]] and [[nuclear]] lung [[scintigraphy]]. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''3.''' If PAH is identified but its causes are not fully recognized, additional testing should include the following:<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''a.''' [[Pulmonary function test]]s with volumes and [[diffusion capacity]] (diffusing capacity of the lung for [[carbon monoxide]]). ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''b.''' [[Pulmonary embolism]]-protocol [[CT]] with parenchymal lung windows. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''c.''' Additional testing as appropriate to rule out contributing causes of PAH. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''d.''' [[Cardiac catheterization]] at least once, with potential for [[vasodilator]] testing or anatomic intervention, at a center with expertise in catheterization, PAH, and management of CHD-PAH. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
|} | |||
{| class="wikitable" | |||
{| | |||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon"| [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | |||
|- | |- | ||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''1.''' It is reasonable to include a 6-minute walk test or similar nonmaximal cardiopulmonary [[exercise test]] as part of the functional assessment of patients with [[CHD]]-[[PAH]]. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''<nowiki>"</nowiki> | |||
| | |||
|} | |} | ||
==== | ==References== | ||
{{reflist|2}} | |||
[[Category:Cardiology]] | |||
[[Category:Congenital heart disease]] | |||
[[Category:Pediatrics]] | |||
[[Category:Disease]] | |||
[Disease | |||
Latest revision as of 05:20, 27 January 2020
Eisenmenger’s syndrome Microchapters |
Diagnosis |
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Eisenmenger’s syndrome ACC/AHA Guidelines for Evaluation of Patients |
Treatment |
Eisenmenger’s syndrome diagnostic study of choice On the Web |
American Roentgen Ray Society Images of Eisenmenger’s syndrome diagnostic study of choice |
Eisenmenger’s syndrome diagnostic study of choice in the news |
Risk calculators and risk factors for Eisenmenger’s syndrome diagnostic study of choice |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Abdelrahman Ibrahim Abushouk, MD[2], Priyamavada Singh, MBBS [3], Kristin Feeney, B.S. [4]
Overview
2018 ACC/AHA Guidelines for the Management of Adults With Congenital Heart Disease (DO NOT EDIT)[1]
Class I |
"1. Care of adult patients with CHD-related PAH should be performed in centers that have shared expertise and training in both ACHD and PAH. (Level of Evidence: C)" |
"2. The evaluation of all ACHD patients with suspected PAH should include noninvasive assessment of cardiovascular anatomy and potential shunting, as detailed below:" |
"a. Pulse oximetry, with and without administration of supplemental oxygen, as appropriate. (Level of Evidence: C)" |
"b. Chest x-ray. (Level of Evidence: C)" |
"c. ECG. (Level of Evidence: C)" |
"d. Diagnostic cardiovascular imaging via TTE, TEE, MRI, or CT as appropriate. (Level of Evidence: C)" |
"e. Complete blood count and nuclear lung scintigraphy. (Level of Evidence: C)" |
"3. If PAH is identified but its causes are not fully recognized, additional testing should include the following:" |
"a. Pulmonary function tests with volumes and diffusion capacity (diffusing capacity of the lung for carbon monoxide). (Level of Evidence: C)" |
"b. Pulmonary embolism-protocol CT with parenchymal lung windows. (Level of Evidence: C)" |
"c. Additional testing as appropriate to rule out contributing causes of PAH. (Level of Evidence: C)" |
"d. Cardiac catheterization at least once, with potential for vasodilator testing or anatomic intervention, at a center with expertise in catheterization, PAH, and management of CHD-PAH. (Level of Evidence: C)" |
Class IIa |
"1. It is reasonable to include a 6-minute walk test or similar nonmaximal cardiopulmonary exercise test as part of the functional assessment of patients with CHD-PAH. (Level of Evidence: C)" |
References
- ↑ Stout KK, Daniels CJ, Aboulhosn JA, Bozkurt B, Broberg CS, Colman JM et al. (2019) 2018 AHA/ACC Guideline for the Management of Adults With Congenital Heart Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation 139 (14):e698-e800. DOI:10.1161/CIR.0000000000000603 PMID: 30586767