Syncope resident survival guide: Difference between revisions
Jump to navigation
Jump to search
Line 24: | Line 24: | ||
===Syncope in the Context of Transient [[LOC]]=== | ===Syncope in the Context of Transient [[LOC]]=== | ||
{{familytree/start}} | {{familytree/start}} | ||
{{familytree | | | | | | | | | {{familytree | | | | | | | A01 | | |A01= Determine if there was [[LOC]] }} | ||
{{familytree | {{familytree | | | |,|-|-|-|^|-|-|.| | | }} | ||
{{familytree | | | B01 | {{familytree | | | B01 | | | | | B02 | | |B01= '''Yes:''' <br> <br> <div style="float: left; text-align: left;"> ❑ It had a rapid onset? <br> ❑ It was of short duration? <br> ❑ Did the patient had a spontaneous <br> complete recovery? </div> |B02='''No:''' <br> <div style="float: left; text-align: left;height: 6em; width: 20em; padding:1em;"> ❑ [[Cataplexy]] <br> ❑ Drop attacks, falls <br> ❑ Functional /psychogenic pseudosyncope <br> ❑ [[TIA]] of carotid origin </div>}} | ||
{{familytree | |,|-|^|-|.| | | | | | | | | }} | {{familytree | | |,|-|^|-|.| | | | | | | | | }} | ||
{{familytree | C01 | | C02 | | | | | | |C01=''' | {{familytree | | C01 | | C02 | | | | | | |C01='''No to ≥ 1:''' <br> (exclude the following before <br> proceeding with syncope evaluation) <br> <div style="float: left; text-align: left;"> ❑ [[Coma]] <br> ❑ Aborted [[Sudden Cardiac Death|SCD]] <br> ❑ [[Epilepsy]] | ||
{{familytree | | | |,|-|^|-|.| | | | | | }} | :❑ Perform neurological evaluation | ||
{{familytree | | | E01 | | E02 | | |E01= Non traumatic |E02= Traumatic }} | :❑ Perform tilt testing, preferably with concurrent EEG <br> and video monitoring if doubt of mimicking epilepsy <br> | ||
{{familytree | | | | | ❑ Metabolic disorders: | ||
{{familytree | | | | :❑ [[Hypoglycemia]] | ||
:❑ [[Hypoxia]] | |||
:❑ [[Hyperventilation]] with [[hypocapnia]] <br> | |||
❑ [[Intoxication]] <br> ❑ Vertebrobasilar [[TIA]]</div> |C02='''Yes:''' <br> <br> ❑ Transient [[LOC]]}} | |||
{{familytree | | | | |,|-|^|-|.| | | | | | }} | |||
{{familytree | | | | E01 | | E02 | | |E01= Non traumatic |E02= Traumatic }} | |||
{{familytree | |,|-|-|+|-|-|-|.| | | | | | | | | }} | |||
{{familytree |F01 | |F02 | | F03 | | | ||F01='''Syncope''' | F02=[[Seizure]] |F03= Psychogenic }} | |||
{{familytree/end}} | {{familytree/end}} | ||
Revision as of 20:48, 28 February 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Karol Gema Hernandez, M.D. [2]
Definition
Syncope is defined as a transient loss of consciousness due to cerebral hypoperfusion, characterized by a rapid onset, a short duration and a spontaneous complete recovery.
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
Management
Syncope in the Context of Transient LOC
Determine if there was LOC | |||||||||||||||||||||||||||||||||||
Yes: ❑ It had a rapid onset? ❑ It was of short duration? ❑ Did the patient had a spontaneous complete recovery? | No: | ||||||||||||||||||||||||||||||||||
No to ≥ 1: (exclude the following before proceeding with syncope evaluation) ❑ Coma ❑ Aborted SCD ❑ Epilepsy
❑ Metabolic disorders:
❑ Vertebrobasilar TIA | Yes: ❑ Transient LOC | ||||||||||||||||||||||||||||||||||
Non traumatic | Traumatic | ||||||||||||||||||||||||||||||||||
Syncope | Seizure | Psychogenic | |||||||||||||||||||||||||||||||||
Diagnostic Flowchart in Patients with Suspected Syncope
Syncope | T-LOC non syncopal | ||||||||||||||||||||||||||||||||||||||||||||||
Certain diagnosis: Treat as according | Uncertain etiology | ❑ Confirm with specific test: OR ❑ Consult with specialist | |||||||||||||||||||||||||||||||||||||||||||||
If arrhythmic cause identified: (EPS) | Risk stratification | ||||||||||||||||||||||||||||||||||||||||||||||
Determine if there are any high risk criteria: ❑ Severe structural or CAD ❑ Clinical orECG features suggesting arrhythmic syncope: -Syncope during exertion or supine -Palpitations at the time of syncope -Family history ofSCD -Non-sustained VT -Conduction abnormalities with QRS >120 ms -Sinus bradycardia -Pre-exited QRS complex -Prolonged or short QR interval -Brugada pattern -ARVC ❑ Important comorbidities: -Severe anemia -Electrolyte intolerance | |||||||||||||||||||||||||||||||||||||||||||||||
❑ If yes: High risk | ❑ If no: Low risk | ||||||||||||||||||||||||||||||||||||||||||||||
Immediate in-hospital monitoring: In bed or telemetry | |||||||||||||||||||||||||||||||||||||||||||||||
Low risk, recurrent syncopes: ❑ Cardiac or neurally mediated tests as appropriate: -Holter if >1 episode/week -ELR if interval between episodes <4 weeks Delayed treatment guided by ECK documentation | Low risk, single syncope | ||||||||||||||||||||||||||||||||||||||||||||||
❑ If suspicion of structural heart disease: Echocardiography | Was it in high risk setting? | ||||||||||||||||||||||||||||||||||||||||||||||
If yes: Treat as according | No structural heart disease | Yes | No: No further evaluation | ||||||||||||||||||||||||||||||||||||||||||||
Tilt testing | |||||||||||||||||||||||||||||||||||||||||||||||
Treatment of Syncope
Reflex and orthostatic intolerance | Cardiac | Unexplained and high risk SCD | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Unpredictable or high- frequency | Predictable or low frequency | Cardiac arrythmias SCD | Structural (cardiac or pulmonary) | i.e. CAD, HOCM, ARV, channelopathies | |||||||||||||||||||||||||||||||||||||||||||||||||||
Consider specific therapy or delayed treatment based by ECG documentation | Education, reassurance, avoidance of triggers | Specfic therapy of the culprit arrythmia | Treatment of underlying disease | Consider ICD therapy | |||||||||||||||||||||||||||||||||||||||||||||||||||
Algorithms based in 2009 ESC Guidelines for the Diagnosis and Management of Syncope. [3]
Do's
- Tilt testing is indicated when it is of clinical value to demonstrate susceptibility to reflex syncope to the patient.
- Tilt testing should be considered to discriminate between reflex and OH syncope.
- Perform tilt testing if psychiatric disease.
- Tilt testing may be considered for differentiating syncope with jerking movements from epilepsy.
- If syncope happened after standing up position, there should be documentation with active standing or tilt testing in order to diagnose OH.
- Perform CSM if patient >40 years with syncope of unknown aetiology after initial evaluation.
- If multiple unexplained falls; perform tilt testing.
- Consider ILR before embarking on cardiac pacing in patients with suspected or certain reflex syncope presenting with frequent or traumatic syncopal episodes.
- Evaluate neurologically if syncope is due to ANF, to evaluate underlying disease.
Don'ts
- Don't perform carotid sinus massage (CSM) in patients with previous TIA or stroke within the past 3 months and in patients with carotid sinus bruits (except if carotid sinus Doppler studies excluded significant stenosis.
- Don't use tilt testing for assessment of treatment.
- Don't perform isoproterenol tilt testing in patients with ischaemic heart disease.
- Don't use ATP test as a diagnostic test to select patients for cardiac pacing, owing to lack of correlation with spontaneous syncope,.
- Don't perform EPS if there is already indication for ICD in patients with ischemic heart with suspected arrhythmic cause.
- Don't perform EPS in patients with normal ECK, no heart disease, and no palpitations.
References
- ↑ Khoo, C.; Chakrabarti, S.; Arbour, L.; Krahn, AD. (2013). "Recognizing life-threatening causes of syncope". Cardiol Clin. 31 (1): 51–66. doi:10.1016/j.ccl.2012.10.005. PMID 23217687. Unknown parameter
|month=
ignored (help) - ↑ Kapoor, WN. (2000). "Syncope". N Engl J Med. 343 (25): 1856–62. doi:10.1056/NEJM200012213432507. PMID 11117979. Unknown parameter
|month=
ignored (help) - ↑ Task Force for the Diagnosis and Management of Syncope. European Society of Cardiology (ESC). European Heart Rhythm Association (EHRA). Heart Failure Association (HFA). Heart Rhythm Society (HRS). Moya A; et al. (2009). "Guidelines for the diagnosis and management of syncope (version 2009)". Eur Heart J. 30 (21): 2631–71. doi:10.1093/eurheartj/ehp298. PMC 3295536. PMID 19713422 Check
|pmid=
value (help).