Sandbox vidit3: Difference between revisions
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'''Diagnostic criteria''' </div> | '''Diagnostic criteria''' </div> | ||
---- | ---- | ||
❑ '''Cardiovascular''' | |||
: ❑ [[Arrhythmia]] and cardiac ischemia-related [[syncope]] is diagnosed by [[EKG]] specific findings ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]]) | : ❑ [[Arrhythmia]] and cardiac ischemia-related [[syncope]] is diagnosed by [[EKG]] specific findings ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]]) | ||
: ❑ Cardiovascular syncope is diagnosed when [[syncope]] presents with [[structural heart disease]] ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]])<br> | : ❑ Cardiovascular syncope is diagnosed when [[syncope]] presents with [[structural heart disease]] ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]])<br> | ||
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: ❑ Diagnosed when [[syncope]] occurs after standing up and there is documentation of [[OH]]. ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]])<br> | : ❑ Diagnosed when [[syncope]] occurs after standing up and there is documentation of [[OH]]. ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]])<br> | ||
❑ '''Reflex''' | ❑ '''Reflex''' | ||
: ❑ [[Vasovagal syncope]]: if is precipitated by emotional distress and is associated with typical [[ | : ❑ [[Vasovagal syncope]]: if is precipitated by emotional distress and is associated with typical [[prodrome]]. ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]]) | ||
: ❑ Situational [[syncope]]: if occurs during or after specific [[Vasovagal syncope#Triggers|triggers]]. ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]]) | : ❑ Situational [[syncope]]: if occurs during or after specific [[Vasovagal syncope#Triggers|triggers]]. ([[ESC#Classes of Recommendations|Class I; Level of Evidence: C]]) | ||
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'''Risk stratification''' | '''Risk stratification''' | ||
---- | ---- | ||
'''Determine if there are any high risk criteria:''' <br> | '''Determine if there are any high risk criteria:''' <br> ❑ Severe [[structural heart disease]] <br> ❑ [[CAD]]<br> ❑ Clinical or [[ECG]] features suggesting arrhythmic syncope: <br> | ||
: ❑ [[Syncope]] during exertion or [[supine]] | : ❑ [[Syncope]] during exertion or [[supine]] | ||
: ❑ [[Palpitations]] at the time of [[syncope]] | : ❑ [[Palpitations]] at the time of [[syncope]] | ||
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❑ Important comorbidities: | ❑ Important comorbidities: | ||
: ❑ Severe [[anemia]] | : ❑ Severe [[anemia]] | ||
: ❑ [[Electrolyte disturbance]] | : ❑ [[Electrolyte disturbance]] </div> | ||
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Revision as of 17:34, 26 March 2014
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❑ Prodrome:
❑ Chest pain (suggestive of cardiovascular syncope)
❑ Activity prior to LOC: (suggestive of cardiovascular or reflex syncope)
❑ Bowel or bladder incontinence (suggestive of reflex syncope) Inquire about medications intake:
Obtain a detailed past medical history:
❑ Cardiovascular disease:
❑ Neurological diseases: ❑ Metabolic disorders (diabetes) ❑ Recent trauma
Identify possible triggers: Suggestive of cardiovascular or orthostatic hypotension
Examine the patient
Vitals
Respiratory Cardiovascular
Neurologic
❑ Glasgow coma scale
Order labs and tests
❑ Glucose (rule out hypoglycemia)
Confirm diagnosis of syncope
Must have this 3 characteristics: ❑ Short duration
❑ Rapid onset ❑ Complete spontaneous recovery
Diagnostic criteria
❑ Cardiovascular
❑ Orthostatic hypotension (OH)
❑ Reflex
Determine if there are any high risk criteria:
❑ Important comorbidities:
Consider alternative diagnoses:
|
Drug | Adult dosage |
---|---|
Inhaled Short Acting β Agonists (SABA) | |
Albuterol/Bitolterol/Pirbuterol a) Nebulizer solution b) MDI | ♦ 2.5-5 mg every 20 minutes for 3 doses, then 2.5-10 mg every 1-4 hours as needed or 10-15 mg/hour continuously. ♦ 4-8 puffs every 20 mins upto 4 hours, then every 1-4 hours as needed. |
Levalbuterol a) Nebulizer solution b) MDI | ♦ 1.25-2.5 mg every 20 mins for 3 doses, then 1.25-5 mg every 1-4 hours as needed. ♦ 4-8 puffs every 20 mins upto 4 hours, then every 1-4 hours as needed. |
Anticholinergics | |
Ipratropium bromide a) Nebulizer solution b) MDI | ♦ 0.5 mg every 20 mins for 3 doses, then as needed. ♦ 8 puffs every 20 mins as needed for upto 3 hours. |
Ipratropium with albuterol a) Nebulizer solution (each 3 ml containing 0.5 mg ipratropium and 2.5 mg albuterol) b) MDI (each puff contains 18 mcg ipratropium and 90 mcg albuterol) | ♦ 3 ml every 20 mins for 3 doses, then as needed. ♦ 8 puffs every 20 mins as needed for 3 hours |
Systemic corticosteroids | |
Prednisone/Prednisolone/Methylprednisolone | ♦ 40-80 mg/day in 1 or 2 divided doses until peak expiratory flowrate (PEF) reaches 70% of personal best. |
Clinical course | Unstable |
---|---|
Physical examination | Signs of heart failure |
Functional class | IV |
6MWD | Less than 400 m |
Echocardiogram | RV Enlargement |
Hemodynamics | RAP high CI low |
BNP | Elevated/Increasing |
Treatment | Intravenous prostacyclin and/or combination treatment |
Frequency of evaluation | Q 1 to Q 3 months |
FC assessment | Every clinic visit |
6MWT | Every clinic visit |
Echocardiogram2 | Q 6 to Q 12 months/center dependent |
BNP | center dependent |
RHC | Q 6 to Q 12 months or clinical deterioration |