Wednesday, August 22, 2012

Management of VF arrest

Passive rewarming

  • Temperature is very important during rewarming as temperature commonly overshoots normal. Warming the patient too quickly or allowing continued shivering causes dangerous electrolyte shifts, leading to potentially lethal arrhythmias. 
  • Controlled rewarming of 0.15° to 0.5° C per hour is recommended. 
  • To maintain tight temperature control throughout rewarming a neuromuscular blockade is usually employed.  
  • Careful fluid monitoring during rewarming is crucial because of the vasodilation that accompanies a body temperature rise. Volume replacement may be needed to prevent fluid deficit and hypotension.
  • Electrolytes shift out of the cells back into the serum during rewarming, so frequent electrolyte monitoring is needed during this phase to prevent critically elevated levels. Slow, controlled rewarming allows the kidneys to excrete excess potassium, preventing hyperkalemia. 
  • Hypoglycemia can occur during rewarming as the insulin resistance of earlier hypothermia phases diminishes. Glucose levels must be monitored frequently, with insulin titration and dextrose boluses used as needed to maintain the patient within ordered ranges.

References

  • http://www.americannursetoday.com/article.aspx?id=8014&fid=7986
  • http://ccforum.com/content/16/S2/A25/ 

Wednesday, May 4, 2011

DCR

DCR = cardioversion (direct current reversion)

References

Pantoprazole infusion

For actively bleeding ulcers give pantoprazole bolus followed by infusion.
  • LOading dose: Pantoprazole 80mg IV in 100ml of NaCl 0.9% or 5% glucose over 20 - 30 minutes
  • Infusion:
    • Pantoprazole 200mg in Dextrose 5% 500mL at 20mL/hr (each mL is 0.4mg , 20mL/hr = 8mg/hr, 1mg =2.5mL)
    • Pantoprazole 80mg in N/Saline 100mL at 10mL/hr (each mL is 0.8mg , 10mL/hr = 8mg/hr,1mg=1.25mL)

References

Tuesday, January 25, 2011

Blood Gas normal values

 





































ArterialVenous
pH7.35-7.457.3-7.35
pCO235-4545-46 (good representation of ventilation)
pO280-10020-80 (uninterprable)
SaO295-100
HCO3-22-28
BE+/- 3

 

Tuesday, December 7, 2010

Resources for lumbar puncture

  • http://www.med.uottawa.ca/procedures/lp/index.htm
  • http://www.articlealley.com/article_596234_17.html
  • http://www.unboundmedicine.com/harrisons/ub/view/Harrisons-Manual-of-Medicine/148408/all/Lumbar_Puncture,

Tuesday, November 30, 2010

Resources for central line insertion

Central lines in general

  • http://egret.psychol.cam.ac.uk/medicine/Central_line_insertion.pdf
  • http://www.nda.ox.ac.uk/wfsa/html/u12/u1213_01.htm
  • http://www.proceduresconsult.com/medical-procedures/central-venous-line-placement-AN-procedure.aspx

Internal jugular lines

  • http://www.anwresidency.com/simulation/guide/ij.html

Sunday, May 9, 2010

AMIs and thrombolysis

ECG changes indicating AMI

  • High probability of MI: persistent ST elevation of ≥ 1 mm in two contiguous limb leads or ST-segment elevation of ≥ 2 mm in two contiguous chest leads or the presence of new LBBB.
  • Intermediate probability of MI: are ST depression, T-wave inversion, and other nonspecific ST-T wave abnormalities.
  • Q waves = old MI

DDxes

Management options

  • Patients with persistent ST elevation should be considered for reperfusion therapy (thrombolysis or primary PCI).
  • Those without ST elevation will be diagnosed with either NSTEMI if cardiac marker levels are elevated or with unstable angina if serum cardiac marker levels provide no evidence of myocardial injury. Patients presenting with no ST-segment elevation are not candidates for immediate thrombolytics but should receive anti-ischemic therapy and may be candidates for PCI urgently or during admission.

Medical Management

  • Aspirin (300 mg) should be given unless already taken or contraindicated (grade A recommendation), and should preferably be given early (eg, by emergency or ambulance personnel).
  • Clopidogrel should be given in addition to aspirin for patients undergoing PCI with a stent (loading-dose of 300–600 mg), or for fibrinolytic therapy (300 mg). Clopidogrel 75 mg daily should be continued for at least a month after fibrinolytic therapy, and for up to 12 months after stent implantation, depending on the type of stent.
  • Antithrombin therapy to inhibit the coagulation cascade, and for patients underdoing PCI. For patients getting streptokinase, whether to heparinise depends on the anti-thrombotic agent. Clexane (enoxaparin) bolus should be dosed at 0.75 mg/kg.
  • Administer a platelet glycoprotein (GP) IIb/IIIa-receptor antagonist (eptifibatide, tirofiban, or abciximab) in addition to aspirin and unfractionated heparin, to patients with continuing ischemia or with other high-risk features and to patients in whom PCI is planned.
  • An ACE inhibitor (Captopril) should be given orally within the first 24 hours of STEMI to patients with anterior infarction, pulmonary congestion, or left ventricular ejection fraction (LVEF) less than 40% in the absence of hypotension.
  • An angiotensin receptor blocker (valsartan or candesartan) should be administered to patients with STEMI who are intolerant of ACE inhibitors and who have either clinical or radiological signs of heart failure or LVEF less than 40%.

Contraindications for fibrinolytic use in STEMI

Absolute contraindications:
  • Prior intracranial hemorrhage (ICH)
  • Known structural cerebral vascular lesion
  • Known malignant intracranial neoplasm
  • Ischemic stroke within 3 months
  • Suspected aortic dissection
  • Active bleeding or bleeding diathesis (excluding menses)
  • Significant closed-head trauma or facial trauma within 3 months
Relative contraindications:
  • History of chronic, severe, poorly controlled hypertension
  • Severe uncontrolled hypertension on presentation (SBP >180 mm Hg or DBP >110 mm Hg)
  • Traumatic or prolonged (>10 min) CPR or major surgery less than 3 weeks
  • Recent (within 2-4 wk) internal bleeding
  • Noncompressible vascular punctures
  • For streptokinase/anistreplase - prior exposure or prior allergic reaction to these agents
  • Pregnancy
  • Active peptic ulcer
  • Current use of anticoagulant (eg, warfarin sodium) that has produced an elevated international normalized ratio (INR) >1.7 or prothrombin time (PT) >15 seconds

Follow-up Patient Care

  • Patients should continue to receive beta-blockers, nitrates, and heparin, as indicated.
  • ACE inhibitors have been shown to improve survival rates in patients who have experienced an MI. In the acute setting, afterload reduction from ACE inhibitors may reduce the risk of CHF and sudden death.

References