http://www.med-ed.virginia.edu/pda/refcards/HemLab/index.htm
All basic info about lab values.
J Apinyawat; A pharmacist in northern Michigan gathering some quick references that may come in handy when needed especially for hospital pharmacist.
Thursday, August 20, 2009
Friday, April 10, 2009
Antibiotic dosing in CRRT patients

Continuous renal replacement therapy or CRRT is frequently used to treat patients with acute renal failure or chronic renal failure.
Ref: University of Pennsylvania Health System - Renal Electrolyte and Hypertension Division
http://www.uphs.upenn.edu/renal/important%20pdf%20II/CRRT%20antibiotic%20dosing.pdf
Sunday, March 22, 2009
UCSF: Infectious Diseases Management Program
Updated antimicrobial guideline in Adults, Pediatrics.
Latest updated 03/06/09
Very good for quick reference. Click Here
Latest updated 03/06/09
Very good for quick reference. Click Here
Sunday, February 22, 2009
The Heart dot Org - part of WebMD
contains anything from ACS, HTN, HF to surgery guideline
plus related news update quite often
http://www.theheart.org/
good for practical guidelines and cool Video CME lectures
plus related news update quite often
http://www.theheart.org/
good for practical guidelines and cool Video CME lectures
Wednesday, February 18, 2009
U of Penn - Department of Medicine - Educational Resources
http://www.uphs.upenn.edu/medicine/education/residents/educationalResources/index.html [not working]
http://pennfm.pbworks.com/Intern-Survival-Guide
Intern Survival Guide
Clinical Guidelines
Textbooks and Journals
Other Links
2006
http://pennfm.pbworks.com/Intern-Survival-Guide
Intern Survival Guide
Clinical Guidelines
Textbooks and Journals
Other Links
2006
L-Carnitine in VPA overdose
L-carnitine supplementation is recommended for patients with CNS depression, evidence of hepatic dysfunction, and hyperammonemia with dosing ranging from 50 to 100 mg/kg/day up to a maximum dose of 2 g/day.
L-carnitine's mechanism of action is thought to be related to its ability to decrease elevated ammonia levels, which may contribute to development of coma in VPA toxicity. Its use remains investigational but can be considered in patients (such as ours) with coma, elevated ammonia levels, and hepatic dysfunction.[1] In our patient, we elected to start her on L-carnitine at 100 mg/kg/day in an attempt to correct her hyperammonemia and encephalopathy. This therapy was continued until her serum ammonia and VPA levels had normalized.
Other Tx for VPA overdose;
Supportive, naloxone, hemodialysis, hemoperfusion
Ref: Medscape
http://www.medscape.com/viewarticle/445062_print
L-carnitine's mechanism of action is thought to be related to its ability to decrease elevated ammonia levels, which may contribute to development of coma in VPA toxicity. Its use remains investigational but can be considered in patients (such as ours) with coma, elevated ammonia levels, and hepatic dysfunction.[1] In our patient, we elected to start her on L-carnitine at 100 mg/kg/day in an attempt to correct her hyperammonemia and encephalopathy. This therapy was continued until her serum ammonia and VPA levels had normalized.
Other Tx for VPA overdose;
Supportive, naloxone, hemodialysis, hemoperfusion
Ref: Medscape
http://www.medscape.com/viewarticle/445062_print
Saturday, December 27, 2008
Notes from Dr. RW
http://doctorrw.blogspot.com/
A hospitalist from Akansas - good blog for interesting med related news summary/review/clinical trials ect.
A hospitalist from Akansas - good blog for interesting med related news summary/review/clinical trials ect.
Friday, December 12, 2008
Tuesday, December 9, 2008
Sunday, September 21, 2008
Narc Conversion Guide
http://www.nhhpco.org/opioid.htm
New Hampshire Hospice and Palliative Care Organization
This Opioid Use Guidelines have been prepared by the NHHPCO Palliative Care Clinicians Special Interest Group as part of their 'Best Practices Project'.
Steps to Rotate or Change Opioids
1. Calculate 24 hr dose of current drug.
2. Translate that to equianalgesic 24 hr dose of oral morphine.
3. Calculate 24 hr equianalgesic dose of new drug and reduce dose to 50-75% of calculated dose if pain is well controlled; use 100% otherwise.
4. Divide to attain appropriate interval and dose for new drug.
5. Always have breakthrough dosing available while making changes.
New Hampshire Hospice and Palliative Care Organization
This Opioid Use Guidelines have been prepared by the NHHPCO Palliative Care Clinicians Special Interest Group as part of their 'Best Practices Project'.
Steps to Rotate or Change Opioids
1. Calculate 24 hr dose of current drug.
2. Translate that to equianalgesic 24 hr dose of oral morphine.
3. Calculate 24 hr equianalgesic dose of new drug and reduce dose to 50-75% of calculated dose if pain is well controlled; use 100% otherwise.
4. Divide to attain appropriate interval and dose for new drug.
5. Always have breakthrough dosing available while making changes.
Sunday, August 24, 2008
OHSU Pharmacy Pearls (Guidelines)
http://www.ohsu.edu/medicine/residency/handouts/pharmpearls/
Aminoglycoside in Dialysis pts, Conivaptan, ICU drugs, Electrolyte replacement ect
Aminoglycoside in Dialysis pts, Conivaptan, ICU drugs, Electrolyte replacement ect
Saturday, August 23, 2008
LMWH Bridging
http://www.med.umich.edu/cvc/services/site_anticoag/healthprof.html
From U of M Cardiovascular Center
From U of M Cardiovascular Center

Thursday, August 21, 2008
A review of warfarin dosing and monitoring
Mariamma Kuruvilla, PharmD and Cheryle Gurk-Turner, RPH
The goal of anticoagulant therapy with warfarin is to administer the lowest effective dose of the drug to maintain the target international normalized ratio (INR). Warfarin, a vitamin K antagonist, is an oral anticoagulant indicated for the prevention and treatment of venous thrombosis and its extension and the prevention and treatment of the thromboembolic complications associated with atrial fibrillation. Warfarin has also been used to prevent recurrent transient ischemic attacks and to reduce the risk of recurrent myocardial infarction, but data supporting these indications are inconclusive at this time (1).
The goal of anticoagulant therapy with warfarin is to administer the lowest effective dose of the drug to maintain the target international normalized ratio (INR). Warfarin, a vitamin K antagonist, is an oral anticoagulant indicated for the prevention and treatment of venous thrombosis and its extension and the prevention and treatment of the thromboembolic complications associated with atrial fibrillation. Warfarin has also been used to prevent recurrent transient ischemic attacks and to reduce the risk of recurrent myocardial infarction, but data supporting these indications are inconclusive at this time (1).
Warfarin inhibits the synthesis of clotting factors II, VII, IX, and X, as well as the naturally occurring endogenous anticoagulant proteins C and S (2). The anticoagulant and antithrombotic activity of warfarin depends on the clearance of functional clotting factors from the systemic circulation once the drug is administered (2, 3). The earliest changes in INR are typically seen 24 to 36 hours after administration of the dose. The antithrombotic effect of warfarin is not present until approximately the fifth day of therapy, which is dependent on the clearance of prothrombin (1, 2).
Initiation of warfarin therapy is challenging, since the pharmacodynamic response is delayed and difficult to predict. Because prothrombin has a half-life of around 50 hours, loading doses of warfarin are of limited value (4). In clinical practice, loading doses (e.g., 7.5 mg or more per day) of warfarin may increase the patient's risk of bleeding complications early in therapy by eliminating the production of functional factor VII (2, 5). Administration of loading doses may place a patient in a hypercoagulable state due to a severe depletion of protein C (2). The administration of a loading dose is a possible source of prolonged hospitalization secondary to dramatic rises in the INR value that may necessitate the administration of vitamin K (5). If a rapid anticoagulant effect is required, an initial dose of heparin or a low molecular-weight heparin should be used and overlapped with warfarin for approximately 4 to 5 days. Once the INR is therapeutic for at least 2 days, the supplemental anticoagulation treatment may be discontinued. (more)Tuesday, August 5, 2008
Thursday, July 10, 2008
Saturday, May 17, 2008
Saturday, March 8, 2008
Monday, February 25, 2008
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