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Target Audience: Mandatory for Clinical Team Members / Open to all Healthcare Providers
Estimated Time of Completion: 8 minutes

Access module

Target Audience: All Staff
Estimated Time of Completion: 30 minutes

Access module

Target Audience: All Staff
Estimated Time of Completion: 30 minutes

Access module

The 2025 Accreditation and Standards packages are now ready. Staff are to complete appropriate sections based on the descriptions available on the self-learning module. Other interested stakeholders (i.e. emergency response services, diagnostic services who work within our service delivery organization) are welcome to also complete the packages. If you have questions please contact your site program educator.

Please print and post this poster as deemed appropriate for staff use.

Submitted by: Tara Stewart, Manager – Clinical Initiatives and Mentorship

Please be advised the following monographs have been updated on the Drug Monographs page. For IV Parenteral Drug Manual holders, please add/replace/discard as indicated.

REPLACE ADULT Monograph:
Discard the old monograph, PRINT (using the hyperlink) & replace with the new monograph in the Adult Parenteral Drug Monograph Manual as listed below:

Medication/TopicApproved Changes
ampicillinReconstitution: Added 1g vials of Auro and Eugia brands NOT MINI BAG PLUS compatible
caspofunginAvailable as: Added CANCIDAS (Merck brand) and Juno brand, Fresenius Kabi brand: Store at room temperature.
Reconstitution: Added Table
IV Intermittenet: Added Table
Max/Single Daily Dose increased to 150mg
DAPTOmycinAdded: Juno Brand
desmopressionAdded: Cushings Diagnostic Test, hyponatremia
Compatability: Added Unknown compatibility with Ringer’s lactate and D5W
dextroseIV Infusion: Changed 500mL to 400mL D50W
DOPamineSoft Low Dose Limit: Decreased to 0.5mcg
IV Infusion: Added Increase by 1 to 5 mcg/kg/min every 10 minutes
enoxaparinOther Names: Added Redesca
Available As: Added 150mg PFS
Dosage: Under Non STEMI/unstable angina patients (regardless of age), maximum dose increased to 150 mg and added Exact dosage will depend if using multi dose vial or pre-filled syringes, and if the CrCl is less than 30 mL/min give daily,
Under STEMI (with te-necteplase) patients less than 75 years old: Added dose banding table. Pulmonary Embo-lism (PERT protocol)
Maximum single subcutaneous dose 150 mg
Additional Notes: Updated
EPINEPHrineDosage: Hypotension refractory to dopamine/dobutamine: Added Increase by doubling the dose (or by 0.02 mcg/kg/min) every 3 to 15 minutes until desired effect
Bradycardia: Added Initial 2 to 10 mcg/minute. Usual range 8 to 40 mcg/minute
esmololAdditional Notes: Limited data for use beyond 24 hours
fentaNYLCompatability: Added Ringers Lactate
Ferric DerisomaltoseGeneric Name changed from iron isomaltoside to Ferric Derisomaltose
Dosage: Updated Table
flumazenilAdded: Contact the Manitoba/Ontario Poison Control Centre at 1-855-776-4766
fondaparinuxNew Monograph
fosphenytoinDosage: Added mg
furosemideAdministration Policy: Added IM Injection
IV Infusion changed 20mg/hour to 40 mg/hour
IV bolus maxium changed from 20mg/minute to 40mg/minute
gentamicinIV Intermittent: Dose changed 100mL to 100mg
glucagonDosage: Removed beta blocker or calcium channel blocker overdose and anaphylaxis sections
inFLIXimabIV Intermittent: Added 0.2 micron filter
ketamine LOWDosage: IV bolus/IV intermittent changed 0.6mg/kg to 0.5mg/kg
Dosage: IV infusion changed 0.15mg/kg/hour to 0.25mg/kg/hour
metoprololDosage: Updated Acute treatment of arrhythmias section
pantoprozoleIV intermittent: Added JAMP brand NOT MINI BAG PLUS compatible
piperacillin-tazobactamReconstitution Dilution Administration: Added 4.5 g vials of Auro and Eugia brands are NOT MINI BAG PLUS compatible
protamine sulfateDosage: Added maximum of 50mg protamine per dose
SUFentanilIV Infusion: Added non-PVC
sugammadexUpdated precautions and additional notes

Submitted by: Cécile Dumesnil, Manager – Pharmacy
For more info. contact: 204-371-5952 or

CADHAM PROVINCIAL LABORATORY

Beginning January 1, 2025, new cases of syphilis detected by Cadham Provincial Laboratory (CPL) using serologic techniques will no longer be routinely confirmed by Treponema pallidum particle agglutination (TPPA).

All syphilis serologic investigation tends to begin with the CMIA syphilis screen test. As a rule, syphilis cases (beyond the early incubation period) will be positive by CMIA syphilis screen test. All screen test positive individuals will then have syphilis titres checked using the Rapid Plasma Reagin (RPR) test. Most new cases of syphilis have mid- to high RPR titres, and in the past have uniformly confirmed using TPPA. TPPA confirmation will no longer routinely be performed on these types of specimens.

TPPA confirmation will continue to be routinely be performed in the following circumstances:

  • CMIA screen positive but RPR negative specimens
  • Borderline CMIA positive specimens, regardless of RPR titre

Retrospective studies of recent CPL syphilis serology indicates that these scenarios benefit the most with the addition of TPPA confirmation.

In general terms, there should be little to no impact to clinicians or public health practitioners with this change. If you feel you have a case that requires further investigation with TPPA, please contact CPL or the CPL physician on-call to discuss.

References/Resources:
Please refer to the CPL Guide to Services (G2S) for collection and submission information.

More Information:
CPL G2S website
Manitoba Syphilis Protocol

Contact Information:
Paul Van Caeseele, MD
Medical Director, Cadham Provincial Laboratory | Shared Health
204-945-6456 or email

Submitted by: Loreley Fehr, Manager, Health Services – Public Health-Healthy Living

Overview:

  • Production of hydroxocobalamin kits was temporarily suspended due to an investigation into a possible deviation relating to a risk of microbial contamination.
  • Lot number 2413, expiry date 30-Oct-2026 was manufactured during this time period and is potentially impacted.
  • Based on risk assessment provided by the manufacturer, Health Canada has made the decision to authorize distribution of the affected batch as the risk of microbial contamination is considered minimal.

Note the following guidelines:

  • Reserve hydroxocobalamin for patients with clinical signs of acute intoxication in a context suggestive of exposure to cyanide: cardiac arrest, shock, respiratory distress, coma, high lactic acidemia (>8 mmol/L)
  • Hydroxocobalamin should not be used in the absence of hypoxia.
  • Any signs/symptoms suggestive of systemic infection should trigger blood cultures and antibiotic therapy.

Supply of hydroxocobalamin kit (CYANOKIT) is constrained and conservation measures need to be implemented in order to avoid stock depletion.

Effective immediately: hydroxocobalamin is to be restricted for use in clinical situations requiring antidote for cyanide poisoning. Alternative treatment to consider for vasoplegic syndrome or refractory hypotension is methylene blue at a suggested dose of 1.5 to 2 mg/kg IV administered once over 20 to 60 minutes.

Please not that serotonin syndrome may occur in patients taking serotonergic agents and concomitant use of methylene blue.

Thank you for your support of the ongoing efforts to manage drug supply issues.

For questions, please contact your site pharmacy or please contact Rizwan Ahmed at or Libby Gair at

Submitted by: Pharmacy Program

Supply of dextrose 50% prefilled syringes 50 mL has stabilized in the Canadian market and is freely available. Inventory is sufficient to use without restriction.

Thank you for your support of the ongoing efforts to manage drug supply issues.

For questions, please contact your site pharmacy or please contact Rizwan Ahmed at or Libby Gair at

Submitted by: Pharmacy Program

QR is short for Quick Response – a graphic allowing the user to scan via a personal device connecting them to relevant information. QR codes are used on print publications (i.e. handouts, pamphlets, posters) and not intended for online content/links.

TIPS:

  • Make sure the QR code is visible and can be easily scanned. If it’s too small or blurry, it won’t work.
  • Test the QR code to make sure it works before you use it.
  • Be sure to include a call to action with your QR code. Tell people what they need to do or what will happen after they scan it, ie. access more info., etc.
  • Make sure the content you’re linking to is mobile-friendly. If it’s not, people won’t be able to view it properly on their phones. As a result, it will defeat the whole purpose of using a QR code in the first place.

For more publication tips, please reference the Southern Health-Santé Sud Graphic Standards Manual.

Submitted by: Communications
For more info. contact: Sylvie Robidoux or Kristine Crocker

clipart graphics of people communicating online
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