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Category Archives: Webinar

26th July 2022 – CME Webinar: Bare Bones of Flaming Joints

Wednesday, June 22nd, 2022 | claly44p | No Comments

Want to know the latest on inflammatory arthropathy? – well tune in on the 26th July at 730pm and I think we will answer most, if not all of your questions!
Register in advance for this meeting:

After registering, you will receive a confirmation email containing information about joining the meeting.

For more information contact Dr Lucinda Thatcher, Rural CME Convenor

Rural CME Webinar Mon 4th April 7:30pm – Acute Dermatology

Tuesday, March 29th, 2022 | claly44p | 1 Comment

Hi there,

You are invited to a Zoom meeting.

Apr 4, 2022 07:30 PM Auckland, Wellington

Acute dermatology from a rural dermatologist’s perspective

David Young, Consultant Dermatologist, Southern Dermatology

Topic: Acute rashes and skin reactions 

Register in advance for this meeting:

https://otago.zoom.us/meeting/register/tJUtcOCpqDMpGtY5tC70EaExHvjR5Yu7Mje3

After registering, you will receive a confirmation email containing information about joining the meeting.

For more details contact: Dr Lucinda Thatcher, CME Convenor lucinda.thatcher@otago.ac.nz

Webinar # 6: Wahine and Pepi – Obstetric emergencies in rural places

Sunday, May 16th, 2021 | Rory | No Comments

Webinar now up on YouTube if you want to watch (and didn’t make it to the session.)

Celia’s Slides

Brendan’s Slides

 

Audio only version is also available on podcast player of your choice.

Available on iTunes or any other podcast apps


 

There was an additional question that has been subsequently been answered:

Can you ask Celia/Brendan for advice about navigating responsibilities with midwives in acute situations? Who’s responsible for what?

From Brendan:

It’s a very good question and I suspect trickier in the acute situation in rural areas.

In larger units the team is called and in essence a ‘referrla of care’ has happened at that point and thus the obstetric team has ‘taken responsibility and lead the team.

I think this is how to interpret s88 and the specific NZ legislation (which has some very specific provisions that guide when care is handed over to an ‘obstetrician’). I know this provision fairly well as we’ve sort clarity (and with Celia’s help) have this extended to include Extended scope docs like Alan and myself.

What is less clear to me is exactly the scenario described where there isn’t an obs doctor. I’d have thought therefore that the primary responsibility remains with the LMC.

BUT this is a slightly different question to “who’s responsible for what” – and a bit like a trauma I suspect that the colleges would advocate for good communication and team based care. I think it’s a tricky as we’re used to being the point of referral and normally if we’re asked to be involved we’ve assumed that we are the team lead. I guess the problem becomes if the outcome is sub-optimal then how will the HDC view it??

Webinar # 4: Diabetes management

Thursday, August 20th, 2020 | Rory | No Comments

Diabetes management with Dr. Alex McCleod and Sharon Sandilansd, hosted by Dr. Matilda Hamilton. The link is below and is available on YouTube. The audio is also available via podcast on the Leaning on Fenceposts podcast via iTunes or wherever you listen to your podcasts (may take a few hours to become available).

Show notes:

Type I Diabetes & HHS

  • Type I diabetes
    • More common onset in the young
    • However, can occur any stage in life & second peak later in life
    • Will often present with higher sugars than a Type II diabetic
    • High glucose directly toxic to pancreas
      • Explains ‘honey-moon’ phase when Type I treatment starts, pancreatic function temporarily improves
    • Glucose spikes around meals, as opposed to Type II with higher basal BSL (although can develop post-prandial highs too)
  • HHS = Hyperglycaemic Hyperosmolar State (previously called HONK)
    • Profound metabolic derangement
    • Profound dehydration
    • Require large volumes & treatment underlying illness
    • Higher glucose levels than DKA/not acidotic/not ketosis
  • Continuous glucose monitoring
    • Available in NZ, not funded

Insulin in acute illness

  • Use novorapid for correction (NOT actrapid, it is actSLOW and lasts around 8 hours)
  • Novorapid – quick acting, 3 hours action
  • No insulin is as good as our native insulin – rapid onset/offset
  • Consider stopping metformin during acute illness and starting insulin
  • Don’t forget to restart metformin before discharge!
  • BSL monitoring during admission: pre-meal, pre-bed, 0200 (monitor for hypos) +/- post-meal (?post-prandial highs)
  • Suggested regime for basal/bolus regime during admission
    • Australian Subcutaneous Insulin Chart
    • Total daily insulin requirement = 0.5 units/kg
      • Split this 50:50 basal & bolus
    • Basal Wt(kg/4) = basal insulin requirement
    • Pre-meal blous = remaining daily insulin requirement/3
    • Example: 100kg woman
      • Estimated total daily dose = 0.5*100 = 50 units
      • Basal requirement = 100/4 = 25 units (note this is half daily dose)
      • Bolus doses = 25/3 = 8 units (8 units pre meal)
      • 25 units (basal) + 8 units + 8 units + 8 units = 50 units (daily dose)
    • Correction factors
      • These are doses of insulin given pre-meal (based on the BSL) that are added onto the usual pre-prandial (bolus) dose
      • Correction factor calculated 100/total daily dose (eg. Case above 100/50 = 2). The correction factor is the expected reduction in BSL for every unit of inulin. (For cases expect BSL to drop by 2 for every unit of insulin).
      • For example this patient may have BSL target of ~ 10.Pre meal BSL 20.  Want to drop BSL by 10, therefore add correction factor of 5 units onto usual pre-meal insulin.
    • Reviewing insulin dosing during acute admission
      • Add up previous 24 hours insulin requirement, then split this 50:50, adjusting the basal and bolus doses accordingly.

Insulin for long-term treatment:

  • When to start?
    • Not reaching target HbA1c despite ma oral therapy
    • Targets
      • Younger patients HbA1c ~50
      • Slightly older ~ 64
      • Elderly more lenient – must avoid hypos!
    • Continue metformin once on insulin
      • Improves insulin sensitivity
    • Options: long-acting vs mixed vs basal bolus
      • Need BSL profile to guide prescribing eg. Post-prandial highs may be indication for mixed insulin
      • Patient factors – eg. May opt for most simple option = safest
    • Mixed insulin – a note
      • Mixture or short-acting & intermediate acting
      • Last ~ 8 hours, therefore often BD dosing

Diabetic Medications – the old & the new

  • Metformin
    • Reduce oral absorption of glucose
    • Increase glucose uptake by cells, by increasing insulin sensitivity
    • Reduce liver production of glucose
    • Main side effect – GI upset
  • Sulfonylureas
    • Being phased out
    • Augment insulin secretion
    • Risk hypoglycaemia
  • GLP-1 receptor agonists (glucagon-like- peptide)/incretin mimetics
    • Increase insulin production when BSL elevated
    • Slow gastric emptying (can cause nausea)
    • Increase weight loss
    • Injection only
    • Not really available in Aotearoa
  • DPP – 4i, enzyme blocker
    • Reduce glucagon & increase insulin
    • Reduce weight
    • Vildaglitpin = Galvus (available in NZ)
    • Galvumet = vildagliptin + metformin
  • SGLT2 – inhibitors (Flozins)
    • NZ dapagliflozin (Forxiga) (not funded)
    • CKD/CVD benefits
    • Probably add on therapy for heart failure
    • Enhances renal excretion of glucose
    • Increase risk of UTIs and thrush
    • Risk DKA with relatively normal BSL

Non-pharmaceutical management = the important stuff

  • Remember the importance of advice around:
    • Diet to reduce glucose intake
    • Exercise to improve insulin sensitivity
  • Engage patients with appropriate services (eg. Free annual diabetic review, Kaupapa Māori services)
  • Walk beside your patients and be gentle on them – diabetes is a long, hard road.

Podcast:

Available on iTunes or any other podcast apps