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Global Obesity Academy: Applying Obesity Guidelines to Adjust Therapy

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Description

This program is supported by an independent education grant from Lilly. This online education program has been designed for healthcare professionals globally.

Prefer to read instead? Read our Key Clinical Summary here.

In this 15-minute on-demand session, leading expert Sue Pedersen, MD, explores the critical phase of reassessing and adjusting long-term obesity treatment when initial goals are not met. As the lead author of the Obesity Canada Clinical Practice Guidelines, Dr. Pedersen utilizes the latest global and Canada-specific updates to guide therapeutic decision-making.

Accreditation: AffinityCE designates this activity for 0.25 AMA PRA Category 1 Credit™

To ensure global accessibility, this content is available in multiple languages. Please click on your preferred option below to watch the talk on its corresponding page:

Session Highlights

  • Pharmacotherapy Initiation: Initiate long-term, evidence-based obesity treatment by utilizing pharmacotherapy to support health behavior changes, as lifestyle changes alone are often insufficient for sustained weight loss and complication improvement.
  • Timely Therapeutic Adjustment: Apply international guidelines to systematically reassess therapy when treatment goals are not met, considering contributing factors (like adherence or dosing) and implementing escalation by adding or substituting medications.
  • Medication Selection: Determine suitable medications by using a decision tool that weighs the agent's efficacy (average weight loss) and benefits for patient-specific comorbidities (e.g., T2D, OSA, OA).
  • Patient-Centric Goals: Identify treatment goals, such as achieving the "best weight" or optimizing complications, in partnership with the patient, ensuring patient values and preferences guide medication choice.

Who Should Watch

  • Primary Care Physicians
  • Primary Care Team
  • Nurse Practitioners
  • Physician Assistants

Presented by

Sue D. Pedersen, MD, FRCPC – Specialist in Endocrinology and Metabolism; American Board of Obesity Medicine; Clinical Lecturer, University of Calgary. Dr Pedersen’s clinical research and leadership in national and global obesity pharmacotherapy trials, as well as her authorship of the Canadian Obesity Clinical Practice Guidelines, have shaped evidence-based strategies for diabetes and obesity management.

Continuing Education Information

Commercial support: This activity received monetary support through an independent education grant from Lilly.

This continuing education activity will be provided by AffinityCE and MedAll. This activity will provide continuing education credit for physicians. A statement of participation is available to other attendees.

Disclosures

Dr Sue Pedersen has disclosed financial relationships within the past 24 months with the following ineligible companies: AstraZeneca, Bausch, Eli Lilly, Novo Nordisk, Janssen, Boehringer, Sanofi, Merck, Abbott, Dexcom, HLS, GSK, Bayer, Pfizer, AbbVie, Roche, Amgen, Prometic, and Regeneron. These relationships include honoraria, participation on advisory boards or speakers’ bureaus, and involvement in research and clinical trials.

These disclosures are made in accordance with ACCME standards to ensure transparency and objectivity in continuing education. Dr Pedersen intends to discuss non-FDA uses of drug products and/or devices only in relation to products for which she has no financial relationships. She will disclose to the audience when this discussion takes place.

AffinityCE staff, MedAll staff, as well as planners and reviewers, have no relevant financial relationships with ineligible companies to disclose.

Mitigation of Relevant Financial Relationships

AffinityCE adheres to the ACCME’s Standards for Integrity and Independence in Accredited Continuing Education. Any individuals in a position to control the content of a CME activity, including faculty, planners, reviewers, or others, are required to disclose all relevant financial relationships with ineligible companies. Relevant financial relationships were mitigated by the peer review of content by non-conflicted reviewers prior to the commencement of the program.

Activity Accreditation for Health Professions

Physicians

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of AffinityCE and MedAll. AffinityCE is accredited by the ACCME to provide continuing medical education for physicians.

AffinityCE designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Physician Assistants

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of AffinityCE and MedAll. AffinityCE is accredited by the ACCME to provide continuing medical education for physicians.

AffinityCE designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credits™. Physician assistants should claim only the credit commensurate with the extent of their participation in the activity.

Nurse Practitioners

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of AffinityCE and MedAll. AffinityCE is accredited by the ACCME to provide continuing medical education for physicians.

AffinityCE designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credits™. Nurse practitioners should claim only the credit commensurate with the extent of their participation in the activity.

Nurses & Other Professionals

All other health care professionals completing this continuing education activity will be issued a statement of participation indicating the number of hours of continuing education credit. This may be used for professional education CE credit. Please consult your accrediting organization or licensing board for their acceptance of this CE activity.

System Requirements

Mobile device (e.g., large-format smart phone; laptop or tablet computer) or desktop computer with a video display of at least 1024 × 768 pixels at 24-bit color depth, capable of connecting to the Internet at broadband or faster speeds, with a current version Internet browser and popular document viewing software (e.g., Microsoft Office, PDF viewer, image viewer) installed. Support for streaming or downloadable audio-visual materials (e.g., streaming MP4, MP3 audio) in hardware and software may be required to view, review, or participate in portions of the program.

Unapproved and/or off-label use disclosure

AffinityCE/MedAll requires CE faculty to disclose to the participants:

  • When products or procedures being discussed are off-label, unlabeled, experimental, and/or investigational (not US Food and Drug Administration [FDA] approved); and
  • Any limitations on the information presented, such as data that are preliminary or that represent ongoing research, interim analyses, and/or unsupported opinion.

CME Inquiries

For all CME policy-related inquiries, please contact us at ce@affinityced.com.

Participation Costs

There is no cost to participate in this program.

This continuing education activity is active starting November 26th 2025 and will expire on May 5th 2027. Estimated time to complete this activity: 15 minutes.

Learning objectives

Apply international and country-specific obesity guidelines to reassess therapy response and escalate or adjust treatment.

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Computer generated transcript

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The following transcript was generated automatically from the content and has not been checked or corrected manually.

Hello, everyone, and thank you so much for joining us today for the Global Obesity Academy International Program. My name is Doctor Sue Peterson. I'm an endocrinologist and obesity medicine specialist in Calgary, Canada, and I'm delighted to take you through this presentation that I've developed for you today. These are my disclosures. OK, let's now move into our second objective, which is to discuss how to reassess and adjust therapy when targets of treatment are not being met. So, polling question here again for you. What are the most appropriate targets of obesity treatment? Is it health benefits? Is it percentage weight loss? Is it treatment targets that the patient decides, Quality of life improvement, or is it as determined in partnership with the patient and the healthcare professional? I'll give you a few seconds. Wonderful. Thank you so much for your responses. So the best answer to this question here was E, as determined in partnership between the patient and the healthcare professional. So, let's talk about that in the context of Sabine. So Sabine is 62. She's retired. She has a past history of severe obstructive sleep apnea, doesn't tolerate CPAP. She has knee osteoarthritis, controlled hypertension, hypothyroidism, and obesity. And here we see her medication list for these conditions, and that includes semaglutide, 2.4 mg weekly, which she's taking for weight management. If we look at her lab and assessment, we see that her BMI is 34. Her waist to height ratio is elevated at 0.64. Her waist circumference also is elevated at 100 centimeters. She has a good A1C, BP controlled. She is well replaced on her thyroid hormone with a normal range TSH. Little bit of elevation in triglycerides, very common, and she's uh got a little bit of chronic kidney disease actually based on today's lab with a GFR of 55. So, in terms of her history, she started semaglutide about 9 months ago, uh, tolerated it well, uh, titrated her way up. Her targets of treatment that were identified in partnership with our healthcare professional and Sabine were improvement in her knee pain. She wants her knees to hurt less. We'd like her sleep apnea to improve, and Sabine says, I'd like to lose at least 15% of weight. That is an important treatment goal for me. So we incorporate that into the treatment paradigm. So, her response to Semelatide over 9 months has been a little improvement in knee pain. Her sleep apnea has improved a little bit as well. It's now in the high moderate range, and she's lost about 5% weight, and her weight has plateaued. So, what if my patient's not responding to treatment? So, here we have a case of Sabine where we're not meeting the goals of treatment. We've had some benefit, but we haven't really substantially improved her sleep apnea. We can likely do more. Um, we have not met her weight loss goals which were very important to her as a target of treatment, and she'd like some improvement. in her knee pain as well. So, the first thing is not to assume that we're not getting benefits in health with the weight loss because health improvements can be realized with less weight loss. But here, we're seeing that we have not had the weight loss that she would like and we have not met the treatment goals for her obesity-related health issues. So, if goals of treatment aren't being met, that doesn't necessarily mean that the medication isn't working. There's other things we need to think about first. Does our patient have continued access to treatment? If they're paying out of pocket, can they still afford it? Is the dose adequate for the desire to Effect? Are there adherence challenges or tolerance challenges? Is she encountering barriers to health behavior change? Are there other psychosocial issues or medical issues or medications maybe that have been started that have been causing weight gain? So we need to go through all of these things with her. After assessing these factors, if we feel that the goals of treatment are not being met on the maximum tolerated dose, we can revisit the pillars of obesity treatment, those being psychological support, pharmacotherapy, and bariatric surgery, and we can consider adding or substituting another medication or intervention to the patient's treatment. So as Sabine hasn't met health targets nor her weight loss goals, are there alternatives to her current treatment? Well, surmount 5 was a direct head to head comparison of semeglutide versus rezepetide for weight management. They found that the average weight reduction was 20.2% with terzepetide at the maximum tolerated dose of 10. 15 mg weekly versus 13.7% with semelutide at the maximum tolerated dose of 1.7 or 2.4 mg weekly. And Sabine wants to lose 15% weight. On the right, we see that 65% of people achieve this with repetide versus 40% of people with semelutide. Now, for obstructive sleep apnea, which Sabine has, there's robust evidence for trazepetide in particular to improve sleep apnea in people on and not on positive airway pressure therapy. The reglutide can actually also provide a modest improvement in sleep apnea along with a modest weight loss. Sabine's not On CPAP, so she'd be similar to the patients here on the left in the terpeide study, where there was a marked reduction of 25 events per hour versus 5 with placebo and accompanied by an average of nearly 18% weight loss. So this would fit, fit really well with Sabine's treatment goals. Sabine also has osteoarthritis, where the only obesity medication showing benefit is semaglutide with a significant greater reduction in the Womack pain scale with semaglutide versus placebo, and with a 13.7% mean weight reduction with semaglutide. But she's already on semaglutide. She's on maximum dose, she's tried it, she's adherent, and it hasn't worked for her, so we should move on to something else. So it's really hard to think through all these trials in a busy clinic day. But with our Obesity Canada clinical Practice guideline decision tool, we can really quickly look at the rows here on obstructive sleep apnea and on osteoarthritis, and the weight loss at the bottom because that's one of Sabine's treatment goals, and we see that terzepeide becomes the best. Choice. She hasn't succeeded with semaglutide, so we'll see if trazepetide provides a better success. So, we suggest switching semaglutide to repetide, and Sabine would really like to do that. Now, as to what dose to switch to, well, that depends on current tolerance of semaglutide and what dose of semaglutide the patient's currently taking. There aren't any specific data currently to guide us on this, only clinical experience. As she's tolerating semaglutide well, I would suggest switching to tezepetide 5 mg, or you could even switch to 7.5 mg weekly and titrate. But typically, I would err on the more conservative side. I'd probably switch Sabine to 5 mg weekly. Now, remember, there's some important things we have to watch here as we are switching to terpetide and then potentially titrating terpetide. She has hypertension. And remember that hypertension medication needs may decrease even before substantial weight loss with highly effective GLP-paced therapies. So we need to have her watching her BP at home and be careful to adjust BP medication. If she's having a reduction in BP, she might not need as much BP medication with the switch to trazepeide. Now, thyroid hormone needs can also decrease with weight loss, and that's really important. Again, we don't have any data to guide us on a specific evidence-based approach here, but what I typically do is check thyroid hormone levels every 2 months for the 1st 6 months or sometimes even monthly if the patient has health conditions where they may be more sensitive to changes in thyroid hormone like coronary artery disease. Disease. And I always recheck one month after any dose change in thyroid hormone. At 6 months, we can evaluate what's the current trajectory of weight loss. If it is slowed, then we might be able to move the thyroid hormone level checks to less frequently, like every 3 months. But remember, this is very individualized and it's important to make these monitoring decisions individually based on the patient.