2023-2024 Education Roundtable Series

Group Photo Of Professional Colleagues Working Together In Clinical Analysis Laboratory
Clinical Chemist Working
Clinical Chemist Group
Clinical Chemist in Lab
Clinical Chemist in Lab
Clinical Chemist Group
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Clinical Chemist in Lab
1Save today! Club members are entitled to join any or all of the Roundtables. Register once only and automatically receive an invitation for each Roundtable and access to the slides and recordings of past roundtables for the current year.

  • Registration is by pre-payment only using the online registration form.
  • Each registration is restricted to one (1) phone line; you may have as many participants using that line as you wish.  You are welcome to sign up more than one (1) phone line but each line must be a separate registration and payment.
  • Participants will be sent a link to the zoom session.

2023-2024 SCHEDULE

Date Time (Eastern) Presenter(s) Topic
1. September 21,2023 14:00 Shirley Li Approaches to Ensure the Equivalence of Patient Results within One Healthcare System
2. October 5, 2023 14:00 Cody Lewis Using big data to derive thyroid hormone reference intervals and optimize a TSH testing algorithm
3. October 19, 2023 11:30 Jonathan Genzen Maximizing Efficiency in Processing and Specimen Distribution Through Laboratory Automation
4. November 2, 2023 11:30 Andre Mattman, Lawrence de Koning & Brian Lam Unusual and Unexpected Cases in Clinical Chemistry
5. November 16, 2023 14:00 Kelly Doyle Estimating Reference Intervals from Routine Laboratory Data – Application of the refineR and TMC R Packages
6. December 14, 2023 11:30 Jessica Boyd Opioids and Gabapentin
7. January 18, 2024 11:30 Khosrow Adeli TBA – Overview of IFCC Activities and Experience as President
8. February 1, 2024 11:30 Allison Venner & Vathany Kulasingam TBA – LIS Implementation
9. February 15, 2024 11:30
10. February 29, 2024 11:30 Wes Schreiber Joint presentation with Archives Committee
11. March 7, 2024 14:00 Cristiana Stefan & Daniel Beriault TBA – Drug Checking Program
12. March 21, 2024 11:30 Michael Reid & Amy Pyle Eilola TBA – Preanalytical Considerations in Pediatric Testing
13. April 4, 2024 14:00 Christopher McCudden TBA – Use of AI in CKD Management
14. April 18, 2024 11:30 Lei Fu TBA – Pre-eclampsia Testing in a Tertiary Care Centre
15. May 2, 2024 11:30 TBD Fellows in Training – Presentations/Journal Clubs
16. May 16, 2024 14:00
17. May 30, 2024 14:00

 

09-21-23: Approaches to Ensure the Equivalence of Patient Results within One Healthcare System

#1. September 21, 2023 Approaches to Ensure the Equivalence of Patient Results within One Healthcare System
Speaker: Jieli Shirley Li, Co-Director of Clinical Chemistry & Toxicology Laboratory/Assistant Professor of Pathology, The Ohio State University

Jieli Shirley Li, MD, PhD, holds the position of Assistant Professor-Clinical within the Department of Pathology and serves as Co-Director of the Clinical Chemistry & Toxicology Laboratory.  Dr. Li obtained her MD and PhD degrees from the Shanghai Jiao-Tong University School of Medicine and completed her fellowship training in clinical chemistry at the MD Anderson Cancer Center.  Her professional interests center around enhancing laboratory tests for the in vitro diagnosis, prognosis, and treatment planning of cancer, endocrine disorders, and cardiovascular diseases.  Dr. Li has authored over 40 scientific articles and contributions as an Ad Hoc reviewer for 20 different scientific journals.  She also plays a vital role in participating in guidelines writing for the Clinical & Laboratory Standards Institute (CLSI) and serving on the Expert Panel Committee of CLSI.  Furthermore, Dr. Li contributes to the field as an inspector for the College of American Pathologists (CAP) and is actively involved with CAP’s Chemistry Committee.

Overview: There are 8 clinical laboratories in multiple locations in the Ohio State University Wexner Medical Center.  The standardization in pre-analytical, analytical and post-analytical phases in all the 8 labs dramatically improve quality, lower cost, provide better efficiency and equivalence of patient results, as well as cross-training of staff members.  These gains carry over to improved quality of care and patient satisfaction.  The approaches/experience to bringing standardization will also be shared and discussed.
Objectives: At the conclusion of this session, participants will be able to:
1) Describe the advantages of standardization in clinical laboratory services, including but not limited to instrumentation, quality management and workflows.
2) Address common challenges encountered in the process of implementing laboratory standardization
3) Implement practical approaches to assess the comparability of patient results within one healthcare system.

10-05-23: Using big data to derive thyroid hormone reference intervals and optimize a TSH testing algorithm

#2 October 5, 2023 Using big data to derive thyroid hormone reference intervals and optimize a TSH testing algorithm
Speaker: Cody Lewis, Assistant Professor, Clinical Biochemist, University of Saskatchewan / Saskatchewan Health Authority

Cody Lewis is currently a Clinical Biochemist working for the Saskatchewan Health Authority with an academic appointment at the University of Saskatchewan. He oversees the general chemistry laboratory at St Paul’s Hospital and co-leads point of care testing in Saskatoon. Additionally, Cody has interests in testing associated with endocrine disorders. Prior to joining the team in Saskatoon, Cody completed his fellowship training 2021 in Calgary Alberta. Before that, he obtained a PhD in Cancer Sciences from the University of Alberta and an MSc from the University of Lethbridge.

Overview: Physicians use reference intervals (RIs) to interpret laboratory results. Laboratories and analytical platforms often have different RIs. Alberta laboratories are striving to standardize RIs across the province, which includes thyroid hormones. To estimate RIs and to develop a reflex TSH testing algorithm, indirect sampling of “big data” was utilized. Data was analyzed by three statistical models: Bhattacharya, refineR, and non-parametric. TSH upper limits were highly variable depending on the model, ranging from 4.70 to 6.50 mIU/L. To refine estimated limits, a panel of adult and pediatric endocrinologists was engaged. The final decision took into account the percentage of normal matched free-T4 results. The standardization of thyroid RIs and the development of a new testing algorithm were achieved by this approach.
Objectives: At the conclusion of this session, participants will be able to:
1) Discuss the impact of implementing a sub-optimal reference intervals (RIs)
2) Define big data and appreciate how it can be used to estimate RIs
3) Recognize the limitation of deriving RIs via indirect sampling methods and discuss options for refining estimated limits

10-19-23: Maximizing Efficiency in Processing and Specimen Distribution Through Laboratory Automation

#3. October 19, 2023 Maximizing Efficiency in Processing and Specimen Distribution Through Laboratory Automation
Speaker: Jonathan Genzen

Dr. Jonathan Genzen is a professor at the University of Utah Department of Pathology. He serves as Chief Medical Officer at ARUP Laboratories, a not-for-profit enterprise of the University of Utah. He previously served as ARUP’s Chief Operations Officer. Dr. Genzen completed his undergraduate education at Northwestern University, and then both his Ph.D. and M.D. training at the University of Chicago. He joined ARUP Laboratories in 2013.

Dr. Genzen is a medical director in ARUP’s chemistry division and is medical director of ARUP’s laboratory automation team. His clinical and research focus is on automated clinical chemistry, process improvement initiatives, and the impact of laboratory regulatory proposals on patient care.

Overview: This lecture will describe how pre-analytical and post-analytical automation can help to improve efficiency and quality across small, medium, and large size clinical laboratories.  It will also discuss emerging technologies in use across manufacturing settings that also can provide benefits to clinical laboratories, including software solutions called robotic process automation.  The benefits of standardization will be emphasized across solutions presented.
Objectives: At the conclusion of this session, participants will be able to:
1) Understand the importance of automation in pre-analytical processing to reduce the risk of pre-analytical error.
2) Describe the benefits of standardization for routine aliquots and in molecular infectious disease testing.
3) Explain how robotic process automation can lead to clinical laboratory efficiency and process improvement.

11-02-23: Unusual and Unexpected Cases in Clinical Chemistry

#4. November 2, 2023 Unusual and Unexpected Cases in Clinical Chemistry
Speakers: Andre Mattman, MD, FRCPC, Medical Biochemist, St. Paul’s Hospital Chemistry Laboratory / Vancouver General Hospital Adult Metabolic Diseases Clinic

  • Division Head Chemistry Lab St Paul’s Hospital, Vancouver, BC since 2019
  • Physician consultant Adult Metabolic Diseases Clinic, Vancouver General Hospital since 2006.
  • Member of the multiple physicians and the environmental groups including Doctors for Planetary Health and the Royal College of Canada working group on CanMeds 2025 Planetary Health competencies.
    • Past Chair, Royal College of Canada National subspecialty committee in medical biochemistry.

Lawrence de Koning, Associate Professor and Clinical Biochemist, University of Clagary, Alberta Precision Laboratories and Alberta Children’s Hospital

Dr. Lawrence de Koning completed a PhD in Health Research Methodology from McMaster University in 2009, and concurrent postdoctoral fellowships in nutritional epidemiology and clinical chemistry at Harvard University from 2009-2012. He became board certified by the American Board of Clinical Chemistry in 2013 and a fellow of the Canadian Academy of Clinical Biochemistry in 2015. Dr. de Koning works as a pediatric clinical biochemist at Alberta Children’s Hospital, a consultant clinical biochemist for Rockyview General Hospital and has numerous clinical and research interests including biomarkers and epidemiology of pediatric and perinatal conditions, laboratory quality improvement, cardiovascular disease, and nutrition.

Ka Hang Brian Lam, University of California, Los Angeles

Overview: Three cases of oxalate nephropathy will be reviewed.

CASE 1:  Presented by Dr. Mattman:  Investigation of oxalate nephropathy

Oxlate nephropathy may be caused by primary and secondary etiologies. The investigation of oxalate nephropathy is complicated by the impact of nephropathy on oxalate concentrations in blood and urine. Nonetheless, oxalate nephropathy is responsive to etiology specific therapy – in some cases readily responsive – and so the laboratory’s role in documenting the etiology is an important piece of patient recovery.

At the conclusion of this session, participants will be able to:
1) Identify the common causes of acquired oxalate nephropathy.
2) Recognize that there are primary hyperoxaluria conditions which have distinct gene specific treatments (that area also distinct as compared to the acquired causes).
3) Identify the laboratory tests of utility in diagnosing primary and secondary hyperoxaluria

CASE 2: Presented by Dr. de Koning: Critically high ammonia in an adolescent girl

This session will review a case of repeatedly elevated plasma ammonia levels in an adolescent girl which were caused by specimen platelet contamination. Topics covered will include ammonia metabolism, urea cycle disorders, ammonia analysis, and the many preanalytical causes of elevated ammonia and how to minimize them.

At the conclusion of this sessions, participants will be able to
1) Describe the metabolism of ammonia
2) Understand the clinical manifestations of urea cycle disorders and appropriate treatments
3) Cite a number of common preanalytical causes for elevated ammonia, and identify ways to prevent them.

CASE 3: Presented by Dr. Bam: A suspected case of carbon monoxide poisoning consistent with fentanyl toxicity

This lecture sill describe a case of fentanyl poisoning that was consistent with carbon monoxide poisoning.
At the conclusion of this session, participants will be able to:
1) Understand the clinical presentation of fentanyl toxicity
2) Understand the diffence between a traditional opiate immunoassay methold and a synthetic fentanyl opioid immunoassay method.

11-16-23: Estimating Reference Intervals from Routine Laboratory Data – Application of the refineR and TMC R Packages

#5. November 16, 2023 Estimating Reference Intervals from Routine Laboratory Data – Application of the refineR and TMC R Packages
Speaker: Kelly Doyle, PhD, D(ABCC), FAACC. University of Utah School of Medicine, Department of Pathology and ARUP Laboratories, Salt Lake City, UT

Dr Doyle is a board‐certified clinical chemist and is an Associate Professor of pathology at the University of Utah. He is associate Director of the Clinical Chemistry Fellowship program and serves as the Medical Director of Special Chemistry and Endocrinology at ARUP Laboratories. He has a special interest in laboratory science education, the application of mass spectroscopy, and quality management.

Overview: The aim of this presentation is to describe the application of modernized indirect reference interval approaches, based on ready to use R packages refineR and TMC. Reference intervals are an integral component for result interpretation and are a regulatory requirement of laboratory medicine practice. Establishing RIs using the traditional approach by direct sampling is complicated by insufficient access to patients within varying interval partitions (e.g., pediatrics), and adoption or transferring of RIs is hindered by lack of assay standardization and unique population demographics. However, indirect sampling techniques using laboratory database results have significant practical advantages compared to direct sampling methods. The use of stored patient data can offer a faster and less costly means to developing RIs.
Objectives: At the conclusion of this session, participants will be able to:
1) Summarize the establishment and use of reference intervals in clinical laboratory practice.
2) Discuss the application of direct and indirect methods to determine population/sex/age-based reference intervals.
3) Describe the use of indirect methods refineR and TMC in estimating reference intervals from stored results.