Matthew Weir

Matthew Weir

Principal Investigator

Biography

Dr. Matthew Weir is an Associate Professor at Schulich School of Medicine & Dentistry and the newly appointed Dr. Adam Linton Chair in Kidney Health Analytics. He holds key clinical leadership roles as the Medical Director of the Kidney Care Centre and the Hemodialysis Unit at University Hospital, London Health Sciences Centre. With an MSc in Epidemiology and Biostatistics, Dr. Weir specializes in health administrative database research, collaborating with the Ontario Renal Network to improve kidney care through integrated knowledge translation.

Active Clinical Studies

(14)

Publications (since 2022)

Updated Feb 09, 2026

Research Profile

Research Areas

Study Types

Methods & Approaches

2025click to view publications

Risk for Scrotal Surgery After Laparoscopic Donor Nephrectomy : A Population-Based Cohort Study.

Garg AX, McArthur E, Sontrop JM, Boudville N, Connaughton DM, Cuerden MS, Feldman LS, Lam NN, Lentine KL, Nguan C, Parikh CR, Segev DL, Sener A, Smith G, Wang C, Weir MA, Yohanna S, Young A, Naylor KL

Ann Intern Med · 2025

Researchers in Ontario, Canada, found that men who donated a kidney through laparoscopic surgery had a significantly higher risk of requiring scrotal surgery later in life compared to men who did not donate. Over a 20-year period, nearly 14 percent of donors underwent surgery to treat fluid collection in the scrotum, most commonly a procedure called a hydrocelectomy. These findings highlight a specific long-term surgical risk for male living kidney donors that may occur several years after the initial donation.

Validity of the International Classification of Diseases, 10th Revision codes for lithium toxicity in adult patients at hospital admission: a cohort study in Canada.

Ahmadi F, Muanda FT, Ehiwario J, McArthur E, Jandoc R, Slater J, Vasudev A, Weir MA, Clark EG, Rej S, Herrmann N, Garg AX

BMJ Open · 2025

Researchers in Ontario evaluated the accuracy of hospital diagnostic codes for identifying lithium toxicity by comparing them to actual blood laboratory results. The study found that while these codes were moderately effective at identifying patients with high lithium levels, they sometimes flagged patients whose levels were below the toxic threshold. These findings help clarify how reliably health database records can be used to track and study lithium-related complications in the healthcare system.

High-Throughput Computing to Detect Harmful Drug-Drug Interactions in Older Adults: Protocol for a Population-Based Cohort Study.

Rostamzadeh N, Sharma R, Abdullah SS, McArthur E, Chalabianloo N, Sontrop JM, Weir MA, Sedig K, Garg AX, Muanda FT

JMIR Res Protoc · 2025

This is a protocol for an ongoing study that describes the design of a research project using high-performance computing to screen millions of potential drug combinations for harmful interactions in older adults. Researchers will use health records from Ontario to compare patients taking two specific medications against those taking only one, tracking over 70 different health outcomes such as hospitalizations and mortality. This automated approach aims to identify dangerous drug-drug interactions much faster than traditional methods to improve prescribing safety and inform regulatory decisions.

Cost-Utility Analysis of Accelerated and Standard Strategies for Renal Replacement Therapy Initiation.

Round J, Akpinar I, Yan C, Patel N, van Katwyk S, Montgomery C, Wald R, Bagshaw SM, STARRT-AKI Investigators

JAMA Netw Open · 2025

This economic evaluation used data from a large clinical trial linked with health databases in Alberta to compare the costs and health outcomes of starting dialysis early versus waiting for standard clinical triggers in critically ill patients with severe acute kidney injury. While waiting to start dialysis was slightly more expensive, it resulted in better quality of life and longer survival for patients over the long term. The findings suggest that a standard approach to starting dialysis is more cost-effective in the Canadian healthcare system than an accelerated approach.

PRevEnting FracturEs in REnal Disease-1 (PREFERRED-1): protocol for a pilot study of a pragmatic, randomised controlled trial of denosumab for the prevention of fragility fractures in haemodialysis.

Clemens KK, Cowan A, Dixon S, Naylor K, Weir MA, Thain J, Khan T, Silver S, Molnar AO, Sultan N, Holden RM, Hiremath S, Wald R, Kitchlu A, Arnold J, Field B, Garg AX

BMJ Open · 2025

This is a protocol for an ongoing pilot study that will assess the feasibility of conducting a larger trial to determine if the medication denosumab can prevent bone fractures in patients receiving hemodialysis. Researchers will recruit at least 60 high-risk patients across Ontario to evaluate how well the study procedures work and whether the treatment can be safely integrated into routine care. The findings will help determine if a full-scale study is possible to test a new strategy for reducing the high rate of fragility fractures in this population.

Spironolactone versus placebo in patients undergoing maintenance dialysis (ACHIEVE): an international, parallel-group, randomised controlled trial.

Walsh M, Collister D, Gallagher M, Mark PB, de Zoysa JR, Tyrwhitt J, Tennankore K, Reis G, Xavier D, Liu WJ, Zuo L, Wang AY, Félix C, Sola L, Arici M, Villanueva R, Jha V, Précoma D, Rabbat CG, Alavudeen SS, Faruqui AR, López-Flecher M, Pyne L, Wald R, Yuan F, Balasubramanian K, Lee SF, Kuptsova A, Christou C, Devereaux PJ, ACHIEVE Investigators

Lancet · 2025

Researchers conducted a large international trial to determine if the medication spironolactone could reduce the risk of heart failure or cardiovascular death in patients receiving long-term dialysis. The study was stopped early for futility after finding no significant difference in heart-related deaths or hospitalizations between patients taking spironolactone and those taking a placebo. These results suggest that daily use of this specific medication does not provide the expected cardiovascular benefits for the maintenance dialysis population.

A study of older adults in Ontario found that taking the antibiotic clarithromycin while also using certain blood pressure medications, known as angiotensin receptor blockers, was associated with a higher risk of hospital visits for high potassium levels and acute kidney injury compared to taking azithromycin. This risk of high potassium was even greater for individuals with pre-existing reduced kidney function. These findings suggest a significant drug interaction occurs because clarithromycin interferes with the body's ability to transport and eliminate these blood pressure medications through the liver.

Clinical Outcomes and Health Care Utilization in Patients with Advanced Chronic Kidney Disease not on Dialysis After the Onset of the COVID-19 Pandemic in Ontario, Canada.

Wang C, Kang Y, Dixon SN, Jeyakumar N, Scott Brimble K, Garg AX, Blake PG, Stukel TA, Oliver MJ, Al-Jaishi A, Clemens KK, Fu L, Ip J, McKenzie S, Moist L, Molnar AO, Muanda-Tsobo F, Reich M, Roshanov P, Silver SA, Wald R, Weir MA, Yau K, Young A, Naylor KL

Can J Kidney Health Dis · 2025

Researchers in Ontario, Canada, found that deaths among people with advanced chronic kidney disease increased by eight per cent during the first 21 months of the COVID-19 pandemic. Despite this increase in mortality, hospital admissions and emergency room visits for these patients actually decreased, suggesting a significant disruption in how they accessed medical care. Interestingly, visits to kidney specialists remained stable throughout the pandemic, and there was no significant change in the number of patients needing to start urgent dialysis.

Researchers examined the steps required to receive a kidney transplant across different regional renal programs in Ontario, Canada, and found significant geographic disparities in access. Patients in Northern Ontario were much less likely to be referred for transplant evaluation, find potential living donors, or be placed on the deceased donor waitlist compared to those in Toronto. These findings highlight that even within a publicly funded health care system, a patient's location can greatly influence their ability to receive a kidney transplant.

SGLT2 Inhibitors and Risk for Hyperkalemia Among Individuals Receiving RAAS Inhibitors.

Wing S, Ray JG, Yau K, Jeyakumar N, Abdullah S, Luo B, Cherney DZI, Harel Z, Hundemer GL, Mavrakanas TA, Molnar AO, Odutayo A, Perl J, Young A, Charytan D, Weir M, Wald R

JAMA Intern Med · 2025

A study of older adults in Ontario, Canada, found that starting a sodium-glucose cotransporter 2 inhibitor was associated with a lower risk of developing high potassium levels in those already taking medications that affect the renin-angiotensin-aldosterone system. Patients who began this new treatment were also less likely to stop their existing blood pressure and kidney-protective medications. These findings suggest that adding this class of drugs may help manage a common side effect of standard kidney and heart treatments in routine clinical practice.

Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic.

Schott C, Alajmi M, Bukhari M, Relouw S, Wang J, McIntyre AD, Baker C, Colaiacovo S, Campagnolo C, Almada Offerni G, Blake PG, Chiu M, Cowan A, Garg AX, Gunaratnam L, House AA, Huang SS, Iyer H, Jain AK, Jevnikar AM, Johnson J, Lotfy K, Moist L, Rehman F, Roshanov PS, Sultan N, Weir MA, Basharat P, Florendo-Cumbermack A, Khan T, Thain J, Kidd K, Kmoch S, Bleyer AJ, Bhangu J, Hegele RA, Connaughton DM

Genes (Basel) · 2025

In a study of 125 adults aged 50 and older with chronic kidney disease, researchers found that genetic testing identified a specific cause of disease in 38% of patients. The highest success rate for diagnosis occurred in those aged 50 to 54, with various forms of glomerular disease being the most common findings. These genetic results led to changes in medical treatment and clinical management, suggesting that age alone should not be a barrier to accessing genetic testing for kidney disease.

Clinical Outcomes and Healthcare Utilization in Patients Receiving Maintenance Dialysis After the Onset of the COVID-19 Pandemic in Ontario, Canada.

Naylor KL, Jeyakumar N, Kang Y, Dixon SN, Garg AX, Al-Jaishi A, Blake PG, Chanchlani R, Fu L, Harel Z, Ip J, Kitchlu A, Kwong JC, Nesrallah G, Oliver MJ, Stukel TA, Wald R, Weir M, Yau K

Can J Kidney Health Dis · 2025

Researchers in Ontario, Canada, compared the health outcomes of over 31,000 dialysis patients before and during the first three years of the COVID-19 pandemic. While death rates were significantly higher during specific months of the pandemic, the overall mortality rate over the entire 36-month period was not substantially higher than expected. Interestingly, hospitalizations and emergency room visits decreased during the pandemic, yet there was no corresponding increase in deaths unrelated to COVID-19.

Time to Renal Replacement Therapy Initiation in Critically Ill Patients With Acute Kidney Injury: A Secondary Analysis of the Standard Versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Trial.

Jeong R, Bagshaw SM, Ghamarian E, Harvey A, Joannidis M, Kirkham B, McAuley D, Ostermann M, Quenot JP, Young PJ, Wald R, STandard vs. Accelerated initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Investigators

Crit Care Med · 2025

Researchers analyzed data from a large clinical trial to determine if waiting longer to start dialysis in critically ill patients with severe acute kidney injury affected their recovery. The study found that longer delays in starting dialysis were not associated with an increased risk of death, though there was a potential link between longer delays and a higher likelihood of remaining dependent on dialysis at 90 days. These findings suggest that for patients without urgent medical needs, a strategy of waiting to see if the kidneys recover naturally does not appear to worsen survival outcomes.

2024

Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada.

Schott C, Arnaldi M, Baker C, Wang J, McIntyre AD, Colaiacovo S, Relouw S, Offerni GA, Campagnolo C, Van Nynatten LR, Pourtousi A, Drago-Catalfo A, Lebedeva V, Chiu M, Cowan A, Filler G, Gunaratnam L, House AA, Huang S, Iyer H, Jain AK, Jevnikar AM, Lotfy K, Moist L, Rehman F, Roshanov PS, Sharma AP, Weir MA, Kidd K, Bleyer AJ, Hegele RA, Connaughton DM

Kidney Int Rep · 2024

Researchers evaluated the impact of a specialized kidney genetics clinic in Canada by providing genetic testing to 300 patients with chronic kidney disease who met specific referral criteria. The study found that using a standardized testing process identified a genetic cause for kidney disease in one-third of the families, with results typically delivered within three months of assessment. These genetic findings frequently led to changes in clinical management, though the researchers noted a significant delay of over ten years between a patient's initial kidney disease diagnosis and their eventual genetic evaluation.

The Global Kidney Patient Trials Network and the CAPTIVATE Platform Clinical Trial Design: A Trial Protocol.

Kotwal SS, Perkovic V, Jardine MJ, Kim D, Shah NA, Lin E, Coggan S, Billot L, Vart P, Wheeler DC, de Boer IH, Zhang H, Hou FF, Sugawara Y, Marion J, Lewis RJ, Berry LR, McGlothlin A, Jha V, De Nicola L, Gorriz JL, Heerspink HJL, GKPTN and CAPTIVATE Investigators

JAMA Netw Open · 2024

This report describes the design of an ongoing global registry and an associated adaptive platform clinical trial aimed at identifying new treatments for people with chronic kidney disease. The registry tracks patient health and outcomes across multiple countries to identify eligible participants for the trial, which will test various medications and combinations to slow the decline of kidney function. The study uses an innovative trial structure that allows researchers to efficiently evaluate multiple therapies simultaneously using a shared placebo group.

Anticoagulation for Patients with Atrial Fibrillation Receiving Dialysis: A Pilot Randomized Controlled Trial.

Harel Z, Smyth B, Badve SV, Blum D, Beaubien-Souligny W, Silver SA, Clark E, Suri R, Mavrakanas TA, Sasal J, Prasad B, Eikelboom J, Tennankore K, Rigatto C, Prce I, Madore F, Mac-Way F, Steele A, Zeng Y, Sholzberg M, Dorian P, Yan AT, Sood MM, Gladstone DJ, Tseng E, Kitchlu A, Walsh M, Sapir D, Oliver MJ, Krishnan M, Kiaii M, Wong N, Kotwal S, Battistella M, Acedillo R, Lok C, Weir M, Wald R

J Am Soc Nephrol · 2024

Researchers conducted a pilot study in Canada and Australia to see if it is feasible to run a large trial comparing warfarin, apixaban, and no anticoagulation in patients on dialysis with atrial fibrillation. The study successfully met its goals for patient recruitment and treatment adherence, despite challenges posed by the pandemic. These results demonstrate that a larger, definitive trial can be conducted to determine the safest and most effective way to prevent strokes in this high-risk population.

Higher dose antiviral therapy for herpes infections is associated with a risk of serious adverse events in older adults with chronic kidney disease.

Olar P, Garg AX, Weir MA, Ahmadi F, McArthur E, Lam NN, Sontrop JM, Muanda FT

Pharmacol Res Perspect · 2024

In older adults with chronic kidney disease, starting oral antiviral medications for herpes at higher doses was associated with a nearly fourfold increased risk of acute kidney injury compared to lower doses. While the overall absolute risk of a serious kidney event remained low at less than one percent, the risk was significantly higher when measured using hospital laboratory data rather than diagnostic codes alone. These findings suggest that careful dose adjustment of these medications is important for patient safety in the context of reduced kidney function.

An Environmental Scan of Canadian Kidney Transplant Programs for the Management of Patients With Graft Failure: A Research Letter.

Slominska A, Gaudio K, Shamseddin MK, Lam NN, Ho J, Vinson A, Mainra R, Hoar S, Fortin MC, Kim SJ, DeSerres S, Prasad GVR, Weir MA, Cantarovich M, Sandal S

Can J Kidney Health Dis · 2024

This study conducted an environmental scan of adult kidney transplant programs across Canada to understand how they manage patients whose kidney transplants are failing. Researchers found significant variations and gaps in care, particularly regarding psychological support, structured preparation for returning to dialysis, and multidisciplinary care. The findings highlight a lack of standardized protocols and a need for evidence-based guidelines to improve outcomes for this complex patient group.

Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6.

Schott C, Dilliott AA, Wang J, McIntyre AD, Son S, Colaiacovo S, Baker C, Gunaratnam L, House AA, Susan Huang SH, Iyer H, Johnson J, Lotfy K, Masellis M, Munoz DP, Rehman F, Roshanov PS, Swartz RH, Weir MA, Hegele RA, Connaughton DM

Gene · 2024

Researchers analyzed genetic data from patients with chronic kidney disease to investigate why many develop severe hardening of the arteries, known as vascular calcification. They identified specific mutations in the ABCC6 gene in several families, suggesting that inherited genetic factors may directly contribute to this cardiovascular complication. Identifying these genetic causes early could eventually help doctors use targeted therapies to prevent vascular damage and reduce the risk of death in kidney disease patients.

Thirty-day risk of digoxin toxicity among older adults co-prescribed trimethoprim-sulfamethoxazole versus amoxicillin: A population-based cohort study.

Muanda FT, Weir MA, Ahmadi F, McArthur E, Sontrop JM, Abdullah SS, Urquhart BL, Sadeghi H, Kim RB, Garg AX

Pharmacotherapy · 2024

In older adults taking digoxin, starting a course of the antibiotic trimethoprim-sulfamethoxazole was associated with a nearly sixfold higher risk of hospitalization for digoxin toxicity compared to starting amoxicillin. While the absolute risk of this complication remained low at less than one percent, the interaction is clinically significant because digoxin has a narrow safety range. Physicians should consider using alternative antibiotics or reducing the digoxin dose when these medications must be used together.

Researchers in Ontario, Canada, found that people living with HIV who were on dialysis had a significantly lower chance of receiving a kidney transplant compared to those without HIV when accounting for the risk of death. Despite this disparity in access, the study found that long-term transplant success and survival rates were similar between patients with and without HIV. These findings highlight a potential inequity in access to transplantation for individuals living with HIV despite comparable clinical outcomes after the procedure.

A woman who donated a kidney was later found to have a genetic mutation for Alport Syndrome that had initially been classified as a finding of uncertain significance. Five years after her donation, a re-evaluation of her genetic data and family history led to the discovery that the mutation was likely disease-causing, explaining her unexpected decline in kidney function. This case highlights the importance of periodically re-examining genetic test results, especially for potential living kidney donors, as scientific understanding of specific mutations evolves over time.

Regional Practice Variation and Outcomes in the Standard Versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Trial: A Post Hoc Secondary Analysis.

Vaara ST, Serpa Neto A, Bellomo R, Adhikari NKJ, Dreyfuss D, Gallagher M, Gaudry S, Hoste E, Joannidis M, Pettilä V, Wang AY, Kashani K, Wald R, Bagshaw SM, Ostermann M, STandard vs. Accelerated initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Investigators

Crit Care Explor · 2024

Researchers analyzed data from a large international trial to compare how doctors in different regions manage severe acute kidney injury in intensive care units. They found significant differences in fluid management and the timing and type of dialysis used, with patients in Australia and New Zealand showing higher survival rates at 90 days compared to those in North America and Europe. These findings highlight how regional variations in clinical practice may influence recovery and survival for critically ill patients.

Impact of Donation After Circulatory Death on Outcomes of Expanded Criteria Donor Kidney Transplants.

Alsolami E, Lotfy K, Alkhunaizi A, Cuerden M, Weir MA, House AA

Transplant Proc · 2024

Researchers compared the success of kidney transplants from older or higher-risk donors based on whether the organ was donated after circulatory death or brain death. They found that kidneys donated after circulatory death had significantly higher rates of initial function delay and a higher risk of graft failure within the first three years. Despite these differences in organ survival, there was no significant difference in overall patient survival between the two groups.

This is a protocol for an ongoing study that describes a new approach to identifying drug safety signals in older adults with chronic kidney disease using high-throughput computing and automation. Researchers will use administrative health databases in Ontario to conduct over 700 automated cohort studies, comparing the risk of 74 different acute health outcomes between new users of various medications and non-users. By analyzing these risks across different levels of kidney function, the study aims to more efficiently detect adverse drug reactions in this vulnerable population.

2023

Low-Dose Methotrexate and Serious Adverse Events Among Older Adults With Chronic Kidney Disease.

Muanda FT, Blake PG, Weir MA, Ahmadi F, McArthur E, Sontrop JM, Urquhart BL, Kim RB, Garg AX

JAMA Netw Open · 2023

A study of older adults in Ontario, Canada, found that those with chronic kidney disease who started low-dose methotrexate had double the risk of serious adverse events, such as sepsis or lung and liver toxicity, compared to those starting hydroxychloroquine. This risk was even higher for individuals with more advanced kidney impairment, particularly those with an estimated glomerular filtration rate below 45. These findings suggest that the potential for severe complications should be carefully weighed against the benefits when prescribing methotrexate to patients with reduced kidney function.

Initiation of continuous renal replacement therapy versus intermittent hemodialysis in critically ill patients with severe acute kidney injury: a secondary analysis of STARRT-AKI trial.

Wald R, Gaudry S, da Costa BR, Adhikari NKJ, Bellomo R, Du B, Gallagher MP, Hoste EA, Lamontagne F, Joannidis M, Liu KD, McAuley DF, McGuinness SP, Nichol AD, Ostermann M, Palevsky PM, Qiu H, Pettilä V, Schneider AG, Smith OM, Vaara ST, Weir M, Dreyfuss D, Bagshaw SM, STARRT-AKI Investigators

Intensive Care Med · 2023

Researchers analyzed data from a large clinical trial to compare whether starting treatment with continuous dialysis or intermittent dialysis led to better outcomes for critically ill patients with severe acute kidney injury. After adjusting for differences between the two groups, they found that patients who began with continuous therapy had a lower risk of being dead or still requiring dialysis 90 days later. This benefit was primarily due to a significant reduction in the number of patients who remained dependent on dialysis treatments.

Investigation of N,N,N-Trimethyl-L-alanyl-L-proline Betaine (TMAP) as a Biomarker of Kidney Function.

Sidor NA, Velenosi TJ, Lajoie GA, Filler G, House AA, Weir MA, Thomson BK, Garg AX, Renaud JB, McDowell T, Knauer MJ, Tirona RG, Noble R, Selby N, Taal M, Urquhart BL

ACS Omega · 2023

Researchers developed a new laboratory test to measure a molecule called TMAP in the blood and evaluated its potential as a marker for kidney function across several patient groups. The study found that TMAP levels were significantly higher in patients with chronic kidney disease and those receiving dialysis compared to healthy individuals, with levels rising as the kidney's filtering capacity declined. Because TMAP was also found in other species and even in maple tree sap, it appears to be part of a biological process that is widely conserved across nature.

Hypocalcemia Risk of Denosumab Across the Spectrum of Kidney Disease: A Population-Based Cohort Study.

Cowan A, Jeyakumar N, McArthur E, Fleet JL, Kanagalingam T, Karp I, Khan T, Muanda FT, Nash DM, Silver SA, Thain J, Weir MA, Garg AX, Clemens KK

J Bone Miner Res · 2023

A study of older adults in Ontario found that while the overall risk of developing low blood calcium after starting the medication denosumab is low, it increases significantly for those with advanced kidney disease or those on dialysis. For patients with the lowest kidney function, nearly one in four experienced mild low calcium and about fifteen percent experienced severe cases. These findings suggest that kidney function and baseline calcium levels are critical factors for doctors to monitor when prescribing this bone-strengthening treatment.

The effect of micro-particle curcumin on chronic kidney disease progression: the MPAC-CKD randomized clinical trial.

Weir MA, Walsh M, Cuerden MS, Sontrop JM, Urquhart BL, Lim YJ, Chambers LC, Garg AX

Nephrol Dial Transplant · 2023

This randomized trial investigated whether a highly absorbable form of curcumin could slow the progression of chronic kidney disease in adults with high levels of protein in their urine. Researchers found that taking 90 milligrams of micro-particle curcumin daily for six months did not significantly improve kidney function or reduce protein leakage compared to a placebo. These results suggest that this specific curcumin formulation does not provide measurable benefits for managing albuminuric chronic kidney disease over a short-term period.

Trimethoprim-sulfamethoxazole and the risk of a hospital encounter with hyperkalemia: a matched population-based cohort study.

Hwang YJ, Muanda FT, McArthur E, Weir MA, Sontrop JM, Lam NN, Garg AX

Nephrol Dial Transplant · 2023

A study of adults aged 66 and older in Ontario, Canada, found that starting the antibiotic trimethoprim-sulfamethoxazole was associated with a more than threefold increased risk of hospitalization for high potassium levels compared to starting amoxicillin. This risk was significantly higher for individuals with pre-existing reduced kidney function, and the medication was also linked to higher rates of acute kidney injury. These findings highlight the importance of monitoring kidney function and potassium levels when prescribing this common antibiotic to older patients.

2022

Impact of renal-replacement therapy strategies on outcomes for patients with chronic kidney disease: a secondary analysis of the STARRT-AKI trial.

Bagshaw SM, Neto AS, Smith O, Weir M, Qiu H, Du B, Wang AY, Gallagher M, Bellomo R, Wald R, STARRT-AKI Investigators

Intensive Care Med · 2022

This study examined whether having pre-existing chronic kidney disease affects the outcomes of different timing strategies for starting dialysis in patients with sudden, severe kidney failure. Researchers found that for patients who already had chronic kidney disease, starting dialysis early led to a three times higher risk of remaining dependent on dialysis after 90 days compared to a more standard, watchful approach. In contrast, the timing of dialysis initiation did not affect long-term dialysis dependence or survival for patients who had healthy kidney function before their acute illness.

A Bayesian reanalysis of the Standard versus Accelerated Initiation of Renal-Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial.

Zampieri FG, da Costa BR, Vaara ST, Lamontagne F, Rochwerg B, Nichol AD, McGuinness S, McAuley DF, Ostermann M, Wald R, Bagshaw SM, STARRT-AKI Investigators

Crit Care · 2022

Researchers re-examined data from a large international trial to determine if starting dialysis earlier in critically ill patients with acute kidney injury provided any benefit. Using advanced statistical modeling, they found a very low probability that early dialysis improves survival and noted that patients in the early-start group actually spent fewer days alive and free from dialysis. These results support the current practice of waiting for standard clinical indications before beginning kidney-replacement therapy.

Association of Higher-Dose Fluoroquinolone Therapy With Serious Adverse Events in Older Adults With Advanced Chronic Kidney Disease.

Muanda FT, Sood MM, Weir MA, Sontrop JM, Ahmadi F, Yoo E, Kim RB, Silverman MS, Knoll GA, Garg AX

JAMA Netw Open · 2022

This study of older adults in Ontario with advanced chronic kidney disease found that those prescribed higher doses of fluoroquinolone antibiotics had a higher risk of serious side effects compared to those given lower doses. These adverse events included hospital visits for nervous system or psychiatric disorders, dangerously low blood sugar, and tendon or collagen-related issues. While the overall risk of these complications remained low at less than two percent, the findings highlight the importance of careful dose adjustment based on kidney function.

Initiation Dose of Allopurinol and the Risk of Severe Cutaneous Reactions in Older Adults With CKD: A Population-Based Cohort Study.

Bathini L, Garg AX, Sontrop JM, Weir MA, Blake PG, Dixon SN, McArthur E, Muanda FT

Am J Kidney Dis · 2022

A study of older adults with chronic kidney disease in Ontario found that starting allopurinol at a dose higher than 100 milligrams per day more than doubled the risk of being hospitalized for a severe skin reaction compared to starting at a lower dose. These results support the practice of using lower initial doses of this medication in patients with reduced kidney function to minimize the risk of dangerous side effects. While higher starting doses were also linked to an increase in overall hospitalizations, there was no significant difference in the risk of death between the two groups.

Fracture Risk of Sodium-Glucose Cotransporter-2 Inhibitors in Chronic Kidney Disease.

Cowan A, Jeyakumar N, Kang Y, Dixon SN, Garg AX, Naylor K, Weir MA, Clemens KK

Clin J Am Soc Nephrol · 2022

Researchers compared the risk of bone fractures between older adults in Ontario starting sodium-glucose cotransporter-2 inhibitors and those starting dipeptidyl peptidase-4 inhibitors. The study found no significant difference in fracture risk between the two medication groups over one year, regardless of the patient's baseline kidney function. These findings suggest that this class of diabetes medication does not increase the risk of skeletal injuries in patients with chronic kidney disease.

Back to team