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Do GLP-1 Drugs Cause Blood Clots After Surgery? 1.6% Against 3.0%

A matched hip-replacement cohort found clots in 1.6% of GLP-1 users against 3.0%. Eighteen events separate the two groups.

Neil Sanders8 min read
Clots within 90 days of a hip replacementon a GLP-11.6%matched controls3.0%1,262 per group — so roughly 20 events against 38Every five-year mechanical outcome was flat.

The one study that counted them found fewer, not more. Deep vein thrombosis at 90 days ran 1.6% against 3.0% in matched hip-replacement patients [1]. That is a relative risk of 0.53, 95% CI 0.31 to 0.89, p = 0.014. The absolute gap is 1.4 percentage points. It is reassurance, not a reason to buy anything. The wound side of the same question is in what happens to a surgical wound.

The hip replacement cohort

Adults having a first hip replacement between 2003 and 2023 were pulled from a claims database. Three or more GLP-1 prescriptions in the prior year counted as exposed. Matching on demographics, conditions and lab values left 1,262 patients per side.

Two ninety-day outcomes separated. Clots ran 1.6% against 3.0%. Readmission ran 1.1% against 2.8%, a relative risk of 0.40, 95% CI 0.22 to 0.71, p = 0.001.

Those rates come to roughly 20 clots against 38. The paper does not print the counts. That is arithmetic from its own percentages, and 18 events is a thin margin.

Most of the study found nothing

Revision survival at five years was 94.6% against 95.5%, p = 0.674. Joint infection was 94.7% against 94.4%, p = 0.465. Other ninety-day outcomes did not separate either.

That flatness is the useful part. The reason people worry about a GLP-1 before an operation is delayed stomach emptying under anesthesia. This cohort did not find worse outcomes. The timing question is handled in whether you have to stop before surgery.

Heart surgery: four trials, 446 patients

Four randomized trials of liraglutide around cardiac surgery were pooled [2]. Thirty-day mortality came out at 0.42, interval 0.06 to 2.81. That rests on four deaths across both arms.

Any complication ran 0.92, interval 0.74 to 1.14. Cardiac events ran 1.08. Hypoglycemia ran 0.85, interval 0.34 to 2.13. Nausea and vomiting came out at 3.01, interval 0.26 to 35.27.

An interval reaching 35 is not a result. None of those numbers rules anything in or out. It is the difference between finding no effect and failing to look hard enough to see one.

Spinal fusion: no complication difference either

A claims analysis matched 425 semaglutide users against 2,514 controls having anterior lumbar interbody fusion [3]. Complication rates did not differ at 90 days or at two years. Users stayed 0.6 days less.

The cost fields moved a long way. Same-day surgical costs ran roughly $10,400 lower and 90-day costs roughly $9,700 lower. Complications were identical, so a smoother recovery did not buy that. Claims amounts are billed or reimbursed sums, not what anyone paid. That gap is tracked in what a GLP-1 saves the system.

Who is in the exposed group

Three filled prescriptions in a year. That is a filter, not a randomization. It selects people who tolerated the drug, afforded it, and kept going.

Most buyers do not, as the refill records in how long people stay on a GLP-1 show. Whatever makes someone a persistent filler probably also makes them a better surgical patient. Matching on database codes cannot see that.

What a buyer takes from this

Nothing to act on. The clot finding is a single moved endpoint among many. The complication nulls are the sturdier half, and they say the operation looks the same.

What one prevented event is worth is a separate calculation, set out in the cost per event prevented. Nobody should read a surgical benefit into a monthly price.

Frequently asked

Do GLP-1 drugs cause blood clots after surgery?
The one cohort that counted them found fewer. Deep vein thrombosis at 90 days after a hip replacement ran 1.6% in GLP-1 users against 3.0% in matched controls, a relative risk of 0.53.
Is that a clot-prevention effect?
The authors say it should not be read that way. Several thromboembolic endpoints were tested and one moved, and they ask for a prospective study before anyone attributes prevention to these drugs.
How many events is that difference built on?
Roughly 20 clots against 38, by arithmetic from the published percentages on 1,262 patients per side. Eighteen events is a thin margin.
What about heart surgery?
Four randomized trials covering 446 patients produced intervals too wide to read. Thirty-day mortality came out at 0.42 with an interval from 0.06 to 2.81, resting on four deaths in total.
Did anything get worse?
Not in these cohorts. Revision and joint infection at five years did not separate, and a lumbar fusion cohort showed no complication difference at 90 days or two years.

Sources

  1. [1] Diab AR, et al. (2026). Preoperative GLP-1 receptor agonist use and outcomes after total hip arthroplasty: a matched cohort study Hip International. PMID 42725550
  2. [2] Gamal I, et al. (2026). Safety and Glycemic Efficacy of Perioperative Liraglutide in Cardiac Surgery: A Systematic Review and Meta-Analysis of Randomized Controlled Trials Cardiology in Review. PMID 42693519
  3. [3] Ng MK, Mastrokostas PG, Tabbaa A, Razi A, Johnson M, Said M (2026). Semaglutide Use Is Associated With Decreased Length of Stay and Hospital Costs in Patients Undergoing Anterior Lumbar Interbody Fusion: A Retrospective Cohort Study Orthopedics. PMID 41636429

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