Pilot Study of Atorvastatin for Orthopedic Surgery Patients

Phase 2

Completed

Conditions: Myocardial Ischemia
Hip Fracture
Inflammation

Interventions: Drug: Atorvastatin
Drug: Placebo

Registration Number: NCT02197065

Lead Sponsor: Hospital for Special Surgery, New York

Brief Summary: Up to 35% of hip fracture patients have been shown to experience heart injury after surgery, and as many as 10% have a heart attack or die in the three months after surgery. Hip and knee arthroplasty patients are also at risk of cardiovascular complications. Patients who have these complications have higher levels of inflammation postoperatively. Statins (such as atorvastatin/Lipitor) lower cholesterol and also lessen inflammation. Both of these effects are important in preventing heart attacks. Statins have been shown to reduce the risk of heart attacks in non-surgical patients, and to protect from heart attacks in patients having heart surgery. Whether statins can prevent heart attacks in orthopedic patients is not known.

In this pilot study the investigators will treat 30 orthopedic surgery patients (hip fracture, hip or knee arthroplasty) with either atorvastatin or placebo (a capsule with no study drug). Patients will start the study drug prior to surgery and take it for 45 days after surgery. Neither the doctors nor the patients will know whether they are taking atorvastatin or placebo. The investigators will look for evidence of inflammation and heart injury after surgery. The investigators hypothesize that atorvastatin will lessen the degree of postoperative inflammation found in these patients. In this study, the investigators will use a very sensitive test of heart injury that can detect problems even when patients have no symptoms. The investigators hypothesize that this test will demonstrate silent heart injury in over 50% of the hip fracture patients and over 30% of arthroplasty patients in our study.

The results of this trial will help us to develop a larger study in 1000 hip fracture and joint replacement patients to determine whether atorvastatin protects orthopedic surgery patients from heart injury and other complications of surgery.

Detailed Description: * Thirty statin-naïve patients ≥ 65 years of age admitted to New York Presbyterian Hospital or Hospital for Special Surgery with an acute hip fracture, or for elective hip or knee arthroplasty will be randomized in a 1:1 ratio to atorvastatin 40 mg daily or matching placebo.

* Atorvastatin will be initiated at least 4 hours prior to hip fracture surgery, or 4 days prior to arthroplasty, and will be continued until postoperative day (POD) 45.

* Patients will be assessed daily in the hospital for adverse events.

* Patients will be contacted by telephone weekly for four weeks after surgery and again on POD 45 and POD 90.

* Patients will mail back study medication bottles on POD 45 for pill counts to assess compliance.

* High sensitivity cardiac troponin I (hs-cTnI) will be measured pre-operatively (prior to atorvastatin therapy) and on POD 2.

* High sensitivity C-reactive protein (hs-CRP), and a panel of cytokines (IL-1β, IL-2, IL-2r, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12, IL-13, IL-17, tumor necrosis factor (TNF)-α, interferon (IFN)-γ, and soluble (s)CD-40L) will be measured preoperatively and on POD 2.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 20

Inclusion Criteria

Hip fracture or elective hip or knee arthroplasty
Age 65 years or older
Life expectancy > 3 months

Exclusion Criteria

Pathological hip fracture due to cancer
Currently taking a statin, or took a statin within the last 30 days
Previous statin intolerance
Acute myocardial infarction or unstable angina
History of myocardial infarction, acute coronary syndrome, angina, coronary/arterial re-vascularization
Hip fracture patients with peripheral arterial disease
Hip fracture patients with history of stroke or transient ischemic attack.
Muscle disorder
Serious liver disease or alanine aminotransferase > 3x upper limit of normal
Serious renal disease (creatinine clearance <30cc/min)
Treatment with HIV protease inhibitor or Hepatitis C protease inhibitor
Treatment with erythromycin, clarithromycin, niacin or azole antifungal agent
Pregnant, planning to become pregnant, or breastfeeding

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Atorvastatin	Atorvastatin	Atorvastatin 40mg daily starting at least 4 hours prior to hip fracture surgery, or 4 days prior to hip or knee arthroplasty, and continued until postoperative day 45.
Sugar pill	Placebo	Sugar pill (placebo) daily starting at least 4 hours prior to hip fracture surgery, or 4 days prior to hip or knee arthroplasty, and continued until postoperative day 45.

Primary Outcome Measures

Name	Time	Method
Peri-operative Rise in High Sensitivity C-reactive Protein (Hs-CRP)	Change from preoperative to post-operative day 2	The change in the level of hs-CRP from baseline to POD2 in 20 orthopedic patients randomized (1:1) to atorvastatin 40mg versus placebo.
Percentage of All Enrolled Patients With a Peri-operative Rise in High-sensitivity Cardiac Troponin I	change from preoperative to postoperative day 2	The percentage of orthopedic patients with a ≥ 10 pg/mL rise in high-sensitivity cardiac troponin I (hs-cTnI) from baseline pre-operatively to post-operative day (POD)2

Secondary Outcome Measures

Name	Time	Method
Peri-operative Rise in Interleukin-6 (IL-6) Levels	Change from preoperative to postoperative day 2	The change in the level of IL-6 from baseline to POD2 in 16 arthroplasty patients randomized (1:1) to atorvastatin 40mg versus placebo.

Trial Locations

Locations (2): New York Presbyterian Hospital (Cornell)
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New York, New York, United States
Hospital for Special Surgery
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New York, New York, United States