September 2021 Print Issue

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IN THE NEWS

SEPTEMBER 2021 / GENERAL SURGERY NEWS

Bariatric Surgery Decreases Hospital al Admissions for Diastolic Heart Failure By KATE O’ROURKE

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ariatric surgery decreases the number of hospital admissions for diastolic heart failure in severely obese patients, according to new research presented at the 2021 annual meeting of the American Society for Metabolic and Bariatric Surgery (abstract A008). According to David Funes, MD, a research fellow at Cleveland Clinic in Weston, Fla., who presented the research, for more than 16 years, the objective of medical therapy in diastolic heart failure has been to decrease hospital admissions and mortality. Unfortunately, all randomized trials have failed to demonstrate efficacy of medical therapy in these important clinical outcomes. Dr. Funes said the only medication that has proven modest impact to prevent hospitalizations in this patient population is candesartan. In the new study, the researchers’ primary objective was to evaluate the hypothesis that bariatric surgery is associated with a decrease in hospital admissions for diastolic heart failure in severely obese patients. The researchers conducted a retrospective analysis of the National Inpatient Sample database from the years 2010 to 2015, dividing patients into those with and without a history of bariatric surgery. They analyzed all covariates associated with morbidity and mortality for diastolic heart failure including hypertension, diabetes mellitus, smoking, coronary artery disease, race, age and sex. The multivariate logistic regression analysis demonstrated that the patients who did not undergo bariatric surgery were at a significantly higher risk for being admitted for acute and chronic diastolic heart failure. “Patients in the control group with no history of hypertension were almost five times more likely to be admitted for acute diastolic heart failure,” Dr. Funes said. “Furthermore, the odds of prevalence for chronic diastolic heart failure were two times higher in the control group when compared to their counterparts in the control group. … The multivariate logistic regression analysis demonstrated that the odds of hospitalization for diastolic heart failure, specifically for patients with a history of coronary artery disease, was almost three times higher in the control group when compared to the surgical group.” Tammy Kindel, MD, PhD, an associate professor and the director of the bariatric surgery program at the University of Wisconsin–Milwaukee, who served

as the discussant of the study, pointed out h that heart failure with preserved ejection fraction (HFpEF) is closely associated with obesity and w hypertension and is now representing 50% of casess of heart failure. She said it

is a distinct pathophysiologic phenotype from heart failure with reduced ejection fraction. “HFpEF has significant morbidity and mortality, as mentioned, and there really is no effecti tive medical treatment cap capable of reducing heart

failure–related mortality,” Dr. Kindel said. “Although it would seem that obesity treatment would be essential, there really are minimal studies demonstrating that weight loss, in any form, can modify diastolic dysfunction in HFpEF patients. Your group has really added an important article to the literature where there is a true void and considerable knowl■ edge gap.”

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LEARN MORE AT WWW.EXPAREL.COM Indication EXPAREL® (bupivacaine liposome injectable suspension) is indicated for single-dose infiltration in patients aged 6 years and older to produce postsurgical local analgesia and in adults as an interscalene brachial plexus nerve block to produce postsurgical regional analgesia. Safety and efficacy have not been established in other nerve blocks.

routes of administration: epidural, intrathecal, regional nerve blocks other than interscalene brachial plexus nerve block, or intravascular or intra-articular use. The potential sensory and/or motor loss with EXPAREL is temporary and varies in degree and duration depending on the site of injection and dosage administered and may last for up to 5 days, as seen in clinical trials.

Important Safety Information EXPAREL is contraindicated in obstetrical paracervical block anesthesia. Adverse reactions reported in adults with an incidence greater than or equal to 10% following EXPAREL administration via infiltration were nausea, constipation, and vomiting; adverse reactions reported in adults with an incidence greater than or equal to 10% following EXPAREL administration via interscalene brachial plexus nerve block were nausea, pyrexia, and constipation. Adverse reactions with an incidence greater than or equal to 10% following EXPAREL administration via infiltration in pediatric patients six to less than 17 years of age were nausea, vomiting, constipation, hypotension, anemia, muscle twitching, vision blurred, pruritus, and tachycardia. If EXPAREL and other non-bupivacaine local anesthetics, including lidocaine, are administered at the same site, there may be an immediate release of bupivacaine from EXPAREL. Therefore, EXPAREL may be administered to the same site 20 minutes after injecting lidocaine. EXPAREL is not recommended to be used in the following patient populations: patients <6 years old for infiltration, patients younger than 18 years old for interscalene brachial plexus nerve block, and/or pregnant patients. Because amide-type local anesthetics, such as bupivacaine, are metabolized by the liver, EXPAREL should be used cautiously in patients with hepatic disease.

Warnings and Precautions for Bupivacaine-Containing Products Central Nervous System (CNS) Reactions: There have been reports of adverse neurologic reactions with the use of local anesthetics. These include persistent anesthesia and paresthesia. CNS reactions are characterized by excitation and/or depression. Cardiovascular System Reactions: Toxic blood concentrations depress cardiac conductivity and excitability, which may lead to dysrhythmias, sometimes leading to death. Allergic Reactions: Allergic-type reactions (eg, anaphylaxis and angioedema) are rare and may occur as a result of hypersensitivity to the local anesthetic or to other formulation ingredients. Chondrolysis: There have been reports of chondrolysis (mostly in the shoulder joint) following intra-articular infusion of local anesthetics, which is an unapproved use. Methemoglobinemia: Cases of methemoglobinemia have been reported with local anesthetic use.

Warnings and Precautions Specific to EXPAREL Avoid additional use of local anesthetics within 96 hours following administration of EXPAREL. EXPAREL is not recommended for the following types or ©2021 Pacira BioSciences, Inc. Parsippany, NJ 07054 PP-EX-US-6517 03/21

Please refer to brief summary of Prescribing Information on adjacent page. For more information, please visit www.EXPAREL.com or call 1-855-793-9727. Reference: 1. Data on File. 6450. Parsippany, NJ: Pacira BioSciences, Inc.; January 2021.

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