Moffitt Cancer Center Advances Patient Standard of Care by Introducing Needleless Blood Draws

March 24, 2021

Moffitt Cancer Center has adopted a new needle-free method of blood collection for patients in treatment who often need to undergo repeated needle sticks in a day, becoming the first cancer center in Florida to offer this pain-free technology as part of its world-class cancer care.

In its continuing efforts of being at the forefront of innovation, last year the cancer center piloted the needle-free PIVO™ procedure from vascular access technology pioneer Velano Vascular. Since then, thousands of needle sticks have been avoided.

“A needle stick may seem inconsequential, but when repeated numerous times a day on a cancer patient with fragile veins who already carries a significant physical and emotional burden, it can be traumatic,” said Jane Fusilero, vice president and chief nursing officer at Moffitt Cancer Center. “This one seemingly small change, to remove the needle from blood collection, is making an enormous difference to our patients and team members alike. What used to be a dreaded, painful experience because of needles is now met with relief and smiles — a transformation that is positive and should be the expectation for patients fighting this disease.”

Moffitt is adopting this novel procedure across its inpatient population in an effort to bring more humanity to a common yet critical medical procedure, and to do so through a safer alternative to drawing blood from central lines and ports.

“This is a dramatic improvement in how a cancer center can approach vein access with our patients,” said Fusilero. “By shifting collection with this novel needle-free procedure to a traditional peripheral IV line, we’ve been able to significantly enhance our already high quality of care — eliminating pain and discomfort, optimizing practice efficiency, and reducing risk — all while enhancing the patient experience.”

This new standard of care enables what is known as one-stick hospitalization, a practice now in place at many leading health systems around the country. Moffitt Cancer Center is adopting the standard in its fight against cancer.

 

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”
Exit mobile version