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The Operating Theatre Journal February 2022

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(Continued)

New Type of Medical Helicopter

Provides Intensive Care in Transit

The research concluded that doctors as well as patients need to be

convinced of the negative consequences of keeping an inaccurate

diagnosis in records. Some felt it was an issue in the hospital setting,

rather than in primary care. Highlighting the negative impacts could

lead to more open discussions between patients and their GPs.

The benefits of testing for penicillin allergy also need to be stressed,

the study found. Doctors need more information about how to arrange

testing for patients.

What’s next?

Both doctors and patients need to understand the potential harms

associated with having penicillin allergy wrongly noted in medical

records. Healthcare professionals could be encouraged to supply more

detail in medical records about the initial reaction to penicillin. They

also need support to de-label low-risk patients in primary care. Decision

aids and algorithms might help to establish whether a medication has

caused harm, and whether testing is needed.

The current study was part of a larger project called ALABAMA (Allergy

Antibiotics and Microbial Resistance). Other research by the same team

is aiming to find clinically- and cost-effective ways of correcting a false

record about penicillin allergy. As part of this work, the researchers

are looking to make allergy testing more efficient. It currently requires

two visits. The team are exploring ways of testing for allergy in a single

visit.

You may be interested to read

This NIHR Alert is based on: Wanat M, and others. Management of

penicillin allergy in primary care: a qualitative study with patients and

primary care physicians. BMC Family Practice 2021;22:112

Another paper from the same team: Wanat M, and others. Patient and

primary care physician perceptions of penicillin allergy testing and

subsequent use of penicillin-containing antibiotics: a qualitative study.

The Journal of Allergy and Clinical Immunology: In Practice 2019;7:1888-

1893

Funding: This work was funded by the NIHR under its Programme

Grants for Applied Research Programme.

Conflicts of Interest: The study authors declare no conflicts of interest.

Disclaimer: NIHR Alerts are not a substitute for professional medical

advice. They provide information about research which is funded or

supported by the NIHR. Please note that views expressed in NIHR Alerts

are those of the author(s) and reviewer(s) and not necessarily those of

the NHS, the NIHR or the Department of Health and Social Care.

Karolinska University Hospital will be the first in Sweden to have a new

type of medical helicopter that can provide the sickest patients with

advanced care, even in the air. The helicopter can bring patients from

all over the country to Karolinska.

A contract for the operation and delivery of an Agusta Westland 139

(AW 139) helicopter has been signed by the supplier, Babcock, and

Karolinska. Karolinska will get access to a temporary helicopter in

March, 2022, and at the beginning of 2023, the permanent helicopter

will be delivered.

- Karolinska will be the first hospital in Sweden to have this type of

helicopter, which is unique, as the on-board staff can provide the

sickest patients with on-board medical care in a way that has not been

possible until now, such as ECMO care, says Lars Falk, operational

manager of Intensive Care and Transport, and continues:

- With the new helicopter, we can reach hospitals faster because we

don’t have to reload like we do now when flying planes.

Another advantage of the AW 139, which is considerably larger, heavier,

and has much more space than a regular ambulance helicopter, is that

it is built to withstand very severe weather conditions.

- In addition, it has its own de-icing system that allows it to withstand

severe winter weather and storms. All in all, the helicopter basically

functions as a flying intensive care unit, says Lars Falk.

HideBabcock Agusta Westland (AW 139)

• Can fly with a total weight of 7 tonnes

• Rotor diameter is 13.8 metres

• Length, 16.7 metres

• Space for 4 staff and 1 patient on board

• Extra-large windows for maximum visibility during missions

GI Supply Receives CE Mark for its EverLift® Submucosal Lifting Agent

New EverLift® medical device now available to physicians

across Europe

GI Supply Inc. today announced its EverLift® Submucosal Lifting Agent

has been awarded a CE Mark and is now available for use by physicians

across Europe. EverLift is a new device for the lift of polyps, adenomas,

early-stage cancers and other gastrointestinal lesions prior to their

excision with a snare or other appropriate endoscopic device1.

EverLift facilitates endoscopic resection procedures such as endoscopic

mucosal resection (EMR) or endoscopic submucosal dissection (ESD),

during examinations in the upper and the lower gastrointestinal tract.

EverLift is GI Supply’s first medical device to be awarded a CE Mark

under the new EU Regulation 2017/745 on Medical Devices (MDR).

EverLift gained FDA clearance in October 2020.

EverLift is the only pre-filled Submucosal Lifting Agent available in

both 5mL and 10mL syringes, providing physicians with the flexibility

to use only what they need whether lifting small or large lesions. In

addition, the sterile pre-filled syringe reduces the time and infection

risk associated with preparing a hospital-mixed solution.

The darker blue colour of EverLift is used to identify the perimeter of

lesions enabling a safe and complete resection, reducing the risk of

recurrent lesions. Following resection of a lesion, the darker colour

helps endoscopists identify potential injuries to the muscle layer.

“Lifting agents aid in safer resections for patients. EverLift provides

a pliable yet reliable cushion for resection and darker blue hues. The

single serve dosing helps reduce waste for everyday polypectomies.” –

Dr. Taavi Reiss, Assistant Professor of Clinical Medicine LSU Health and

Director of Interventional GI Metropolitan Gastroenterology Associates.

EverLift is cellulose based, creating a hypertonic solution with an

absorption rate slower than other currently available agents2. EverLift

provides gastroenterologists with a long and stable lift during their

resection procedures.

“This is an effective lifting agent for endoscopic resection that is

offered in convenient and cost-effective packaging.” – Prof. Douglas

Rex, Director of Endoscopy at Indiana University Hospital, Indianapolis.

“The CE Mark for EverLift enables us to reach more physicians around

the world. Many gastroenterologists will be familiar with our Spot®

Ex Endoscopic Tattoo, and we have used our extensive experience in

injection solutions to develop a unique lifting agent which will enhance

their ability to safely resect lesions,” said GI Supply Senior Marketing

Manager Simon Humphrey-Adam.

View the product video here: bit.ly/OTJEverLift

Further information contact: Simon Humphrey-Adam, International

Marketing Manager, s.humphrey-adam@gi-supply.com, 07974 319 541

www.gi-supply.com.

1. EverLift Instruction for Use G55-006 Rev 08, Nov 2021; G59-007

Rev 07, Nov 2021

2. Based on ex-vivo bench top studies and not in clinical use.

Data on file

Find out more 02921 680068 • e-mail admin@lawrand.com Issue 377 February 2022 25

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