The Operating Theatre Journal February 2022
The Operating Theatre Journal February 2022
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
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