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legal and regulatory approvals.<br />
Besides precision dosing<br />
apps, BaseCase Portal can also<br />
be used for diverse purposes<br />
such as providing education<br />
and facilitating collaboration.<br />
Examples include apps that<br />
provide product information,<br />
inform on guidelines and<br />
treatment pathways, and track<br />
the progress of global studies.<br />
As BaseCase Portal is a<br />
white label solution, it can be<br />
tailored to reflect each clients’<br />
brand identity, Certara informs.<br />
BTG launches<br />
cryoablation<br />
system<br />
BTG plc has announced the<br />
global launch of the ICEfx<br />
Cryoablation System. ICEfx,is<br />
an updated version of the<br />
existing Visual ICE system is<br />
designed for interventional<br />
radiologists who want to<br />
offer their patients minimally<br />
invasive treatment options.<br />
It allows physicians to<br />
provide safe and efficient<br />
cryoablation procedures,<br />
facilitating precise and<br />
effective treatment without<br />
the need for surgery or<br />
repeated radiation treatments.<br />
The advanced cryoablation<br />
technology is currently<br />
supporting a number of active<br />
clinical research studies in<br />
bone, kidney, lung, pain, and<br />
prostate, the company said.<br />
BTG Interventional<br />
Oncology delivers IO ablation<br />
solutions across multiple<br />
physician specialties.<br />
Stent to seal<br />
coronary artery<br />
tears cleared<br />
The US FDA has cleared PK<br />
Papyrus Covered Coronary<br />
Stent System, a device to<br />
treat acute coronary artery<br />
perforations or tears in the<br />
blood vessels of the heart.<br />
A coronary artery<br />
perforation can occur during<br />
Percutaneous Coronary<br />
Guide XT system for<br />
visualization of DBS<br />
Guide XT System for<br />
visualization of deep<br />
brain stimulation (DBS)<br />
was launched in Europe,<br />
said Boston Scientific<br />
Corporation.<br />
The Guide XT System<br />
is built for directionality<br />
that utilizes patientspecific<br />
anatomy and<br />
stimulation field modeling.<br />
This technology provides<br />
physicians with 3-D image<br />
planning capability and<br />
when used in conjunction<br />
with the Vercise DBS<br />
Systems, enables physicians<br />
to personalise and optimise<br />
DBS treatment.<br />
DBS treats movement<br />
disorder symptoms in<br />
patients with Parkinson’s<br />
disease, dystonia or essential<br />
tremor. The procedure<br />
stimulates a targeted<br />
Intervention (PCI) procedures.<br />
The PK Papyrus Stent<br />
System is a balloonexpandable<br />
covered coronary<br />
stent and delivery system.<br />
The device is advanced into<br />
the perforated coronary<br />
artery vessel using a balloon<br />
catheter, similar to the<br />
one used during the PCI<br />
procedure. Once the PK<br />
Papyrus stent is implanted,<br />
it provides a physical barrier<br />
to seal the tear in the artery<br />
wall while still allowing<br />
region of the brain through<br />
implanted leads that are<br />
powered by a device called<br />
an implantable pulse<br />
generator (IPG).<br />
The Guide XT System<br />
automatically detects<br />
the location of the<br />
leads, implanted by a<br />
neurosurgeon, in the<br />
imaging of the brain.<br />
Following the implant, a<br />
clinician programmes a<br />
patient’s device and the<br />
Guide XT System can be<br />
used to help visualize<br />
the stimulation field and<br />
efficiently determine the<br />
most appropriate settings for<br />
each patient.<br />
Guide XT was developed<br />
in partnership with<br />
Brainlab AG, a softwaredriven<br />
medical technology<br />
company.<br />
blood to flow through the<br />
device to the heart muscle.<br />
Successful sealing of a<br />
coronary perforation with the<br />
PK Papyrus Covered Coronary<br />
Stent System can be a lifesaving<br />
procedure without the<br />
need for open-heart surgery.<br />
The FDA reviewed realworld<br />
survey data from<br />
80 patients who received<br />
PK Papyrus stents to treat<br />
coronary artery perforations.<br />
PK Papyrus stents were<br />
successfully delivered to the<br />
perforation site in 76 of the<br />
80 patients (95 percent), and<br />
the device successfully sealed<br />
the perforation in 73 patients<br />
(91.3 percent), according to<br />
US FDA.<br />
Micro pump for<br />
Parkinson’s gets<br />
CE mark<br />
Sensile Medical AG, a<br />
Swiss medical technology<br />
company, said its wearable<br />
micro pump has received CE<br />
certification from EU.<br />
The micro pump is<br />
designed to be used in<br />
the treatment of advanced<br />
Parkinson’s disease. The<br />
handy-sized, discreet<br />
pump has got easy to use<br />
features such as automatic<br />
filling with liquid medicine.<br />
Technologies such as colour<br />
display, charging unit and data<br />
storage help enhance therapy<br />
management.<br />
A personally<br />
programmable basal profile<br />
enables treatment to be<br />
optimized for Parkinson’s<br />
patients and ensures that they<br />
receive the precise dosage<br />
they need. Likewise for the<br />
bolus rate: A patient can<br />
cause the device to deliver<br />
a bolus at just one touch of<br />
a button. Sensile’s patented<br />
SenseCore micro rotary<br />
piston pump in the device<br />
ensures safe, precise drug<br />
delivery, eliminating flow rate<br />
calculations.<br />
86 / FUTURE MEDICINE / <strong>NOVEMBER</strong> <strong>2018</strong>