Doseme.com.au
INTRODUCTORY BROCHURE The DoseMe Platform
The DoseMe® Platform
Personalised Medicine: Making Complex Simple
What is DoseMe®?DoseMe is an easy-to-use Bayesian dose-individualisation platform designed for clinicians and healthcare practitioners
to optimise patient care. DoseMe currently supports several classes of drugs, including antibiotics, anti-coagulants, and
chemotherapeutic agents. DoseMe supports label or guideline-based dosing as well as dose-individualisation.
Why Dose-Individualise?Adverse drug events on average require 4.6 additional hospital days, at a cost of approximately $10,000.1 For the commonly
used antibiotic, gentamicin (which makes up approximately 7% of total hospital antibiotic use2), the effects of adverse
dosing events include nephrotoxicity and vestibular damage. These each occur in conservatively 2-3% of patients, but
likely significantly more.3,4 For large tertiary hospitals, conservatively assuming 2-3%, this is approximately $3 million per
annum for each hospital, just for gentamicin. In fact, other drugs such as warfarin have substantially higher adverse drug
Appropriate methods of dose adjustment and individualisation have been shown to reduce adverse drug events by
75-80%.5 Furthermore, Bayesian dose individualisation has been shown to significantly extend life for patients undergoing
Finally, computerised dose individualisation has been mandated by the 2010 Australian Therapeutic Guidelines for the use
of aminoglycosides. Gentamicin toxicity is a known issue to the legal community, with some law firms specialising in these
Drug SupportDoseMe currently supports the following drugs:
• Amikacin (adults and paediatric)
• Itraconazole (adults and paediatric)
• Busulfan (adults and paediatric)
• Methotrexate (adults and paediatric)
• Ciclosporin (adults)
(adults and paediatric)
• Enoxaparin (adults)
• Tobramycin (adults and paediatric)
• Gentamicin (adults and paediatric)
• Vancomycin (adults and paediatric)
• Factor VIII (adults and paediatric)
• Voriconazole (adults)
• Flucloxacillin (adults and paediatric)
(adults and paediatric)
New drugs are being added continually, and DoseMe can support specific drugs on request. DoseMe does not limit the
number of compartments or the types and kinds of covariates supported in drug models.
Clinically TestedDoseMe has undergone multiple trials for both accuracy and usability. DoseMe was found in a recent study to be the most
accurate individualised dosing method tested, having both the lowest bias and highest precision.9
These trials report extremely positive findings, both for clinical outcomes, and DoseMe's ease-of-use. DoseMe was initially
developed in conjunction with clinical and research staff in the Royal Brisbane and Womens' Hospital – the largest teaching
hospital in the southern hemisphere – for both clinical and research purposes. DoseMe has been piloted at multiple hos-
pitals across Australia and Eur
These programmes [iPad and web-interface] provide easy to use dosing
"support for these difficult to dose medications… We have found the
DoseMe software very straightforward for doctors to use. "
- Professor and Clinical Pharmacologist, Brisbane
Bates DW, Spell N, Cullen DJ, Burdick E, Laird N, Petersen LA, et al. The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention
Study Group. JAMA. 1997;277(4):307-11.
CHRISP. Antimicrobial Utilisation Report to Queensland Health Medicines Advisory Committee. May 2012.
Selimoglu E. Aminoglycoside-induced ototoxicity. Curr Pharm Des. 2007;13(1):119-26. Review.
Selby NM, Shaw S, Woodier N, Fluck RJ, Kolhe NV. Gentamicin-associated acute kidney injury. QJM. 2009 Dec;102(12):873-80.
Executive summary of disease management of drug hypersensitivity: a practice parameter. Joint Task Force on Practice Parameters, the American Academy of
Allergy, Asthma and Immunology, and the Joint Council of Allergy, Asthma and Immunology. Ann Allergy Asthma Immunol. 1999;83:665-700
Evans WE, Relling MV, Rodman JH, Crom WR, Boyett JM, Pui CH. Conventional compared with individualized chemotherapy for childhood acute lymphoblastic
leukemia. N Engl J Med. 1998 Feb 19;338(8):499-505
Keith S. Douglass & Associates, L.L.P. http://www.gentamicin.com/legal-issues
Oshman & Mirisola, LLP. http://www.oshmanlaw.com/pharmaceutical_litigation/gentamicin.html
Hennig S, Stiller F, Teo B, Staatz C. Comparing methods for once daily tobramycin exposure predictions in children with cystic fibrosis. PAGANZ 2014.
Designed for the ClinicDoseMe has been designed from the ground-up
to seamlessly fit into a clinical workflow. DoseMe
supports use by the bedside (iPads / iPhones),
the desktop (web interface), as well as integrating
into existing patient management software.
(Cloud or Physical)
DoseMe supports industry standard integration
languages, including HL7, and is currently being
extended to provide dosing recommendations
(after physician approval) to patient phones.
Custom integration services are also available to
suit whatever clinical requirements you may have.
Schematic of DoseMe's logical architecture.
Fully SupportedDoseMe is a fully-supported product 24x7, with both phone and online support. DoseMe has partnered with a leading
global IT solution provider, allowing DoseMe to provide world-wide support, localisation, and implementation services.
Performance and availability of the DoseMe Platform is continually monitored, so you can rely on DoseMe being there when
you need it.
A Regulated Medical DeviceDosing support software is considered a regulated medical device in much of the world. DoseMe
has obtained CE marking, TGA approval, and hopes to shortly file for FDA approval. Designed and
built to comply with these requirements from the beginning, DoseMe gives you confidence that
you're using software developed and maintained to the rigorous standards appropriate for a clinical
Every time a new DoseMe installation occurs, or an update is prepared for release, a large set of validation tests (thousands)
are automatically performed to ensure that DoseMe remains numerically precise. Before releasing updates, user acceptance
testing of DoseMe is also undertaken – making sure DoseMe's interface is suitable for clinical practice.
Every model incorporated in DoseMe goes through rigorous review by an expert pharmacometrician.
Cloud-Based and ScalableDoseMe is a cloud-based solution that can be deployed and
made available immediately, without requiring lengthy and
difficult IT compatibility projects. However, we do support
integration with in-house systems if required. DoseMe scales
seamlessly, supporting 1 to more than 100,000 patients.
Safe & SecureDoseMe Pty Ltd is committed to safe and secure data
storage and transmission.
• DoseMe encrypts all communication using bank-grade
• We comply with data security and privacy legislation.
Our privacy policy is available on our website.
• All servers used by a given clinic are hosted in the same
jurisdiction, simplifying your legal requirements.
For More InformationTo learn more about DoseMe, please feel free to contact the DoseMe team with any questions
or for a demonstration. In the past, DoseMe has presented to specific clinical units (e.g. renal
units), mixed-speciality audiences (e.g. grand rounds), as well as to research and management
DoseMe evaluation accounts are available free on request. Send us an email or give us a call to
get started with personalised medicine today.
T +61 7 3151 3033
M +61 421 979 896
Copyright 2015 DoseMe Pty Ltd. All rights reserved. DoseMe is a trademark of DoseMe Pty Ltd. All other trademarks mentioned herein are the sole property of their respective owners.
Source: https://doseme.com.au/assets/files/doseme_technology.pdf
Your GP or Endocrinologist may also check: What do I need to know about my medication? Kidney function The aim of treatment is to abolish symptoms – not Phosphate and magnesium levels to restore ‘normal' calcium levels in the blood. Vitamin D levels In the absence of PTH, higher levels of calcium are found in the urine for a given blood calcium level.
MODELLING THE SPATIAL-TEMPORAL EVOLUTION OF THE 2009 A/H1N1 INFLUENZA PANDEMIC IN CHILE URGERA, GERARDO CHOWELLB, PEP MULETC, AND LUIS M. VILLADAD Abstract. A spatial-temporal transmission model of 2009 A/H1N1 pandemic influenzaacross Chile, a country that spans a large latitudinal gradient, is developed to characterizethe spatial variation in peak timing of the 2009 A/H1N1 influenza as a function of spatialconnectivity assumptions across Chilean regions and the location of introduction of the virusinto the country. The resulting model is a SEIR (susceptible-exposed-infected-removed)compartmental model with local diffusion and optional non-local terms to describe themigration of individuals of the S, E and R classes and the effect of a "hub region". Thismodel is used along with epidemiological data to explore the spatial-temporal progressionof pandemic influenza in Chile by assuming a range of transmission scenarios. Numericalresults indicate that this relatively simple model is sufficient to characterize the south-northgradient observed during the 2009 influenza pandemic in Chile, and that the "hub region"corresponding to the capital region plays the critical role in keeping the population wellmixed in a relatively short period of time.