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Testimonials

Since Tri-Solfen® was commercially launched, over 150 million lambs have been treated and over 80% of Australian wool growers are now using Tri-Solfen for their sheep. Here’s what some of them have to say…

‘We have used pain relief for two years now and seen real production gains. We are concerned for the welfare of our animals and will continue to use pain relief to ensure they get the best care.’

Clinton Wise– Wililoo Merino Stud, Woodanilling, W.A.

'It easy to see the difference pain relief makes. Before, lambs would walk away hunched up, even taking a couple of hours to walk back to the paddock. Now they run straight back to Mum and start suckling,” says Rod. “My wool is now sold under the Better Choices brand. I see this as a definite advantage. I think it will be an advantage in the long run, to both me and the industry as a whole.'

Rod Miller– Glenpaen Merino Stud, Horsham, Vic

'After being treated with pain relief my lambs were more content and less stressed. As farmers we are sincere in looking after the welfare of our animals and using pain relief demonstrates this.'

Richard Coole– Frankland, W.A.

'We have been using pain relief for the past three years. We’re impressed by reduced bleeding in the mulesing wound immediately after application. Lambs run straight back to find the ewe, which has dramatically reduced our mortality rates. Flock management, post lamb marking is easier due to the effect of pain relief and the scab healing faster.'

Ryan & Malcom O’Dea– Peepingee Merino Stud, Narrogin, W.A.

'Using pain relief eases the stress and allows lambs to mother up and move back to the paddock easier with faster weight gains.'

Kent Lummis– Waverley Downs, Gilgandra, NSW

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Patent Portfolio

Country Species Patent
Australia Sheep Granted
Australia Horses, Dogs, Lab animals Granted
Australia Cattle Granted
Australia Humans Granted
New
Zealand
Sheep,
Cattle
Granted
New
Zealand
Horses, Dogs, Lab animals Granted
EU Humans Granted
EU Pig, Sheep,
Cattle
Granted
USA Dogs, Horses, Lab animals Granted
USA Humans Granted
USA Pig, Sheep,
Cattle
Granted
Canada Horses, Dogs, Lab animals Granted
Canada Cattle,
Pig
Granted
Canada Humans Granted

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Advisory Board

Ian Page

Non-Executive Director

Ian is Chief Executive Officer of Dechra Pharmaceuticals, which has a 33% shareholder in Medical Ethics. He joined National Veterinary Services, Dechra’s former services business in 1989 and joined the Board of Dechra in 1997. In October 2010, Ian was appointed as Non-Executive Chairman of Sanford DeLand Asset Management.

Dr Chris Roberts

Human Wound and Regulatory Advisor

Chris has over 20 years’ line management experience of heading clinical research teams. He was previously global head of Smith & Nephew clinical support and market development, where he managed global clinical Phase II and III programmes in the management of venous and pressure ulcers.

Lieutenant Colonel Professor Steven Jeffery

Medical Specialist Advisor

Steve has over 15 years’ experience in military plastic surgery. In 2011 he was awarded the Military Civilian Partnership Award for ‘Regular of the Year’, as well as receiving the Wounds UK ‘Key Contribution’ award and the Smith and Nephew ‘Customer Pioneer of the Year’ award. He has also been awarded Fellowship of the Royal College of Surgeons of England ad eundum. He is an expert adviser to NICE Medical Technologies Evaluation Programme. Steve co-founded the Woundcare 4 Heroes charity, which is already making a big difference to the wound care of both serving and veteran personnel.

Dr Matthew Bayfield

Medical Specialist Scientific Director

Dr Matthew Bayfield, Head of Cardiothoracic Surgery, Strathfield Private Hospital and VMO Cardiothoracic Surgeon, Royal Prince Alfred Hospital.

Professor Peter Windsor

Veterinarian Research Advisor

Peter is a registered specialist veterinary surgeon in New South Wales and an emeritus Professor at Sydney University. He holds a BVSc (Hons), PhD, DVSc and diploma from the European College of Small Ruminant Health Management.

Dr Julian Braidwood

Global Regulatory Affairs Advisor

Julian has held leadership roles and managed international clinical projects with Grampian. He was previously Regulatory Affairs Manager at Novartis Animal Health. He is the Founder and Managing Director of Triveritas, where he is responsible for a team of 40 animal health specialists across the EU and the US.

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Medi-Solfen® technology has the potential to deliver a rapid onset

Surgical debridement uses sharp instruments (such as a scalpel, scissors and other sharp instruments) to remove necrotic tissue from the wound bed, either at the patient’s bedside or in specialised clinics. The advantages of such approaches include excellent control over the selection of tissue type to be removed and how much tissue to remove. It is the fastest way to achieve a clean wound bed and an increased frequency of debridement of this kind has the potential to speed up the healing process1,2 which presents clinical, patient and economic advantages. A major disadvantage is that the use of sharp instruments may be painful for the patient. The pain type is described as procedural/operative pain which by definition causes pain that results from routine procedures such as dressing changes or wound cleansing, or is associated with significant wound interventions, such as biopsies or debridement3. Rapid control of such pain will impact on the patient’s overall experience of the procedure and also improve subsequent compliance to attend future events of this nature and adhere to dressing changes. It is possible that patients will deny future consent for the sharp debridement if the first experience was painful. This poses difficulties in providing optimal care and in achieving healing in a timely manner. Delayed healing eventually creates additional costs and deterioration in the patient’s quality of life. Some anaesthetic containing creams such as EMLA can take up to 1 hour post application to attain sufficient levels of anaesthesia to allow the debridement process to commence. This extends considerably the procedure duration times, levels of anticipation surrounding what the patient may be expecting to happen (especially if pain has been encountered in previous visits) and affect resource utilisation strategies within the clinical facility. With the increasing number of venous ulcers being treated questions can be raised about the ability of healthcare professionals to meet, for example, CQUIN wound care goals with the additional timings required for routine but essential procedures such as debridement4.

Having access to a proven, rapid onset, multimodal anaesthetic gel with additional bacterial agents and adrenaline such as Medi-Solfen® allows faster turnaround times for debridement procedures within any clinic situation. This will positively impact on clinical resource utilisation initiatives increasing productivity. The rapid onset of effective anaesthesia also offers great benefits to the patient, avoiding previous negative experiences associated with pain and making the overall experience more accommodating to enhance overall compliance with treatment. This also aligns itself to the UK NHS advocating a patient- centred approach, an approach that promotes physical comfort, including pain management5.

References

  1. Steed DL, Donohoe D, Webster MW, Lindsley L (1996) Diabetic Ulcer Study Group. Effect of extensive debridement and treatment on the healing of diabetic foot ulcers. J AmColl Surg; 183(1): 61-64.
  2. Wilcox JR, Carter MA and Covinton S (2013) Frequencies of debridement and time to heal. A retrospective cohort study of 312744 wounds. JAMA Dermatol; 149(9): 1050- 1058.
  3. Brown A. (2014) Strategies to reduce or eliminate wound pain. Nursing times; 110 (15): 13-15.
  4. Commissioning for Quality and Innovation (CQUIN). Guidance for 2017-2019 Publications Gateway Reference 06023. Nov 2016
  5. NHS Paper summarising Patient experience Framework (2011). Gateway reference 17273.