14 April 2014

My take on the 10th Australian Lymphology Association Conference in Auckland, Day 1

Where to begin.  Well, let's just say there is no way I'm going to cover even a fraction of what I saw/heard at the 10th Australian Lymphology Association Conference, there was just so much content. I've counted that there were 39 presentations in three days, one of those was broken into case studies with different presenters being allocated 2 minutes (in one hour there were 12 presentations)! So I'll go for the stand-out highlights for me and I'll do a few different posts over the next week or so to not bombard you with too much info.

I attended three workshops - we got to choose those when we registered and two of them I found fantastic.  The first was on Differential Diagnosis of Lymphoedema, presented by my favourite, Prof Neil Piller of Flinders University, and Vaughan Keeley of the Royal Derby Hospital, UK.  Was really pleased that they focussed on lipoedema and the difficulties of diagnosing some cases.

I found the presentations by Dr Hiroo Suami of the University of Texas MD Anderson Cancer Centre to be very interesting and amazingly upbeat and humourous (quite difficult I reckon when showing slides of cadavers).  He has pioneered The Lymphosome Concept, a way of "visualising the lymphatic system using hydrogen peroxide and a radio-opaque medium injected into cadavers then using radiographs and three-dimensional computed tomography scans to see how and where lymphatic fluid flows, which vessels, nodes and territories it uses.  Fascinating.  He also talked about surgical treatment for lymphoedema, including creating new channels to increase the capacity to transport lymph fluid; liposuction or lymphovenous shunting, lymphatic graft and vascularised lymph node transfer.

One of the most interesting things I heard was in one of the "breakaway sessions" of four talks.  It was by another of my favourite presenters, Alex Munnoch, of Ninewells Hospital in the UK.  He noted that surgical staff who perform long surgeries often complain of leg discomfort and oedema, so they set up a small trial to see whether T.E.D. stockings (those beautiful white stockings you are given when you've had some surgery in hospital) have an effect on the level of oedema.  One leg was randomised (by the flipping of a coin, very scientific criteria indeed!) to wear a T.E.D. stocking and the control leg (the other side) would receive no compression at all.  Fluid levels were measured before and after the surgeries.  40 legs were studied in all with an average operating time of 9.5 hours.  Results?  T.E.D. stockings were found to reduce the increase of fluid and interestingly, when they tried the experiment using compression stockings instead of T.E.D. stockings the degree of oedema increased!  What!! That was a surprise indeed.  He conceded that such a small study was perhaps not conclusive and more study was definitely warranted.

On the first day there I also attended presentations on head and neck lymphoedema management; lymphoedema and osteopathic care; reducing oedema after lower limb cellulitis; wounds and lymphoedema; and case study presentations on things such as; TRAM flap reconstruction; layered compression garments; liposuction; bioimpedance spectroscopy; kineseotape post radiotherapy; yellow nail syndrome .... the list goes on.

My head was swimming by the end of the day, that's for sure.

If you'd like more info on any of the topics I mentioned, please leave me a comment and I'll add some more infomation.  To access more information about lymphoedema and it's treatment, visit the ALA website here.

But it wasn't all hard work - here's a photo from the closing ceremony of two of my favourites ... Prof Piller and Alex Nunnoch, good on them for getting into the spirit of things!

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Prof Neil Piller and Alex Munnoch, letting their hair down

0 comments on “My take on the 10th Australian Lymphology Association Conference in Auckland, Day 1”

  1. Are there any print outs of info given during this conference.... Obviously some great speakers and i am sure they would have shared a lot of info that would interest those of us who have lymphedema.... Thanks

    1. Hi Helen, no,they don't give handouts (I think probably because there are too many attendees, over 250 this year, so too difficult to co-ordinate photocopying for that number of talks). The ALA does eventually put them up on their website, but in a restricted area. I'll keep an eye out for when they are put up and we can have a chat then about what you'd like more info about. As it is, I probably came back with an extra kilo of papers, but more from the product side of things - lots of compression options, skin care and that sort of thing.

      1. Thanks... I believe the ALA has voted to allow limited membership to those with Lymphedema... I hope this goes ahead as i think it would be really good... Going to MT Wilga about end of May ... Work on that lower back of thigh area!! Fun!!

          1. No I would have to pay each separate appointment as a long Physio!! But at MT Wilga as long as I stay in my health cover pays 100%... Plus I do feel they have a lot more experience there with bandaging and are well set up and in the past it has really helped... Plus laser and a gym program.. maquarie cannot offer me any of that they are really only set up for basic MLD... So will be having a two week holiday in Hornsby!!! Lots of books, films and writing... Will let you know how i go..😃😃

          2. A holiday in Hornsby ... sounds like a movie title. They are really the place to go to get it all done, you won't know yourself by the end. Hope you're taking photos along the way. I'm sure you can pick their brains about the Coban bandaging as well.

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