Let's Understand

 

Wound Care Library

GO BACK
Cullen's Circle Evidence

Disclaimer

The product information on this page is not intended to be used by health care professinoals or users in the United States and may not comply with the regulatory standards of the United States – please click the link above for product information in respect of products used in the United States

 

Cullens CircleCullen's circle


The insights that we have today (many of which we now consider self-evident) have not always been as clear. An insight has always started somewhere, started by someone who began to think about a notion, concept or another complex process. It also takes time before new insights are actually generally accepted. This also applies to insights about wound care.


The composition of wound exudate in chronic and acute wounds is totally different

Attention was first devoted to the wound exudate environment more than 10 years ago, with a publication by Schultz and Mast (1996). In this publication, it was clearly demonstrated that the composition of the wound exudate of chronic wounds differs significantly from the exudate in 'acute' wounds (see figure 1).


MMPs and the chronic wound

During the first couple of days after injury quite a bit of 'housekeeping' has to take place and that is primarily undertaken by a group of proteins (enzymes) called MMPs. MMPs are needed for recovery and, in an acute wound the role of the MMPs suddenly comes to an end. This is not the case in a chronic wound. If the wound continues to break down, then the MMP level will rise excessively and it will often not repair at all. The wound has become complicated.

 

 

MMPs and The Chronic Wound Graph

 

Figure 1

The origin of the vicious circle


During the years following the publication by Schultz and Mast, it became evident that the MMPs result in a some kind of vicious circle for the complicated wound. Damaged cells produce the MMPs, but in addition they also provide nutrients for bacteria, which are liberated by the bacteria by producing of MMPs, i.e. they dissolve their surrounding space and use that as nutrition. Also, the environment that is introduced by wound dressings can be harmful to the wound. We have already known for a long time that dry gauzes are very harmful to the tissue and also to the cells (Wood, 1976) as yet.

If we are all conscious of that, then we should also be able to find a way out of this situation. In other words, if we combat damage, physiological imbalance and the micro-organisms, we have found something that could lead to the problem being resolved (and thus exiting the vicious circle).


What does the vicious circle look like?


The evidence that has been collated to date for the existence and continuation of a complicated wound can be clearly shown in a picture of a vicious circle (figure 2):

 

vicious circle

 

 

 

 

 

 

 

 

 

 

 

 

 

Figure 2: the vicious circle

Because it is a vicious circle, it doesn’t matter where you start to read. However, let us start, for example, with the proteases (predominantly MMPs) that are released when cells (fibroblasts, keratinocytes, macrophages, etc.) are damaged. These MMPs not only damage the newly formed tissue, but growth factors (being proteins themselves) are also destroyed.

Bacteria are greatly attracted to damaged tissue. Bacteria also produce MMPs in order to release the nutrients from the cells/tissues. The micro-organisms also excrete toxins, through which increasingly larger numbers of leucocytes have to be mobilised to the area of the wound. The leucocytes try to kill the bacteria, also resulting in serious damage to the 'normal' cells and tissues. And this is what makes the circle "vicious", because the damaged cells again produce yet more MMPs.

It becomes even easier if we simplify figure 2 to the figure shown below:

 

 

Figure 3: roundabout

Figure 3 shows a road sign that we all know: that of a roundabout. A roundabout is also rather like a vicious circle - after all, you could continue to drive around it for as long as you want to. However, a roundabout does offer exits, and is therefore, different from a real vicious circle, from which an exit doesn’t seem evident or possible.

Intuitively, as a car driver we know that when we enter a roundabout, there will always be a time at which we can leave the roundabout again. You would also receive rather strange looks if you arrive at work late and say that you have just driven around the roundabout for several hours because you weren’t able to find the exits!

If we consider this, why do we therefore frequently not find the exits when treating a wound? Even in that case, we are aware of them: damage, imbalance and micro-organisms.

 

Leaving the vicious circle

Using the Clean, Close and Cover model discussed above, it is easy to explain why, based on these insights, it is possible to close wounds that have sometimes existed for a very long time (years):

  • The use of antimicrobial agents (i.e. SILVERCEL™) can result in a significant reduction in microbes, which can, therefore, also no longer produce their toxins and MMPs.
  • The introduction of the ideal moist conditions (such as, for example, with TIELLE™) will ensure that the cells can once again do their job and do not fall prey to the barren situations that dryness or soaking wet conditions introduce.
  •  Finally, the physiological imbalance can (on the basis of evidence) be abolished through the management of MMP levels.


In short, the seemingly complex model in figure 2 can be illustrated in a simpler model shown as follows in figure 4. There are three possible ways out of the vicious circle!

 

 

 

Cullens Circle figure 2

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Figure 4: Three ways out of the circle

Published: December 2007 by R. Legerstee, RN, MSc in Wound Healing & Tissue Repair

References:


Pourhassan S, Clinical evidence for the effort of sequential use of wound treatments using a “Clean, Close and Cover” approach. EWMA 2009.

Snyder R.  – Clinical evaluations of PGP and SNA

Disclaimer

The product information on this page is not intended to be used by health care professinoals or users in the United States and may not comply with the regulatory standards of the United States – please click the link above for product information in respect of products used in the United States

 

BACK TO TOP
 
 
Let's Heal™ is the unique system developed by Systagenix which represents the world's first integrated wound healing system,
allowing the clinician to "test and treat" wounds at the point of care.
With a wealth of clinical and scientific evidence that is hard to match, and a team of professionals continuing to raise the standards of innovation and expertise, we are committed to developing wound care solutions to help wounds heal, fast.
Meet the Systagenix Leadership Team, Clinical Advisory Board, and Board of Directors
Systagenix sales and marketing teams provide support in over 100 countries worldwide. For dedicated wound healing education and services, contact Systagenix directly to make an appointment now.
 
 

Media Centre

Next Step

Enlarge | Next

Now Playing: WOUNDCHEK™ Protease Status Specimen Collection (Serena's Technique)

Description:
1. Prior to swabbing, cleanse the wound with sterile saline to remove all loose debris, remains of therapeutic agents and necrotic tissue.
2. Ensure that complete hemostasis has been achieved before obtaining the specimen. Do not perform sharp wound debridement prior to sample collection.
3. Moisten wound area to be swabbed with a few (up to five) drops of saline. Care should be taken not to flood the wound with excessive saline.
4. Avoid swabbing areas that contain blood, necrotic material, thick slough or fibrinous tissue.
5. Using a sterile swab provided in the kit, collect the wound fluid sample by pressing the head of the swab flat against the base of the wound and gently rolling it back and forth several times while applying pressure. Continue rolling the swab head until fully coated and discoloured by wound fluid.
6. Test fresh sample swabs as soon as possible after collection. Follow test procedure instructions
.

Disclaimer
The product information on this page is not intended for, or to be used by health care professionals or users in the United States

Video footage kindly provided by SerenaGroup

SerenaGroup, 311 Pennsylvania Ave. West, Warren, PA 16365, USA, For more information email: Systagenix.

close

Your Comments

WOUNDCHEK™ Protease Status Specimen Collection (Serena's Technique)

Description:
1. Prior to swabbing, cleanse the wound with sterile saline to remove all loose debris, remains of therapeutic agents and necrotic tissue.
2. Ensure that complete hemostasis has been achieved before obtaining the specimen. Do not perform sharp wound debridement prior to sample collection.
3. Moisten wound area to be swabbed with a few (up to five) drops of saline. Care should be taken not to flood the wound with excessive saline.
4. Avoid swabbing areas that contain blood, necrotic material, thick slough or fibrinous tissue.
5. Using a sterile swab provided in the kit, collect the wound fluid sample by pressing the head of the swab flat against the base of the wound and gently rolling it back and forth several times while applying pressure. Continue rolling the swab head until fully coated and discoloured by wound fluid.
6. Test fresh sample swabs as soon as possible after collection. Follow test procedure instructions
.

Disclaimer
The product information on this page is not intended for, or to be used by health care professionals or users in the United States