FOR THE MANAGEMENT OF RENAL FAILURE IN CATS AND DOGS
2
Chronic renal failure in cats and dogs
Chronic renal failure (CRF) is characterised by the presence of irreversible structural lesions, and is generally considered, at least in clinical cases, to be progressive which ultimately result in the death. Therapy is thus aimed at ameliorating the clinical signs and systemic complications associated CRF, and slowing the progressive decline of renal function. CRF is a frequent cause of death in cats and particularly geriatric cats and in dogs.
1. Initial lesionsThe initial lesion causes reduction in the nephron population. It may be caused by toxic or infectious agents. In most instances it remain unnoticed until CRF has been diagnosed.
MAIN LESIONS CAUSING CRFCongenital in origin AcquiredAmyloidosis GlomerulopathyPolykistosis Interstitial nephropathyDysplasia Pyelonephritis
2. Clinical symptoms Clinical symptoms are usually noticed when the kidneys have lost 70% of their initial mass. Uraemia is the clinical state towards which all generalised renal diseases converge. The symptoms are attributed to the numerous uraemic toxins. Most of them emanate from the catabolism of proteins.
LIST OF THE MAJOR URAEMIC TOXINSUrea PhenolsCreatinine “Middle molecules”PTH HormonsIndoles SkatolsAmines acids Aliphatic aminesGuanidine compounds
The clinical symptoms are not pathognomonic and are different in dogs and in cats. Complementary biochemical analysis is needed to assess the exact diagnosis. Anorexia and digestive problems are frequent in cats: it makes changing their diet more diffi cult.
MOST FREQUENT CRF SYMPTOMS (RANKED BY DECREASING FREQUENCY)IN CATS IN DOGSAnorexia Polyuria – polydypsiaLethargy VomitingWeight loss DiarrhoeaPolyuria – polydypsia Weight lossVomiting
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3. PrognosisAnimals with CRF often survive for many months or years with a good quality of life. The diagnosis is more difficult in dogs because the symptoms occur later. Compensatory mechanisms of the body maintain a state of biochemical homeostasis despite significant renal dysfunction. As renal failure progresses, the animals are forced to live in a narrowed state of physiologic activity. A uraemic crisis may be suddenly precipitated by decreased intake of nutrients or water, development of concomitant diseases or administration of certain drugs.
PROGRESSION OF CRF: ROLE OF THE COMPENSATORY MECHANISMS
Chronic renal failure is an inherently progressive disease. Its progression either results from continuing renal damage induced by the nephropathy or from mechanisms independent of the initiating lesion and responsible for the spontaneous self perpetuation of the disease.
MECHANISMS OF COMPENSATORY ADAPTATION
• Hyperfiltration model: compensatory hyperfiltration and intraglomerular hypertension occur initially as adaptive responses to reduction in nephrons but eventually leads to progressive proteinuria, glomerular sclerosis and loss of functional nephrons.
• Nephrocalcinosis causes tubulo-interstitial injury characterised by tubular atrophy and dilation, interstitial fibrosis and interstitial inflammation. Excess PTH, caused by hyperphosphataemia, promotes too great flux of calcium into these cells, thus activating enzymes that destroy phospholipids, proteins, and nucleic acids. These effects result in cell dysfunction and death.
(according to D.J. Polzin and C.A. Osborne)
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CRF: Prolongation of life expectancy in cats and dogsManagement of compensatory mechanisms
Improving the health status and slowing down the progression of the disease is an important goal of treatment of CRF.
Reduction of phosphataemia: the corner stone of CRF treatment.
Reducing phosphaetaemia has been shown to prolong life expectancy in cats and dogs whatever the stage of the disease.
Reduction of protein intake: proven ineffective on survival time
Dietary protein restriction has been reported to have no effect on survival time. (1), (4), (5). The benefi ts of low protein diets seen in cases of advanced CRF (ie animals with moderate to severe azotemia and showing clinical signs of uraemia such as anorexia, weight loss, vomiting, diarrhoea and constipation) are non-renal. Low protein diets benefi t the patients condition (they will feel better) but do not prevent the progression of renal lesions or halt the decline in renal function.
Reduction of glomerular hypertension: limited to the most severe cases
Vasodilators which specifi cally target the efferent arteries of the glomerulus should help in decreasing intraglomurular hypertension thus limiting glomerular sclerosis.
Some preliminary results indicate they are probably effective in the most severs cases (Urine Protein to Creatine ration >0.8).
1. Reduction of phosphataemia in dogs (1)
Regression analysis model of effects of dietary P on glomerular filtration rate
Months
RFG laitini t necre
P
High P
04 8 12 16 20 24
20
40
60
80
100
120 Low P
Survival time
Months
srovivrus fo srebmu
N
High P
Low Prot
High Prot
Low P
00 2 4 6 8 10 12 14 16 18 20 22 24
4
8
12
16
20
24
(Finco and coll. 1992) (Finco and coll. 1992)
Dogs fed with low phosphorus diets show better glomerular fi ltration rate.
They also enjoy a signifi cant prolonged survival. Protein has no effect.
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2. Reduction of phosphataemia in cats (3)
The life expectancy of cats with borderline naturally occurring CRF is 2.5 times longer when they are fed with phosphate restricted diets in combination, with phosphate binders.
0,0
0,5
1,0
1,5
2,0
2,5
Evolution of phosphataemia
Initial
NormalPhosphateDiet group
Mid survival
)l/lpm
m( aimetahps oh
P
RestrictedPhosphateDiet group
* **
Mean cats survival
s yaD
Normal PhosphateDiet group
Restricted PhosphateDiet group
0
200
600
400
800
264
633
0
50
100
150
200
250
Evolution of plasma PTH
Initial
*NormalPhosphateDiet group
Mid survival
)lm/gp( noitartnecnoc a
msalp HT
PRestrictedPhosphateDiet group
* p<0.01 vs NPD Group
** p<0.002 vs initial diagnosis
* p<0.015 vs initial diagnosis
The Kaplan-Meier survival curves show a highly significantdifference between the 2 groups (p=0.0036)
(Elliott and coll. 2000)(Elliott and coll. 2000)
(Elliott and coll. 2000)
(1) Effects of dietary phosphorus and protein in dogs with renal failure. Delmar R. Finco, Scott A. Brown, Wayne A. Crowell, Robert J. Duncan, Jeanne A. Barsanti, Samuel E. Bennett. 1992 Am. Journ. Vet. Res. 53, 2264-2271.
(2) Effects of phosphorus/calcium-restricted and phosphorus/calcium-replete 32% protein diets in dogs with chronic renal failure . Delmar R. Finco, Scott A. Brown, Wayne A. Crowell, Carlotta A. Groves, Robert J. Duncan, Jeanne A. Barsanti. 1992 Am. Journ. Vet. Res. 53, 157-163.
(3) Survival in cats with naturally occurring chronic renal failure: effect of dietary management. J. Elliott, J. M. Rawlings, P. J. Markwell, P. J. Barber. 2000 Journ. Small Anim. Pract. 41, 235-242.
(4) Protein and calorie effects on progression of induced chronic renal failure in cats. Delmar R. Finco, Scott A Brown, Cathy A. Brown, Wayne A. Crowell, Gregory Sunwold, Tanya L. Cooper. 1998 Am. Journ. Vet. Res. 59, 575-581.
(5) Long term renal responses to high dietary protein in dogs with 75% nephrectomy. John L. Robertson, Michael Goldshmidt, David S. Kronfeld, John E. Tomaszewski, Gary S. Hill and Kennetth C. Bovee. 1986, Kidney International, 29, 511-519.
Ipakitine is a combination of calcium carbonate + chitosan (cellulose fi bre). They are synergistic in preventing the absorption of substances which exacerbate renal failure. Calcium phosphate-binding agents, when administered with meals substantially decrease intestinal absorption of phosphates.
Ipakitine is a bland off white powder with no discernable taste. It is mixed in to food at meal time. It is a very small dose (1 g/5 kg body weight) important for long term administration to cats with CRF.
1. Calcium carbonate: the phosphate eliminator agent
• Calcium carbonate belongs to the short list of substances commonly used in human medicine to bind phosphate in patients with CRF:
Intestinal phosphorus binding agents Approximate daily Recommended dose Aluminium hydroxide 30 to 90mg/kg/day Aluminium carbonate 30 to 90mg/kg/day Aluminium oxide 30 to 90mg/kg/day Calcium carbonate 90 to 150mg/kg/day
• Calcium carbonate is considered safe without long term side effects at the prescribed dose. On the other hand Aluminum salts are reported to accumulate in bones and brain which may be deleterious when used in long term treatment.
2. Chitosan: a naturally derived polysaccharide; similar to plant cellulose
• Chitosan is a polysaccharide derived from chitan which is extracted from the shells of crabs. It is a naturally occurring substance chemically similar to the plant fi bre cellulose.
• Shown to reduce blood urea and creatinine levels in laboratory animals and humans.
• Prolongs the phosphate –binding properties of calcium in the gastro – intestinal tract.
• Binds and blocks absorption of uraemic toxins.
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Ipakitine – calcium phosphate binder for cats and dogs
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Ipakitine, a proven effi cacy in reducing phosphataemia in cats
Ipakitine was the subject of a comparative study at the Veterinary University of Vienna in 2003 (6). It was aimed at assessing Ipakitine effi cacy in reducing phosphataemia and uraemia. It involved both healthy young cats and cats with early stage naturally occurring chronic renal failure.
1. Ipakitine reduces phosphorus blood concentration
IPAKITINE LOWERS PHOSPHORUS ABSORPTION IN NORMAL CATS
Ipakitine action upon phosphatemia
etar ytili bits egiD
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
*
0,0
0,2
0,4
0,6
0,8
1,0
1,2
1,4
1,6
1,8
* significant difference p < 0.05 (Wagner and coll. 2004)
Apparent digestibility of phosphates
etar y tilibitsegiD
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
0
5
10
15
20
25
30
35
40
45
*
* significant difference p < 0.05 (Wagner and coll. 2004)
IPAKITINE LOWERS PHOSPHATAEMIA IN CATS WITH CRF
In cats with CRF, Ipakitine decreases the serum phosphorus concentration from 1.7mmol/l (above the normal range) to 1.1 mmol/l (within the normal range).
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Ipakitine, a proven effi cacy in reducing uraemia in cats
2. Ipakitine reduces uraemia in cats with CRF
Ipakitine action upon uraemia
)ld/gm ( ai
m earU
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
*
0
10
20
30
40
50
60
70
80
90
* significant difference p < 0.05 (Wagner and coll. 2004)
(6) Effects of a dietary chitosan and calcium supplement on Ca and P metabolism in cats. E. Wagner, I. Schwendenwein, J. Zentek, BMTW 117: 7/8 (2004)
3. Ipakitine: lack of side effectsAll other biological parameters (TP, AST, ALT, WBC, RBC, Hk, MCV, MCH, MCHC) remained at a normal level and especially blood calcium concentration which did not change during the 35 days of the trial.
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When to prescribe Ipakitine?
1. Early symptoms of CHF: initiate prophylactic treatment
Reducing plasma phosphorus blood concentration is now considered as the primary goal in CRF treatment. It should take place even before the reduction of protein intake.
2. Moderate symptoms of CRF: pragmatic treatment, an alternative to renal diets
Once azoatemia has been diagnosed, it is advised to lower the protein intake in order to relieve clinical symptoms. Nevertheless, anorexia is a very common clinical symptom for CRF and the main one for cats. In many cases it is very diffi cult or even impossible to make the cat change its usual diet towards a less palatable renal diet.
• ‘Ipakitine – a palatable powder for mixing with food, a change of the diet may not required at this stage of CRF.’
• Clinical studies indicate Ipakitine reduces phosphataemia and uraemia
Ipakitine is a practical treatment option that enables the veterinarian to address to the main objectives of the treatment of CRF: an increase in survival time and improved health status of the patient.
3. Moderate to severe chronic renal failure: essential treatment to support renal diets
At this point in the evolution of CRF, renal diets will not limit the level of phosphataemia. Phosphate – binders are indicated block dietary phosphate uptake from the gastro- intestinal tract.
Ipakitine is a veterinary phosphate-binder which has been researched and developed for cats and dogs. Effi cacy, palatability and safety have been the cornerstones of the product’s development.
Ipakitine may be used in combinations with ACEi’s which are indicated in the later stage of CRF.
Progression of renal failure
Time (years)
Death
IpakitineIpakitine or renal feed
Ipakitine and renal feed
Ipakitine and renal feed and/or ACEis
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Summary : Ipakitine is a palatable, cost effective phosphate-binder for management of CRF in cats and dogs
1. Chronic renal failure”• An important life threatening disease of cats and dogs
• A degenerative, progressive disease which requires regular monitoring and treatment.
• Clinical symptoms become evident when there is a signifi cant loss of the kidney’s mass. The symptoms differ in cats and dogs.
• Compliance with prescribed and dispensed treatments important for optimum clinical outcome.
• Early and aggressive treatment improves longevity of the patient.
2. Increasing life expectancy in pets with CRF• Reducing phosphataemia is the corner stone for the treatment of CRF.
It has been clinically proven in dogs and in cats.
• Protein reduction has no effect on survival time.
• Use of vasodilators should be limited to the most severe cases.
Mean cats survival
s yaD
Normal PhosphateDiet group
Restricted PhosphateDiet group
0
200
600
400
800
264
633
(Elliott and coll. 2000)
Survival time
Months
srovivrus fo srebmu
N
High P
Low Prot
High Prot
Low P
00 2 4 6 8 10 12 14 16 18 20 22 24
4
8
12
16
20
24
(Finco and coll. 1992)
In Cats In Dogs
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IPAKITINE …
3. Ipakitine mode of action• Calcium carbonate is proven as a phosphate-binder, in human medicine with little or
no toxicity or side effects.
• Chitosan binds phosphates and various uraemic toxins.
4. Ipakitine palatability• A high level of acceptance and palatability has been demonstrated. Published clinical
studies confi rm Ipakitine effectively binds and block absorption of dietary phosphates.
5. Ipakitine effi cacy• Ipakitine has shown its potential in decreasing both phosphataemia and urea
in cats with CRF.
6. Ipakitine use• Ipakitine can be used in all stages of CRF.
Ipakitine action upon phosphatemia
etar yti libitsegiD
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
*
0,0
0,2
0,4
0,6
0,8
1,0
1,2
1,4
1,6
1,8
* significant difference p < 0.05 (Wagner and coll. 2004)
Ipakitine action upon uraemia
)ld/gm( ai
mea rU
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
*
0
10
20
30
40
50
60
70
80
90
* significant difference p < 0.05 (Wagner and coll. 2004)
Progression of renal failure
Time (years)
Death
IpakitineIpakitine or renal feed
Ipakitine and renal feed
Ipakitine and renal feed and/or ACEis
Ipakitine action upon phosphatemia
etar yti libitsegiD
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
*
0,0
0,2
0,4
0,6
0,8
1,0
1,2
1,4
1,6
1,8
* significant difference p < 0.05 (Wagner and coll. 2004)
Ipakitine action upon uraemia
)ld/gm( ai
mea rU
Maintenance dietwithout Ipakitine
Maintenance dietwith Ipakitine
*
0
10
20
30
40
50
60
70
80
90
* significant difference p < 0.05 (Wagner and coll. 2004)
Progression of renal failure
Time (years)
Death
IpakitineIpakitine or renal feed
Ipakitine and renal feed
Ipakitine and renal feed and/or ACEis
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Ipakitine compositionFine white powder made of :
Calcium carbonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10%
Chitosan (=crab shell extracts) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8%
Lactose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82%
Ipakitine dose rate1g for 5kg body weight, twice a day, preferably combined with feed.
Ipakitine presentations50g packs with a 1g measure
150g packs with a 1g measure
300g packs with a 2.5g measure
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