Saturday, 6 April 2019

Summer management of Dogs

"Summer is here and you need to do extra care with necessary precaution to protect your dog from heat stroke .

SUMMER MANAGEMENT OF DOGS
As you need air conditioners and coolers to cool your body temperature, sunglasses to protect your eyes, sunscreen to protect your skin, cold water and food to lower body temperature in summer, So in the same ways your Dogs also need such contrivances in summers which prevent them from dehydration and sunburn.

If Dog parents can't do extra care with necessary precautions during high temperature in summer their Dog may suffer or even die due to heat stroke or organ failure when temperature of Dog reaches above 43°C

"KEEP THINGS IN MIND THAT WHAT NOT TO DO WITH YOUR DOGS IN SUMMER"

SUMMER MANAGEMENT OF DOGS
            1. Don't leave your Dog in vehicle even if it is parked in the cooler place.

SUMMER MANAGEMENT OF DOGS
2. Always provide fresh,clean adequate amount of water to your Dog.
SUMMER MANAGEMENT OF DOGS
3. Always travel with your Dog in well ventilated vehicle and avoid travelling in the middle of the day when temperature is too high.
SUMMER MANAGEMENT OF DOGS
4. Avoid excessive running and exercise during day time when temperature is too high.


"KEEP THINGS IN MIND THAT WHAT TO DO WITH YOUR DOGS IN SUMMER"

1. Keep your Dog inside home with proper air conditioning or fans to provide sufficient amount of air circulation.

2. Always provide two bowls of water in case one is knocked over.

3. Always provide unrestricted access to fresh, clean water sources and added few ice cubes in it so that your Dog will remain hydrated.

3. Wet Dog food can help in increasing water intake during summers so  you can feed wet Dog food to your Dog.

4.   Exercise your Dog early morning or evening when the temperature is cooler.  


TYPES OF DOGS SUSCEPTIBLE TO HEAT STROKE

1. Brachycephalic breed ( pushed in nose) like Pugs, Bulldogs, Boston Terrier with Golden Retrievers and Labrador which are prone to laryngeal paralysis are also susceptible to heat stroke as well.

2. Dogs which are suffering from cardiac and respiratory diseases. 

3. Geriatric(elderly) or ill Dogs. 

4. Obese Dogs.

5. Dogs which are recently transferred to hotter climates.

6. Dogs which are caged or under poor ventilated areas.  

7. Dogs which do excessive running and exercise in high temperature.

8. Dogs which are suffered previously with heat stroke could be at higher risk of getting heat stroke again. 

DOGS VS HUMANS
1. "The only effective method of cooling/thermoregulation in Dogs is panting. Humans who sweat almost from everywhere because they have sweat glands, called apocrine glands, associated with every hair follicle on their body but Dogs only produce sweat on areas not covered with fur, such as the nose and paw pads." 

2. Dogs can't ask about feeling a need to drink to you when they are too hot.

3.They won't stop playing until there body can't take any more because Dogs are so eager to please their parents.

SYMPTOMS OF HEAT STROKE
1. An anxious expression or staring appearance
1. Heavy panting and raspy breathe
2. Excessive salivation
3. Elevated rectal temperature
4. Skin feels warmer than usual
5. Bright red gums
6. lying flat on cool surfaces
7. Collapsing, stumbling or falling down
8. Vomiting
9. Seizures

HEAT STROKE EFFECTUATE
1. Brain damage (Temporary or sometimes permanent).
2. Muscle Damage. 
3. Bleeding disorders.  
4. Organ failure if body temperature exceeds than 43°C
5. Lungs, liver and kidney failure.
6. Ulceration of stomach and intestine.
7. Death 

THINGS YOU CAN DO AT HOME IF YOU SUSPECTED THAT YOUR DOG HAS HAD HEAT STROKE 

SUMMER MANAGEMENT OF DOGS


TREATMENT BY VETERINARIAN

1. Cold water enema
2. Intravenous fluid (isotonic crystalloid at shock dose i.e. 90 ml/kg for dogs).
3. Seizures should be treated with appropriate anticonvulsants (diazepam, phenobarbital, propofol). 
4. Cerebral edema may be treated with mannitol or corticosteroids. Corticosteroids also would benefit a patient with upper airway edema.
5. Antibiotic therapy should be instituted to protect gastrointestinal tract.
6. Avoid non-steroidal anti-inflammatory drugs. 

OUTCOMES
The key to successful management and treatment includes rapid recognition with protocols aimed at rapid cooling and support of the affected body systems. Heat stroke can result in multi-organ dysfunction that can be life-threatening.



















Tuesday, 2 April 2019

Clinical signs and diagnosis of Canine Atopic Dermatitis: An Update




INTRODUCTION
Atopic dermatitis in dogs is defined as: “A genetically-predisposed inflammatory and pruritic allergic skin disease with characteristic clinical features”. It is associated most commonly with Ig E antibodies specific for environmental allergens such as house dust mites and grass pollen”
Canine Atopic Dermatitis (CAD) is a frequent disease of skin associated with release of inflammatory mediators with estimated prevalence of around 10% (Hillier et al., 2001). Though the exact cause is unknown, it is commonly associated with IgE antibodies to environmental allergens. The primary clinical signs, erythema and pruritus is associated with lesions at ear pinna, paws, ventral abdomen, inguinal and axillary regions (Herbert et al., 2006). Though the diagnosis of atopic dermatitis is based on ruling out other etiological causes, Intra dermal allergic skin test (IDST) is still the gold standard diagnostic procedure. Though the literature on canine atopy is available, reports on long term research particularly on diagnosis using Intra dermal allergic skin test (IDST) and therapy is dearth in India. Hence, the present paper puts on record for the first of its kind clinical study from India.
Cutaneous adverse food reaction (CAFR) and CAD have been historically considered as two different conditions. In fact, CAFR includes both immune mediated and non-immune-mediated food intolerances and may be associated with a wide range of clinical signs such as gastro-intestinal disturbances, urticaria, angioedema, and signs mimicking those of atopic dermatitis. The present article will consequently describe the clinical features and diagnostic methods of dogs affected by CAD from whatever cause. The clinical signs and diagnostic methods of food allergy are however beyond the scope of this article.

SIGNALMENT OF CAD DOGS

Some studies reported predisposition for male, female or for neither sex. However, some sex predispositions were detected in some breed such as golden or Labrador retrievers (more female) or Boxer (more male). The typical age at onset of CAD is reported to be between 6 months and 3 years. We have however recently shown that about 78% of CAD present with clinical signs before three years of age. It does mean that every fifth CAD dog develops the first clinical signs later in life.

HISTORY OF CAD DOGS

Information regarding the history of the affected dog should be recorded carefully. Some important questions have already been mentioned (age at onset, breed, familial predisposition) but some others such as seasonality, presence of “pruritus sine material” (pruritus with no skin changes) at onset, efficacy of previous treatment, should be asked before any clinical examination. Clinical signs of CAD may be seasonal or not but seasonality is often present at onset (42-75%).  Approximately 80% of dogs with seasonal signs are symptomatic in spring or summer while the others exhibit signs in winter or autumn. It should be mentioned that some dogs with non-seasonal disease do exhibit worsening of clinical signs during one specific season. Pruritus must be present and its absence rules out the diagnosis CAD.
In fact, some CAD dogs do exhibit initially pruritus. This feature was recorded in 61% of affected dogs in recent study. As well, 43% of CAD dogs presented first with an episode of otitis externa. In comparison, associated conjunctivitis blepharitis is very much rarer. CAD dogs are often treated with glucocorticoids and responses to such therapy should be evaluated carefully.
 It is also shown in the study that 78% of CAD dogs responded adequately to such treatment. In the first stages of the disease, the pruritus responds well and readily to the administration of reduced amount of glucocorticoid (i.e. 0.3-0.5mg/kg Prednisolone daily). In chronic cases however, the development of secondary bacterial or yeast infections usually corresponds with a poorer response to such treatment. Last but not least, we have also showed that 82% of atopic dogs spend most of their time indoor. This suggests that prolonged exposure to house dust mites may trigger or worsen CAD clinical signs.

CLINICAL SIGNS OF CAD

Although very frequent, CAD may be difficult to diagnose owing to the lack of pathognomonic signs and the protean clinical picture. Erythema and pruritus are however virtually always present and often represent the first clinical signs. However, mild pruritus may remain unrecognized by the owner and the veterinarian may sometimes rely on indirect proofs of pruritus such as the presence of excoriations or saliva-coloured hairs. Most of the signs are actually due to self-trauma and/or secondary infections. In fact, small erythematous papules, which are considered the primary lesion of CAD, are rarely observed in CAD dogs.
The practitioner will usually observe the consequences of the inflammation and pruritus, namely excoriations and self-induced alopecia and/or the signs of the secondary bacterial infection (papules, pustules, crusts, erosions) and/or the symptoms of secondary yeast dermatitis (epidermal hyperplasia, hyperpigmentation, lichenification).
 Recurrent or chronic skin or ear infections are very frequently observed in CAD Most of these signs are however not specific at all and the distribution of these lesions is consequently more helpful. The most often affected areas are the pinnae (58%), the axillae (62%), the abdomen (66%), the front (79%) and hind feet (75%), the lips (42%) and the perineal area (43%). Unfortunately, all these areas are rarely simultaneously affected in the same individual, except in chronic cases.  Dermatological (pyotraumatic dermatitis, interdigital fi stulae)  and non dermatological signs are sometimes associated with CAD and their presence should reinforce the suspicion. Spring/summer conjunctivitis, for example, is presented in approximatively 20% of CAD dogs while gastro-intestinal signs (soft stools, diarrhea, vomiting) are recognized in 26% of FIAD dogs.
Clinical signs of FIAD dogs differ very slightly from those of classical, environment-induced AD. In fact, in our study, statistically significant differences were only uncovered for gastro-intestinal signs, seasonality, cortico-sensible pruritus and pruritus sine material (less frequent in FIAD dogs). As well, more FIAD dogs show the fi rst clinical signs early in life (less than one year) or, on the contrary, rather late (more than 6 years of age).

DIAGNOSIS OF CAD

The diagnosis of CAD is based on the history (age at onset, seasonality, pruritus sine material at onset, familial or breed predisposition, previous response to glucocorticoids), the development of the disease (seasonality, “wax and wane” character, development of secondary skin infections) and the lesional pattern.
A diagnosis of CAD should however never been made, as long as resembling diseases such as fleas, ectoparasites (sarcoptic mange) and primary skin infections have not been ruled out. Depending on the clinical presentation and the age of the affected dog, some other differentials, i.e.demodicosis, dermatophytosis, cheyletiellosis, cutaneous lymphoma should be properly ruled out. It should also be mentioned that the histological aspect of allergic skin is usually not specific and that his test is consequently not adequate to make the diagnosis.
It may be indicated, however, to perform skin biopsies in some instances, to rule out some differentials such as cutaneous lymphoma, for example. As well, allergy testing (serological evaluation of allergen-specific Ig E and intradermal skin testing) are not regarded as criteria for the diagnosis of CAD. This is because numerous healthy dogs are sensitized to environmental allergens and are consequently positive (poor specificity of this criterion) and ALD and some FIAD dogs are deemed negative. These tests should consequently be only carried out to identify the offending allergens (i.e. to choose the allergens for allergen specific immune therapy: desensitization). In the same way, in order to identify FIAD dogs, a 6-to 8-week elimination diet and a subsequent challenge with the previous food should be carried out in all dogs with clinical signs of CAD. Several sets of criteria have been proposed for the diagnosis of CAD.
CRITERIA FOR THE DIAGNOSIS OF CANINE ATOPIC DERMATITIS AND ASSOCIATED SENSITIVITY AND SPECIFICITY.
1. Age at onset < 3years
2. Mostly indoor
3. Corticosteroid-responsive pruritus
4. Chronic or recurrent yeast infections
5. Affected front feet
6. Affected ear pinnae
7. Non –affected ear margins
8. Non-affected dorso-lumbar area
Sensitivity when 5 criteria are fulfilled: 85%
Specificity when 5 criteria are fulfilled: 79%
Sensitivity when 6 criteria are fulfilled: 58%
Specificity when 6 criteria are fulfilled: 88 %

SUMMARY
Canine Atopic Dermatitis (CAD) is the most frequent canine dermatosis. It has been defined by the International Task Force on Canine Atopic Dermatitis (ITFCAD) as a “genetically predisposed inflammatory and pruritic allergic skin disease with characteristic clinical features associated with IgE antibodies most commonly directed against environmental allergens”.  ITFCAD-revised nomenclature for veterinary allergy also takes into account dogs with clinical signs of atopic dermatitis but no demonstrable allergen-specific IgE (Intradermal tests and/or serology).

REFERENCES
1. Favrot, C., Steffan, J., Seewald, W., & Picco, F. (2010). A prospective study on the clinical features of chronic canine atopic dermatitis and its diagnosis.Veterinary dermatology, 21(1), 23-31.
2. DeBoer, D. J., & Hillier, A. (2001). The ACVD task force on canine atopic dermatitis (XV): fundamental concepts in clinical diagnosis. Veterinary immunology and immunopathology, 81(3), 271-276
3. Nambi, A. P., & Kavitha, S. (2013). Canine atopic dermatitis. Intas Polivet,14(2), 236-24
4. Bensignor, E. (2010). [Canine atopic dermatitis]. Bulletin de l'Academie nationale de medecine, 194(7), 1357-1364.
5. Olivry, T., & Mueller, R. S. (2003). Evidencebased veterinary dermatology: a systematic review of the pharmacotherapy of canine atopic dermatitis.Veterinary dermatology, 14(3), 121-146.

Gastrointestinal Endoscopy in Dogs


Gastrointestinal Endoscopy in Dogs


Introduction
Endoscopy is a Greek word comprising of “Endo” for Inner and “Skopein” to view or observe with a purpose and Fiberoptic endoscopy is a noninvasive technique for evaluating the lumen and mucosa of the gastrointestinal tract of dogs. It is a fundamental method for investigation of the digestive tract, and is important in the diagnosis and prognosis of a variety of gastrointestinal disorders.
It is indicated mainly if history and physical examination of a patient reveals abnormalities in the area of the gastrointestinal tract. In addition to this further investigations like plan and contrast radiography, ultrasonography and functional tests may permit tentative diagnosis. Until recently clinician had been limited in their ability to diagnose GI diseases morphologically because of the need to carry out an exploratory laparotomy in order to obtain biopsy samples and has been largely replaced by endoscopy.

THORACOCENTESIS AS DIAGNOSTIC AND THERAPEUTIC TOOL IN DOGS



THORACOCENTESIS

Introduction

Thoracocentesis is the name given to the clinical technique where by fluid or air is removed from thoracic cavity.

1. Thoracocentesis may be diagnostic to determine whether air or fluid is present and to characterize the nature of the fluid obtained.

2. Thoracocentesis also can be therapeutic when removing large volumes of air or fluid to allow pulmonary re-expansion and correction of hypoxemia  and orthopnea.

3. Rapid stabilization in immediate respiratory distress due to the accumulation of air or fluid in the pleural space.

When the findings of the thoracic auscultation or percussion are suggestive of pleural effusion then thoracocentesis is  performed  to -

Ø  To Confirm the presence of pleural effusion.

Ø  Provide a specimen for examination which provide a diagnosis or guide the therapeutic plan .

Ø  Therapeutically drain a large of pleural fluid is present.

 THORACOCENTESIS IN DOGS

Materials needed:
Ø  Sterile Needle
Ø  Cat, 18-23 gauge
Ø  Dog, 18-21 gauge
Ø  Scalp Vein
Ø  A flexible polythene catheter with removable needle
Ø  Syringe- Usually 10-30ml so that large volumes of fluid/air can be collected.

Technique

1. Clip the hair and clean the skin at the proper location and each rib marked with an overlay of red ink.
THORACOCENTESIS IN DOGS

2Palpate the 13th rib, and then the 12th interspace immediately in front of it.‘Walk’ your fingers cranial ly from one interspace to the next, counting 11-10-9-8-7 as you go, to identify the 7th and 8th interspaces.
THORACOCENTESIS IN DOGS

3. Once you’ve identified the desired location, advance the needle through the skin. As soon as the needle enters the subcutaneous space, pull back on the plunger to apply 1-2 cc’s of vaccum. You should be able to feel the plunger tugging against your fingers.
THORACOCENTESIS IN DOGS

4. Never advance the needle deeper than you think the pleural space is your main goal is to avoid lacerating the lung in animals that in fact have no pleural space fluid or air.

5.Withdraw the needle as soon as you get a positive tap (loss of  vacuum observation of fluid), and proceed to a therapeutic tap.

6. While maintaining a strong suction, advance the needle through the chest wall at the leading (cranial) edge of the rib behind it. The instant the needle enters the pleural cavity , you will either lose the vacuum (in the case of pneumothorax as shown here) or observe the entry of fluid into the needle barrel (in the case of pleural fluid accumulation).
THORACOCENTESIS IN DOGS

THORACOCENTESIS IN DOGS


     Fluid Analysis

EDTA tube
a. Total protein concentration
b. Specific gravity
c.Total nucleated and red cell counts, and cytology.

Plain tube
a. Bacteriological examination
b. Other biochemical tests e,g,  triglycerides and cholesterol
c.  Smears should be prepared immediately after collection.

 Type of effusion

1. Pure transudate
a. Low protein level in the plasma (hypoproteinemia)
b. Congestive cardiac failure 

2. Modified transudate
a. High venous and capillary hydrostatic presure
b. Congestive heart failure
c. Obstruction of vein and/or lymphatics –intrathoracic mass 

3. Chylous effusions
a. Thorax –rupture of the thoracic duct
b. Intrathoracic lymphagiectasia
c. Obstruction or trauma

4. Haemorrhagic exudates
a. Thoracic trauma
b. Intrathoracic tumour

5. Exudates
1. Septic
a. Foreign body
b. Penetratign wound of the thorax, oesophagus or airway

2. Non-septic
a. Negative culture 
b. Immune-mediated process
c. Parasitic or neoplastic process

Thoracocentesis is very effective and safe procedure  in diagnosing conditions of the thoracic cavity in dogs and requires no special equipment. Thoracocentesis often makes the difference between life and death in dogs with severe disease. 



CHOCOLATE TOXICITY IN DOGS



IS CHOCOLATE SAFE FOR OUR PETS ??

Chocolate contains substances known as methylxanthines (specifically caffeine and theobromine), which dogs are far more sensitive to than people.  The onset of theobromine poisoning is usually marked by severe hyperactivity.

What Makes Chocolate Toxic to Dogs?


In general, though, the darker and more bitter the chocolate the greater the danger. Different types of chocolate contain varying amounts of methylxanthines. A small amount of chocolate will probably only give your dog an upset stomach with vomiting or diarrhea. With large amounts, theobromine can produce muscle tremors, seizures, an irregular heartbeat, internal bleeding or a heart attack. 
CHOCOLATE TOXICITY IN DOGS

Why Isn't Chocolate Toxic to Humans?


Humans can break down and excrete methylxanthines such as theobromine much more efficiently than dogs.

What Should I Do if My Dog Ate Chocolate?


If you know your dog has ingested chocolate , or has any of the symptoms below, contact your veterinarian right away.

Remember, with any poisoning, it’s always cheaper, less invasive, and has a better prognosis/outcome if you treat early. 

"Once your dog has already developed clinical signs and is affected by the poison, it makes difficult for veterinarian to treat easily." 

Symptoms of concern include:
CHOCOLATE TOXICITY IN DOGS
  • Vomiting
  • Diarrhea
  • Increased body temperature
  • Increased reflex responses
  • Muscle rigidity
  • Rapid breathing
  • Increased heart rate
  • Low blood pressure
  • Seizures
  • Advanced signs (cardiac failure, weakness, and coma)

Treatment
Your dog should be seen immediately by your veterinarian to find out if there is immediate care that you begin with. It is common practice to induce vomiting and control any seizures, should they occur. In the meantime, you will need to keep your dog cool, calm, and in a quiet space.

Fluids will be given to keep your dog to keep it hydrated as its condition improves. To avoid any further problems, it should be fed a bland diet for several days.

Prevention

It is crucial to your pet’s health to keep chocolate products out of their reach, as there is no antidote to chocolate toxicity.

Summer management of Dogs

"Summer is here and you need to do extra care with necessary precaution to protect your dog from heat stroke . As you need air ...