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Small Animal Clinical Pharmacology - CYF MEDICAL DISTRIBUTION

Small Animal Clinical Pharmacology - CYF MEDICAL DISTRIBUTION

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DIURETICS<br />

metabolic acidosis due to poor perfusion. Despite the<br />

increase in net acid excretion, urinary pH falls slightly<br />

after furosemide administration, while urine specific<br />

gravity is generally reduced to around 1.006–1.020.<br />

In addition to its diuretic effects, furosemide acts as<br />

a mild systemic venodilator, decreasing systemic venous<br />

pressure before diuresis takes place (especially after<br />

intravenous administration). Furosemide decreases renal<br />

vascular resistance. Thus, it acutely increases renal<br />

blood flow (in the order of 50%) without changing<br />

glomerular filtration rate.<br />

Furosemide increases thoracic duct lymph flow in<br />

dogs following high doses (8–10 mg/kg IV). This<br />

effect is independent of renal function as it occurs in<br />

nephrectomized animals. The basis for this effect is<br />

unexplained.<br />

Furosemide acts as a bronchodilator in humans,<br />

horses and guinea-pigs. It can be administered as an<br />

inhalant in humans with asthma. Its bronchodilatory<br />

effects in dogs and cats are unknown. If it does have<br />

bronchodilatory effects in cats and dogs, it could have<br />

beneficial effects in cats with asthma and in dogs with<br />

chronic bronchitis but its use should not replace conventional<br />

therapy for these diseases. It does, however,<br />

offer an explanation for why some dogs with chronic<br />

valve disease that are not truly in heart failure and are<br />

coughing due to chronic bronchitis (small airway<br />

disease) may experience a reduction in their cough when<br />

treated with furosemide. Thus resolution or improvement<br />

of a cough following trial therapy with furosemide<br />

does not prove the patient was in heart failure. One<br />

needs to document radiographic resolution of a characteristic<br />

infiltrate in the therapeutic trial of this nature.<br />

It is important that dogs with heart disease (preclinical)<br />

that will not benefit from furosemide are not administered<br />

the drug chronically.<br />

Formulations and dose rates<br />

Furosemide is available in oral (tablets, suspensions) and parenteral<br />

formulations.<br />

CANINE<br />

Chronic heart failure<br />

1 mg/kg PO q.12 h for mild heart failure to 5 mg/kg q.8 h (doses<br />

should be separated by at least 3 h but do not have to be exactly 8 h)<br />

for severe heart failure. When this dose fails to keep the patient free<br />

of clinical signs of congestion a second diuretic may be added (see<br />

hydrochlorothiazide). The need for the addition of a rescue diuretic is<br />

clinically relatively rare. In general, the goal with furosemide is to use<br />

the minimum dose necessary to keep the patient free of clinical signs<br />

of congestion. Dogs with mitral regurgitation secondary to CVD that<br />

are refractory to furosemide administration may also benefi t from the<br />

administration of a systemic arteriolar dilator, such as amlodipine or<br />

hydralazine.<br />

Acute heart failure<br />

Severe pulmonary edema requires immediate intensive intravenous<br />

or intramuscular administration in dogs. Intravenous is preferred if<br />

feasible.<br />

FUROSEMIDE DOSE SCHEDULE FOR SEVERE LIFE-THREATENING<br />

CARDIOGENIC PULMONARY EDEMA IN THE DOG<br />

• Dependent on severity of respiratory clinical signs<br />

• Guided by resting respiration rate with oxygen supplementation<br />

and thoracic radiographs when available<br />

• For severe life-threatening cardiogenic pulmonary edema in the<br />

dog:<br />

Initial dose: 4–6 mg/kg IV (IM if IV not feasible)<br />

Then: 2–4 mg/kg IV q.1 h (or 1 mg/kg min CRI) until resting<br />

respiration rate (RR) ↓ by 20%<br />

Then: 2–4 mg/kg IV q.2 h (or 0.5 mg/kg min CRI) until resting RR ↓<br />

by 50%<br />

Then: 2–4 mg/kg IV q.6–8 h (discontinue CRI at this time)<br />

Then: switch to oral 2–4 mg/kg q.8–12 h<br />

Note: For less severe edema use the lower end of the dose range and<br />

in older patients who are concurrently azotemic reduce the lower<br />

range doses in the schedule by 50%.<br />

If dogs with respiratory distress fail to demonstrate a trend for<br />

improvement (reduced respiration rate) following 4–6 doses or 4–6 h<br />

of a furosemide CRI alternative differentials for respiratory distress<br />

should be considered and/or additional heart failure therapy should<br />

be initiated.<br />

FELINE<br />

Chronic heart failure<br />

1 mg/kg PO every 1–3 d (mild heart failure) to 2 mg/kg twice to three<br />

times daily (severe heart failure) in most cases (doses should be<br />

separated by at least 3 h but do not have to be exactly 8 h). In general<br />

the goal with furosemide is to use the minimal dose necessary to keep<br />

the patient free of clinical signs of congestion. Some cats that are not<br />

amenable to oral administration may benefi t from chronic clientadministered<br />

subcutaneous injections. A higher oral dose may be<br />

considered in some cats that are not responding to a conventional<br />

dose. The need for the addition of rescue diuretics in the cat is<br />

exceedingly rare.<br />

Acute heart failure<br />

Severe pulmonary edema requires immediate intensive intravenous<br />

or intramuscular administration in cats. Intravenous is preferred if<br />

feasible.<br />

FUROSEMIDE DOSE SCHEDULE FOR SEVERE LIFE-THREATENING<br />

CARDIOGENIC PULMONARY EDEMA IN THE CAT<br />

• Dependent on severity of respiratory clinical signs<br />

• Guided by resting respiration rate with oxygen supplementation<br />

and thoracic radiographs when available<br />

• For severe life-threatening cardiogenic pulmonary edema in the<br />

cat:<br />

Initial dose: 2–4 mg/kg IV (IM if IV not feasible)<br />

Then: 1–2 mg/kg IV in 1–2 h<br />

Then: 1–2 mg/kg IV in 2–4 h if resting respiration rate is not ↓ by<br />

50%<br />

Then: switch to oral at 1–2 mg/kg q.8–12 h once RR reduced by<br />

50%<br />

391

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