Hypertension in Cats and Dogs
Waltham/OSU Symposium, Small Animal Cardiology, 2002
Rebecca L. Stepien, DVM, MS, Diplomate ACVIM (Cardiology)
University of Wisconsin

PREVALENCE AND IMPORTANCE OF SYSTEMIC HYPERTENSION

"Systemic hypertension" (HT) refers to the persistent elevation of systemic blood pressure. Chronic elevation of systemic blood pressure results in damage to multiple end-organ systems; some of this damage may be clinically obvious but some may be insidious. Blood pressure is discussed in terms of systolic and diastolic values. In people, combined HT (systolic and diastolic values elevated), isolated systolic and isolated diastolic HT have differing morbidity and mortality rates. Little information about the prevalence and importance of isolated systolic or diastolic HT in dogs and cats is available1-3, but it is clear that HT occurs in these species and is a cause of significant morbidity in some animals.

Systemic hypertension is typically classified as primary ("essential") HT or secondary HT. Some veterinary clinicians have attempted to distinguish essential HT from idiopathic HT (i.e., systemic HT in the absence of overt, clinically apparent causal disease). Use of the term "idiopathic" acknowledges that there may be a causal disease (e.g., renal disease) that is responsible for the HT but that the causal disease is in a pre-clinical phase4,5. In cases where the underlying disease is rare (e.g., pheochromocytoma), discovery of the cause of the HT is dependent on the thoroughness of the diagnostic testing.

Sporadic cases of apparent essential HT in dogs have been published6-9 but the majority of hypertensive dogs and cats have developed HT as a complication of another systemic disease. The prevalence of HT varies with the population studied.

Cats

The prevalence of HT in the general feline population is unknown but HT is common in some subpopulations. Chronic renal failure is the disease most commonly associated with HT in cats; HT has been documented in 20-65% of cats with this condition4,10,11. Up to 86% of hyperthyroid cats had blood pressures above the normal range of values in one early clinical study11, but more recent anecdotal evidence suggest that the prevalence rate of HT in hyperthyroid cats today is much lower (~7-10%12), perhaps due to increased screening and earlier detection of hyperthyroidism (i.e., before hypertensive complications develop). Detection of the true prevalence of HT in thyrotoxic cats is also complicated by the presence of concurrent renal insufficiency in many of these cats. Advanced age alone does not appear to be a significant risk factor for feline HT11,13 but the risk of chronic renal disease or hyperthyroidism is higher in older cats. Breed and sex do not appear to be significant risk factors for HT in cats.

Dogs

The prevalence of HT in the general canine population appears to be low14,15, but as is the situation in cats, prevalence of HT is much higher in certain populations. Numerous studies support chronic renal disease (especially glomerular disease), hyperadrenocorticism (HAC) and diabetes mellitus (DM) as the most common diseases associated with HT in dogs. Most studies report the prevalence of HT as 60-90% in dogs with chronic renal failure1,6,16,17. Similar prevalence values are reported for dogs with HAC (70-80%)1,18. Systemic HT is documented less frequently in dogs with DM (reported prevalence of HT: 25-45%)1,2. Less common conditions associated with HT in dogs include pheochromocytoma, acromegaly, primary hyperaldosteronism and use of hypertensive medications such as phenylpropanolamine. Although small increases in blood pressure have been documented with increasing age in dogs in one study15, other studies found age and blood pressure were not significantly correlated3,19. Healthy sight hounds (e.g., greyhounds, deerhounds) have a higher normal range of blood pressures; normal resting blood pressure values may be up to 15 mmHg higher than other breeds of similar size15,20. Male dogs tend to have slightly higher blood pressure readings than females but the difference is unlikely to be clinically significant15.

Development of HT in cats and dogs is almost always associated with the concurrent presence of one or more identifiable underlying diseases. The search for an underlying condition responsible for the development of HT is an essential component of the diagnosis of HT in cats and dogs.

SYSTEMIC EFFECTS OF SYSTEMIC HYPERTENSION

Clinical signs of HT are frequently not apparent until catastrophic damage has occurred (Figure 1).

Figure 1.

External ophthalmic examination of a cat with severe hyphema and retinal detachment secondary to systemic hypertension.


 

Earlier in the course of HT, subtle clinical signs of elevated blood pressure may be masked by the clinical signs of the underlying condition or the pet's owner reports no clinical signs. In many cases, the possibility of HT is investigated based on the suspicions of the clinician when suggestive clinical findings are present or a disease associated with HT is suspected or diagnosed. Several organ systems are recognized as "target organ systems" typically sustaining damage in the presence of chronic HT (Table 1, Figure 2).

Table 1. End-Organ Effects of Hypertension41-44

Organ or System

Effect of HT

Effects More Likely

Comments

Kidneys

 Enhanced rate of decline of renal function

 Promotion of glomerulosclerosis

 Nephron loss

 Enhancement of proteinuria

If SBP > 160 mmHg

 Often difficult to determine whether renal disease is a cause or effect of HT in clinical patients

Eyes

 Exudative retinal detachment

 Retinal or vitreal hemorrhage, hyphema

 Retinal edema or papilledema

 Retinal vessel tortuosity

If SBP > 180 mmHg

 Referred to as "hypertensive retinopathy/choroidopathy"

Brain

 Disruption of blood flow autoregulation

 Fibrinoid arteriolar necrosis

 Thrombosis with subsequent hypoxic damage

 Cerebral swelling/edema

If SBP > 180 mmHg acutely

 Clinical signs result from ischemic stroke and/or hemorrhagic damage

Heart

 Concentric LV hypertrophy leads to increased wall stress and promotes ischemia

 Secondary murmurs/gallop rhythms

Unknown

 Pulse pressure or systolic pressure most reliable indicator of CV risk (human)

 In cats, cardiac changes may resolve with successful antihypertensive therapy

HT: hypertension, SBP: systolic blood pressure, LV: left ventricular, CV: cardiovascular

Figure 2.

Post-mortem cardiac specimen from a dog with left ventricular hypertrophy secondary to chronic systemic hypertension due to protein-losing glomerulopathy. Chronic valvular changes due to endocardiosis are also present.


 

DIAGNOSIS OF SYSTEMIC HYPERTENSION

Patient Selection

Multiple clinical studies of different methods of measuring blood pressure in conscious animals indicate that the most commonly-used non-invasive techniques yield results that are precise (i.e., repeatable) but of variable accuracy15,19,21-23. Blood pressure values exceeding normal ranges for the species may be viewed differently in the two populations of patients most likely to have blood pressure measured: patients screened as part of a yearly "wellness" exam, and patients presented with clinical signs suggestive of or systemic diseases known to be associated with HT.

"Screening" Examinations on Healthy Patients

Routine blood pressure measurement in asymptomatic patients that do not have a disease associated with HT is controversial. Some authors have suggested that individual dogs have "characteristic" blood pressures22; routine evaluation on every patient would establish a "normal" blood pressure for that animal. Theoretically, a significant increase in blood pressure from one measurement period to the next would trigger a more detailed diagnostic work-up to search for a cause. Tests that are highly sensitive (i.e., high probability that an affected patient will have an abnormal test result) are usually recommended for screening a population of low prevalence (in this case, a healthy clinical population). Tests of high sensitivity carry a higher risk of false positive findings, so most clinicians recommend that healthy patients with apparently elevated blood pressure have this finding confirmed on multiple test occasions before proceeding with a diagnostic work-up or therapy.

Diagnostic Blood Pressure Measurements in Patients at Risk for Hypertension

Patients with clinical signs of HT or a disease that increases the risk of HT should have their blood pressure measured at the time of initial diagnosis. Risk factors for canine and feline hypertension differ from risk factors for human hypertension. Ocular hemorrhage, retinal hemorrhage or detachment, neurologic signs such as depression, obtundation or seizures, the presence of renal disease or findings of unexplained left ventricular hypertrophy should result in blood pressure evaluation in both species. In cats, a diagnosis of hyperthyroidism should include blood pressure evaluation. Screening blood pressure measurements in any cat with left ventricular hypertrophy is required before a diagnosis of idiopathic hypertrophic cardiomyopathy can be made with confidence. In dogs, in addition to the findings listed above for both species, a diagnosis of HAC, DM, acromegaly, pheochromocytoma or primary hyperaldosteronism should result in blood pressure evaluation. In all cases, evidence of ocular damage typical of HT or neurologic manifestations of HT is considered an emergency and treated as such with a goal of rapid reduction of blood pressure prior to pursuit of further diagnostics. Measurement of elevated blood pressure on one occasion is diagnostic for HT when clinical signs are present24.

Methods of Measuring Blood Pressure

Invasive Blood Pressure Measurement

Invasive blood pressure measurement involves arterial puncture (for acute measurement) or arterial cannulation with use of a blood pressure monitor providing pressure tracings19. Invasive blood pressure measurement provides a direct reflection of true intra-arterial pressure, but can be cumbersome for clinical use. With rare exception, direct blood pressure monitoring is used for anesthetic or acute critical care monitoring or in research situations.

Oscillometric Blood Pressure Measurement

Oscillometric blood pressure measurement is a common and useful technique that relies on detection of arterial pulsation through the use of an automatically inflating and deflating cuff that is wrapped around a distal limb or tail19,25,26. Oscillometric techniques have been shown to accurately track trends in blood pressure over time in conscious dogs22, but individual measurements obtained oscillometrically may underestimate direct systolic blood pressure measurements by up to 5-20 mmHg19,23,27. Oscillometric diastolic pressure results in conscious dogs are poorly correlated to invasively measured diastolic pressure19,23.

Doppler methods of Blood Pressure Measurement

Doppler blood pressure measurement using piezoelectric crystal detection of arterial pulsation with a hand-inflated cuff is a commonly-used and useful method of blood pressure measurement19, and is the preferred method in cats13. Accuracy is dependent on user experience and meticulous attention to technique, and diastolic pressures can be difficult to discern in some animals.

Photoplethysmographic Blood Pressure Measurement

The photoplethysmographic method of blood pressure measurement estimates blood pressure based on attenuation of infrared radiation as a method of estimating arterial volume28. Although this method is commonly used for people, studies of its accuracy in conscious dogs and cats are not available.

General Measurement Recommendations

Noninvasive blood pressure measurement is preferred in most clinical situations. For acute blood pressure measurement in conscious animals, the current recommendations of the American College of Veterinary Medicine Hypertension Consensus Panel12 include the following:

 Standardize the procedure in the clinic-blood pressure should be measured the same way in every patient

 Doppler is currently the recommended method for cats, oscillometric or Doppler methods can be used for dogs

 Cuff size: ~ 40% of circumference of limb or tail

 Position cuff level with right atrium for readings

 Discard first reading, then use mean of 3-5 measurements with 30 seconds to one minute between readings

 Patient considerations

 Blood pressure measurements should be obtained prior to any other patient manipulation29

 Client presence to calm the animal can be helpful to calm the patient

 The patient should be conscious, calm and in sternal or lateral recumbency

 A few minutes of acclimation to the position is recommended

Interpretation of Results

Comparable normal values generated using direct and indirect methods in cats11,13,29-33 and dogs17,19,25,34,35 are available. Some authors have suggested that blood pressures greater than two standard deviations from the mean normal values should be considered diagnostic for hypertension3,13, but relatively small increases in renal blood pressure may have detrimental effects on end organ function (e.g., progressive glomerular disease) and many clinicians find these guidelines too conservative. Current recommendations for both species suggest that systolic blood pressure >160 mmHg or diastolic blood pressure >95 mmHg measured by any method are reasonable values at which concern is warranted12,24. General guidelines for interpretation of systolic blood pressure (SBP, mmHg) are expressed in terms of risk of end-organ damage and are associated with recommendations for further action12:

 SBP < 150/95: minimal risk-no further diagnostics indicated

 SBP 150/95 --> 160/100: low risk

 Confirm by repeated measurement if no clinical signs or compatible disease

 Search for underlying disease

 Monitor over time if no disease found

 SBP 160/100 --> 180/120: moderate risk

 Careful search for underlying disease

 Therapy warranted if clinical signs are present

 Consider therapy if no clinical signs but rapid resolution of underlying disease is not anticipated

 Monitor over time if no disease found

 SBP > 180/120: high risk

 If ocular or neurologic signs are present --> treat first, then proceed with diagnostic work-up for underlying disease

 If high risk associated disease is present --> therapy is indicated

 If no clinical signs and no associated disease --> recheck frequently: if consistently abnormal, consider therapeutic trial of antihypertensive medication

TREATMENT OF SYSTEMIC HYPERTENSION

Despite the large number of drugs available to treat hypertension in people, therapy of systemic hypertension in dogs36 and cats37-39 is still under-researched in the clinical population. Recommendations are frequently based on anecdotal information and theoretical concerns, especially in dogs. As controlled clinical trials accumulate, better information regarding rational choices of antihypertensive medications will guide clinical decision-making.

Emergency Therapy of Hypertension

Emergency therapy of HT in dogs in cats is primarily guided by the level of concern generated by clinical signs in the patient. Rapid oral (e.g., hydralazine) or intravenous therapy with vasodilating agents is warranted (Table 2). Nitroprusside or acepromazine can be used intravenously for rapid reduction of blood pressure; the short half-life of nitroprusside makes it easy to titrate to effect (i.e., hypotension can be quickly rectified by decreasing the infusion rate). Acepromazine is available in most clinics and can be used in an emergency situation, but the longer lasting effects of the drug make it harder to titrate to effect. Higher doses of acepromazine may result in over-sedation, hypotension and compromise of renal function, especially in geriatric patients.

Table 2. Medications used to treat systemic hypertension in cats and dogs*

Medication

Dose

Comment

Acepromazine

D/C: 0.03-0.1 mg/kg IV

 Start with low dose and use to effect.

 Use with extreme caution in geriatric patients and Boxers.

 Monitor heart rate and blood pressure closely

Atenolol

D: 0.25-1 mg/kg PO q12hr

C: 3 mg/kg PO q12hr (or 6.25-12.5 mg/cat PO q12hr)

 Most useful in conjunction with another antihypertensive agent

 May be particularly useful in cases of hyperthyroidism or pheochromocytoma

 Monitor for bradycardia at higher doses

Propranolol

D: 0.2-1 mg/kg PO q8hr

C: 0.4-1.2 mg/kg PO q8hr

 Titrate dose to effect, especially in combination with other antihypertensive medications

 May be particularly useful in cases of hyperthyroidism or pheochromocytoma

 Monitor for bradycardia at higher doses

Nitroprusside

D/C: 1-5 µg/kg/min IV as constant rate infusion

 Use only if constant arterial pressure monitoring available

 Titrate to effect

 Monitor closely for hypotension

 Protect medication from light

Hydralazine

D: 0.5 mg/kg PO (initial dose), 0.5-2.0 mg/kg PO q12hr

C: 2.5 mg/cat PO q12-24hr

 Titrate to effect

 Monitor for hypotension

Amlodipine

D: 0.5-1 mg/kg PO q24hr

C: 0.625-1.25 mg/cat q24hr

 Risk of adverse effects increases with doses higher than recommended range

Enalapril

D: 0.5 mg/kg PO q12-24hr

C: 0.25-0.5 mg/kg PO q12-24hr

 Monitor renal function

Benazepril

D/C: 0.25-0.5 mg/kg PO q24hr

 Monitor renal function

*underlying diseases should be treated simultaneously in most cases

Chronic Therapy of Hypertension

A diet moderately restricted in sodium content is a reasonable recommendation for patients with HT and may assist in the control of blood pressure. Diuretics are not currently recommended as monotherapy for therapy of HT. Some patients may respond to discontinuation of other medications that tend to raise blood pressure (e.g., phenylpropanolamine). In patients receiving fluid therapy, reductions in the amount of fluid administered may allow for easier management of HT with vasodilating medications, but renal function should be monitored closely.

Chronic Therapy of Hypertension in Cats

Amlodipine besylate (a long-acting dihydropyridine calcium antagonist) is the current antihypertensive medication of choice for cats12,38-40. Beta-blocking agents such as atenolol or propranolol may be useful adjunctive therapy, especially in hyperthyroid cats, but beta-blocking agents are less successful when administered alone for management of HT. Angiotensin-converting enzyme inhibitors (e.g., enalapril or benazepril) have proven to be variable in their efficacy in controlling hypertension in cats but may have other beneficial effects (e.g., aldosterone antagonism) in these patients37. Other oral agents such as hydralazine may be useful in some situations but have not undergone wide clinical study.

Chronic Therapy of Hypertension in Dogs

Angiotensin-converting inhibitors are useful for therapy of HT related to protein-losing renal diseases in dogs, decreasing both blood pressure and renal protein loss36. The antihypertensive effect of these medications in dogs with HT secondary to other diseases appears to be variable, but ACEIs are usually well tolerated and can be initiated as a therapeutic trial in non-emergency HT patients. If response to ACEI alone is inadequate, other drugs may be added or substituted. Amlodipine besylate is commonly used for control of HT in dogs but higher doses may be needed to obtain clinical effects as compared to cats. Adverse effects may be seen at higher doses and caution is advised when increasing amlodipine doses for blood pressure control in dogs. When standard doses of amlodipine are not controlling blood pressure sufficiently, addition of an ACEI or beta-blocking agent may be helpful.

Diagnosis and therapy of HT in dogs and cats can be challenging. Careful assessment of all body systems is merited whenever HT is diagnosed. Conversely, the possibility of HT should be investigated whenever suspicious clinical signs or diseases known to be associated with HT are diagnosed in a clinical patient.

References

1.  Rapoport GS, Stepien RL. Direct arterial blood pressure measurement in 54 dogs presented for systemic hypertension screening 1998-2001 (abstract). 11th Congress, European Society of Veterinary Internal Medicine 2001;62.

2.  Struble AL, Feldman EC, Nelson RW, Kass PH. Systemic hypertension and proteinuria in dogs with diabetes mellitus. J Am Vet Med Assoc 1998;213:822-825.

3.  Remillard RL, Ross JN, Eddy JB. Variance of indirect blood pressure measurements and prevalence of hypertension in clinically normal dogs. Am J Vet Res 1991;52:561-565.

4.  Syme HM, Barber PJ, Markwell PJ, Elliott J. Prevalence of systolic hypertension in cats with chronic renal failure at initial evaluation. J Am Vet Med Assoc 2002;220:1799-1804.

5.  Maggio F, DeFrancesco TC, Atkins CE, et al. Ocular lesions associated with systemic hypertension in cats: 69 cases (1985-1998). J Am Vet Med Assoc 2000;217:695-702.

6.  Littman MP, Robertson JL, Bovee KC. Spontaneous systemic hypertension in dogs: Five cases (1981-1983). J Am Vet Med Assoc 1988;193:486-494.

7.  Bovee KC, Littman MP, Crabtree BJ, Aguirre G. Essential hypertension in a dog. J Am Vet Med Assoc 1989;195:81-86.

8.  Bovee KC, Littman MP, Saleh F, et al. Essential hereditary hypertension in dogs: a new animal model. J Hypertens 1986;4:S172-1.

9.  Tippet TE, Padgett GA, Eyster G, et al. Primary hypertension in a colony of dogs. Hypertension 1987;9:49-58.

10. Stiles J, Polzin DJ, Bistner SI. The prevalence of retinopathy in cats with systemic hypertension and chronic renal failure or hyperthyroidism. J Am Anim Hosp Assoc 1994;30:564-572.

11. Kobayashi DL, Peterson ME, Graves TK, et al. Hypertension in cats with chronic renal failure or hyperthyroidism. J Vet Intern Med 1990;4:58-62.

12. Hypertension Consensus Panel, American College of Veterinary Internal Medicine. Current recommendations for diagnosis and management of hypertension in cats and dogs (report). Dallas, TX, 20th Annual Veterinary Medical Forum, 2002.

13. Sparkes AH, Caney SMA, King MCA, Grufydd-Jones TJ. Inter- and intraindividual variation in Doppler ultrasonic indirect blood pressure measurements in healthy cats. J Vet Intern Med 1999;13:314-318.

14. McCubbin JW, Corcoran AC. Arterial pressures in street dogs: Incidence and significance of hypertension. Proc Soc Exp Biol Med 1953;84:130-131.

15. Bodey AR, Michell AR. Epidemiological study of blood pressure in domestic dogs. J Sm Anim Pract 1996;37:116-125.

16. Anderson LJ, Fisher EW. The blood pressure in canine interstitial nephritis. Res Vet Sci 1968;9:304-313.

17. Cowgill LG, Kallet AJ. Recognition and management of hypertension in the dog In: Kirk, RW and Bonagura, JD, eds. Current Veterinary Therapy VIII: Small Animal Practice. Philadelphia: W.B. Saunders Company; 1983;1025-1028.

18. Ortega TM, Feldman EC, Nelson RW, et al. Systemic arterial blood pressure and urine protein/creatinine ratio in dogs with hyperadrenocorticism. J Am Vet Med Assoc 1996;209:1724-1729.

19. Stepien RL, Rapoport GS. Clinical comparison of three methods to measure blood pressure in nonsedated dogs. J Am Vet Med Assoc 1999;215:1623-1628.

20. Schneider HP, Truex RC, Knowles JO. Comparative observations of the hearts of mongrel and greyhound dogs. Anat Rec 1964;149:173-180.

21. Brown S, Haberman C, Morgan J. Evaluation of Doppler ultrasonic and oscillometric estimates of blood pressure in conscious dogs (abstract). 19th Annual Veterinary Medical Forum 2001;845.

22. Bodey AR, Michell AR. Longitudinal studies of reproducibility and variability of indirect (oscillometric) blood pressure measurements in dogs: evidence for tracking. Res Vet Sci 1997;63:15-21.

23. Bodey AR, Michell AR, Bovee KC, Buranakurl TG. Comparison of direct and indirect (oscillometric) measurement of arterial blood pressure in conscious dogs. Res Vet Sci 1996;61:17-21.

24. Cowgill LD. Systemic hypertension: Overview & importance. Proceedings, 19th Annual Veterinary Medical Forum 2001;107-108.

25. Kallet AJ, Cowgill LD, Kass PH. Comparison of blood pressure measurements obtained in dogs by use of indirect oscillometry in a veterinary clinic versus at home. J Am Vet Med Assoc 1997;210:651-654.

26. Bodey AR, Young LE, Bartram DH, et al. A comparison of direct and indirect (oscillometric) measurements of arterial blood pressure in anaesthetised dogs, using tail and limb cuffs. Res Vet Sci 1994;57:265-269.

27. Brown S, Haberman C, Morgan J. Evaluation of Doppler ultrasonic and oscillometric estimates of blood pressure in cats (abstract). J Vet Intern Med 2001;15:281.

28. Binns SH, Sisson DD, Buoscio DA, Schaeffer DJ. Doppler ultrasonographic, oscillometric sphygmomanometric, and photoplethysmographic techniques for noninvasive blood pressure measurement in anesthetized cats. J Vet Intern Med 1995;9:405-414.

29. Belew AM, Barlett T, Brown SA. Evaluation of the white-coat effect in cats. J Vet Intern Med 1999;13:134-142.

30. Brown SA, Langford K, Tarver S. Effects of certain vasoactive agents on the long-term pattern of blood pressure, heart rate, and motor activity in cats. Am J Vet Res 1997;58:647-652.

31. Bodey AR, Sansom J. Epidemiological study of blood pressure in domestic cats. J Small Anim Pract 1998;39:567-573.

32. Mishina M, Watanabe T, Fujii K, et al. Non-invasive blood pressure measurements in cats: Clinical significance of hypertension associated with renal failure. J Vet Med Sci 1998;60:805-808.

33. Klevans LR, Hirkaler G, Kovacs JL. Indirect blood pressure determination by Doppler technique in renal hypertensive cats. Am J Physiol 1979;237:H720-H723.

34. Chalifoux A, Dallaire A, Blais D, et al. Evaluation of the arterial blood pressure of dogs by two noninvasive methods. Can J Comp Med 1985;49:419-423.

35. Coulter DB, Keith JC. Blood pressures obtained by indirect measurement in conscious dogs. J Am Vet Med Assoc 1984;184:1375-1378.

36. Grauer GF, Greco DS, Getzy DM, et al. Effects of enalapril vs. placebo as a treatment for canine idiopathic glomerulonephritis. J Vet Intern Med 2000;14:526-533.

37. Steele JS, Henik RA, Stepien RL. Effects of ACE-inhibition on blood pressure and the renin-angiotensin-aldosterone system in cats with hypertension associated with chronic renal disease. Vet Therap 2002;3:157-166.

38. Henik RA, Snyder PS. Treatment of systemic hypertension in cats with amlodipine besylate. J Am Anim Hosp Assoc 1997;33:226-234.

39. Snyder P. Amlodipine: a randomized, blinded clinical trial in 9 cats with systemic hypertension. J Vet Intern Med 1998;12:157-162.

40. Henik RA. Systemic hypertension and its management. Vet Clin NA, Sm Anim Prac 1997;27:1355-1372.

41. Brown SA. Systemic hypertension: Kidney as a target organ. Proceedings, 19th Annual Veterinary Medical Forum 2001;117-118.

42. Bagley RS. Systemic hypertension: Brain as a target organ. Proceedings, 19th Annual Veterinary Medical Forum 2001;111-112.

43. Davidson MG. Systemic hypertension: The eye as a target organ. Proceedings, 19th Annual Veterinary Medical Forum 2001;113-114.

44. Atkins CE. Systemic hypertension: The heart as a target organ. Proceedings, 19th Annual Veterinary Medical Forum 2001;115-116.

Speaker Information
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Rebecca L. Stepien, DVM, MS, Diplomate ACVIM (Cardiology)
University of Wisconsin


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