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Postural hypotension

Orthostatic hypotension (also known as postural hypotension and, colloquially, as head rush) is a sudden fall in blood pressure that occurs when a person assumes a standing position. more...

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Medicines

Symptoms

Symptoms, which generally occur after sudden standing, include dizziness, lightheadedness, blurred vision, and syncope (temporary loss of consciousness).

Causes

It may be caused by hypovolemia (a decreased amount of blood in the body), resulting from the excessive use of diuretics, vasodilators, or other types of drugs, dehydration, or prolonged bed rest. It can be a side effect of certain anti-depressants, such as tricyclics. The disorder may be associated with Addison's disease, atherosclerosis (build-up of fatty deposits in the arteries), diabetes, and certain neurological disorders including Shy-Drager syndrome and other forms of dysautonomia.

Treatment and management

When orthostatic hypotension is caused by hypovolemia due to medications, the disorder may be reversed by adjusting the dosage or by discontinuing the medication. When the condition is caused by prolonged bed rest, improvement may occur by sitting up with increasing frequency each day. In some cases, physical counterpressure such as elastic hose or whole-body inflatable suits may be required (such as Jobst stockings). Dehydration is treated with salt and fluids.

The prognosis for individuals with orthostatic hypotension depends on the underlying cause of the condition.

Medical management

Some drugs that are used in the treatment of orthostatic hypotension include fludrocortisone (Florinef), erythropoietin and midrodrine.

Lifestyle advice

Some suggestions for minimizing the effects include:

  • Checking blood pressure regularly with a home monitoring kit. Check when lying flat and when standing as well as when symptoms occur.
  • Standing slowly rather than quickly, as the delay can give the blood vessels more time to constrict properly. This can help avoid incidents of syncope.
  • Maintaining an elevated salt intake, through sodium supplements or electrolyte-enriched drinks. A suggested value is 10 g per day; overuse can lead to hypertension and should be avoided.
  • Maintaining a proper fluid intake to prevent the effects of dehydration.
  • As eating lowers blood pressure, eating multiple smaller meals rather than fewer larger meals. Taking extra care when standing after eating.

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Tolerance to tacrine, arterial hypotension and leuko-araiosis in Alzheimer's disease
From Age and Ageing, 9/1/98 by Florence Lebert

SIR--The baroreflex regulation of blood pressure is modulated by cholinergic systems [1]. Alzheimer's disease (AD) is more often associated with sympathetic dysfunction than fronto-temporal lobe dementia, in which the cholinergic system is relatively spared [2]. In patients with AD, orthostatic hypotension is associated with the severity of the cognitive decline--possibly because of chronic hypoperfusion of the white matter [3]. Orthostatic hypotension could also influence the response to cholinesterase inhibitors; Velnacrine non-responders had a more severe decrease in systolic postural blood pressure before treatment than responders [4].

Amar et al. [5] reported a high rate of withdrawal from tacrine in patients with AD with leuko-araiosis, especially because of agitation. We examined a possible relationship between tolerance to tacrine, orthostatic blood pressure and leuko-araiosis in patients with AD. Forty-one consecutive patients with AD with mild or moderate dementia were included. They were free from heart disease, diabetes mellitus or delirium. They were not taking any drugs with hypotensive side effects. Drug dosage had been stable for at least 1 month before the start of the study. Median age was 73.9 years (range 57-88), the median Mini-Mental State Examination score [6] was 19.6 (range 29-9) at baseline. Leuko-araiosis was ,assessed on computed tomography scan using Rezek's score [7].

Patients received 40 mg/day of tacrine for 6 weeks, 80 mg/day for 6 weeks, then 120 mg/day. Orthostatic hypotension (defined according to Bannister's criteria [8]) was noted at baseline and after 2 weeks of tacrine at 120 mg/day. The Mann-Whitney U-test was used for statistical analysis. Thirty-six patients were treated with tacrine without obvious side effects. Five patients (14%) were withdrawn prematurely: three because of gastritis and nausea, one because of agitation and one because of abnormal liver function tests. The age of withdrawn patients was higher than that of the others [80.2 years (73-88) versus 73.1 years (57-87); U = -1,97, P = 0.04]. The Rezek score did not differ between the groups: in withdrawn patients it was between 0 and 15 points. Seventeen patients had orthostatic hypotension: none was withdrawn. However, systolic blood pressure in supine position was significantly lower in withdrawn patients [123.6 mmHg (110-150) versus 142.6 mmHg (118-182); U = -2,43, P = 0.01]. Furthermore, orthostatic hypotension disappeared whilst on tacrine in 13 patients (42% versus 10%).

In conclusion, it appears that patients with low blood pressure have a lower tolerance of tacrine and that tacrine has an effect on orthostatic hypotension. A relationship between blood pressure dysregulation, cognitive decline, tolerance to anticholinesterase drugs in AD and white matter changes should be further investigated. Anticholinesterase drugs might also benefit patients with AD by decreasing orthostatic hypotension.

We would like to thank Didier Leys for his comments on this work.

[1.] Brezenoff HE. Cardiovascular regulation by brain acetylcholine. Fed Prac 1984; 43: 17-20.

[2.] Hasenbroekx C, Lebert F, Pasquier F et al. Autonomic failures in Alzheimer's disease and in frontotemporal dementia. Neurobiol Aging 1996; suppl. 17: S88.

[3.] Englund E, Brun A, Gustafson X et al. A white matter disease in dementia of Alzheimer's type--clinical and neuropathological corretater. Int J Geriatr Psychiatr 1989; 4: 87-102.

[4.] Pomara N, Deptula D, Singh R. Pretreatment postural blood pressure drop as a possible predictor response to the cholinesterase inhibitor velnacrine (HP 029) in Alzheimer's disease. Psychopharmacol Bull 1991; 27: 301-7.

[5.] Amar K, Wilcock GK, Scot M et al. The presence of leuko-araiosis in patients with Alzheimer's disease predicts poor tolerance to tactine, but does not discriminate responders from non-responders. Age Ageing 1997; 26: 25-9.

[6.] Folstein ME Folstein SE, McHugh PR. Mini Mental State: practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 1975; 12: 189-98.

[7.] Rezek DL, Morris JC, Fulling KH et al. Periventricular white matter lucencies in senile dementia of the Alzheimer type and in normal aging. Neurology 1987; 37: 1365-8.

[8.] Bannister R, Mathias CJ. Autonomic Failure, third edition. Oxford: Oxford University Press, 1993.

FLORENCE LEBERT, CAROLE MOULY, FLORENCE PASQUIER

Memory Disorders Unit,

University Hospital of Lille (CHRU-Hopital B),

Lille, France

Fax: (+33) 3 28 43 47 98

COPYRIGHT 1998 Oxford University Press
COPYRIGHT 2000 Gale Group

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