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Published on: March 21, 2013
Clinostatic hypertension and orthostatic hypotension
1Emergency and Accident Department, Medicine Unit, Ospedale S. Maria Nuova, Florence, Italy. alfonso.lagi@asf.toscana.it
Insights
The Hyp-Hyp phenomenon links clinostatic hypertension (CH) and orthostatic hypotension (OH), affecting many patients. Early diagnosis and tailored management are crucial for preventing symptoms and end-organ damage.
Area of Science:
- Cardiology
- Neurology
Background:
- The Hyp-Hyp phenomenon, characterized by the association of clinostatic hypertension (CH) and orthostatic hypotension (OH), affects a significant percentage of hypertensive and OH patients.
- CH/OH poses clinical challenges due to troublesome symptoms, end-organ damage, and management difficulties.
Purpose of the Study:
- To review the international literature on the clinical problem of CH.
- To outline optimal diagnostic work-up and tailored treatment strategies for patients with CH/OH.
Main Methods:
- A systematic literature review was conducted using MEDLINE.
- Key topics included diagnostic work-up, association with dysautonomic failure and syncope, and treatment options for CH/OH.
Main Results:
- Standard OH diagnosis involves assessing cardiac autonomic function.
- Midodrine is FDA-approved for OH treatment; short-acting antihypertensives at bedtime may help severe CH.
- Further research is needed on the link between CH/OH, dysautonomic failure, and syncope.
Conclusions:
- Clinical diagnosis of the Hyp-Hyp phenomenon is feasible, but identifying the underlying cause is challenging.
- Establishing simple diagnostic standards for identifying patients at risk of dysautonomic impairment is recommended for targeted work-up.
Background:
The association of clinostatic hypertension (CH) and orthostatic hypotension (OH) is described as the "Hyp-Hyp phenomenon," and it has been found in about 5.5% of hypertensive patients and in up to 50% of patients with OH. The importance of CH/OH in clinical practice is mainly due to the presence of troublesome symptoms, end-organ damage, and difficulties in its clinical management.
Hypothesis:
The review focuses on the clinical problem of CH and review the international literature for the best management, including the diagnostic work-up and the taylored treatment for this kind of patients.
Methods:
A systematic review of the literature was conducted through MEDLINE research to focus the main controversial issues about CH/OH. Included topics: (1) the diagnostic work-up, (2) the association with dysautonomic failure and syncope, and (3) the treatment options and prevention of end-organ damage.
Results:
Current standard reference for OH diagnosis includes functional assessment of the cardiac vagal nervous system and the sympathetic adrenergic system. The association with dysautonomic failure and with syncope needs further investigation. Pharmacologic treatment of OH is aimed at controlling symptoms rather than restoring normotension. Midodrine is the only medication that has been put to multicenter placebo-controlled trial and subsequently approved by the U.S. Food and Drug Administration (FDA) for OH treatment. Short-acting oral antihypertensive agents at bedtime should be considered in patients with severe, sustained CH.
Conclusions:
Data obtained from the literature review showed that clinical diagnosis of the Hyp-Hyp phenomenon is relatively simple, but it remains more difficult to establish the causal disease. In our opinion, it is advisable to define simple diagnostic standards for the selection of patients at risk of dysautonomic impairment so that a subsequent highly specific diagnostic work-up could be initiated.
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