| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
1 Dept of Geriatric Medicine, and 2 Dept of Urology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
To the Editors:
In a recent issue of the European Respiratory Journal, Vazir et al. 1 demonstrated that spectral analysis of heart rate variations (HRV) may be useful as a "rule-out test" for sleep-disordered breathing (SDB) in patients with mild-to-moderate congestive heart failure (CHF). This is an interesting approach to the diagnosis of SDB in CHF patients without sleepiness. As CHF patients with Cheyne–Stokes respiration (CSR)/central sleep apnoea (CSA) are often asymptomatic, this noninvasive approach may be effective to rule out SDB in patients. However, we feel that there are a number of problems with the article by Vazir et al. 1.
First, HRV analysis cannot be applied in patients with arrhythmia, including atrial fibrillation (AF). In a group of patients with CHF, it has been demonstrated that there is a considerable association between AF and CSA 2. Thus, AF may be a feature of CHF with CSR/CSA. As AF is very common in CHF with CSR/CSA, it is difficult for HRV analysis alone to rule out the majority of patients with both AF and SDB. Furthermore, paroxysmal AF (PAF) can occur during the night in patients with sleep apnoea and in those of increased age 3. The presence of PAF episodes and frequent ventricular ectopy may impair the analysis of HRV in patients with CHF.
Secondly, there is the problem of the causal relationship between AF and CSR/CSA. It has been suggested that the risk factors for CSR/CSA are male sex, AF, aged >60 yrs and hypocapnia. AF may therefore be a causal factor for CSR/CSA. In this scenario, CHF patients with AF have a high risk for CSR/CSA. In addition, treatment of arrhythmia with atrial overdrive pacing (AOP) may also have some beneficial effects on sleep apnoea itself 4. Although obstructive sleep apnoea syndrome predisposes to clinically significant cardiac rhythm disturbances that can be successfully controlled by nasal continuous positive airway pressure, AOP has no significant effect on the respiratory variables, including the apnoea/hypopnoea index 5. Therefore, the causal relationships between AF and CSR/CSA are not simple.
Thirdly, CHF patients are often treated with antihypertensive agents. These agents also have some effect on HRV results. It has been reported that a sympathetic activation during the day and a decrease in parasympathetic activity during the night after therapy with a calcium channel blockade, amlodipine, correlated with increases in plasma noradrenaline (NA). In contrast, therapy with an angiotensin II receptor blocker, telmisartan, significantly increased parasympathetic activity without changes in NA during the night and day 6. It has also been suggested that treatment with a nonselective ß-adrenergic blocking agent, carvedilol, in CHF restores both autonomic balance and the ability to increase reflex vagal activity 7. Thus, the treatment strategy for CHF with antihypertensive agents has a great impact on HRV analysis.
Autonomic disturbances and central nervous system abnormality also cause SDB and cardiac dysfunction 8. Patients with neurological disorders and CHF may not undergo HRV analysis.
The large number of CHF patients cannot all be examined in sleep laboratories, so alternative methods of screening for SDB may be required for CHF patients in AF. Although pulse oximetry may underestimate nondesaturated CSA, it still has an advantage over HRV monitoring in terms of convenient and widely available methods. Thus, CHF patients with negative results in SDB judged by pulse oximetry should be analysed with HRV.
In two previous studies 9, 10, sleep apnoea patients had markedly decreased heart rate variability and increased blood pressure variability. These variability abnormalities are characteristic of patients with hypertension. The abnormalities in cardiovascular variability may exaggerate ventricular function and contribute to development of AF and other cardiovascular diseases 9, 10. Although cardiovascular variability and HRV abnormality are features of CHF with SDB, the clinical significance of HRV analysis for screening SDB may be limited.
Because an ideal screening test should have a high sensitivity with a reasonable specificity, we believe that the conclusion drawn by Vazir et al. 1 should be changed to: "spectral analysis of heart rate variations may be useful as a noninvasive rule-out test for sleep-disordered breathing in patients with congestive heart failure without arrhythmia."
REFERENCES
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
