Skip to main content
British Heart Journal logoLink to British Heart Journal
. 1992 Aug;68(2):205–211. doi: 10.1136/hrt.68.8.205

Repeatability of measurements and sources of variability in tests of cardiovascular autonomic function

Gillian P Lawrence 1, Philip D Home 2, Alan Murray 1
PMCID: PMC1025016  PMID: 1389739

Abstract

Objective—To determine the repeatability and sources of variability of clinical tests of cardiovascular autonomic function.

Design—The commonly used electrocardiographic related tests of autonomic function were studied. Two repeat measurements of all tests were made on all subjects on four separate days over a four week period.

Subjects—Ten normal subjects with no known autonomic dysfunction were investigated.

Main outcome measures—These were deep breathing (subject seated and supine), Valsalva manoeuvre, standing up from lying position, and normal relaxed breathing (subject supine). During the tests the electrocardiogram and respiratory pattern were recorded by computer. Beat to beat RR intervals were measured automatically from the electrocardiogram, and from these the results of the tests were calculated.

Results—Variance analysis showed significant between subject variability for all tests (p < 0·005), but some tests showed a much smaller relative within subject variability than others. Average repeatability data (within subject SD) for each test were calculated, and included deep breathing sitting (maxmin) RR (46 ms), Valsalva ratio (0·17), and lying to standing RR ratio (0·11). These compare with between subject SDs of 65 ms, 0·38, and 0·13 respectively, at mean values of 305 ms, 1·92, and 1·15 respectively. The data highlighted one subject with the poorest repeatability, whose electrocardiogram turned out on closer inspection to be under atrial rather than sinus control at times. Poor repeatability in the other subjects was related to variability in the respiratory pattern, and in the deep breathing test, repeat variability was significantly correlated (r = 0·79) with variability in the respiratory amplitude (p < 0·05).

Conclusions—Repeatability data should be available to each laboratory carrying out autonomic function tests. The data provided in this study could be used as a baseline. Poor repeatability highlights the need to re-examine the test procedures, or the test data from specific subjects. Variability of respiratory pattern is associated with poor repeatability, and so careful instructions on respiration should be given to each subject before the tests.

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baldwa V. S., Ewing D. J. Heart rate response to Valsalva manoeuvre. Reproducibility in normals, and relation to variation in resting heart rate in diabetics. Br Heart J. 1977 Jun;39(6):641–644. doi: 10.1136/hrt.39.6.641. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Clark C. V., Mapstone R. Age-adjusted normal tolerance limits for cardiovascular autonomic function assessment in the elderly. Age Ageing. 1986 Jul;15(4):221–229. doi: 10.1093/ageing/15.4.221. [DOI] [PubMed] [Google Scholar]
  3. Dyrberg T., Benn J., Christiansen J. S., Hilsted J., Nerup J. Prevalence of diabetic autonomic neuropathy measured by simple bedside tests. Diabetologia. 1981 Mar;20(3):190–194. doi: 10.1007/BF00252626. [DOI] [PubMed] [Google Scholar]
  4. Ewing D. J., Borsey D. Q., Bellavere F., Clarke B. F. Cardiac autonomic neuropathy in diabetes: comparison of measures of R-R interval variation. Diabetologia. 1981 Jul;21(1):18–24. doi: 10.1007/BF03216217. [DOI] [PubMed] [Google Scholar]
  5. Ewing D. J., Campbell I. W., Clarke B. F. Assessment of cardiovascular effects in diabetic autonomic neuropathy and prognostic implications. Ann Intern Med. 1980 Feb;92(2 Pt 2):308–311. doi: 10.7326/0003-4819-92-2-308. [DOI] [PubMed] [Google Scholar]
  6. Ewing D. J., Campbell I. W., Murray A., Neilson J. M., Clarke B. F. Immediate heart-rate response to standing: simple test for autonomic neuropathy in diabetes. Br Med J. 1978 Jan 21;1(6106):145–147. doi: 10.1136/bmj.1.6106.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ewing D. J., Clarke B. F. Diagnosis and management of diabetic autonomic neuropathy. Br Med J (Clin Res Ed) 1982 Oct 2;285(6346):916–918. doi: 10.1136/bmj.285.6346.916. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ewing D. J., Martyn C. N., Young R. J., Clarke B. F. The value of cardiovascular autonomic function tests: 10 years experience in diabetes. Diabetes Care. 1985 Sep-Oct;8(5):491–498. doi: 10.2337/diacare.8.5.491. [DOI] [PubMed] [Google Scholar]
  9. Fisher B. M., Frier B. M. Usefulness of cardiovascular tests of autonomic function in asymptomatic diabetic patients. Diabetes Res Clin Pract. 1989 Feb 15;6(2):157–160. doi: 10.1016/0168-8227(89)90121-6. [DOI] [PubMed] [Google Scholar]
  10. Griffiths C. J., Gilmartin J. J., Gibson G. J., Murray A. Measurement of chest wall movement; design, performance and clinical use of a four-channel magnetometer instrument. Clin Phys Physiol Meas. 1983 Nov;4(4):363–371. doi: 10.1088/0143-0815/4/4/001. [DOI] [PubMed] [Google Scholar]
  11. Levin A. B. A simple test of cardiac function based upon the heart rate changes induced by the Valsalva maneuver. Am J Cardiol. 1966 Jul;18(1):90–99. doi: 10.1016/0002-9149(66)90200-1. [DOI] [PubMed] [Google Scholar]
  12. Murray A., Ewing D. J., Campbell I. W., Neilson J. M., Clarke B. F. RR interval variations in young male diabetics. Br Heart J. 1975 Aug;37(8):882–885. doi: 10.1136/hrt.37.8.882. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mustonen J., Länsimies E., Uusitupa M., Talwar S., Hyödynmaa S., Kärkkäinen A. Testing of autonomic cardiovascular regulation--methodological considerations. Clin Physiol. 1989 Jun;9(3):249–257. doi: 10.1111/j.1475-097x.1989.tb00977.x. [DOI] [PubMed] [Google Scholar]
  14. O'Brien I. A., O'Hare P., Corrall R. J. Heart rate variability in healthy subjects: effect of age and the derivation of normal ranges for tests of autonomic function. Br Heart J. 1986 Apr;55(4):348–354. doi: 10.1136/hrt.55.4.348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. SHARPEY-SCHAFER E. P., TAYLOR P. J. Absent circulatory reflexes in diabetic neuritis. Lancet. 1960 Mar 12;1(7124):559–562. doi: 10.1016/s0140-6736(60)92773-2. [DOI] [PubMed] [Google Scholar]
  16. Sampson M. J., Wilson S., Karagiannis P., Edmonds M., Watkins P. J. Progression of diabetic autonomic neuropathy over a decade in insulin-dependent diabetics. Q J Med. 1990 Jun;75(278):635–646. [PubMed] [Google Scholar]
  17. Smith S. A. Diagnostic value of the Valsalva ratio reduction in diabetic autonomic neuropathy: use of an age-related normal range. Diabet Med. 1984 Nov;1(4):295–297. doi: 10.1111/j.1464-5491.1984.tb01976.x. [DOI] [PubMed] [Google Scholar]
  18. Smith S. A. Reduced sinus arrhythmia in diabetic autonomic neuropathy: diagnostic value of an age-related normal range. Br Med J (Clin Res Ed) 1982 Dec 4;285(6355):1599–1601. doi: 10.1136/bmj.285.6355.1599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Smith S. E., Smith S. A. Heart rate variability in healthy subjects measured with a bedside computer-based technique. Clin Sci (Lond) 1981 Oct;61(4):379–383. doi: 10.1042/cs0610379. [DOI] [PubMed] [Google Scholar]
  20. Sundkvist G., Almér L. 0., Lilja B. Respiratory influence on heart rate in diabetes mellitus. Br Med J. 1979 Apr 7;1(6168):924–925. doi: 10.1136/bmj.1.6168.924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Wheeler T., Watkins P. J. Cardiac denervation in diabetes. Br Med J. 1973 Dec 8;4(5892):584–586. doi: 10.1136/bmj.4.5892.584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Wieling W., van Brederode J. F., de Rijk L. G., Borst C., Dunning A. J. Reflex control of heart rate in normal subjects in relation to age: a data base for cardiac vagal neuropathy. Diabetologia. 1982 Mar;22(3):163–166. doi: 10.1007/BF00283745. [DOI] [PubMed] [Google Scholar]

Articles from British Heart Journal are provided here courtesy of BMJ Publishing Group

RESOURCES