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Ann Thorac Surg 2002;73:1028
© 2002 The Society of Thoracic Surgeons


Correspondence

Problems in the evaluation of thymectomy for myasthenia gravis: Reply

Jason M. Budde, MDa, Joseph I. Miller, Jr, MDa

a Division of Cardiothoracic Surgery, Emory University School of Medicine, 1365 Clifton Rd, NE, Atlanta, GA 30322, USA

e-mail: jmille6331{at}aol.com

To the Editor

We thank Dr Jaretzki and colleagues for their constructive criticism of our study [1]. We also acknowledge here, as we have done in our report, the tireless work done by the Task Force of the Myasthenia Gravis Foundation of America in designing research guidelines [2]. They will no doubt greatly facilitate the standardization of future studies concerning a very important topic: thymectomy for myasthenia gravis (MG).

We agree that our classification of "improvement"—decreased number or severity of symptoms with the same or less medications—involves a measure of subjectivity on the part of both the clinician and the researcher. We would point out that the Task Force, in its guidelines, "sees no alternative but to accept the inherent imprecision of a clinical classification" in assessing MG [2]. In addition, some permutation of symptom severity and medication use has been employed as a postoperative assessment in most MG studies, many of which we have cited in our article [36]. As such, we feel that to reject the validity of this assessment—admittedly not perfectly objective—would thereby reject the findings of most studies ever conducted concerning MG and thymectomy.

We also acknowledge that our table comparing remission and improvement rates has not undergone any statistical comparison (though Jaretzki and colleagues have in their study [3]), and have not implied that such was the case. Concerning the issue of patient pool (or "denominator," as stated in the letter), we included only one nonoperative study [5], as some measure of the remission rates occurring in nonthymectomized MG. We feel that this is clearly indicated in our table, and that there should be no suggestion of mixing populations.

Finally, our use of the Osserman classification pertains to preoperative assessment only, and was tested by us, in our multivariate analysis, as a potential predictor of response. Therefore we used it as originally designed—to describe typical clinical patterns—and not to describe changes in disease severity, as suggested by the letter.

We look forward to seeing results of thymectomy studies using the new guidelines recently developed by the Task Force (guidelines which, we may add, were published after our study was completed and accepted for presentation).

References

  1. Budde J.M., Morris C.D., Gal A.A., Mansour K.A., Miller J.I., Jr Predictors of outcome in thymectomy for myasthenia gravis. Ann Thorac Surg 2001;72:197-202.[Abstract/Free Full Text]
  2. Jaretzki A., III, Barohn R.J., Ernstoff R.M., et al. Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America. Ann Thorac Surg 2000;70:327-334.[Free Full Text]
  3. Jaretzki A., III, Penn A.S., Younger D.S., et al. "Maximal" thymectomy for myasthenia gravis. Results. J Thorac Cardiovasc Surg 1988;95:747-757.[Abstract]
  4. Venuta F., Rendina E.A., De Giacomo T., et al. Thymectomy for myasthenia gravis: a 27-year experience. Eur J Cardiothorac Surg 1999;15:621-624.[Abstract/Free Full Text]
  5. Ferguson M.K. Transcervical thymectomy. Semin Thorac Cardiovasc Surg 1999;11:59-64.[Medline]
  6. Masaoka A., Yamakawa Y., Niwa H., et al. Extended thymectomy for myasthenia gravis patients: a 20-year review. Ann Thorac Surg 1996;62:853-859.[Abstract/Free Full Text]

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This Article
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