Bp. Madden et al., IS ROUTINE POSTOPERATIVE SURVEILLANCE FOR CYTOMEGALOVIRUS-INFECTION FOLLOWING HEART-TRANSPLANTATION NECESSARY, European journal of cardio-thoracic surgery, 14(1), 1998, pp. 15-17
Objective: Cytomegalovirus infection (CMV) is an important cause of mo
rbidity and mortality following cardiac transplantation. The purpose o
f the present study was to ascertain whether routine post-operative sc
reening for CMV infection influenced clinical management. Methods: Lab
oratory and case notes of 220 patients who received cardiac transplant
ation between November 1986 and October 1996 were reviewed. The range
of follow-up was one to 120 (median 36) months. CMV surveillance invol
ved blood tests for early antigen detection weekly for the first 6 pos
t-operative weeks, fortnightly thereafter until the end of the third p
ost-operative month and every 6 weeks to the end of the first post-ope
rative year. Otherwise monitoring was performed if the patients had cl
inical symptoms suggestive of CMV infection. CMV sere-negative IgG rec
ipients (R) of sere-positive IgG donor (D) organs and/or blood product
s received hyper-immune gammaglobulin for the first three post-operati
ve months. Four patient groups were noted, namely R+D+ (59 patients),
R+D- (70 patients), R-D+ (35 patients) and R-D- (56 patients). Results
: CMV antigenaemia was present in 40% (89) of patients and 48% (43) of
these patients developed clinical features of CMV infection and recei
ved ganciclovir therapy. The distribution of clinical CMV infection re
quiring treatment was 25% (9/35) in the R+D- group, 50% (16/32) in the
R+D+ group and 85% (18/22) in the R-D+ group. None of the patients in
the R-D- group developed CMV antigenaemia. Forty six (52%) patients w
ho were CMV antigen positive but who did not develop symptoms were not
treated with ganciclovir and have remained well. Conclusion: Our resu
lts suggest that routine screening for CMV following cardiac transplan
tation is unnecessary. Surveillance did not result in the instigation
of treatment for CMV unless there were associated clinical features of
CMV infection. (C) 1998 Elsevier Science B.V. All rights reserved.