Echocardiographic assessment of pulmonary hypertension in Gaucher's disease

被引:76
作者
Elstein, D
Klutstein, MW
Lahad, A
Abrahamov, A
Hadas-Halpern, I
Zimran, A
机构
[1] Shaare Zedek Med Ctr, Gaucher Clin, IL-91031 Jerusalem, Israel
[2] Shaare Zedek Med Ctr, Dept Med, IL-91031 Jerusalem, Israel
[3] Shaare Zedek Med Ctr, Dept Cardiol, IL-91031 Jerusalem, Israel
[4] Shaare Zedek Med Ctr, Dept Pediat, IL-91031 Jerusalem, Israel
[5] Shaare Zedek Med Ctr, Dept Diagnost Radiol, IL-91031 Jerusalem, Israel
关键词
D O I
10.1016/S0140-6736(98)10194-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Enzyme therapy has been shown to decrease the signs and symptoms of Gaucher's disease. A few patients, however, develop pulmonary hypertension on such treatment. We investigated the frequency of pulmonary hypertension in Gaucher's disease. Methods We studied 134 adults with type 1 Gaucher's disease, including 73 patients on enzyme replacement, with echocardiography. We measured tricuspid incompetence (TI) with continuous-wave doppler. Pulmonary hypertension was indicated by a TI gradient of more than 30 mm Hg. Findings Nine (7%) patients had pulmonary hypertension: all were treated and six had undergone splenectomy. Chest radiographs confirmed the presence of pulmonary hypertension in these patients as well as in most patients with TI gradients of 25-29 mm Hg. Interpretation The confounding effects of disease severity and splenectomy in many treated patients precluded definitive conclusion of cause and effect. Nonetheless, we found an unexpectedly high rate of pulmonary hypertension and recommended routine echocardiographic monitoring of all treated and untreated patients with type 1 Gaucher's disease. We also suggest consideration of treatment withdrawal if the TI gradient progresses to more than 30 mm Hg.
引用
收藏
页码:1544 / 1546
页数:3
相关论文
共 13 条
[1]   Appetite-suppressant drugs and the risk of primary pulmonary hypertension [J].
Abenhaim, L ;
Moride, Y ;
Brenot, F ;
Rich, S ;
Benichou, J ;
Kurz, X ;
Higenbottam, T ;
Oakley, C ;
Wouters, E ;
Aubier, M ;
Simonneau, G ;
Begaud, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (09) :609-616
[2]   REPLACEMENT THERAPY FOR INHERITED ENZYME DEFICIENCY - MACROPHAGE-TARGETED GLUCOCEREBROSIDASE FOR GAUCHERS-DISEASE [J].
BARTON, NW ;
BRADY, RO ;
DAMBROSIA, JM ;
DIBISCEGLIE, AM ;
DOPPELT, SH ;
HILL, SC ;
MANKIN, HJ ;
MURRAY, GJ ;
PARKER, RI ;
ARGOFF, CE ;
GREWAL, RP ;
YU, KT .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (21) :1464-1470
[3]  
DAWSON A, 1995, CLIN RES, V43, P277
[4]   PRIMARY PULMONARY-HYPERTENSION IN PATIENTS WITH CLASSIC HEMOPHILIA [J].
GOLDSMITH, GH ;
BAILY, RG ;
BRETTLER, DB ;
DAVIDSON, WR ;
BALLARD, JO ;
DRISCOL, TE ;
GREENBERG, JM ;
KASPER, CK ;
LEVINE, PH ;
RATNOFF, OD .
ANNALS OF INTERNAL MEDICINE, 1988, 108 (06) :797-799
[5]  
Harats D, 1997, ACTA HAEMATOL-BASEL, V98, P47
[6]   Pulmonary function abnormalities in type I Gaucher disease [J].
Kerem, E ;
Elstein, D ;
Abrahamov, A ;
Ziv, YB ;
HadasHalpern, I ;
Melzer, E ;
Cahan, C ;
Branski, D ;
Zimran, A .
EUROPEAN RESPIRATORY JOURNAL, 1996, 9 (02) :340-345
[7]  
LEE RE, 1988, LAB INVEST, V58, pA54
[8]  
Rich S, 1997, HEART DIS TXB CARDIO, P780
[9]   GAUCHERS DISEASE OF LUNG CAUSING SEVERE PULMONARY HYPERTENSION WITH ASSOCIATED ACUTE RECURRENT PERICARDITIS [J].
ROBERTS, WC ;
FREDRICKSON, DS .
CIRCULATION, 1967, 35 (04) :783-+
[10]   Gaucher cells in pulmonary-capillary blood in association with pulmonary hypertension [J].
Ross, DJ ;
Spira, S ;
Buchbinder, NA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (05) :379-381