Influence of pathophysiology, severity, and cost on the medical management of gastroesophageal reflux disease

被引:12
作者
Reynolds, JC
机构
关键词
economics; gastroesophageal reflux; gastrointestinal drugs; gastrointestinal motility;
D O I
10.1093/ajhp/53.22_Suppl_3.S5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This article summarizes the pathophysiology of gastroesophageal reflux disease (GERD) and the wide spectrum in disease and symptom severity as they influence the selection of cost-effective treatment strategies. The vast majority of patients with GERD have mild symptoms, no gross endoscopic evidence of esophagitis, and little risk of developing complications. More than 85% of patients with GERD symptoms have uncomplicated disease. Diffuse ulcerations or complications (grade III or IV esophagitis) occur in only 3.5% of patients <65 years of age. However, some patients with GERD can develop severe complications, including esophageal obstruction, significant blood loss, and, in rare circumstances, perforation. Furthermore, adenocarcinoma of the esophagus, which is increasing in incidence faster than any other cancer, is caused by GERD. Although severe ulcerations are uncommon in young patients, they occur in 20-30% of patients over age 65. Patients with ulcerative esophagitis are not only more prone to develop complications, they are also more resistant to treatment. Cost-effective medical management of GERD must take into account the wide spectrum of symptom and disease severity. Therapy consists of both nonpharmacologic treatment and the appropriate use of medications from several classes of drugs, either alone or in combination. Traditionally, prokinetic agents or histamine receptor antagonists have been used as primary therapy; proton-pump inhibitors are reserved for more resistant cases. The rationale for this and for alternative approaches is discussed.
引用
收藏
页码:S5 / S12
页数:8
相关论文
共 80 条
[11]   THE INCIDENCE OF ADENOCARCINOMA IN COLUMNAR-LINED (BARRETTS) ESOPHAGUS [J].
CAMERON, AJ ;
OTT, BJ ;
PAYNE, WS .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (14) :857-859
[12]   DUODENOGASTROESOPHAGEAL REFLUX - RELATIONSHIP TO PH AND IMPORTANCE IN BARRETTS-ESOPHAGUS [J].
CHAMPION, G ;
RICHTER, JE ;
VAEZI, MF ;
SINGH, S ;
ALEXANDER, R .
GASTROENTEROLOGY, 1994, 107 (03) :747-754
[13]  
CLOUD ML, 1991, AM J GASTROENTEROL, V86, P1735
[14]  
CLOUD ML, 1990, DIGEST DIS SCI, V37, P865
[15]   HISTAMINE-2-RECEPTOR ANTAGONISTS IN GASTRO-ESOPHAGEAL REFLUX [J].
COLINJONES, DG .
GUT, 1989, 30 (10) :1305-1308
[16]   BASAL ACID OUTPUT AND GASTRIC-ACID HYPERSECRETION IN GASTROESOPHAGEAL REFLUX DISEASE - CORRELATION WITH RANITIDINE THERAPY [J].
COLLEN, MJ ;
JOHNSON, DA ;
SHERIDAN, MJ .
DIGESTIVE DISEASES AND SCIENCES, 1994, 39 (02) :410-417
[17]  
COLLINS BJ, 1987, HEPATO-GASTROENTEROL, V34, P113
[18]   ROLES OF GASTRIC-ACID AND PH IN THE PATHOGENESIS OF GASTROESOPHAGEAL REFLUX DISEASE [J].
DENT, J .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1994, 29 :55-61
[19]   OMEPRAZOLE V RANITIDINE FOR PREVENTION OF RELAPSE IN REFLUX ESOPHAGITIS - A CONTROLLED DOUBLE-BLIND TRIAL OF THEIR EFFICACY AND SAFETY [J].
DENT, J ;
YEOMANS, ND ;
MACKINNON, M ;
REED, W ;
NARIELVALA, FM ;
HETZEL, DJ ;
SOLCIA, E ;
SHEARMAN, DJC .
GUT, 1994, 35 (05) :590-598
[20]   MECHANISMS OF GASTRO-ESOPHAGEAL REFLUX IN PATIENTS WITH REFLUX ESOPHAGITIS [J].
DODDS, WJ ;
DENT, J ;
HOGAN, WJ ;
HELM, JF ;
HAUSER, R ;
PATEL, GK ;
EGIDE, MS .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (25) :1547-1552