CHAPTER 35 • GASTROENTEROLOGY 207
therapy fails, it is important not only to consult gas-
troenterology, but also the specialty that would evaluate
for extraintestinal complications. In the face of a clas-
sic history and normal physical examination, it is rea-
sonable to institute empiric therapy in a stepwise
fashion (Fig. 35-2).
- Persistent symptoms despite behavioral interventions
warrant medical therapy. Episodic complaints are
treated with over-the-counter(OTC) antacids or an
H-2 receptor antagonist(H2RA) as needed. This can
beadvanced to prescription-strength H2RA therapy if
control is insufficient. Should symptoms continue
after 6 weeks of H2RA therapy, neither continuing
therapy nor increasing the dose are likely to achieve
control (Kahrilas, Fenerty, and Joelsson, 1999). At
this point, it was previously common practice to con-
sider add-on therapy with a prokinetic agent to
improve LES tone, gastric emptying, and peristalsis.
These agents all have side effects that make them
undesirable for use in athletes. Bethanechol has gen-
eralized cholinergic effects. Metoclopramide has a
high incidence of fatigue, restlessness, tremor, and
tardive dyskinesia, making it a poor choice for any-
thing more than sporadic use. Cisapride, formerly the
prokinetic agent of choice, was found to be associated
with arrhythmia development, especially with con-
comitant use of macrolides, imidazoles, or protease
inhibitors (Wysowski and Bacsanyi, 1996). This dis-
covery led to severe prescribing restrictions in the
United States.
- In individuals who fail to respond to H2RAs, standard-
dose proton pump inhibitors (PPI) are the treatment of
choice. PPIs provide more rapid relief of symptoms
(Bardhan et al, 1999) and are more likely than H2RAs
to heal and prevent recurrence of erosive esophagitis
(Chilba et al, 1997). The agents in this class are equally
efficacious in controlling heartburn and have similar
healing and relapse rates (Caro, Salas, and Ward,
2001). Because reported differences in initial bioavail-
ability and antisecretory potency are not clinically sig-
nificant with long-standing use, one PPI cannot be
recommended over another (Williams et al, 1998). If
the response to episodic treatment is generally favor-
able but symptoms are occurring on a more chronic
basis, maintenance therapy is beneficial. Because their
efficacy is dose-dependent, PPI therapy can be stepped-
up to control symptoms. Failure to respond to high dose
PPI therapy requires gastroenterologist evaluation to
rule out complications of GERD. In the absence of find-
ings consistent with reflux disease, further GI testing
FIG. 35-2 Therapeutic Pyramid
for Exercise-Related Gastroeso-
phageal Reflux Disease.