M. Sarli et al., TREATMENT OF POST MENOPAUSAL OSTEOPOROSIS WITH INTRAVENOUS PAMIDRONATE IN PATIENTS WITH ESOPHAGOGASTRIC PATHOLOGY, Medicina, 58(5), 1998, pp. 446-452
Pamidronate is an effective inhibitor of bone resorption; for this rea
son it is used in the treatment of high bone turnover diseases and ost
eoporosis. Because of potential gastric and esophagic side effects the
ir oral use is limited in patients with active pathology in these orga
ns. With the aim to evaluate the usefulness and to establish the ideal
schedule of treatment of intravenous pamidronate, we assayed pamidron
ate infusions (APDIV) in 20 postmenopausal women with active gastroeso
phagical diseases. Ten of these patients received 30 or 45 mg weekly u
ntil they achieved an average dose of 157.50 +/- 9.28 mg/year in one m
onth (range: 120-180 mg) (Group A). Another comparable ten women's gro
up received 30 or 45 mg every three months or 90 mg every six months;
the achieved average dose in this group was 166.50 +/- 6.87 mg/year (r
ange: 120-180 mg) (Group B). All patients received 1 000 mg elemental
calcium daily. Bone mineral density in lumbar spine significantly incr
eased in both groups, but this increment (Delta DMO%) was higher in gr
oup B. Bone mineral density in femoral neck was only increased in grou
p A. Parathyroid hormone (iPTH) significantly increased at the third m
onth but returned to basal values at the end of the year in both group
s. Parameters of bone remodeling such as osteocalcin (BGP), pyridinoli
ne and deoxipyridinolin decreased progressively and remained low at th
e end of the year. The treatment was well tolerated: only two patients
in group A and one in Group B experienced fever and pseudoflu syndrom
e; phlebitis was present in one patient in the second group. In conclu
sion, intravenous Pamidronate is an effective and safe treatment for p
ostmenopausal osteoporosis specially in these patients with esophagico
r gastric disorders, Future trials are needed to clarify the ideal dos
e and schedule of treatment.