Clinical effect of sulbactam/ampicillin on community-acquired pneumonia with positive Streptococcus pneumoniae urinary antigen test
Niro OKIMOTO, Koichi UCHIDA, Tadashi KATOH, Hisataka TANAKA
Toshikiyo HAYASHI, Takeyuki KURIHARA, Naoyuki MIYASHITA
Department of General Internal Medicine 1, Kawasaki Hospital, Kawasaki Medical School,2-1-80, Nakasange, Kitaku, Okayama, 700-8505, JapanABSTRACT We investigated the efficacy of intravenous penicillin (sulbactam/ampicillin: SBT/ABPC) in adult patients with positive Streptococcus pneumoniae urinary antigen test requiring hospitalization. We administered 3g of SBT/ABPC intravenously in the morning and evening for 7-14 days to 32 adult community-acquired pneumonia patients with positive Binax NOW® S. pneumoniae urinary antigen. Clinical efficacy, bacteriological efficacy, and side effects of these patients were prospectively examined. We observed clinical efficacy in a total of 28 of 32 patients (87.5%); 24 of 26 moderate patients (92.3%), and four of six severe patients (66.7%). Side effects were drug eruption, increased GOT, increased AMY, and decreased WBC, observed in one patient each; however, all were mild. SBT/ABPC is extremely useful in patients with positive S. pneumoniae urinary antigen test requiring hospitalization
Key words: Stereptococcus pneumoniae urinary antigen test,sulbactam/ampicillin INTRODUCTION SUBJECTS AND METHODS
The JRS guidelines for the management
of community-acquired pneumonia in adults
Subjects were 32 patients with adult community-
recommend intravenous penicillin drip if
acquired pneumonia and positive S. pneumoniaeStreptococcus pneumoniae urinary antigen test
urinary antigen test who underwent treatment at
shows positive. Therefore, we examined the clinical
Kawasaki Hospital, Kawasaki Medical School from
efficacy of intravenous penicillin (sulbactam/
ampicillin: SBT/ABPC) in patients with adult
community-acquired pneumonia and positive
Adult community-acquired pneumonia patients
S. pneumoniae urinary antigen test requiring
with positive urinary antigen for S.pneumoniae
(Binax NOW® S. pneumoniae) were administered
Department of General Internal Medicine 1, Kawasaki
Hospital, Kawasaki Medical School, 2-1-80, Nakasange, Kitaku, Okayama, 700-8505, Japan
3g of SBT/ABPC intravenously in the morning
and evening for 7-14 days. Then clinical efficacy,
bacteriological efficacy, and side effects of these patients were prospectively examined. This study
was approved by the clinical trial review committee
Chronic obstructive pulmonary disease
Subjects were 20 males and 12 females aged 40
Severity by A-DROP system was moderate in 26
COPD (chronic obstructive pulmonary disease)
was observed in four subjects, bronchial asthma
in three, bronchiectasis in three, cerebrovascular
(1)PISP
(2)PRSP
diseases in five, hypertension in five, diabetes mellitus in three, and hypothyroidism in one.
Clinical efficacy was observed in a total of 28
of 32 (87.5%) patients; 24 of 26 (92.3%) moderate
patients, and in four of six (66.7%) severe patients.
Efficacy was observed in three patients (PISP two,
PRSP one) with penicillin-resistant S. pneumoniae.
With regard to sensitivity of penicillin-G , MIC ≦2
μg , MIC =4μg , and MIC ≧8μg were judged
Bacteriological efficacy (Table 4) PSSP 19 strains, PISP two strains, and PRSP one
DISCUSSION
strain were isolated, and all were eradicated.
S. pneumoniae is the most frequently observed
microorganism in adult community-acquired
Clinical adverse reaction was drug eruption in
pneumonia, accounting for 25-39% of patients with
one patient (3.1%). Abnormal laboratory findings
pneumonia requiring hospitalization. Pneumonia
were increased GOT, increased AMY, and decreased
caused by S. pneumoniae is a potentially-severe
WBC in one patient each; however, all were mild,
and there were no patients whose treatment was
Gram staining and culture are useful in diagnosis.
discontinued, or who received treatment for adverse
Recently, S. pneumoniae urinary antigen test has
been widely used in the clinical setting for rapid diagnosis. The JRS guidelines for the management of community-acquired pneumonia in adults
Okimoto N, et al. : sulbactam/ampicillin on Streptococcus pneumoniae pneumonia
recommend S. pneumoniae urinary antigen test to
32 (87.5%) patients; 24 of 26 (92.3%) moderate
identify the causative organism. S. pneumoniae
patients, and four of six (66.7%) severe patients.
urinary antigen test (Binax NOW® S. pneumoniae)
Furthermore, in terms of bacteriology, all strains
is the method to detect urinary capsule antigen for
composed of PSSP (19 strains), PISP (two strains),
S. pneumoniae by immunochromatography. It has
and PRSP (one strain) were eradicatd.
higher sensitivity than sputum or blood culture,
Although the MIC of penicillin-G was as high as
with a sensitivity of 70-80% and a specificity of 80-
4μg10) for PISP and PRSP, administration of 3 g
90%2-5). The JRS guidelines also recommend
of SBT/ABPC b. i. d. was efficacious for penicillin-
intravenous penicillin for patients with positive
S. pneumoniae urinary antigen test requiring
Side effects were drug eruption, increased GOT,
increased AMY, and decreased WBC in one patient
Therefore, we evaluated the efficacy of
each; however, all were mild, showing high safety.
intravenous penicillin (sulbactam/ampicillin: SBT/
The results of Metaanalysis11) also showed high
ABPC) in patients with positive S. pneumoniae
urinary antigen test requiring hospitalization. SBT/
As shown above, intravenous penicillin
ABPC is ABPC compounded with a β-lactamase
(sulbactam/ampicillin: SBT/ABPC) for patients
inhibitory agent that exhibits a strong antibacterial
with positive S. pneumoniae urinary antigen test
requiring hospitalization is extremely useful.
Subjects were 26 moderate and 6 severe patients aged 40 to 91 years (72.8±15.5years). Many
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Greg E. Sharon, M.D. Priya J. Bansal, M.D. DRUG ALLERGY A drug allergy, or an allergic drug reaction, is an unexpected drug PENICILLIN: reaction that results from a specific immune system response Penicillin is the most prevalent allergy causing medication, with to a medication. Past tolerance to a medication is no guarantee that approximately 10% of patients reporting being p
Summary of DDMAC Enforcement Correspondence January 2007 In January 2007, FDA’s Division of Drug Marketing, Advertising and Communications (DDMAC) posted one warning letter and two untitled letters on its website.1 The letters addressed the issues below. This summary describes only DDMAC’s allegations. It does not reflect the recipient’s response or analysis by Covington & Burli