13 - 208 - eficácia e segurança de sultamicilina.indd
Rev Bras Otorrinolaringol2006;72(1):104-11ORIGINAL ARTICLE Efficacy and safety of Sultamicillin (Ampicillin/ Sulbactan) and Amoxicillin/ Clavulanic Acid in the treatment of upper respiratory tract infections in adults - an open-label, multicentric, randomized trial João Batista Ferreira1, Priscila Bogar Rapoport2, Eulália Sakano3, Arthur Octávio De Ávila Kós4,
Key words: ampicillin, sulbactan, amoxicillin, clavulanic, in-
Otávio B. Piltcher5, Shirley Shizue Nagata Pignatari6, Sebastião Diógenes Pinheiro7, Marcos Mocellin8
Upper respiratory tract infections are the most common
causes of medical visits in children and adults, demanding massive use of antibiotics. Bacterial resistance caused by beta- lactamase is one of the most serious problems in this matter. Sultamicillin, a double pro-drug of Ampicillin/Sulbactan, is a potent beta-lactamase inhibitor which can face this challenge. Aim: evaluate efficacy, safety and tolerability of Ampicillin/Sulbactan compared to Amoxicillin/Clavulanate in upper respiratory tract infections in adults. Methods: 102 patients were enrolled and randomized to receive Ampicillin/Sulbactan or Amoxicillin/Clavulanate during 10 days. They were evaluated 10 and 30 days after treatment to learn about the therapeutic response. Results: There were no differences between the two groups respecting cure at the end of treatment (visit 2) or at the end of the study (visit 3). Cure ratio was 61.7% and 93.2% (visits 2 and 3) in the Amoxicillin/Clavulanate group compared to 64.4% and 97.4%, respectively, in Ampicillin/Sulbactan group. The adverse events ratio for the two groups was the same (p=0.940). The number of patients with diarrhea was greater in the group of patients receiving Amoxicillin/Clavulanate (70.6%) than in the group receiving Ampicillin/Sulbactan (29.4%) (p=0.0164). Conclusions: Ampicillin/Sulbactan is as safe and efficient as Amoxicillin/Clavulanate in the empiric treatment of upper respiratory infections in adults. The low occurrence of diarrhea in the group receiving Ampicillin/Sulbactan needs confirmation in other studies.
1 Assistant Professor, Head of the Otolaryngology Department – Surgery Department – Medical School of the UFG.
2 PhD in Otolaryngology by the Medical School of the USP, Full Professor of Otolaryngology of the Medical School of the ABC.
3 Head of the Rhinology Department of the Otolaryngology Service of the UNICAMP.
4 Associate Professor of Otolaryngology by the Universidade Federal do Rio de Janeiro. Full Professor of the Federal University of Rio de Janeiro.
5 Physician hired by the Otolaryngology Department of the University Hospital of Porto Alegre - RS.
6 Assistant Professor of the Otolaryngology and Head and Neck Department - UNIFESP / EPM.
7 PhD in Medicine. Physician from the University of the Walter Cantídio Hospital of the Medical School of Ceará.
8 MSc and PhD from the Paulista School of Medicine – SP. Full Professor of the Otolaryngology
Department of the University of Paraná.
Medical School of the Federal University of Goiás.
Mailing address: João Batista Ferreira - a/c Aline Guerra Rua Ministro Gastão Mesquita 515 ap. 112 Pompéia São Paulo SP 05012-010
Tel (0xx11) 9404-2344 - E-mail: [email protected]
Paper submitted to the ABORL-CCF SGP (Management Publications System) on April 5th, 2005 and accepted on May 24th, 2005.
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
http://www.rborl.org.br / e-mail: [email protected]INTRODUCTION
difficult to have in our settings6-9.
AURTI etiology rests on the knowledge of the
Upper airway infections in children and adults are
habitual flora in the upper airways and the rarely iso-
the most common diseases, and also the most common
lated prevalent micro-organisms. In pharyngo-tonsillitis
reasons for seeking medical consult in primary care. They
the prevalent bacterial agent is the group A hemolytic β
also constitute the major diagnosis that require the use of
streptococcus. In AOM and sinusitis the prevalent micro-
antibiotics. Its diagnosis and treatment have an impact not
organisms are Streptococcus pneumonia, Haemophilus
only from the stand point of population health, but also
from the social and economical stand point, because of
The choice of the antimicrobial agent should be
the cost of medical care, cost of antibiotic used and for the
guided by this knowledge. For clinicians and pediatricians,
loss they represent as far as work and school absenteeism
the choice of antimicrobial agent is a key issue. Right now
are concerned. Taking Acute Otitis Media in children for
the attention of the medical community and the general
instance, American data points towards a total of 16 million
public is directed towards the high cost of medication
visits on this account in the year 2000. These visits gener-
and the growing rates of antibiotic resistance10. Therefore,
ate a total 13 million prescriptions, meaning 802 antibiotic
judicious choice of antimicrobial agents is becoming a
prescribed for each group of 1,000 visits. The cost of each
antibiotic therapy varied from US$ 10 to US$ 100.
Ampicillin/Sulbactan is a combination of antibiotics
The proper use of antibiotics not only in a hospital
made up of ampicillin, a betalactam and sulbactam, a beta-
setting, but also in handling the most common infections in
lactamase inhibitor11. By adding sulbactan we consider-
the community, has been the objective of ever increasing
ably broaden the ampicillin action spectrum, including B
debates, in an attempt to contain the growing resistance
fragilis, Klebsiella sp, S aureus (MS) and H influenza.
rates that have been seen. Great emphasis have been
The betalactam core destruction of penicillin and
given to standardizations published by national entities
cephalosporin by bacterial b-lactamase, constitutes the
and universities, where evidence based approach reviews
clinical most important mechanism of bacterial resistance
the major points related to the diagnosis and treatment of
against these antibiotics. The lack of receptor binding may
infections. Many standardizations have been recently pub-
be caused by: (1) changes in the permeability of the cell
lished about otitis, sinusitis and pharyngo-tonsillitis2-5.
membrane and/or (2) changes in target site biding capacity
The major discussions in these documents are fo-
and (3) enzymatic destruction by antibiotics.
cused on whether or not it is necessary to use antibiotics
The third of these three main causes is the most
in AURTI (acute upper respiratory tract infections) and,
frequent origin of antibiotic inefficacy. Beta-lactamase
specially in non-complicated Acute Otitis Media (AOM).
production causing bacterial resistance is one of the most
The recommendation of initial use of symptomatic medica-
severe problems of clinical practice today. B-lactamase may
tion followed by antibiotics if there is no clinical improve-
be produced either by gram positive or by gram negative
ment with the patient, is based on the high incidence of
bacteria. They destroy the antibiotic Betalactam core, turn-
viral etiology in these pathologies. Notwithstanding, it can
ing them useless. This destruction occurs by the hydrolysis
not be followed in many cases when the decision has to
of the amide bond in the betalactam ring, resulting in the
be made quickly, without the possibility of having the
production of acid derivatives that do not have antibacte-
patient return, as is the case of ER visits. For this reason,
rial properties. Clinical failure appears when a sufficient
great emphasis should be given to aspects that support
number of antibiotic molecules is neutralized12,13.
the most accurate possible diagnosis. And, from then, the
Unasynâ (sultamicillin) is an antibiotic developed
specifically to face these problems14,15. It is an ampicilin
As far as diagnosis is concerned, there is some con-
and sulbactam double pro-drug, a powerful beta-lactamase
sensus: history of acute onset of symptoms; presence of
inhibitor. The ampicillin/sulbactam mechanism of action
exudation/inflammation signs in the middle ear, choanae
depends mainly on the sulbactam bond, a suicide inhibitor,
and nasal cavities or throat; pain, satellite lymph node
with a large number of b-lactamase molecules. Sulbactam
hydrolyzed fragments remain irreversibly bound to this
The difficulties lie on the real possibility of estab-
enzyme, thus forming an inactive complex.
lishing reliable and reproductive parameters to establish
Ampicillin/Sulbactam pharmacokinetic studies have
the presence of inflammatory and/or exudative clinical
shown that the inactive pro-drug is well absorbed in the
signs. The different clinical experiences and the available
intestine. Ampicillin/Sulbactam is hydrolyzed in two com-
technology translate themselves into different diagnostic
pounds in the intestine wall, sulbactam and ampicillin. The
approaches in about 50% of the non-complicated cases.
total ampicillin distributed is approximately twice larger
Particularly in pharyngo-tonsillitis, the germ culture and
when compared to the oral distribution of ampicillin alone.
the quick strep test are recommended, however they are
The high serum level achieved is followed by optimum
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
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ampicillin and sulbactam tissue penetration. And finally,
between days 10 and 13 (V-2 – end of treatment) and
the clearance route for both active drugs is the urine16-18.
between days 26 and 34 (V-3 – end of trial).
The Ampicillin/Sulbactam action spectrum en-
On visit 1, male and female patients older than 12
compasses gram positive coccus and rods, aerobic gram
years and weighing 30 Kg and more were diagnosed as car-
riers of bacterial infections in the ears, nose and/or throat,
Peptococcus and Peptostreptococcus spp, anaer-
concomitant or not, through clinical history and physical
obes, Group B Streptococcus, Enterococcus faecalis,
exam data. Inclusion criteria were defined as follows:
Streptococcus pneumoniae, Streptococcus pyogenes,
• Having at least 3 of the following signs/symptoms
Streptococcus viridans (alpha-hemolytic), C diphtheriae,
for sinusitis patients: bi-phased disease, defined as the
Clostridium spp (Cl tetani, Cl perfringens, Cl botulinum),
presence of two phases of the current disease; purulent
Listeria monocytogenes, Haemophilus influenza, E coli
anterior or posterior rhinorrhea; purulent secretion in the
(over 50% of the strains may be resistant), P mirabilis,
nasal cavity; facial/maxillary or teeth pain; OR
Salmonella spp (S typhimurium may be 30% to 40% resist-
• Having at least 3 of the following signs/symp-
ant), Shigella flexneri, Fusobacterium spp.
toms for otitis patients: local pain, fever of 38°C or more;
The Ampicillin-Sulbactam combination (Sultamicil-
otoscopy findings such as tympanic hyperemia; tympanic
lin) shows marked synergy. The MIC of many ampicillin-
bulging; purulent or mucous-purulent secretion in the
resistant pathogens is reduced, being very similar to those
sensitive organisms of the same species. The ampicillin
• Having at least 4 of the following signs/symptoms
activity against sensitive organisms remains the same19,20.
for pharyngo-tonsillitis patients: sudden onset, intense pain
On the other hand, the production of significant
on swallowing; tonsillar enlargement; tonsillar hyperemia;
quantities of b-lactamase have been associated to ce-
exudate on the tonsils; painful anterior cervical lymph
phalosporin resistance (Cephoxytin is the most powerful
node disease; fever of 38°C or more.
resistance inducer) and to the ureidopenicillins. Incubation
Patients were excluded when mentioned: hypersen-
with sub lethal concentrations of sulbactam clavulanic
sitivity to the trial drugs or to the betalactamic; pregnancy,
acid and numerous betalactam antibiotics has shown that
breast feeding or pregnancy possibility during the trial;
sulbactam did not induce measurable levels of chromo-
specific systemic disease or other medical conditions,
some betalactam, while clavulanic acid induced 30% in
including viral and urinary infections and meningitis that
could interfere in the therapeutic response assessment, in
Therefore, clavulanic acid may cause significant
the absorption of medications, or safety of the trial drug;
induction. This fact is in agreement with the results of an
treatment with any systemic antibacterial drug within 14
in vitro study on the negative R factor of the carbenicillin-
days before the randomization; concomitant participation
resistant P. aeruginosa strains which suggests the existence
in any other investigational drug clinical trial; blood dona-
of an antagonism between the clavulanic acid and azlocillin
tion or blood derivatives for transfusion in the 30 days prior
combination, while adding sulbactam does not seem to
to the treatment with the trial drugs at any time during
affect the penicillin minimum inhibitory concentrations. So
the trial or after 30 days of the trial end; treatment with
far, no antagonism between sulbactan and other betalactam
halopurinol, metrotrexate, probenecide and disulfiram,
or other medications that may interfere on the trial drug
The objective of this trial was to assess Sultamicil-
assessment, and, transaminase values (ALT/SGPT or AST/
lin efficacy, safety and tolerability compared to that of
SGOT) above 3 fold the upper limit of normality (ULN),
Amoxicillin/Clavulanic acid, in the treatment of community
and serum creatinin above 2 times the ULN.
acquired infections of the upper respiratory tract, specially
On visits 1, 2 and 3, the patients underwent a ma-
otitis, sinusitis and pharyngo-tonsillitis.
terial collection for safety exams (Complete blood count, biochemistry and pregnancy test, when indicated) and
general clinical evaluation. Besides all of this, the patients underwent specific evaluation for signs and symptoms
Eight Brazilian research centers participated in this
related to upper respiratory tract infections, which include
study, recruiting 102 patients from March 22, 2002 to July
the same aspects used to confirm the diagnosis.
04, 2003. The protocol design established a comparative, multicentric, open and randomized trial of Ampicillin/Sul-
Evaluation of the clinical response
bactan compared to Amoxicillin/Clavulanic acid. Patients
Efficacy was evaluated based on the clinical re-
were given 375mg bid PO Ampicillin/Sulbactan or 500mg
sponse seen on visits 2 and 3 classified by the investigator
tid PO Amoxicillin/Clavulanic acid after randomization.
The study included 3 medical visits and lasted 34 days,
Cure: absence of all signs and symptoms of the
having one initial visit (V-1), followed by a treatment pe-
disease being studied, described in the inclusion criteria
riod of 10 consecutive days, and 2 later follow up visits
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
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at least one dose of the medication. Only 83 patients
Improvement: presence of at least one of the studied
completed the 30 days of the trial. The reasons why 14
disease signs and symptoms described in the inclusion
patients were taken off the trial are as follows: adverse
criteria, without the need to prescribe another antibiotic
events - 5 patients; removal from the post-informed consent
- 3 patients; loss of follow up - 3 patients; and protocol
Failure: Persistence of one or more signs or symp-
violation - 2 patients. Patient 107 was taken off because
toms of the studied disease described in the inclusion
criteria, or the appearance of new signs and symptoms
Table 1 depicts the traits of the 97 security popula-
of the studied disease and/or the need to add another
tion patients at the trial onset. There was no statistically
antibiotic agent or to change the study therapy.
significant difference among the demographic and clinical traits of the patients belonging to the two groups.
The infection time, in other words, the time span
All adverse events seen or reported were registered
between symptoms onset and diagnosis also did not show
with specifications of the date of onset, the duration, the
significant difference between the groups, varying from 1
severity, the evolution and the possible relation with the
to 40 days with a 4 day median in both groups (Table 1).
trial drug. Altered findings in the lab exams were also
The type of infection presented by patients varied in both
groups, although it was not significant. The Amoxicillin/Clavulanic acid group had a greater incidence of sinusitis
Statistical analysis
and otitis whilst the Ampicilin/Sulbactan group patients
The safety population was formed by 97 patients
had a larger number of pharyngo-tonsillitis.
that took at least one dose of the trial medication. The
Table 2 lists the signs and symptoms that were part
ITT (intention to treat) efficacy population was made up
of diagnostic criteria for each type of infection. Table 3
by the patients who were given at least one dose of the
depicts signs and symptoms of patients along the trial,
assigned treatment and had at least one subsequent clas-
that is, at diagnosis – visit 1 – and their development in
sification of clinical response to the instituted therapy.
In other words, it was made up of 92 patients: all the 97 safety population patients minus the 5 patients who had
Efficacy and clinical answer
unknown clinical response on visits 2 and 3. The efficacy
There were no evidences of differences between
PP population is made up of the patients who received
the two groups in regards to the proportion of patients
at least 6 doses of the assigned treatment and had at least
who did not show cure at treatment end (visit 2) or at
one subsequent clinical response to therapy classification.
trial end (visit 3). In the Amoxicillin/Clavulanic acid
In this study, population PP is formed by the same ITT
group, cure rates were 61.7% and 93.2% on visits 2 and
population patients, because all had at least 6 doses of
3, respectively . In the Ampicilin/Sulbactan group, cure
rates were 64.4% and 97.4%, respectively. Table 4 depicts
For clinical response we created a confidence inter-
Confidence intervals for the difference among cure ratios
val of 95% for the difference in cure and cure + improve-
for both groups, as well as the results of the Fisher exact
ment ratio among the treatment modalities. In order to
test. Four patients had treatment failure on the third visit
compare the average of vital signs along the visits we used
after having reported cure on the second visit. Of these,
the Variance Analysis with Repeated Measures, using the
3 were from the Amoxicillin/Clavulanic acid and 1 from
non-structured co-variance matrix in order to model the
existing correlation among the visits of a same patient. This technique takes into account the incomplete observations
Adverse Effects
and, therefore, does not rule out the patient as a whole if
There were 56 adverse effects along the trial (30
he/she does not have all the observations in all the visits.
in the Amoxicillin/Clavulanic acid group and 26 in the
All the aforementioned analysis require data normality as-
Ampicillin/Sulbactan group). The total number of patients
sumption which was verified and confirmed in all cases.
who had adverse effects was 34, representing 35% of the
Statistical analysis was made by the SAS version 8 software.
total number of participants in the trial. Of these, 17 be-
The adopted significance level was of 0.05.
longed to the Amoxicillin-Clavulanic acid group and 17 to the Ampicillin/Sulbactan group. The ratio of patients who
experience at least one adverse effect was similar in both groups (p = 0.940). Notwithstanding, among the 34 patients who had adverse effects, the ratio of patients with diarrhea
Patient traits
was significant higher in the Amoxicillin-Clavulanic acid
Eight Brazilian centers recruited 102 patients for the
group (70.6%) when compared to the Ampicilin/Sulbactan
trial. Of these, ninety seven started the trial and received
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
http://www.rborl.org.br / e-mail: [email protected]Table 1. Patient characteristics in the beginning of the study: age, gender and race. Table 2. Type of infection; and signs and symptoms at diagnosis
Type of infection and symptoms at diagnosis
Purulent anterior or posterior rhinorrhea
Mucus-purulent secretion in the middle year
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
http://www.rborl.org.br / e-mail: [email protected]Table 3. Proportions (%) of patients who presented one of the following signs/symptoms along the study, according to treatment group
Obstructive nasal secretion, epistaxis, cacosmia
V1: Visit 1 – Study onset V2: Visit 2 – Treatment end V3: Visit 3 – Trial end Table 4. Ratio of cured patients at treatment end (V2) and at trial end (V3). Table 5. Adverse effect of which causality was not ruled out by the investigator.
BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
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the bacteriological cure and S pneumoniae was the most
As to laboratory work up, no relevant alterations
frequently found micro-organism. Other trials show the
were found after the use of trial medications. The altered
comparative performance of Sultamicillin with amoxicil-
values were already present on visit 1 for both groups.
lin alone or in combination with Clavulanic Acid in lower
According to protocol criteria, there was no severe
respiratory tract infections. The clinical response was, once
adverse effect. Only 5 patients were removed from the trial
again, comparable with efficacy rates varying between 84%
because of adverse events (2 on the Ampicillin/Sulbactan
and 94%29. Considering the treatment of otitis in children,
group and 3 on the Amoxicillin-Clavulanic acid group).
Ampicillin/Sulbactan proved to be efficient, with cure
The 9 adverse effects of these 5 patients were: diarrhea
rates above those seen with the use of Cefaclor24. From
– 3 Amoxicillin-Clavulanic acid related events and one
the safety stand point, our study confirms literature reports
Ampicilin/Sulbactan-related event; lethargy – 1 Amoxi-
that Ampicillin/Sulbactan is a well tolerated drug. There
cillin-Clavulanic-acid-related event; irritability – 1 case;
were no severe adverse effects, and in those that really
worsening of tonsillitis – 1 case; worsening of sinusitis
happened, both groups had similar distribution. Only
– 1 case; and abdominal pain – 1 case. Bellow we listed
diarrhea was significantly higher in the Amoxicillin/Cla-
the adverse effects with cause related to the drugs used. 5
vulanic acid group (p=0.016). Gastrointestinal symptoms
Ampicillin/Sulbactan group patients had diarrhea, however
seem to be the most frequent adverse effect related to
only 4 are listed here because the investigator considered
the use of Ampicillin/Sulbactan. In the same way, these
that one was not related to the trial drug.
symptoms and, diarrhea most specifically, are very com-mon with the use of Amoxicillin/Clavulanic acid, making
Concomitant medication
its use rather difficult sometimes, specially by children.
Sixty patients (61.8%) received at least one concomi-
In some measure, our data may have pointed towards a
tant medication. Of these, 29 belonged to the Amoxicillin/
greater tolerability of Ampicillin/Sulbactan in comparison
Clavulanic acid group and 31 to the Ampicillin/Sulbactan
to Amoxicillin/Clavulanic acid, according to what has been
group. Among the drugs used, the most frequent were
reported in the literature30. Other studies must follow in
Dipirone and paracetamol, and there was no difference
order to investigate these aspects, with more cases and
in its use among the two treatment groups.
In short, we have concluded that Ampicilin/Sul-
DISCUSSION
bactan is as efficient and safe as Amoxicillin/Clavulanic acid in the empirical treatment of adult acute upper res-
The results of this trial show the comparable effi-
piratory tract infections, thus representing an important
cacy of Ampicillin/Sulbactan and Amoxicillin/Clavulanic
therapeutic alternative. This lower occurrence of diarrhea
acid combinations in the treatment of acute upper res-
in the Ampicillin/Sulbactan group that has been observed
piratory tract infections in adults. Such results correlate
to literature reports on the use of Ampicillin/Sulbactan combination in the treatment of both upper and lower
There was no significant difference in the propor-
This investigation was financed with resources from
tion of patients who were cured at the end of treatment
and at the end of trial in both groups. In the Ampicillin/Sulbactan group, the cure ratios increased from 64.4%, at
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BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY 72 (1) JANUARY/FEBRUARY 2006
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