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2.
J. bras. pneumol ; 40(6): 669-672, Nov-Dec/2014. graf
Article in English | LILACS | ID: lil-732565

ABSTRACT

Tracheal diverticulum, defined as a benign outpouching of the tracheal wall, is rarely diagnosed in clinical practice. It can be congenital or acquired in origin, and most cases are asymptomatic, typically being diagnosed postmortem. We report a case of a 69-year-old woman who was hospitalized after presenting with fever, fatigue, pleuritic chest pain, and a right neck mass complicated by dysphagia. Her medical history was significant: pulmonary emphysema (alpha-1 antitrypsin deficiency); bronchiectasis; and thyroidectomy. On physical examination, she presented diminished breath sounds and muffled heart sounds, with a systolic murmur. Laboratory tests revealed elevated inflammatory markers, a CT scan showed an air-filled, multilocular mass in the right tracheal wall, and magnetic resonance imaging confirmed the CT findings. Fiberoptic bronchoscopy failed to reveal any abnormalities. Nevertheless, the patient was diagnosed with tracheal diverticulum. The treatment approach was conservative, consisting mainly of antibiotics. After showing clinical improvement, the patient was discharged.


Divertículos da traqueia são evaginações benignas da parede traqueal e raramente diagnosticados na prática clínica. Podem ser congênitos ou adquiridos, e na maioria dos casos são assintomáticos, sendo tipicamente diagnosticados em estudos post-mortem. Relatamos o caso de uma mulher de 69 anos que foi hospitalizada após apresentar febre, fadiga, dor torácica pleurítica e uma massa cervical à direita complicada por disfagia. Tinha antecedentes pessoais de enfisema pulmonar (deficiência de alfa-1 antitripsina), bronquiectasias e tireoidectomia. Ao exame físico apresentava murmúrio vesicular diminuído, hipofonese cardíaca e um sopro sistólico. Laboratorialmente apresentava marcadores inflamatórios elevados, e uma TC mostrou uma massa aérea, multiloculada na parede direita da traqueia, achados confirmados por ressonância magnética nuclear. Realizou ainda uma fibrobroncoscopia que se revelou normal. Assumiu-se o diagnóstico de divertículo da traqueia. O tratamento proposto foi conservador, consistindo principalmente de antibioticoterapia. Após melhora clínica, a paciente recebeu alta.


Subject(s)
Aged , Female , Humans , Anti-Bacterial Agents/therapeutic use , Diverticulum/complications , Tracheal Diseases/complications , alpha 1-Antitrypsin Deficiency/complications , Diverticulum/drug therapy , Magnetic Resonance Imaging , Pulmonary Emphysema , Tomography, X-Ray Computed , Thienamycins/therapeutic use , Tracheal Diseases/drug therapy , Vancomycin/therapeutic use , alpha 1-Antitrypsin Deficiency/drug therapy
4.
Acta cir. bras ; 29(9): 615-621, 09/2014. graf
Article in English | LILACS | ID: lil-722123

ABSTRACT

PURPOSE: To evaluate the treatment outcome of severe peritonitis in rats with increasing age. METHODS: Thirty Wistar rats stratified in three groups: group I - six month-old; group II - 12 month-old; and group III - 18 month-old, underwent autogenously fecal peritonitis (6 ml/kg rat), and were treated with intravenous meropenem. The survival animals were followed-up for 45 days. The variables were expressed by their mean and standard error of the mean (SEM). p<0.05 was used for rejecting the null hypothesis. The study was approved by the Ethics Committee. RESULTS: There was a significant increase in the mortality and morbidity in elderly rats. Of interest, even among young survival rats presenting with severe residual abscesses both in the abdomen and thorax cavities, they present an almost normal life. CONCLUSIONS: The treatment of severe autogenously fecal peritonitis with intravenous meropenem reached reasonable results in rats with six and twelve months of age, even considering residual abscesses on abdomen and thorax cavities. However, the great majority (80%) of elderly rats could not overcome the initial severe infectious challenge, proving that ageing is a very important risk factor for impairing immune response. Thus, sepsis remains a challenging situation, especially in elderly. .


Subject(s)
Animals , Anti-Bacterial Agents/therapeutic use , Peritonitis/drug therapy , Thienamycins/therapeutic use , Administration, Intravenous , Age Factors , Feces , Peritonitis/mortality , Peritonitis/pathology , Rats, Wistar , Reproducibility of Results , Risk Factors , Severity of Illness Index , Sepsis/drug therapy , Time Factors , Treatment Outcome
5.
Indian J Med Microbiol ; 2012 Jul-Sept; 30(3): 350-351
Article in English | IMSEAR | ID: sea-143983

ABSTRACT

Recently, doripenem has been approved for the treatment of nosocomial pneumonia (NP), including ventilator-associated pneumonia (VAP). The E-test was performed to determine the MICs of doripenem and meropenem in 203 endotracheal aspirate isolates that consisted of 140 Acinetobacter calcoaceticus-Acinetobacter baumannii complexes and 63 Pseudomonas aeruginosa. Doripenem showed minimum concentration necessary for inhibition of 50% (MIC 50 ) of P. aeruginosa isolates at 0.38 mg/L which is several times (84.2 times) lower than the corresponding MIC 50 value of >32 mg/L for meropenem. The MIC 50 and MIC 90 were similar for both the drugs against A. baumannii. Thus, P. aeruginosa was consistently more susceptible than the A. baumannii.


Subject(s)
Acinetobacter Infections/drug therapy , Acinetobacter Infections/microbiology , Acinetobacter baumannii/drug effects , Acinetobacter baumannii/isolation & purification , Acinetobacter calcoaceticus/drug effects , Acinetobacter calcoaceticus/isolation & purification , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Carbapenems/pharmacology , Carbapenems/therapeutic use , Humans , Microbial Sensitivity Tests , Pneumonia, Ventilator-Associated/drug therapy , Pneumonia, Ventilator-Associated/microbiology , Pseudomonas Infections/drug therapy , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/isolation & purification , Thienamycins/pharmacology , Thienamycins/therapeutic use
7.
Indian J Med Sci ; 2009 Oct; 63(10) 464-467
Article in English | IMSEAR | ID: sea-145455

ABSTRACT

Enteric fever is endemic in this part of the world, and Widal test is one of the time-honored laboratory tests that are being used for years to diagnose the disease. On the other hand, melioidosis is a newly emerging disease from this region, which is most often misdiagnosed or underdiagnosed by clinicians. It is well accepted that false-positive Widal reactions following certain non-typhoid Salmonella infections may occur commonly. Three cases of high titers of Widal test are described, where melioidosis was the actual diagnosis in every occasion and was never suspected until diagnosed microbiologically. All the patients had shown a partial response to ceftriaxone. Blood and pus cultures grew Burkholderia pseudomallei, whereas Salmonella typhi was not isolated from blood in any patient. With appropriate antibiotics, the patients showed clinical and microbiological improvement with lowering of Widal titers. These 3 cases show that high Widal titer in any patient may mislead the diagnosis of melioidosis, and further laboratory workup should always be done to rule out melioidosis, especially in cases with nonresponsiveness to treatment.


Subject(s)
Adult , Aged , Amoxicillin-Potassium Clavulanate Combination/therapeutic use , Anti-Bacterial Agents/therapeutic use , Anti-Infective Agents/therapeutic use , Burkholderia pseudomallei , Ceftriaxone/therapeutic use , Doxycycline/therapeutic use , False Positive Reactions , Female , Humans , Imipenem/therapeutic use , Male , Melioidosis/diagnosis , Melioidosis/drug therapy , Melioidosis/microbiology , Melioidosis/pathology , Middle Aged , Thienamycins/therapeutic use , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use
8.
Indian J Med Sci ; 2009 Oct; 63(10) 461-463
Article in English | IMSEAR | ID: sea-145454

ABSTRACT

Ciprofloxacin is one of the most commonly used antibacterial agents with relatively few side effects. Serious adverse reactions reported with ciprofloxacin are rare with an incidence of 0.6%. Recently we came across two rare adverse effects of ciprofloxacin, viz. toxic epidermal necrolysis and agranulocytosis. To our knowledge, a total of seven cases have been reported in the literature documenting an association between oral ciprofloxacin administration and toxic epidermal necrolysis. One case of granulocytopenia, four of pancytopenia and fifteen of leucopenia worldwide have been reported. With the use of ciprofloxacin becoming more and more widespread, these two rare but fatal complications of ciprofloxacin should be borne in mind.


Subject(s)
Administration, Oral , Adult , Agranulocytosis/chemically induced , Agranulocytosis/drug therapy , Anti-Bacterial Agents/therapeutic use , Anti-Infective Agents/administration & dosage , Anti-Infective Agents/adverse effects , Ciprofloxacin/administration & dosage , Ciprofloxacin/adverse effects , Stevens-Johnson Syndrome/drug therapy , Stevens-Johnson Syndrome/etiology , Female , Granulocyte Colony-Stimulating Factor/administration & dosage , Granulocyte Colony-Stimulating Factor/therapeutic use , Humans , Leukopenia , Neutropenia , Risk Factors , Sepsis/drug therapy , Thienamycins/therapeutic use
9.
Rev. Inst. Med. Trop. Säo Paulo ; 51(2): 111-113, Mar.-Apr. 2009. ilus
Article in English | LILACS | ID: lil-511833

ABSTRACT

We describe an in vivo evolution of an antimicrobial profile from susceptibility to full-resistance to carbapenems, with heteroresistance as an intermediate stage, in an Acinetobacter baumannii strain. Heteroresistance was characterized by the growth of sub-populations within the susceptibility halo in both disk-diffusion and Etest. PCRs for the main A. baumannii carbapenemases were negative. The exact resistance mechanism, diagnostic methods and clinical relevance of heteroresistance in A. baumannii warrant further investigations. This is the first description of such phenomenon in vivo and the second report of heteroresistance to carbapenems in A. baumannii.


Descrevemos a evolução in vivo, de um perfil de sensibilidade aos antimicrobianos, passando de sensibilidade a resistência total aos antibióticos carbapenêmicos, com um estágio intermediário de heteroresistência em isolado de Acinetobacter baumannii. A heteroresistência foi caracterizada pelo crescimento de sub-população na zona de inibição pelo método de disco-difusão e pelo Etest. PCRs para as principais carbapenemases envolvidas com resistência neste microrganismo foram negativas. O exato mecanismo de resistência envolvido, método diagnóstico e relevância clínica justificam investigação adicional. Esta é a primeira descrição deste fenômeno in vivo e o segundo relato de heteroresistência em A. baumannii.


Subject(s)
Aged , Female , Humans , Acinetobacter Infections/microbiology , Acinetobacter baumannii/drug effects , Anti-Bacterial Agents/pharmacology , Imipenem/pharmacology , Thienamycins/pharmacology , Acinetobacter Infections/drug therapy , Disk Diffusion Antimicrobial Tests , Drug Resistance, Multiple, Bacterial , Imipenem/therapeutic use , Phenotype , Thienamycins/therapeutic use
10.
Indian Pediatr ; 2009 Jan; 46(1): 61-3
Article in English | IMSEAR | ID: sea-7539

ABSTRACT

Serratia marcescens is a well recognized nosocomial pathogen. We report an outbreak with this organism in 8 neonates in a neonatal intensive care unit (NICU). Seven cases were treated successfully with meropenem after the failure of imipenem treatment. Although they have similar anti-microbial effects, meropenem can effectively treat the S. marcescens sepsis resistant to imipenem.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Cross Infection/drug therapy , Disease Outbreaks , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Serratia Infections/epidemiology , Serratia marcescens , Thienamycins/therapeutic use , Turkey/epidemiology
12.
Indian Pediatr ; 2008 Aug; 45(8): 693-4
Article in English | IMSEAR | ID: sea-14902

ABSTRACT

We report two premature infants who developed multiple brain abscesses following Klebsiella pneumoniae infection. Both the cases were diagnosed by ultrasonogram (USG) and cranial tomography. Abscess had intraventricular communication in one case. One infant was managed conservatively while the other required surgical drainage.


Subject(s)
Amikacin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Brain Abscess/drug therapy , Humans , Infant, Newborn , Infant, Premature , Klebsiella Infections/complications , Klebsiella pneumoniae/isolation & purification , Thienamycins/therapeutic use
13.
Arq. neuropsiquiatr ; 65(4a): 1018-1021, dez. 2007. ilus
Article in English | LILACS | ID: lil-470136

ABSTRACT

BACKGROUND: Cerebral abscesses are extremely rare in neonates. Serratia marcescens is an unusual cause of sepsis and neurological spread is especially ominous. PURPOSE: To report the case of a 34-week neonate who developed this rare condition and to discuss diagnostic and therapeutic measures. CASE REPRT: A 34-week male neonate sequentially developed respiratory distress syndrome, early sepsis and necrotizing enterocolitis; later cultures revealed S. marcescens. After deterioration, a cerebral abscess became evident, which revealed S. marcescens. Clinical improvement ensued after high-dose amikacin and meropenem. CONCLUSION: Clinical signs are often non-specific. Proper diagnostic measures, neurosurgical consultation and aggressive antibiotic therapy are essential for these high-risk neonates.


INTRODUÇÃO: Abscessos cerebrais são extremamente raros em neonatos. Serratia marcescens é causadora incomum de sepse nestes pacientes e a disseminação no sistema nervoso central é grave. OBJETIVO: Relatar um prematuro de 34 semanas que desenvolveu esta condição e discutir as medidas diagnósticas e terapêuticas. RELATO DE CASO: Prematuro masculino de 34 semanas desenvolveu síndrome do desconforto respiratório, sepse neonatal e enterocolite necrotizante; hemoculturas revelaram S. marcescens. Após deterioração clínica, evidenciou-se um abscesso cerebral cuja drenagem revelou S. marcescens. Houve melhora após introdução de amicacina e meropenem. CONCLUSÃO: Os sinais clínicos são inespecíficos. Passos diagnósticos apropriados, avaliação neurocirúrgica precoce e antibioticoterapia agressiva são essenciais para estes prematuros.


Subject(s)
Humans , Infant, Newborn , Male , Brain Abscess/microbiology , Diseases in Twins/microbiology , Serratia marcescens , Serratia Infections/microbiology , Amikacin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Brain Abscess/diagnosis , Brain Abscess/drug therapy , Diseases in Twins/diagnosis , Diseases in Twins/drug therapy , Serratia Infections/diagnosis , Serratia Infections/drug therapy , Thienamycins/therapeutic use
14.
The Korean Journal of Laboratory Medicine ; : 338-343, 2007.
Article in Korean | WPRIM | ID: wpr-148430

ABSTRACT

Valproic acid (VPA) is a commonly prescribed anticonvulsant drug for the treatment of various forms of epilepsy. Concomitant administration of VPA and carbapenem antibiotics such as panipenem/ betamipron and meropenem has been reported to decrease the serum level of VPA. We observed seven cases which showed a decrease in serum levels of VPA due to concomitant use of VPA and carbapenem from January 2002 to October 2006 in a 750-bed university hospital, the average decrease of 70.4% was observed. Carbapenem antibiotics administrated concomitantly with VPA were panipenem (1 case), meropenem (3 cases), and imipenem (2 cases), and in one other case imipenem and meropenem were used sequentially. We found the VPA serum levels were significantly decreased with meropenem (n=4) more than with other carbapenem antibiotics (n=4, 89.3% vs. 51.5% decrease, P=0.03). Clinicians should be aware of this potential interaction, pay attention to the failure of seizure control due to decreased serum VPA levels with concomitant use of carbapenem antibiotics, and monitor VPA serum levels for those cases.


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Anti-Bacterial Agents/administration & dosage , Anticonvulsants/administration & dosage , Carbapenems/administration & dosage , Drug Interactions , Drug Therapy, Combination , Epilepsy/drug therapy , Imipenem/therapeutic use , Thienamycins/therapeutic use , Valproic Acid/administration & dosage
16.
Yonsei Medical Journal ; : 1087-1090, 2003.
Article in English | WPRIM | ID: wpr-119964

ABSTRACT

Although there are ever increasing reports of extraintestinal human infections caused by Aeromonads, in both immunocompromised and immunocompetent patients, respiratory tract infections remain uncommon. We describe a case of aspiration pneumonia in an immunocompetent patient with multiple sclerosis, caused by a community acquired, multidrug resistant strain of Aeromonas hydrophila sensitive only to meropenem. The case highlights the clinical significance of Aeromonas hydrophila as a respiratory pathogen, as well as the community origin of multidrug resistance and the utility of newer carbapenems in such cases.


Subject(s)
Adolescent , Female , Humans , Aeromonas hydrophila/physiology , Drug Resistance, Microbial , Drug Resistance, Multiple , Gram-Negative Bacterial Infections/drug therapy , Pneumonia, Aspiration/microbiology , Thienamycins/therapeutic use
17.
Indian J Pediatr ; 2001 Jan; 68(1): 15-9
Article in English | IMSEAR | ID: sea-84798

ABSTRACT

Recently, new broad spectrum carbapenem has been investigated on a world-wide scale for the treatment of moderate to severe infections. In the neonatal intensive care units the extensive use of third generation cephalosporins for therapy of neonatal sepsis may lead to rapid emergence of multiresistant gram-negative organisms. We report the use of meropenem in 35 infants with severe infections due to Acinetobacter baumanii and Klebsiella pneumoniae. All gram negative bacteria were resistant to ampicillin, amoxicillin, ticarcilin, cefazoline, cefotaxime, ceftazidime, ceftriaxone and aminoglycosides. Eighty two percent of the cases (29/35) were born prematurely. Assisted ventilation was needed in 85.7% (30/35). All infants deteriorated during their conventional treatment and were changed to meropenem monotherapy. Six percent (2/35) died. The incidence of drug-related adverse events (mostly a slight increase in liver enzymes) was 8.5%. No adverse effects such as diarrhea, vomiting, rash, glossitis, oral or diaper area moniliasis, thrombocytosis, thrombocytopenia, eosinophilia and seizures were observed. At the end of therapy, overall satisfactory clinical and bacterial response was obtained in 33/35 (94.3%) of the newborns treated with meropenem. Clinical and bacterial response rates for meropenem were 100% for sepsis and 87.5% for nosocomial pneumonia. This report suggests that meropenem may be a useful antimicrobial agent in neonatal infections caused by multiresistant gram negative bacilli. Further studies are needed to confirm these results: Meropenem, newborn, sepsis and nosocomial infection.


Subject(s)
Acinetobacter Infections/drug therapy , Cross Infection/drug therapy , Drug Resistance, Multiple , Female , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Klebsiella Infections/drug therapy , Male , Prospective Studies , Thienamycins/therapeutic use
18.
Southeast Asian J Trop Med Public Health ; 2000 Mar; 31(1): 89-90
Article in English | IMSEAR | ID: sea-33424

ABSTRACT

The recommended treatment for severe melioidosis is ceftazidime or a combination of ceftazidime and trimethoprim-sulfamethoxazole (TMP/SMX). Amoxicillin-clavulanate has been shown to be an effective alternative therapy. In patient who is allergic to penicillin and cephalosporin, imipenem an alternative drug may be used. We described a 10 year-old boy who was diagnosed as septicemic melioidosis and type 1 diabetes mellitus. He developed fever and rash while being given ceftazidime and TMP/SMX. The fever recurred when amoxicillin-clavulanate was administered orally. He was successfully treated with imipenem.


Subject(s)
Amoxicillin-Potassium Clavulanate Combination/adverse effects , Anti-Bacterial Agents/adverse effects , Bacteremia/complications , Ceftazidime/adverse effects , Cephalosporins/adverse effects , Child , Diabetes Complications , Drug Therapy, Combination/adverse effects , Humans , Imipenem/therapeutic use , Male , Melioidosis/complications , Thienamycins/therapeutic use
19.
Arq. bras. med ; 63(6): 487-92, nov.-dez. 1989. tab
Article in Portuguese | LILACS | ID: lil-76939

ABSTRACT

Relata-se a experiência com o uso de imipenem/cilastatina no tratamento de 23 pacientes críticos, internados de janeiro de 1987 a julho de 1988. Quinze (65%) eram do sexo masculino e oito do sexo feminino, com idades variando entre seis meses e 83 anos; os pacientes foram divididos retrospectivamente em dois grupos: imunodeprimidos (10 casos) e näo imunodeprimidos (13). Foi feito o seguimento diário de todos os pacientes e, noc aso de óbito, foi realizada necrópsia. Os agentes etiológicos mais freqüentes foram os bacilos Gram-negativos, mas cocos Gram-positivos foram identificados em quatro casos. Houve predomínio das infecçöes pulmonares (11 casos), acompanhados ou näo de septicemia. Dez pacientes (43% estavam curados no final do tratamento e doze morreram, embora somente três (13%) no decorrência do processo infeccioso. A terapia foi interrompida em um caso, que desenvolveu extenso exantema purpúrico. A vancomicina foi usada associadamente em 11 pacientes, nos quais suspeitou-se de infecçäo por estafilococo multirresistente. No total, a infecçäo foi controlada após o uso de imipenem/cilastina em 18/23 casos (78%). Ressalta-se a importância desta nova droga no tratamento de infecçöes graves, recomendando-se resguardá-la para o uso em protocolos de tratamento de granulocitopênicos com febre, infecçöes em transplantados, infecçöes por agentes só sensiveis ao imipenen, ou na terapia de casos graves, sem agente definido ou com resposta insatisfatória a outros esquemas antimicrobianos


Subject(s)
Infant , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Humans , Male , Female , Critical Care , Bacterial Infections/drug therapy , Lactams/therapeutic use , Thienamycins/therapeutic use , Postoperative Complications/drug therapy , Bacterial Infections/etiology
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