ABSTRACT
Los efectos adversos de medicamentos en general y antimicrobianos en particular, son comunes y esperados de enfrentar durante la atención de los pacientes. La mayoría de ellos consiste en intolerancia, efectos colaterales y secundarios, alergia, idiosincrasia, sobredosis o interacciones farmacológicas indeseables. Durante el empleo de antimicrobianos con fines terapéuticos o preventivos en infecciones documentadas o sospechadas, pueden presentarse efectos adversos inesperados o consecuencias lamentables. Esta publicación revisa siete situaciones en que esto puede acontecer. La terapia antimicrobiana agrava una enfermedad infecciosa o empeora su daño (i.e., tratamiento antimicrobiano precoz de la infección intestinal por Escherichia coli O157:H7); el antimicrobiano al ejercer su efecto causa daño al huésped (reacción de Jarisch Herxheimer en el tratamiento de la sífilis); el antimicrobiano por sí solo es insuficiente para curar la infección ( absceso no drenados, infección relacionada a prótesis sin remoción del cuerpo extraño), el tratamiento antimicrobiano de infecciones no significativas o autolimitadas, el riesgo de efectos secundarios sobrepasa a los beneficios (tratamiento de bacteriuria asintomática en mayores con bajo riesgo de morbiilidad); el tratamiento antimicrobiano temprano en infecciones crónicas no aporta mayor beneficio que una terapia diferida y arriesga las opciones futuras (enfermedad por VIH, hepatitis B); la terapia antimicrobiana restaura la inmunidad deprimida gatillando una respuesta inflamatoria dañina para el huésped (terapia antiretroviral durante una fase precoz de terapia antituberculosa); la terapia antimicrobiana de infecciones intratables o condiciones no infecciosas (Enfermedad de Chagas, condiciones alérgicas o autoinmunes). Además, población especial, más proclive a efectos adversos de fármacos son: el adulto mayor, pacientes con afecciones renales o hepáticas, enfermedad por VIH, mujeres embarazadas y, en general, pacientes que reciben varios medicamentos en forma concomitante
Subject(s)
Humans , Anti-Infective Agents , Anti-Bacterial Agents/adverse effects , Drug Hypersensitivity , Adverse Drug Reaction Reporting Systems , Drug Interactions , Drug-Related Side Effects and Adverse ReactionsABSTRACT
Eight chilean teenagers traveled to Ecuador in january 1999, where they were bitten by mosquitoes, had contact with parakeets and lodged in poorly hygienic places; 6/8 visited for 5-10 minutes the interior of a bat cave. About a week later these 6 began with headache, myalgia and fever that lasted 2-3 weeks. 5/6 had dry cough with no respiratory distress. The index case was seen in the 2nd week of symptoms. A chest x-ray showed multiple nodular infiltrates as in the other five. Two had histoplasma serology, one was negative and the other positive at a low titer; histoplasmine skin test showed induration of 17-27 mm in all six. An acute histoplasmosis with massive exposure was diagnosed and treated with itraconazole for 3 weeks. All became asymptomatic and chest x-rays returned to normal. Histoplasmosis (non existent endogenously in Chile) is, among other geographic and tropical diseases, a risk for chilean travelers. Awareness of this in the general population and development of expertise in these diseases by local health care providers is required
Subject(s)
Humans , Adolescent , Adult , Travel , Disease Outbreaks , Histoplasmosis/epidemiology , Tetracycline/therapeutic use , Fluconazole/therapeutic use , Itraconazole/therapeutic use , Tropical Zone , Fever/etiology , Histoplasma/pathogenicity , Histoplasmin , Histoplasmosis/diagnosis , Histoplasmosis/drug therapy , Chiroptera/microbiology , Radiography, Thoracic , Signs and SymptomsABSTRACT
In the last decade in Chile, there was a large reduction in the rate of communicable diseases, especially typhoid fever, and those preventable through the universal vaccination programs. Exceptions were hepatitis A and Pertussis. The reduction in tuberculosis, has lead the country to a threshold in which the elimination of tuberculosis as a public health problem is reachable. The HIV epidemic is still expanding, at higher rate among women and heterosexual men, keeping drug addiction as a low ranked risk factor. At the end of the century, universal or expanded access to HIV therapy was still not a reality. Cholera was a well controlled emerging infection, but Hantavirus infection has become a major threat in many regions. Syphilis and especially gonorrhea have decreased, but condyloma has increased dramatically. The nosocomial infection scenario has changed somehow, due to more severely ice and complex patients admitted to hospitals. Multiresistant nosocomial pathogens continue expanding (S aureus, fermentor and non fermentor gram negative rods, especially A baumannii). The country has been able to expand control programs to almost all hospitals. Antimicrobial resistance has continued growing. The massive and indiscriminate use of antibiotics, largely responsible for the resistance, grew worse until the sale of antimicrobials in pharmacies was restricted by law. This had a major impact, with important reduction in sales of most, but not all, antibiotics. The impact in resistance rate of this reduction, if any, has yet to be assessed
Subject(s)
Humans , Communicable Diseases , Tuberculosis, Pulmonary , Drug Resistance, Microbial , Sexually Transmitted Diseases , HIV Infections , Cholera/epidemiology , Cross Infection/epidemiology , Disease Notification/statistics & numerical data , Immunization Programs/trendsABSTRACT
Background: Three-drug antiretroviral therapy (ART-3) has reduced complications and improved survival in HIV+ patients. The Chilean Public Health System began dual therapy (ART-2) in 1997, covering approximately 40 percent of patients in need. Aim: To report the results of a follow-up of patients with and without access to ART in a Chilean public hospital. Patient and Methods: Prospective follow-up of patients with ART-2 and 3 (cases) and patients with no access to ART (controls). All patients needed ART but it was available to a minority of them. Selection for ART was at random. Follow-up was between 6-24 months (11/96 to 3/99). Basal and periodic clinical and laboratory parameters were determined. Mortality and occurrence of new AIDS-defining events (ADE) were compared statistically using chi square. Results: One hundred and fifty cases (106 ART2, 28 ART3 and 16 ART2 expanded to ART3) and 166 controls were studied. Basal parameters were similar except prior ART (32.7 and 18.7 percent in cases and controls respectively). Close to 1/3 patients had AIDS. Cases had a mean follow up of 527 days; controls, 478. Six cases (4 percent) (5 in ART-2) and 17 controls (10 percent) died. Mortality x 100/pts/yr was 2.7 in cases and 7.7 in controls, p <0.05. ADE per 100/pts/yr was 21 in cases (24.4 in ART2, 15.1 in TAR3) and 54.5 in controls, p <0.05. Cases had a reduction of: esophageal candidiasis (84 percent), tuberculosis (75 percent), cryptococcosis and toxoplasmosis (66 percent), P carinii pneumonia (55 percent) and bacterial pneumonia (46 percent) and they had fewer hospitalizations (73 percent). Late assessment: 70 of 101 ART-2 patients had changed to ART-3 (1 death); 22 of 101 kept original ART-2 (12 dead, 10 alive), 39 of 43 ART-3 patients were alive and 1 died. Conclusions: Short-term ART-2 and 3 significantly reduced mortality (60 percent and 73 percent) ADE (65 percent and 76 percent respectively) and hospitalizations. Benefits of ART-2 were short lived. Resource-constrained countries cannot depend on weaker than standard ART for proper care of people with HIV disease
Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Zidovudine , Lamivudine , Acquired Immunodeficiency Syndrome/drug therapy , Case-Control Studies , Prospective Studies , AIDS-Related Opportunistic Infections , Anti-HIV Agents , Hospitalization , Acquired Immunodeficiency Syndrome/complications , Acquired Immunodeficiency Syndrome/mortalityABSTRACT
Background: Second generation cephalosporins (CFPs) are more active in the treatment of acute pyelonephritis during pregnancy but their cost is considerably higher than their predecessors. Cefuroxime, a second generation CFP with oral and parenteral presentations, might offer significant advantages and become a first choice antimicrobial in this setting. Aim: To compare the efficacy, safety and cost of cefuroxime and cephradine in the treatment of acute pyelonephritis in pregnancy. Patients and methods: Hospitalized women with 12 to 34 weeks of pregnancy, with clinical and bacteriological diagnosis of acute pyelonephritis, were randomly assigned to receive cefuroxime (Curocef (r), GlaxoWellcome) 750 mg t.i.d, i.v or cephradine 1 g q.i.d., i.v. If the isolated organism was resistant to the assigned drug the patient was excluded. Once patients were afebrile, they were switched to an oral form of the same antimicrobial. They were discharged according to the clinical status and treated for a total of 14 days. Laboratory tests, including urine culture were requested during controls and at the end of follow-up at 28 days. Results: One hundred and one patients were randomized: 49 to receive cephradine and 52 to receive cefuroxime. Patients in the cefuroxime group had fewer febrile days (mean 1.7 vs 2.2, p<0.05), faster clinical recovery (mean 2.7 vs 3.1 days, p<0.05), a higher rate of bacteriological cure at 28 days (78.8 percent and 59.2 percent, p<0.05) and lower rate of failure (21.2 percent vs 40.8 percent p<0.05). The rate of resistance of isolated uropathogens was l4 percent to cephradine and 1 percent to cefuroxime. Conclusions: Cefuroxime can be considered as a first choice option in the treatment of acute pyelonephritis during pregnancy due to its tolerance, microbiological activity and efficacy
Subject(s)
Humans , Female , Adult , Pregnancy Complications, Infectious/etiology , Pregnancy Complications, Infectious/drug therapy , Pyelonephritis/drug therapy , Cefuroxime/pharmacology , Cephradine/pharmacology , Parity , Pyelonephritis/economics , Pyelonephritis/etiology , Urine/microbiology , Prospective Studies , Treatment Outcome , Escherichia coli/isolation & purification , Escherichia coli/drug effects , Escherichia coli/pathogenicity , Health Care Costs/statistics & numerical data , Length of Stay/statistics & numerical dataABSTRACT
Background: Combined antiretroviral therapy (AVR) has shown a protective effect (PE) on morbidity and survival in HIV (+) patients of industrialised countries where triple-drug therapy (ARV-3) is standard. In Chile the public health system began providing double-drug therapy in 1997 (ARV-2) with 2 reverse transcriptase inhibitors. Aim: To assess the impact of ARV in morbimortality of HIV (+) patients in Chile after a year of follow up. Patients and methods: Retrospective case-control (1:1) study. Cases were 97 patients followed during 1997 for 6 or more months and dying during that period. Each case had a control of the same gender and CDC stage, similar age and CD4 count, but surviving a same period of follow up. A comparison of ARV before and during follow up (rate and type) was done. P carinii prophylaxis, pneumococcal immunization at baseline or follow up, frequency of hospital admissions and occurrence of opportunistic infections in both groups were assessed. Odds ratio (OR) for mortality, hospitalisation and opportunistic infections in ARV user, as well as treatment PE were calculated. Results: Twenty four (24.7 percent) cases and sixty six (68 percent) controls received ARV during follow up (p< 0.001), OR was 0.15 (CI 95 percent 0.08-0.3), p < 0.001, the PE was 6.6 for ARV users versus non users, among cases 19 patients received ARV-2 and five received ARV-3. Among controls, 41 patients received ARV-2 and 25 received ARV-3. These differences established an OR of 0.20 (CI 95 percent 0.09-0.04) and a PE of 5 for ARV-2 versus no ARV. For ARV-3 compared with no ARV the OR was 0.08 (CI 95 percent 0.003-0.26), and the PE 12.5. Fifty three (54.6 percent) cases and 13 (13.4 percent) controls required hospital admission, OR 0.49 (CI 95 percent 0.25-0.94), p=0.03, and PE of 2.04 of ARV versus no ARV; 82 (85.3 percent) cases and 50 (51 percent) controls had opportunistic infections, OR 0.5 (CI 95 percent 0.26-0.96), p=0.03 and PE of 2 for ARV versus no ARV. There were no significant differences in prior ARV, prophylaxis and immunisation between cases and controls. Conclusions: This study showed the high impact of ARV in short term morbimortality of HIV(+) patients and the need to implement antiretroviral therapy to all patients as an official health policy. This study did not answer the question of the role, if any, of weaker-than standard antiretroviral therapy
Subject(s)
Humans , Female , Male , Adult , Middle Aged , Protease Inhibitors/pharmacology , Zidovudine/pharmacology , Reverse Transcriptase Inhibitors/pharmacology , Acquired Immunodeficiency Syndrome/drug therapy , Case-Control Studies , Retrospective Studies , AIDS-Related Opportunistic Infections/drug therapy , AIDS-Related Opportunistic Infections/epidemiology , Anti-HIV Agents/pharmacology , Drug Therapy, Combination , Hospitalization/statistics & numerical data , Acquired Immunodeficiency Syndrome/mortalityABSTRACT
El término sepsis es amplio y algo vago, en general se refiere a infecciones graves. Afortunadamente se ha llegado a un grado de consenso de las distintas entidades y se está empezando a hablar en un lenguaje común. Esta revisión, más que analizar esta terminología de consenso y su cada vez mejor caracterización fisiopatológica, se abocará al problema práctico del enfoque terapéutico de infecciones graves, aquellas que habitualmente son vistas en las unidades de cuidados intensivos, con el propósito de fijar un marco de referencia que permita tratar adecuadamente las patologías, optimizar los recursos y analizar críticamente algunos conceptos y prácticas de la especialidad
Subject(s)
Humans , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/pharmacology , Sepsis/drug therapy , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents , Drug Resistance, Microbial , Intensive Care Units , Sepsis/etiologyABSTRACT
Esta revisión pretende entregar un método de análisis de las infecciones pulmonares extrahospitalarias orientada especialmente al diagnóstico etiológico de la enfermedad desde el punto de vista epidemiológico, clínico y de laboratorio
Subject(s)
Pneumonia/diagnosis , Respiratory Tract Diseases/diagnosis , Cross Infection , Pneumonia/drug therapy , Pneumonia/therapy , Respiratory Tract Diseases/drug therapy , Respiratory Tract Diseases/therapySubject(s)
Humans , Communicable Diseases , Poverty , Hantavirus Infections , Anti-Bacterial Agents/therapeutic useABSTRACT
Health Care Workers (HCW) are continually exposed to body fluids from patients. Some of these fluids may carry pathogens potentially transmissible to HCWs if the exposure is considered to be of "high risk" (mainyly percutaneous exposure). The main agents that have been transmitted by occupational exposure are hepatitis B and C viruses and human immunodeficiency virus (HIV). The risk of transmission after risky occupational exposure to these agents is about 2-40 percent, 3-10 percent and 0.2-0.3 percent respectively. This review presents an operational recommendation for the management of HCWs occupationally exposed to patients' body fluids. The recommendations, through a system of algorithms focus in assessing the actual risk of the accident and the body fluid involved, the possibility of the fluid harboring a transmissible pathogen, the susceptibility of the HCW to that pathogen and the post exposure measure to be taken. For hepatitis B, pre exposure immunization is highly recommended and he vaccine in addition to hyperimmune globuline for post exposure prophylaxis is advisable. For risky occupational exposures to HIV counselling is mandatory; the role of post exposure drug prophylaxis is discussed. Hepatitis C can be occupationally transmitted; no known post exposure prophylactic measures are available. Dure to the low incidence of these and other transmissible pathogens in the general population the author's recommendation is that occupational exposure to body fluids from unidentifiable or unknown sources or from patients without clinical evidence of hese infections be considered as low risk, and no baseline or follow up serologic studies or measures besides counselling be taken.For other causes, the serologic follow up for exposed HCWs for each of these infections is presented
Subject(s)
Humans , Universal Precautions , Health Personnel/standards , Occupational Exposure/standards , Biological Pollutants , Containment of Biohazards/standards , Infectious Disease Transmission, Patient-to-Professional/standardsABSTRACT
This paper presents recommendations on the care of HIV infected adults based upon the author's personal experience with close to 700 patients in a multiprofessional pilot center. This medical care has 5 main objectives: 1)Promotion of good health (through standard recommendation of hygiene, health habits and regular checkup) 2)Prevention of infectious complications (through detection of latent pathogens, chemoprophylaxis, vaccination and avoidance of risk exposures). 3)Treatment of complications (mainly infectious, through early diagnosis and proper treatment); 4)Delay of HIV disease progression (through timely and properly chosen antiretroviral therapy) 5)Reduction of HIV disease progression spread from index case of others (through promotion of responsible behavior and avoidance of pregnancy and HIV exposure to others). Studies for evaluating global health and immunologic status and carriage of potential pathogens are discissed as well as the criteria and timing for chemoprofilaxis for tuberculosis and P carinii pneumonia (PCP). Algorithms for the management of major clinical syndromes and presented: diarrhea (afebrile, mostly parasitic, versus febrile, frequently bacterial); pneumonia (lobar mostly bacterial versus interstitial, frequently PCP specially if lymphopenic and not receiving PCP prophylaxis); brain mass lesion (most commonly toxoplasmosis). Finally, the evaluation and diagnostic possibilities of febrile patients is presented, based upon the immunologic status and associated symptoms
Subject(s)
Humans , Male , Female , Carrier State/microbiology , HIV Infections/therapy , HIV Seropositivity/therapy , Pneumonia, Pneumococcal/microbiology , Pneumonia, Pneumococcal/drug therapy , Patient Education as Topic , AIDS-Related Opportunistic Infections/diagnosis , AIDS-Related Opportunistic Infections/therapy , Clinical Laboratory Techniques , Diarrhea/microbiology , Diarrhea/drug therapy , Anti-Bacterial Agents/administration & dosage , Lung Diseases, Interstitial/microbiology , Lung Diseases, Interstitial/drug therapyABSTRACT
En las infecciones puerperales, ha habido un resurgimiento de la virulencia del Streptococcus pyogenes, con la variedad llamada síndrome shock tóxico. Se presenta como severa sepsis con falla orgánica múltiple y generalmente conduce a la muerte de la paciente. La variedad M que produce exotoxina A, B o ambas ha sido el serotipo más frecuentemente aislado en esta infección invasiva. Comunicamos un caso de sepsis puerperal, con síndrome shock tóxico. Esta publicación pretende alertar sobre el posible retorno de esta infección y recordar al obstetra esta grave forma de presentación
Subject(s)
Humans , Female , Adult , Puerperal Infection , Shock, Septic/diagnosis , Streptococcus pyogenes/pathogenicity , Drug Therapy, Combination/therapeutic use , Hysterectomy , Shock, Septic/surgery , Shock, Septic/etiology , Shock, Septic/drug therapy , Streptococcus pyogenes/drug effectsABSTRACT
Es práctica común diagnosticar Fiebre Tifoidea (FT) a base del hemograma tífico (HT), y no en criterios bacteriológicos. Este estudio evaluó la sensibilidad del HT en pacientes (pts) con FT documentada bacteriológicamente y la especificidad para FT en pts que durante su estudio tenían HT. Se definió al HT con 5 parámetros: leucopenia (3500-6500), más de 40% de polimorfonucleares, 6% o más de baciliformes, aneosinofilia y VHS entre 25 y 50 mm. De 50 pts con FT, la mayoría adultos, sólo 13 (26%) tenían los 5 parámetros de HT, 41 (82%) al menos 4 y 49 (98%). Cuarenta y siete pts tenían HT; 25 adultos y 22 niños (sin lactantes). Sólo 14 (30%) tenían FT: 7 de 15 adultos (47%) y 7 de 21 niños (33%) con cuadro febril compatible. Los cuadros febriles no tíficos de adultos HT fueron: pericarditis, lupus, sarampión, colitis isquémica, pielonefritis, tuberculosis, peritonitis y psitacosis. En niños lo más frecuente fue: diarrea infecciosa y neumonía, también hepatitis, linfomas y celulitis. Se concluye que la sensibilidad del HT para FT es alta, pero el examen es poco específico
Subject(s)
Humans , Male , Female , Adult , Blood Chemical Analysis , Typhoid Fever/blood , Blood Sedimentation , Diagnosis, Differential , Leukocyte Count , NeutrophilsABSTRACT
El objetivo de este trabajo fue estudiar las características clínicas del embarazo con infección por virus de inmunodeficiencia humana (VIH) y la transmisión vertical. Se analizaron embarazadas con esta infección, controladas en la Fundación Arriarán, cuya gestación y parto fueron atendidos en la Maternidad del Hospital San Borja Arriarán. Durante la gestación se hizo pesquisa de otras infecciones. La zidovudina (AZT) fue usada según protocolo ACTG 076 en 6 mujeres. En el parto se prefirió la cesárea electiva. Se impidió la lactancia. Se hizo seguimiento de los niños. Diecisiete mujeres tuvieron 19 partos. Presentaron infección genitourinaria 4 pacientes (21,1 por ciento); infecciones no ginecológicas 5 (26,3 por ciento); patología del embarazo 4 (21,1 por ciento); rotura prematura de membranas de término 1 (5,3 por ciento); parto prematuro 3 (15,8 por ciento). El parto fue por cesárea en 15 casos (78,9 por ciento). La transmisión vertical fue 26,3 por ciento (5/19), 33,3 por ciento (5/15) en la cesárea y 16,7 por ciento con tratamiento de AZT. Un niño presentó muerte fetal y trece (68,4 por ciento) están sanos. Ocho mujeres están asintomáticas, tres sintomáticas, cuatro abandonaron controles y dos fallecieron. Es conveniente que la embarazada con infección por VIH use AZT y sea controlada por especialistas para disminuir los factores de riesgo en la transmisión vertical. La cesárea facilita la administración de AZT durante el parto. La lactancia materna debe suprimiese