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1.
J Hosp Med ; 10(6): 390-5, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25809958

RESUMEN

PURPOSE: Common labs such as a daily complete blood count or a daily basic metabolic panel represent possible waste and have been targeted by professional societies and the Choosing Wisely campaign for critical evaluation. We undertook a multifaceted quality-improvement (QI) intervention in a large community hospitalist group to decrease unnecessary common labs. METHODS: The QI intervention was composed of academic detailing, audit and feedback, and transparent reporting of the frequency with which common labs were ordered as daily within the hospitalist group. We performed a pre-post analysis, comparing a cohort of patients during the 10-month baseline period before the QI intervention and the 7-month intervention period. Demographic and clinical data were collected from the electronic medical record. The primary endpoint was number of common labs ordered per patient-day as estimated by a clustered multivariable linear regression model clustering by ordering hospitalist. Secondary endpoints included length of stay, hospital mortality, 30-day readmission, blood transfusion, amount of blood transfused, and laboratory cost per patient. RESULTS: The baseline (n = 7824) and intervention (n = 5759) cohorts were similar in their demographics, though the distribution of primary discharge diagnosis-related groups differed. At baseline, a mean of 2.06 (standard deviation 1.40) common labs were ordered per patient-day. Adjusting for age, sex, and principle discharge diagnosis, the number of common labs ordered per patient-day decreased by 0.22 (10.7%) during the intervention period compared to baseline (95% confidence interval [CI], 0.34 to 0.11; P < 0.01). There were nonsignificant reductions in hospital mortality in the intervention period compared to baseline (2.2% vs 1.8%, P = 0.1) as well as volume of blood transfused in patients who received a transfusion (127.2 mL decrease; 95% CI, -257.9 to 3.6; P = 0.06). No effect was seen on length of stay or readmission rate. The intervention decreased hospital direct costs by an estimated $16.19 per admission or $151,682 annualized (95% CI, $119,746 to $187,618). CONCLUSION: Implementation of a multifaceted QI intervention within a community-based hospitalist group was associated with a significant, but modest, decrease in the number of ordered lab tests and hospital costs. No effect was seen on hospital length of stay, mortality, or readmission rate. This intervention suggests that a community-based hospitalist QI intervention focused on daily labs can be effective in safely reducing healthcare waste without compromising quality of care.


Asunto(s)
Pruebas Diagnósticas de Rutina/estadística & datos numéricos , Economía Hospitalaria , Médicos Hospitalarios/normas , Mejoramiento de la Calidad/normas , Procedimientos Innecesarios/economía , Control de Costos/métodos , Grupos Diagnósticos Relacionados/economía , Pruebas Diagnósticas de Rutina/economía , Pruebas Diagnósticas de Rutina/normas , Registros Electrónicos de Salud/estadística & datos numéricos , Femenino , Humanos , Modelos Lineales , Masculino , Persona de Mediana Edad , Modelos Organizacionales , Evaluación de Resultado en la Atención de Salud/economía , Evaluación de Resultado en la Atención de Salud/estadística & datos numéricos , Alta del Paciente/economía , Mejoramiento de la Calidad/economía , Suecia , Procedimientos Innecesarios/estadística & datos numéricos
2.
J Clin Psychiatry ; 65(11): 1531-6, 2004 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-15554768

RESUMEN

BACKGROUND: The purpose of this study was to examine the effectiveness and tolerability of quetiapine for aggression, hyperactivity, and self-injury in pervasive developmental disorders (PDDs). METHOD: The medical records of all patients with PDDs diagnosed according to DSM-IV criteria and treated with quetiapine were retrospectively reviewed. Patients who received quetiapine for at least 4 weeks and who were not concurrently treated with another antipsychotic or mood stabilizer were included. Improvement was measured with the Clinical Global Impressions-Improvement scale (CGI-I), with response determined by ratings of "much improved" or "very much improved." Data were collected from May 15, 2003 through November 30, 2003. RESULTS: Of 857 records reviewed, 20 patients (16 male, 4 female) (mean +/- SD age = 12.1 +/- 6.7 years; range, 5-28 years) received a quetiapine trial (mean +/- SD dosage = 248.7 +/- 198.4 mg/day; range, 25-600 mg/day) over a mean duration of 59.8 +/- 55.1 weeks (range, 4-180 weeks). Eight (40%) of 20 patients were judged "responders" to quetiapine; the mean CGI-I score for the entire group was 3.0 +/- 1.1 (minimally improved). A statistically significant improvement (p = .002) was found between a mean pretrial CGI-Severity of Illness scale (CGI-S) score of 5.1 +/- 0.6 (markedly ill) and a posttrial CGI-S score of 4.2 +/- 1.1 (moderately ill). Adverse effects occurred in 50% (N = 10) of patients and led to drug discontinuation in 15% (N = 3) of patients. CONCLUSION: Quetiapine was modestly effective for maladaptive behavior in patients with a PDD. Controlled studies are needed to further assess these preliminary findings.


Asunto(s)
Antipsicóticos/uso terapéutico , Trastornos Generalizados del Desarrollo Infantil/tratamiento farmacológico , Dibenzotiazepinas/uso terapéutico , Adolescente , Adulto , Agresión/efectos de los fármacos , Niño , Trastornos Generalizados del Desarrollo Infantil/psicología , Preescolar , Discinesia Inducida por Medicamentos/etiología , Humanos , Hipercinesia/tratamiento farmacológico , Masculino , Escalas de Valoración Psiquiátrica , Fumarato de Quetiapina , Estudios Retrospectivos , Conducta Autodestructiva/tratamiento farmacológico , Índice de Severidad de la Enfermedad , Sueño/efectos de los fármacos , Trastornos del Inicio y del Mantenimiento del Sueño/inducido químicamente , Resultado del Tratamiento , Aumento de Peso/efectos de los fármacos
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