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1.
Am Heart J ; 136(2): 307-13, 1998 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-9704695

RESUMO

BACKGROUND: Patients with chronic obstructive pulmonary disease are usually excluded from intravenous dipyridamole thallium-201 testing. We developed a nurse-administered protocol to screen and pretreat patients so they could be safely tested. METHODS AND RESULTS: We prospectively screened patients referred for intravenous dipyridamole thallium testing and retrospectively reviewed a comparison group of patients who had undergone intravenous dipyridamole testing before our bronchospasm protocol. We studied 492 consecutive patients referred for intravenous dipyridamole thallium testing, separating those with complete data (n = 451) into two groups: group A (n = 72), patients assessed to be at risk for intravenous dipyridamole-induced bronchospasm who received our bronchospasm treatment protocol; and group B (n = 379), patients assessed to be free of risk, who did not receive our bronchospasm protocol. Group C (n = 89) was a retrospective comparison group of patients who had undergone intravenous dipyridamole testing before initiation of the protocol. Patients were considered at risk for an adverse event if any of the following were present: peak flow < or =400 ml at the time of the test (spirometry by nurse) that increased to >400 ml after bronchodilator treatment, wheezing audible with stethoscope, history of chronic obstructive pulmonary disease or asthma or dyspnea on exertion at less than four blocks, or resting respiratory rate >18 breaths/min. The test was considered contraindicated if resting oxygen saturation was <85%, respiratory rate < or =36 breaths/min, or peak flow measured by peak flowmeter <400 ml after bronchodilator inhalant (albuterol or metaproterenol sulfate by spacer) at a dose of up to six puffs. One minute after injections of thallium-201, patients at risk were given 50 mg aminophylline by slow intravenous injection. We looked for major and minor adverse effects and divided them into three categories: (1) minor events (transient headache, abdominal discomfort, or nausea), wheezing (audible by stethoscope but without marked respiratory distress), (2) marked events (severe bronchospasm or severe ischemia defined as wheezing audible with or without stethoscope, respiratory rate >20 breaths/min or increased by 10 from pretest evaluation, oxygen desaturation to <90%, hypoventilation [reduced respiratory rate with decreased mental status], respiratory arrest, chest pain, horizontal ST-segment depression > or =1 mm on the electrocardiogram in any lead, symptomatic hypotension), or (3) other intravenous dipyridamole-induced side effects (persistent headache, dizziness, flushing, nausea, dyspnea, and ischemic chest pain) or anginal equivalent. The protocol properly identified patients with impaired pulmonary function. There was no difference in the frequency of adverse marked events among groups A, B, or C (1 % vs 4% vs 2%, p = 0.25). Patients in group A had more minor side effects than those in group B (53% vs 35%, p = 0.004). Specifically, patients in group A were more likely to wheeze (39% vs 1 %, p = <0.001), but wheezing in group A was self-limited or responded to treatment as described in the protocol. The prevalence of positive thallium-201 scans in group A (44%) compared with group C (49%) was not different (p = 0.15). CONCLUSIONS: A nurse-administered risk assessment and pretreatment protocol (1) properly identified patients with impaired pulmonary function, (2) permitted completion of intravenous dipyridamole testing in patients at risk for bronchospasm without an increased incidence of marked adverse events, and (3) did not appear to influence the interpretation of the thallium test.


Assuntos
Dipiridamol , Pneumopatias Obstrutivas/diagnóstico por imagem , Vasodilatadores , Idoso , Espasmo Brônquico/induzido quimicamente , Espasmo Brônquico/fisiopatologia , Espasmo Brônquico/prevenção & controle , Broncodilatadores/administração & dosagem , Dipiridamol/efeitos adversos , Teste de Esforço , Humanos , Processamento de Imagem Assistida por Computador , Infusões Intravenosas , Pneumopatias Obstrutivas/enfermagem , Pneumopatias Obstrutivas/fisiopatologia , Masculino , Pessoa de Meia-Idade , Avaliação em Enfermagem , Pré-Medicação , Estudos Prospectivos , Cintilografia , Sons Respiratórios/fisiologia , Estudos Retrospectivos , Medição de Risco , Fatores de Risco , Radioisótopos de Tálio , Vasodilatadores/efeitos adversos
3.
Radiology ; 151(3): 785-7, 1984 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-6585860

RESUMO

Bone scans using Tc-99m diphosphonate were found to become abnormal within 2 weeks after laminectomy in less than half of patients regardless of the extent of the operation. The degree of new uptake equaled that of the sacroiliac joints in only one of 19 patients with a normal preoperative scan. However, the Ga-67 citrate scan usually became abnormal (89%) postoperatively. Thus the Tc-99m bone scan may be helpful in detecting postoperative infection.


Assuntos
Radioisótopos de Gálio , Deslocamento do Disco Intervertebral/diagnóstico por imagem , Laminectomia , Infecção da Ferida Cirúrgica/diagnóstico por imagem , Compostos de Tecnécio , Difosfonatos , Humanos , Deslocamento do Disco Intervertebral/cirurgia , Cintilografia , Articulação Sacroilíaca/diagnóstico por imagem , Tecnécio , Fatores de Tempo
4.
Clin Nucl Med ; 9(4): 205-7, 1984 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-6609791

RESUMO

Intrapenile blood pool activity may be a source of artefact in interpreting a gastrointestinal bleeding study employing Tc-99m sulfur colloid or erythrocytes. Proper positioning should avoid a false reading of rectal bleeding.


Assuntos
Hemorragia Gastrointestinal/diagnóstico , Pênis/diagnóstico por imagem , Eritrócitos , Hemorragia Gastrointestinal/diagnóstico por imagem , Humanos , Masculino , Pênis/irrigação sanguínea , Cintilografia , Reto , Enxofre , Tecnécio , Coloide de Enxofre Marcado com Tecnécio Tc 99m
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