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1.
Am J Cardiol ; 54(1): 14-9, 1984 Jul 01.
Article in English | MEDLINE | ID: mdl-6741804

ABSTRACT

The efficacy of intravenous (i.v.) thrombolytic therapy has not been firmly established in comparison with the intracoronary (i.c.) route of administration. In a randomized trial of 28 patients who underwent angiography before and during i.v. and i.c. administration of streptokinase (STK), recanalization was achieved in 73% of patients who received the drug by the i.c. route, compared with 62% of patients who received the drug by the i.v. route (difference not significant). Reopening took 28 minutes for i.c. STK and 39 minutes for i.v. STK. Patients in whom recanalization was successful using either route of administration had shorter euglobulin lysis times and lower fibrinogen levels than did patients in whom it was not successful (p less than 0.05). Bleeding complications were closely correlated with heparinization after thrombolysis rather than with STK itself. These results in a limited patient series suggest that early administration of i.v. STK in the emergency department may yield recanalization rates similar to those for the i.c. route and may benefit myocardial preservation by restoring flow much earlier.


Subject(s)
Myocardial Infarction/drug therapy , Streptokinase/administration & dosage , Aged , Coronary Circulation/drug effects , Coronary Vessels , Creatine Kinase/blood , Humans , Infusions, Intra-Arterial , Infusions, Parenteral , Male , Random Allocation
2.
Am J Med ; 69(5): 690-4, 1980 Nov.
Article in English | MEDLINE | ID: mdl-7192052

ABSTRACT

Of 38 adult patients with idiopathic thrombocytopenic purpura followed an average of more than 12 years, 15 suffered splenectomy failure or postsplenectomy recurrence of thrombocytopenia. Nine of the 15 also received immunosuppressive agents, and four of the nine failed such therapy. In eight of these 15 treatment failures normal or safe platelet counts were achieved in a subsequent three to 12 year period during which they received no therapy. The frequency of spontaneous recovery of satisfactory platelet levels in adults with idiopathic thrombocytopenic purpura in whom treatment failed may have negative implications for very vigorous or longstanding immunosuppressive therapeutic attempts in certain cases.


Subject(s)
Purpura, Thrombocytopenic/therapy , Adolescent , Adult , Aged , Azathioprine/administration & dosage , Child , Cyclophosphamide/administration & dosage , Drug Therapy, Combination , Evaluation Studies as Topic , Female , Follow-Up Studies , Humans , Male , Middle Aged , Platelet Count , Purpura, Thrombocytopenic/blood , Recurrence , Remission, Spontaneous , Splenectomy , Time Factors
3.
Arch Intern Med ; 140(10): 1370-1, 1980 Oct.
Article in English | MEDLINE | ID: mdl-6775611

ABSTRACT

Synotinatuc subclavian vein thrombosis developed in a patient receiving long-term parenteral nutrition. Serial phlebograms showed progression of venous thrombosis, despite therapy with heparin. Fibrinolytic therapy with streptoikinase, monitored in the laboratory by the euglobulin clot lysis time, was strikingly successful and may be the treatment of choice for this condition if certain contraindications are absent.


Subject(s)
Catheterization/adverse effects , Streptokinase/therapeutic use , Subclavian Vein , Thrombosis/etiology , Vena Cava, Superior , Adult , Heparin/adverse effects , Humans , Male , Parenteral Nutrition, Total/adverse effects , Thrombosis/drug therapy
4.
Am J Med ; 66(6): 959-66, 1979 Jun.
Article in English | MEDLINE | ID: mdl-287373

ABSTRACT

The data on 31 patients who fit into the clinical spectrum of subacute myeloid leukemia have been reviewed. The majority of patients were male with a median age of 61 years. The interval from onset of symptoms to actual diagnosis was extremely variable, with a mean of 16 months and a median of six months. Most patients presented with anemia and thrombocytopenia, although the white blood cell count varied from striking leukopenia to marked leukocytosis. Examination of the bone marrow invariably revealed abnormalities of all cell lines with megaloblastoid erythrogenesis and dysplastic megakaryocytopoiesis. Although the white cell line showed prominence of immature forms, there was more maturation than is seen in acute myeloid leukemia. Survival from diagnosis was variable, from less than one month to greater than 68 months, with a median of only six months. Anemia and hepatosplenomegaly were prognosticators of a poor outlook; patients with hepatosplenomegaly in association with either leukocytosis or thrombocytopenia had a particularly poor outlook, with a median survival of only one and a half months. Approximately half the patients received chemotherapy with no demonstrated effect on survival.


Subject(s)
Leukemia, Myeloid/blood , Adolescent , Adult , Aged , Alkaline Phosphatase/blood , Antineoplastic Agents/therapeutic use , Blood Cell Count , Bone Marrow Cells , Hematocrit , Humans , Leukemia, Myeloid/diagnosis , Leukemia, Myeloid/mortality , Leukocytes/enzymology , Middle Aged , Muramidase/blood , Prognosis , Thrombocytopenia/blood
16.
Postgrad Med ; 39(4): 403-6, 1966 Apr.
Article in English | MEDLINE | ID: mdl-5907410
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