RESUMEN
Objective Carbazochrome sodium sulfonate (CSS) has been routinely used to treat bleeding; however, no study has examined the effect of CSS for gastrointestinal bleeding. Therefore, we aimed to investigate the effect of CSS for colonic diverticular bleeding. Methods We performed a nationwide observational study using the Japanese Diagnosis Procedure Combination inpatient database. We identified patients who were admitted for diverticular bleeding from July 2010 to March 2018. Patients who received CSS on the day of admission were defined as the CSS group, and those not receiving CSS were defined as the control group. The primary outcome was in-hospital mortality. Secondary outcomes were length of stay, total costs, and blood transfusion within 7 days of admission. Propensity score matching analyses were performed to compare outcomes between the two groups. Results A total of 59,965 patients met our eligibility criteria. Of these, 14,437 (24%) patients received CSS on the day of admission. One-to-one propensity score matching created 14,379 matched pairs. There was no significant difference in the in-hospital mortality between the CSS and control groups (0.6% vs. 0.5%, respectively; odds ratio: 0.96; 95% confidence interval: 0.72-1.29). The length of stay was longer in the CSS group than in the control group (11.4 vs. 11.0 days, respectively; difference: 0.44; 95% confidence interval: 0.14-0.73). There were no significant differences in the total costs or the proportion of patients receiving blood transfusion between the groups. Conclusions CSS may not reduce in-hospital mortality, length of stay, total costs, or the need for blood transfusion in patients with colonic diverticular bleeding.
Asunto(s)
Adrenocromo/análogos & derivados , Enfermedades del Colon/tratamiento farmacológico , Enfermedades del Colon/mortalidad , Enfermedades Diverticulares/tratamiento farmacológico , Enfermedades Diverticulares/mortalidad , Hemostáticos/uso terapéutico , Adrenocromo/uso terapéutico , Adulto , Factores de Edad , Anciano , Anciano de 80 o más Años , Transfusión Sanguínea , Comorbilidad , Bases de Datos Factuales , Femenino , Gastos en Salud/estadística & datos numéricos , Mortalidad Hospitalaria/tendencias , Humanos , Japón , Tiempo de Internación/estadística & datos numéricos , Masculino , Persona de Mediana Edad , Oportunidad Relativa , Puntaje de Propensión , Estudios Retrospectivos , Factores Sexuales , Factores SocioeconómicosRESUMEN
BACKGROUND: To evaluate gingival inflammation from fixed-dose combinations of vitamin C, vitamin E, lysozyme and carbazochrome (CELC) in the treatment of chronic periodontitis following scaling and root planing. METHODS: One hundred patients were randomly assigned to receive CELC (test) or placebo (control) for the first 4 weeks at a 1:1 ratio, and both groups received CELC for the remaining 4 weeks. Primary outcome was the mean change in the gingival index (GI) after 4 weeks. Secondary outcomes included mean change in GI after 8 weeks and plaque index, probing depth, clinical attachment level, and VAS at 4 weeks and 8 weeks. RESULTS: Ninety-three patients completed the study. The GI in the test group significantly decreased after 4 weeks (p < 0.001) and 8 weeks (p < 0.001). The mean change from baseline in GI significantly decreased in the test group compared to the control group after 4 weeks (p = 0.015). In the GEE model adjusting for age, gender and visits, the test group showed 2.5 times GI improvement compared to the control group (p = 0.022). CONCLUSIONS: Within the study, CELC showed a significant reduction in gingival inflammation compared with a placebo. Other parameters, however, were similar between groups. TRIAL REGISTRATION: KCT0001366 (Clinical Research Information Service, Republic of Korea) and 29 Jan 2015, retrospectively registered.
Asunto(s)
Adrenocromo/análogos & derivados , Antibacterianos/uso terapéutico , Ácido Ascórbico/uso terapéutico , Periodontitis Crónica/tratamiento farmacológico , Muramidasa/uso terapéutico , Vitamina E/uso terapéutico , Adrenocromo/uso terapéutico , Índice de Placa Dental , Raspado Dental , Método Doble Ciego , Quimioterapia Combinada , Líquido del Surco Gingival , Humanos , Inflamación , República de Corea , Estudios Retrospectivos , Aplanamiento de la RaízRESUMEN
OBJECTIVES: To study the effect of carbazochrome sodium sulfonate, an agent that reduces capillary permeability, on refractory chronic prostatitis. METHODS: Patients with prostatitis refractory to at least 8 weeks of routine therapy and with urinalysis positive for microhematuria were considered for the present study. In addition to their prior therapy, the patients received carbazochrome at a dose of 30 mg three times a day. The severity of pain (score 0-10), daytime and night-time frequency, international prostate symptom score, global self-assessment, urine occult blood positivity, and adverse events were assessed after 4 and 8 weeks of treatment, and compared with baseline findings. RESULTS: A total of 50 patients (mean age 68.6 ± 8.5 years) were evaluable. The pain score decreased significantly from 3.2 ± 2.1 at baseline to 1.7 ± 1.4 after 4 weeks of treatment and to 1.1 ± 1.8 after 8 weeks. Daytime and night-time frequency, storage symptoms, post-micturition symptoms, and urine occult blood positivity also significantly improved. More than 36% of the patients gave a global self-assessment rating of "improved" or "better" after both 4 and 8 weeks of treatment. Mild adverse events occurred in three patients; one had nausea and two developed drug rash. CONCLUSIONS: Carbazochrome seems to effectively improve pain as well as storage and post-micturition symptoms in patients with refractory chronic prostatitis.
Asunto(s)
Adrenocromo/análogos & derivados , Hemostáticos/uso terapéutico , Prostatitis/tratamiento farmacológico , Adrenocromo/uso terapéutico , Anciano , Enfermedad Crónica , Humanos , Masculino , Persona de Mediana Edad , Resultado del TratamientoRESUMEN
OBJECTIVE: We report the case of a 47-year-old man with depression who developed acute dyspnea, hypoxemia, and mild hemoptysis after electroconvulsive therapy (ECT). METHOD: Intravenous carbazochrome sodium sulfate hydrate as a hemostatic drug (100 mg/day) was prescribed for 2 days. On the day of ECT, oxygen inhalation (4 L/min) was continued, and SpO2 was maintained at 94-96%. RESULTS: Chest radiography showed improvement in alveolar infiltration. Chest CT 6 days after ECT also confirmed the disappearance of ground glass opacities in the lung fields. CONCLUSION(S): NPE is life threatening and should be recognized as an uncommon adverse event associated with ECT.
Asunto(s)
Trastorno Depresivo/terapia , Terapia Electroconvulsiva/efectos adversos , Edema Pulmonar/etiología , Adrenocromo/análogos & derivados , Adrenocromo/uso terapéutico , Hemostáticos/uso terapéutico , Humanos , Masculino , Persona de Mediana Edad , Edema Pulmonar/diagnóstico por imagen , Edema Pulmonar/tratamiento farmacológico , Tomografía Computarizada por Rayos XRESUMEN
The objective was to quantify the effect of furosemide and carbazochrome on exercise-induced pulmonary hemorrhage (EIPH) in Standardbred horses using red blood cell count and hemoglobin concentration in bronchoalveolar lavage (BAL) fluid. Six healthy Standardbred horses with prior evidence of EIPH performed a standardized treadmill test 4 h after administration of placebo, furosemide, or furosemide-carbazochrome combination. Red blood cell (RBC) counts and hemoglobin concentrations were determined on the BAL fluid. The RBC count in BAL ranges were (2903-26,025 cells/microL), (45-24,060 cells/microL), and (905-3045 cells/microL) for placebo, furosemide, and furosemide-carbazochrome, respectively. Hemoglobin concentration ranges were (0.03-0.59 mg/mL), (0.01-0.55 mg/mL), and (0.007-0.16 mg/mL) for placebo, furosemide, and furosemide-carbazochrome groups, respectively. No significant differences were detected among treatments. However, there was great variability among horses, suggesting that a larger sample size or better selection of horses was needed.
Asunto(s)
Adrenocromo/análogos & derivados , Diuréticos/uso terapéutico , Furosemida/uso terapéutico , Hemorragia/veterinaria , Enfermedades de los Caballos/tratamiento farmacológico , Enfermedades Pulmonares/veterinaria , Condicionamiento Físico Animal/efectos adversos , Adrenocromo/uso terapéutico , Animales , Líquido del Lavado Bronquioalveolar/citología , Estudios Cruzados , Quimioterapia Combinada , Prueba de Esfuerzo/veterinaria , Femenino , Hemorragia/tratamiento farmacológico , Caballos , Enfermedades Pulmonares/tratamiento farmacológico , Masculino , Distribución Aleatoria , Resultado del TratamientoRESUMEN
Electronic database Medline, Embase, Cochrane Library and Lilacs were used to retrieve the clinical trials that will evaluate the various therapeutical options available for management of hemorrhagic dengue. Eight clinical studies were included. Supportive care and symptomatic treatment through hydration and aggressive fluid management, if hypotension develops in the course of disease, are the most important aids to improve survival. Treatment with corticosteroids such as methylprednisolone, hydrocortisone, carbazochorome sodium sulfonate (AC-17) and recombinant activated factor VII did not reduce mortality in children with hemorrhagic dengue. At present, no vaccine or effective antiviral treatment is available for the prevention or treatment of hemorrhagic dengue.
Asunto(s)
Manejo de la Enfermedad , Dengue Grave/terapia , Corticoesteroides/uso terapéutico , Adrenocromo/análogos & derivados , Adrenocromo/uso terapéutico , Antipiréticos/uso terapéutico , Niño , Ensayos Clínicos como Asunto/estadística & datos numéricos , Coloides/uso terapéutico , Colombia , Terapia Combinada , Soluciones Cristaloides , Método Doble Ciego , Quimioterapia Combinada , Factor VIIa/uso terapéutico , Fluidoterapia , Hemorragia/tratamiento farmacológico , Hemorragia/etiología , Hemostáticos/uso terapéutico , Humanos , Soluciones Isotónicas/uso terapéutico , Terapia por Inhalación de Oxígeno , Ensayos Clínicos Controlados Aleatorios como Asunto/estadística & datos numéricos , Proteínas Recombinantes/uso terapéutico , Insuficiencia Respiratoria/etiología , Insuficiencia Respiratoria/terapia , Dengue Grave/complicaciones , Dengue Grave/tratamiento farmacológico , Choque/etiología , Choque/terapiaAsunto(s)
Adrenocromo/análogos & derivados , Desamino Arginina Vasopresina/uso terapéutico , Síndrome de Ehlers-Danlos/complicaciones , Estrógenos Conjugados (USP)/uso terapéutico , Hematoma/tratamiento farmacológico , Adrenocromo/uso terapéutico , Adulto , Transfusión Sanguínea , Terapia Combinada , Quimioterapia Combinada , Hematoma/etiología , Hematoma/terapia , Humanos , Masculino , Recurrencia , Muslo , Ácido Tranexámico/uso terapéuticoRESUMEN
Flavonoids, such as troxerutin, have been shown to be safe and effective agents for the treatment of chronic venous insufficiency. The fixed combination between troxerutin 150 mg and carbazochrome 1.5 mg (Fleboside ampoules) was previously shown to have a good efficacy and safety profile in non-surgical patients with acute uncomplicated hemorrhoids. The purpose of this randomized, double-blind, placebo-controlled study was to investigate the efficacy and tolerability of the active combination in the treatment of post-hemorrhoidectomy patients. 30 patients were randomized to receive one of two treatments: troxerutin 150 mg and carbazochrome 1.5 mg, or placebo, i.m. 3 ml ampoules twice a day for five consecutive days after the surgical procedure, starting from the day of surgery. Efficacy parameters were assessed as follows: at baseline (T1), after the first administration (T2; day of surgery), the second day after the surgical procedure (T3), and the fifth day after the surgical procedure (T4); hemorrhoidal symptoms based on a visual analogue scale (VAS): pain, discharge, bleeding, inflammation, and pruritus; analgesic intake, if any; time to restore a physiological defecation; edema evaluation (based on a four-point scale: 0 = absent; 1 = mild; 2 = moderate; 3 = severe); camera pictures taken at T1 and T4 (in selected patients); and blood coagulation tests. Analysis between treatment groups revealed a highly significant difference at T3 and T4 for the total VAS score (p = 0.007 and p = 0.001, respectively) in favor of the active combination treatment. A statistically significant difference was also observed for bleeding and pruritus at T3 and for these two parameters and both inflammation and edema at T4 (p < 0.001) in favor of the active combination group. No adverse events were reported. Neither the active combination nor placebo affected blood coagulation tests. We conclude that intramuscular administration of the fixed combination of troxerutin 150 mg and carbazochrome 1.5 mg is effective, well tolerated and superior to placebo in improving hemorrhoidal and post-surgical symptoms during the five days following surgery.
Asunto(s)
Adrenocromo/uso terapéutico , Hemorroides/cirugía , Hidroxietilrutósido/análogos & derivados , Hidroxietilrutósido/uso terapéutico , Complicaciones Posoperatorias/tratamiento farmacológico , Vasoconstrictores/uso terapéutico , Adrenocromo/administración & dosificación , Adrenocromo/análogos & derivados , Adulto , Distribución de Chi-Cuadrado , Método Doble Ciego , Combinación de Medicamentos , Femenino , Humanos , Hidroxietilrutósido/administración & dosificación , Inyecciones Intramusculares , Masculino , Persona de Mediana Edad , Estadísticas no Paramétricas , Resultado del Tratamiento , Vasoconstrictores/administración & dosificaciónRESUMEN
This multicenter, double-blind, randomised study was undertaken to determine the efficacy and safety of a combination of troxerutin 150 mg and carbazochrome 1.5 mg compared to carbazochrome alone in patients with acute uncomplicated hemorrhoids. Patients were administered by the intramuscular route (one ampoule) twice daily for one week. Both subjective and objective efficacy variables significantly improved in the combination drug group only, thus demonstrating the rationale for a combination therapy. Treatments were safe and well tolerated either at a local or systemic level.
Asunto(s)
Adrenocromo/uso terapéutico , Hemorroides/tratamiento farmacológico , Hemostáticos/uso terapéutico , Hidroxietilrutósido/análogos & derivados , Hidroxietilrutósido/uso terapéutico , Vasoconstrictores/uso terapéutico , Adrenocromo/administración & dosificación , Adrenocromo/efectos adversos , Adrenocromo/análogos & derivados , Adulto , Método Doble Ciego , Combinación de Medicamentos , Femenino , Hemostáticos/administración & dosificación , Hemostáticos/efectos adversos , Humanos , Hidroxietilrutósido/administración & dosificación , Hidroxietilrutósido/efectos adversos , Masculino , Vasoconstrictores/administración & dosificación , Vasoconstrictores/efectos adversosRESUMEN
The study was designed as double blind, placebo controlled. The patients were treated with 15 mg of iprazochrome daily in three equal doses for eight weeks, or--with equal amount of placebo tablets. The effectiveness was calculated with the use of Migraine Score (MS) by Couch et. al. 44 patients completed the study. In 21 the therapy was positive: 16 out of them were treated with iprazochrome, 5--with placebo. In 23 patients the treatment was negative: 19 out of them took placebo, 4--iprazochrome. Statistical analysis showed significant influence (chi 2 test: p < 0.001; Youle coeff. = 0.88). In iprazochrome group mean decrease of MS was significant after treatment (p < 0.01), but not significantly changed in the placebo group. According to our results iprazochrome was found effective in the prophylaxis of migraine.
Asunto(s)
Adrenocromo/análogos & derivados , Indolquinonas , Trastornos Migrañosos/prevención & control , Antagonistas de la Serotonina/uso terapéutico , Adrenocromo/uso terapéutico , Adulto , Método Doble Ciego , Femenino , Humanos , Persona de Mediana Edad , Estudios RetrospectivosRESUMEN
Migraine belongs to the most frequent idiopathic headaches affecting 5-10% of the population. The knowledge of migraine pathogenesis is as yet insufficient for complete elucidation of its causes. There is no effective drug for all patients which could interrupt the attack or prevent its development. The methods of migraine prevention could be divided into pharmacological and non-pharmacological. Among the drugs used for attack prevention drugs are mentioned known and used since a long time and drugs less commonly used such as riboflavin, sulpiride, alpha-adrenolytic agents. Own experiences are presented with the use of iprasochrom for migraine prevention. Besides pharmacological methods also non-pharmacological methods are discussed which are applied for attack prevention.
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Adrenocromo/análogos & derivados , Indolquinonas , Trastornos Migrañosos/prevención & control , Antagonistas Adrenérgicos alfa/uso terapéutico , Adrenocromo/uso terapéutico , Antagonistas de Dopamina/uso terapéutico , Homeopatía , Humanos , Riboflavina/uso terapéutico , Antagonistas de la Serotonina/uso terapéutico , Sulpirida/uso terapéuticoRESUMEN
OBJECTIVE: We studied the ability of carbazochrome sodium sulfonate (AC-17) to prevent capillary permeability in dengue hemorrhagic fever/dengue shock syndrome. METHOD: A randomized, placebo-controlled trial in 95 children stratified by age and sex was conducted in two hospitals during 1992. AC-17 (n = 45 cases) or B vitamins as placebo (n = 50) were given as a bolus infusion and then as a continuous drip for 24 hours; a total of 300 mg of AC-17 was administered on the first 2 days and 150 mg on the third day. RESULTS: The two groups were comparable in age, sex, duration of illness, and clinical manifestations. No significant difference in shock or pleural effusion was noted between the two groups. Shock developed in 8.9% (4/45) of patients in the AC-17 group and 6% (3/50) in the placebo group (p = 0.44). Pleural effusion was found at 0, 24, 48, and 72 hours after admission in 4.4%, 20%, 31.1%, and 20% in the AC-17 group and 2%, 14%, 28%, and 14% in the placebo group, respectively. CONCLUSION: Administration of AC-17 does not prevent plasma leakage or shock in dengue hemorrhagic fever/dengue shock syndrome.
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Adrenocromo/análogos & derivados , Permeabilidad Capilar/efectos de los fármacos , Hemostáticos/farmacología , Hemostáticos/uso terapéutico , Dengue Grave/tratamiento farmacológico , Adrenocromo/farmacología , Adrenocromo/uso terapéutico , Niño , Preescolar , Femenino , Hospitalización , Humanos , Lactante , Recién Nacido , Tiempo de Internación , Masculino , Dengue Grave/diagnóstico , Dengue Grave/rehabilitación , Insuficiencia del TratamientoRESUMEN
Heavy bleeding often occurs following cementless total knee arthroplasty (TKA) and it is difficult to control. We devised a new method of hemostasis after cementless TKA. In brief, the implant was inserted after coating the exposed surface of the cancellous bone with fibrin glue. Before removal of the tourniquet after completion of the operation a cocktail of hemostatic agents (containing 25 mg of carbazochrome sodium sulfonate and 250 mg of tranexamic acid) in 50 ml of physiological saline was injected into the joint cavity via the drain tube and the drain was clamped for about 30 min after removal of the tourniquet. After removal of the clamp, standard negative pressure suction was performed. This method was used on 84 knees in 42 patients who underwent simultaneous bilateral cementless TKA and 64 knees in 64 patients who underwent unilateral TKA. The mean total amount of blood loss during and after the operation was 235 +/- 178 ml in the unilateral TKA patients and 402 +/- 208 ml in the bilateral TKA patients. No patient required blood transfusions postoperatively. This method was effective for achieving hemostasis after cementless TKA.
Asunto(s)
Artroplastia de Reemplazo de Rodilla/métodos , Hemostasis Quirúrgica/métodos , Adrenocromo/análogos & derivados , Adrenocromo/uso terapéutico , Anciano , Antifibrinolíticos/uso terapéutico , Quimioterapia Combinada , Femenino , Adhesivo de Tejido de Fibrina/uso terapéutico , Hemostáticos/uso terapéutico , Humanos , Masculino , Ácido Tranexámico/uso terapéuticoRESUMEN
A 55-year-old woman, who had systemic amyloidosis associated with multiple myeloma, had sudden development of hematomas of her lip and upper eye lid. There was no evidence of deterioration of multiple myeloma, thrombocytopenia nor deficiency of coagulation factors. Biopsy specimen showed the deposit of amyloid substance in the dermis and perivascular region. The bleeding tendency in this patient with myeloma was likely due to the deposit of amyloid substance in the vascular wall; improvement was achieved with administration of hemostatic agents.
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Amiloide/metabolismo , Amiloidosis/complicaciones , Hematoma/etiología , Adrenocromo/análogos & derivados , Adrenocromo/uso terapéutico , Vasos Sanguíneos/metabolismo , Femenino , Hematoma/tratamiento farmacológico , Hemostáticos/uso terapéutico , Humanos , Persona de Mediana Edad , Mieloma Múltiple/complicaciones , Ácido Tranexámico/uso terapéuticoRESUMEN
Cepharanthin, a kind of alkaloid, has been reported to show a protective effect for leukopenia induced by radiation therapy. In this study, one of three kinds of drugs, Cepharanthin, S-Adchnon (adrenochrome derivative) and Hythiol (L-cysteine), was randomly administered to 94 patients with cancer of the head and neck, the uterine cervix and the lung, during the course of radiotherapy. When Cepharanthin was given, 81.3% of the patients were protected from leukopenia, compared with 51.6% in S-Adchnon and 32.3% in Hythiol. It is suggested that prophylactic use of Cepharanthin may be useful for cancer radiotherapy.
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Adrenocromo/análogos & derivados , Alcaloides/uso terapéutico , Leucopenia/tratamiento farmacológico , Neoplasias/radioterapia , Protectores contra Radiación/uso terapéutico , Radioterapia/efectos adversos , Adrenocromo/uso terapéutico , Bencilisoquinolinas , Cisteína/uso terapéutico , Femenino , Humanos , Leucopenia/etiología , Ensayos Clínicos Controlados Aleatorios como AsuntoRESUMEN
The results obtained in patients suffering from essential epistaxis in paediatric age using a peptide fraction derived from the enzymatic hydrolysis of bovine factor VIII (VUEFFE-Baldacci) are reported. Carbazochrome sodium sulphate was employed for comparison purposes. Vueffe is effective in reducing haemorrhagic episodes without modifying the laboratory parameters investigated.
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Epistaxis/tratamiento farmacológico , Factor VIII/uso terapéutico , Adolescente , Adrenocromo/análogos & derivados , Adrenocromo/uso terapéutico , Niño , Evaluación de Medicamentos , Femenino , Humanos , Masculino , Ensayos Clínicos Controlados Aleatorios como AsuntoRESUMEN
The effect of the serotonin antagonist iprazochrome was studied in 30 patients with atypical facial pain and 10 control nonpain volunteers. The aim of the study was to investigate the effect of a single dose of iprazochrome and of its short-term administration in patients with chronic pain. Twelve of the 30 patients reported increased pain, 16 reported no effect, and two reported pain relief for some hours after taking iprazochrome. None of the controls reported any effect from iprazochrome. Four of the 12 patients who reported increased pain also reported increased pain in distant organs, especially in the joints. A hypothesis of the mechanism is presented and a possible use of iprazochrome as a diagnostic tool is suggested.