Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
1.
Leuk Res ; 116: 106836, 2022 05.
Article in English | MEDLINE | ID: mdl-35405632

ABSTRACT

BACKGROUND: Azacitidine (AZA) is approved for the treatment of high-risk chronic myelomonocytic leukemia (CMML) of myelodysplastic (MD) subtype. Data of response rates using the specific response criteria for this disease are scarce. The aim of this study was to evaluate the response to AZA in patients diagnosed with CMML from the Spanish Registry of Myelodysplastic Syndromes (MDS) applying the overlap myelodysplastic/myeloproliferative neoplasms (MDS/MPN) response criteria. METHODS: We retrospectively studied 91 patients with CMML treated with at least one cycle of AZA from the Spanish Registry of MDS. As it was a real-world study, the response rate was evaluated between cycle 4 and 6, applying the MDS/MPN response criteria FINDINGS: The overall response rate at cycle 4-6 was 58%. Almost half of the patients achieved transfusion independence and one quarter showed clinical benefit, regardless of the CMML French-American-British (FAB) and World Health Organization (WHO) subtypes and CMML Specific Prognosis Scoring (CPSS) risk groups. Toxicity was higher in the MD-CMML subtype. INTERPRETATION: In our series, most CMML patients achieved an overall response rate with AZA according to the overlap-MDS/MPN response criteria regardless of the CMML FAB and WHO subtypes and CPSS risk groups. Thus, AZA may also be a treatment option for patients with the myeloproliferative CMML subtype and those with a lower-risk CPSS, but symptomatic.


Subject(s)
Azacitidine , Leukemia, Myelomonocytic, Chronic , Azacitidine/adverse effects , Azacitidine/therapeutic use , Humans , Leukemia, Myelomonocytic, Chronic/drug therapy , Myelodysplastic Syndromes/diagnosis , Myelodysplastic Syndromes/drug therapy , Myelodysplastic-Myeloproliferative Diseases/drug therapy , Retrospective Studies
2.
ASAIO J ; 47(1): 50-5, 2001.
Article in English | MEDLINE | ID: mdl-11199315

ABSTRACT

The LD-PACE II was designed for use in cardiomyoplasty, aortomyoplasty, and skeletal muscle ventricles. All parameters specified as programmable can be changed in a noninvasive manner (using a programming interface wand connected to a computer using the Windows 95/98 environment). Two new functions may be very useful clinically, based on experimental research. 1. Work-rest regimen. The LD-PACE II is able to deliver alternating periods of muscle contractions and rest. Work and rest periods may be programmed independently between 1 and 120 minutes in increments of 1 minute. The work-rest regimen may be useful clinically if muscle contractions are needed for cardiac assist postoperatively. 2. Night/day regimen. This feature allows for a change in the ratio of muscle contractions according to a patient's activity level. During the day the cardiosynchronization ratio may be set from 1:1 to 1:4, and during the night it may be set for 1:8 to 1:16. This allows the muscle to have a long rest period, prevents overuse, and prolongs battery life. These two new features make this cardiomyostimulator very attractive for cardiomyoplasty in particular. The addition of the work-rest and night-day regimens allow the muscle to rest for periods during the day to prevent overuse, subsequent damage, and potential atrophy.


Subject(s)
Cardiomyoplasty/instrumentation , Heart-Assist Devices , Heart/physiology , Pacemaker, Artificial , Humans , Myocardial Contraction , Prosthesis Design
5.
Rev Clin Esp ; 195(3): 160-3, 1995 Mar.
Article in Spanish | MEDLINE | ID: mdl-7754150

ABSTRACT

The increase in the incidence of tuberculosis infection in the last few years has caused a recurrence of atypical clinical forms, as well as the development of associations and uncommon complications during the clinical course, which include the adult respiratory distress syndrome (ARDS) and septic shock. Three patients with ARDS are here reported; two patients had findings of septic shock and negative serology to human immunodeficiency virus and the only etiological agent documented was M. tuberculosis. The three patients required hemodynamic support and two of them mechanical ventilation. None of the patients survived the episode. Tuberculosis, particularly the disseminated forms, should be considered as possible etiology in high risk patients with septic shock, ARDS or both.


Subject(s)
Respiratory Distress Syndrome/etiology , Shock, Septic/etiology , Tuberculosis, Miliary/complications , Tuberculosis, Pulmonary/complications , Adult , Aged , Aged, 80 and over , Fatal Outcome , Female , Humans , Lung/pathology , Male , Middle Aged , Respiratory Distress Syndrome/diagnosis , Respiratory Distress Syndrome/pathology , Shock, Septic/diagnosis , Shock, Septic/pathology , Tuberculosis, Miliary/pathology , Tuberculosis, Pulmonary/pathology
7.
Rev Clin Esp ; 194(2): 75-80, 1994 Feb.
Article in Spanish | MEDLINE | ID: mdl-8008943

ABSTRACT

Provided here are the descriptions of 18 patients with focal infections caused by Salmonella spp no-typhi occurring in a period of seven years at the Puerta de Hierro Clinic. In all cases, there was at least one local factor, treatment, or underlying illness associated with decreased resistance to infection. Antecedents of severe gastroenteritis were found in seven cases (38 percent). Eighty-three percent had previous or concomitant bacteremia caused by the same serotype of Salmonella isolated in the focal infection. S. enteritidis was the most prevalent serotype (66 percent). The most common localizations were plueropulmonary (5), osteoarticular (5), and intravascular (3). Relapsing infection was demonstrated in five cases. There was 28 percent mortality. Statistically, age greater than 65 years and the absence of surgical intervention were associated with a worse prognosis.


Subject(s)
Salmonella Infections , Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Retrospective Studies , Salmonella/isolation & purification , Salmonella Infections/classification , Salmonella Infections/drug therapy , Salmonella Infections/mortality
8.
Nephron ; 68(2): 262-4, 1994.
Article in English | MEDLINE | ID: mdl-7830868

ABSTRACT

The syndrome of inappropriate secretion of antidiuretic hormone is a common consequence of neurologic and pulmonary infections as well as drug intake and many other clinical situations. Its association with herpes varicella-zoster virus infections is scarcely reported in the literature. It generally appears in immunosuppressed patients suffering from serious underlying diseases. There are also a few cases of syndrome of inappropriate secretion of antidiuretic hormone related to vidarabine use. We report the case of a man infected by human immunodeficiency virus who developed a disseminated herpes varicella-zoster virus infection and symptoms due to hyponatremia caused by antidiuretic hormone excess. The patient was cured with saline hypertonic infusion, water restriction, and intravenous administration of acyclovir. To the best of our knowledge, this is the first case of this association in a human immunodeficiency virus infected patient. We propose the use of acyclovir instead of vidarabine in the management of these situations.


Subject(s)
AIDS-Related Opportunistic Infections/complications , Acquired Immunodeficiency Syndrome/complications , HIV-1 , Herpes Zoster/complications , Inappropriate ADH Syndrome/complications , AIDS-Related Opportunistic Infections/drug therapy , Acyclovir/therapeutic use , Adult , Herpes Zoster/drug therapy , Humans , Hyponatremia/complications , Male , Syndrome
9.
Enferm Infecc Microbiol Clin ; 10(10): 576-80, 1992 Dec.
Article in Spanish | MEDLINE | ID: mdl-1292598

ABSTRACT

BACKGROUND: Tuberculous meningitis accounts for 5% to 12% of all extrapulmonary tuberculosis cases in western-hemisphere population non infected by HIV virus, and carries a high mortality rate. METHODS: We analyze retrospectively 21 patients with tuberculous meningitis in HIV negative patients seen from 1975 to 1989, with emphasis on clinical, laboratory and therapeutic features. RESULTS: In 48% of cases there were not typical meningeal signs, and 61% of patients showed neurological focal signs and/or seizures. CSF examination revealed a clear fluid with high cell counts (mostly lymphocytes), high protein and low sugar levels in 67% of cases. However, the microbiologic examination had a low yield of diagnosis (33%). The clinical course is prolonged, and treatment is usually delayed. Morbidity and mortality were high (34% and 10% of cases). In this study, the use of steroids did not show a significant reduction in mortality nor in neurological sequelae. CONCLUSION: Tuberculous meningitis in HIV negative patients is a chronic infection, without meningeal signs in most cases and linked to a high rate of neurological defects. The microbiologic tests have low yield of diagnosis. Steroid drugs seem to be indicated only if there are additional complications.


Subject(s)
Tuberculosis, Meningeal/epidemiology , Adolescent , Adrenal Cortex Hormones/therapeutic use , Adult , Aged , Aged, 80 and over , Antitubercular Agents/therapeutic use , Biomarkers , Child , Child, Preschool , Disease Susceptibility/immunology , Female , Humans , Incidence , Male , Middle Aged , Nervous System Diseases/etiology , Retrospective Studies , Spain/epidemiology , Tuberculosis, Meningeal/cerebrospinal fluid , Tuberculosis, Meningeal/complications , Tuberculosis, Meningeal/diagnosis , Tuberculosis, Meningeal/drug therapy
10.
Diagn Microbiol Infect Dis ; 15(8): 703-6, 1992.
Article in English | MEDLINE | ID: mdl-1478051

ABSTRACT

Cutaneous aspergillosis is generally associated with immunosuppression, burns, and major trauma. Most cases are acquired by direct inoculation, although cutaneous involvement does occasionally occur with disseminated disease. Surgical wound infections caused by Aspergillus species are very unusual and to our knowledge have not been described in the setting of organ transplantation. We describe two liver transplant recipients who developed wound aspergillosis during a nosocomial outbreak of Aspergillus infection. Infection developed in the second and fourth postoperative week respectively, and in both cases wound appearance mimicked necrotizing fasciitis. Both patients died despite local debridement and antifungal therapy with amphotericin B. Aspergillus must be added to the list of potential pathogens of surgical wounds, especially in the setting of organ transplantation.


Subject(s)
Aspergillosis/microbiology , Aspergillus fumigatus/isolation & purification , Liver Transplantation , Surgical Wound Infection/microbiology , Amphotericin B/therapeutic use , Aspergillosis/therapy , Combined Modality Therapy , Debridement , Female , Humans , Male , Middle Aged , Surgical Wound Infection/therapy
SELECTION OF CITATIONS
SEARCH DETAIL
...