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1.
Rev. invest. clín ; 58(1): 34-38, ene.-feb. 2006. ilus, tab
Article in Spanish | LILACS | ID: lil-632334

ABSTRACT

In two institutions in México, twelve patients were given a second allogeneic stem cell transplantation, using the "Mexican" non-myeloablative preparative regimen. Eight had a malignant condition (six acute leukemias, one myelofibrosis and one myelodysplasia), eleven individuals were allografted twice from the same donor and in one case, cells from two different umbilical cords were used. The median time to conduct the second allograft after the first one was 6 months (range 1-41). The five patients who failed to engraft after the first transplant failed also to engraft after the second one; all of them had been heavily transfused. Only three patients were successfully rescued with the second transplant, two with acute leukemia and one with aplastic anemia. Seven patients are alive 10-41 months (median 35) after the second transplant, but only three (25%) remain disease-free. The 52-month overall survival (SV) of the patients is 58%, whereas the median overall SV has not been reached, being above 52 months. Conducting a second allograft may be useful to rescue some individuals relapsing after a first hematopoietic allotransplant.


En dos instituciones en México se llevaron a cabo doce segundos trasplantes de células hematopoyéticas usando el "método mexicano" de acondicionamiento no mieloablativo. Ocho pacientes tenían una enfermedad maligna (seis leucemias agudas, una mielofibrosis y una mielodisplasia). Once sujetos se retrasplantaron del mismo donador y en un caso se emplearon células hematopoyéticas de dos diferentes cordones umbilicales. La mediana del tiempo transcurrido entre los dos trasplantes fue de seis meses (rango 1 a 41). Los cinco pacientes que no se injertaron con el primer trasplante tampoco se injertaron con el segundo; todos ellos habían sido multitransfundidos antes de los trasplantes. Sólo tres pacientes se pudieron rescatar con el segundo trasplante, dos con leucemia aguda y uno con anemia aplástica. Siete pacientes están vivos 10 a 41 meses (mediana 35) después del segundo trasplante, pero sólo tres (25%) se encuentran libres de enfermedad. La supervivencia (SV) global a 52 meses es de 58%, en tanto que la mediana de SV no se ha alcanzado y es mayor de 52 meses. Hacer un segundo trasplante hematopoyético puede rescatar a algunos pacientes quienes recaen después de un trasplante de médula ósea.


Subject(s)
Adult , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Cord Blood Stem Cell Transplantation , Peripheral Blood Stem Cell Transplantation , Transplantation Conditioning/methods , Acute Disease , Anemia, Aplastic/surgery , Cohort Studies , Cord Blood Stem Cell Transplantation/statistics & numerical data , Disease-Free Survival , Health Care Costs , Hospitals, University/statistics & numerical data , Hospitals/statistics & numerical data , Leukemia/surgery , Mexico , Neural Tube Defects/surgery , Osteopetrosis/surgery , Peripheral Blood Stem Cell Transplantation/statistics & numerical data , Primary Myelofibrosis/surgery , Recurrence , Red-Cell Aplasia, Pure/surgery , Reoperation/statistics & numerical data , Survival Analysis , Treatment Outcome , Thalassemia/surgery , Transplantation, Homologous/statistics & numerical data
2.
Annals of King Edward Medical College. 2005; 11 (4): 507-509
in English | IMEMR | ID: emr-69719

ABSTRACT

The study aims at investigating the complications associated with splenectomy in thalassemic patients It was a prospective clinical study. Sixty Splenectomies were preformed electively after pre-operative preparation in Sir Ganga Ram Hospital, Lahore during the year Jan 2003 to Sep 2005. Complications were categorized into per-operative, early post-operative and late complications. The frequency of per-operative complications was 3%, early post-operative complications were 10% and late complications were 1.6%. The rate of complications has decreased markedly as the patients are well prepared and improved post operative carp has also reduced the post-operative complications. With good perioperative management, splenectomy in children with massive splenomegaly is both safe and effective


Subject(s)
Humans , Male , Female , Thalassemia/surgery , Intraoperative Complications , Postoperative Complications , Splenomegaly/etiology , Splenomegaly/surgery , Vaccination , Hypersplenism , Hematopoiesis, Extramedullary
3.
Article in English | IMSEAR | ID: sea-44498

ABSTRACT

Hemodynamic changes of 50 thalassemic children who had splenectomy under general anesthesia were compared to 40 identical patients who, in addition, received intravenous furosemide 1 mg/kg immediate preoperation. During the anesthetic process, both groups showed a significant increase of heart rate, systolic and diastolic blood pressure more than the preanesthetic values. Hemodynamic variables in the furosemide group declined toward normal range on termination of anesthesia, whereas, the other group's variables were still significantly higher than their control. During the first 24 hours postoperatively, 20 per cent of the furosemide group had blood pressure rising higher than 130/90 mmHg, while 18 per cent was observed in the other group. Antihypertensive drugs were given to reduce the blood pressure in both groups. None of the patients in the furosemide group demonstrated any abnormal neurological symptoms, but 3 out of 50 patients in the other group developed convulsion. We, therefore, conclude that circulatory volume reduction with furosemide does not prevent hypertension during perioperative splenectomy in thalassemic children. However, it's role in prevention of neurological abnormalities needs to be further investigated.


Subject(s)
Chi-Square Distribution , Child , Furosemide/administration & dosage , Hemodynamics/drug effects , Humans , Hypertension/drug therapy , Injections, Intravenous , Postoperative Complications/prevention & control , Splenectomy/adverse effects , Thalassemia/surgery , Treatment Outcome
6.
Article in English | IMSEAR | ID: sea-41361

ABSTRACT

Sixty-nine children with beta-thalassemia/E disease, hemoglobin H disease and beta-thalassemia major who were followed for at least 2 years before and after splenectomy were studied retrospectively for the results of the splenectomy. It was found that. 1. The hematocrit increased significantly in beta-thalassemia/E from 18 to 22 per cent, in hemoglobin H disease from 21 to 34 per cent and in beta-thalassemia major from 14-15 to 18-19 per cent. 2. The requirement of blood transfusions per year decreased significantly from 6 to 2 times in beta-thalassemia/E, 10 to 4-5 times in beta-thalassemia major and no transfusion was needed in hemoglobin H disease. 3. Postoperatively, there was a significant increase (p less than 0.05) in the liver size by the third year in beta-thalassemia/Hb E disease, and in the first year in beta-thalassemia major but the liver-size was decreased significantly by the fourth year in hemoglobin H disease. 4. Within 2 years postoperatively, the growth velocity in height kept up with their presplenectomy period in hemoglobin H and beta-thalassemia major (except two cases). The growth in weight kept up with their presplenectomy period in 40/49 cases (81.63%) in beta-thalassemia/Hb E but there was no change in the weight velocity in hemoglobin H and beta-thalassemia major. 5. There were 5 cases with immediate postoperative complications. Three cases had pneumonia, one case had septicaemia and one case had bleeding at the operative wound. Episodes of URI decreased in the post-operative period. Five cases of bacteremia developed within 6 years post-splenectomy.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Female , Humans , Male , Postoperative Complications , Retrospective Studies , Splenectomy , Thalassemia/surgery
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