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1.
Am J Trop Med Hyg ; 64(3-4): 214-21, 2001.
Article in English | MEDLINE | ID: mdl-11442220

ABSTRACT

A retrospective analysis of the discharge records of 186,131 inpatients admitted to six Ugandan hospitals during 1992-1998 was performed to describe the disease patterns and trends among the population of Northern Uganda. In all hospitals, malaria was the leading cause of admission and the frequency of admissions for malaria showed the greatest increase. Other conditions, such as malnutrition and injuries, mainly increased in the sites affected by civil conflict and massive population displacement. Tuberculosis accounted for the highest burden on hospital services (approximately one-fourth of the total bed-days), though it showed a stable trend over time. A stable trend was also observed for acquired immunodeficiency syndrome (AIDS), which is in contrast to the hypothesis that AIDS patients have displaced other patients in recent years. In conclusion, preventable and/or treatable communicable diseases, mainly those related to poverty and poor hygiene, represent the leading causes of admission and death, reflecting the socioeconomic disruption in Northern Uganda.


Subject(s)
Acquired Immunodeficiency Syndrome/epidemiology , Hospitalization/statistics & numerical data , Hospitalization/trends , Hospitals, District/statistics & numerical data , Poverty , Humans , Malaria/epidemiology , Medical Records , Poverty/statistics & numerical data , Retrospective Studies , Tuberculosis, Pulmonary/epidemiology , Uganda/epidemiology
2.
East Afr Med J ; 78(3): 165-6, 2001 Mar.
Article in English | MEDLINE | ID: mdl-12002060

ABSTRACT

Tumoral calcinosis (TC) is a rare disease of obscure aetiology. In its classic form, it is characterised by solitary or multiple large foci of mineralisation in the soft tissue adjacent to the bone around large joints in the absence of disorders of calcium metabolism and visceral calcification. A case is presented of TC in a 75-year old Kenyan woman.


Subject(s)
Calcinosis/pathology , Hip , Soft Tissue Neoplasms/pathology , Aged , Calcinosis/diagnostic imaging , Calcinosis/surgery , Female , Humans , Radiography , Soft Tissue Neoplasms/diagnostic imaging , Soft Tissue Neoplasms/surgery
5.
Lung Cancer ; 14(2-3): 353-60, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8794416

ABSTRACT

Vinorelbine (VNB) and cisplatin (CDDP) combination regimen was found active in the treatment of advanced non-small cell lung cancer (NSCLC) patients, but significant toxicity was observed. We evaluated the activity and toxicity of this combination administered at lower doses than previously reported. From March 1992 to March 1994, 99 patients (pts) were enrolled in a multicentric Phase II study and received intravenous CDDP at 80 mg/m2 on day 1, associated with intravenous VNB at 25 mg/m2 on days 1 and 8. Cycles were repeated every 3 weeks. The reduced doses led to a consistently lower myelotoxicity (8% Grade III-IV leukopenia) in comparison to two related Phase III studies, recently published. Conversely, the incidence of neurological toxicity was superimposable. Considering all eligible patients, the overall response rate was 28.3%, and this is similar to the results commonly observed employing the most active CDDP containing regimens. In conclusion, CDDP and VNB combination chemotherapy at the schedule performed in the present study led to a reduction of hematologic toxicity, while an appreciable activity was maintained.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Non-Small-Cell Lung/drug therapy , Lung Neoplasms/drug therapy , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Carcinoma, Non-Small-Cell Lung/surgery , Cisplatin/administration & dosage , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Humans , Lung Neoplasms/surgery , Male , Middle Aged , Vinblastine/administration & dosage , Vinblastine/analogs & derivatives , Vinorelbine
6.
Tumori ; 81(4): 299-301, 1995.
Article in English | MEDLINE | ID: mdl-8540131

ABSTRACT

The demonstrated association with hematologic neoplasms may partially account for the poor survival of patients with mediastinal nonseminomatous germ cell tumors (MNSGCT) compared to patients with testicular and retroperitoneal counterparts. It has been shown that the median interval from the diagnosis of MNSGCT to the diagnosis of the hematologic disorders is 6 months, which contrasts sharply with the average time of 2 to 3 years for the development of therapy-related leukemias. The 2 cases herein described, 1 male and 1 female, developed acute M2 leukemia 4 and 2 years after the diagnosis of MNSGCT. In the second patient (the first female ever described), we cannot exclude a pathogenetic role of the PEB regimen (platinum, etoposide, bleomicin), even though the total dose of etoposide administered has been demonstrated to have a mild leukemogenic potential. This is not the case of the first patient, who did not receive adjuvant chemotherapy after the radical resection of primary MNGSCT and developed the hematologic disorder a few months after local recurrence. In conclusion, the time elapsed from chemotherapy administration does not discriminate the hematologic neoplasms associated to MNGSCT from those related to therapy.


Subject(s)
Carcinoma, Embryonal/complications , Leukemia, Myeloid, Acute/complications , Mediastinal Neoplasms/complications , Teratocarcinoma/complications , Teratoma/complications , Adolescent , Adult , Female , Humans , Male
7.
Tumori ; 81(3): 164-8, 1995.
Article in English | MEDLINE | ID: mdl-7571021

ABSTRACT

AIMS AND BACKGROUND: The Childhood Cancer Registry of Piedmont (RTI) periodically updates the life status of each registered child. Given its size, the RTI is the major (albeit geographically limited) Italian source of population-based survival rates of cancer in children. The present report describes time trends in survival of children with acute lymphocytic leukemia (ALL). METHODS: During 1970-87, 429 residents in Piedmont aged 0-14 were diagnosed as having ALL: they have been followed up until 1991. RESULTS: Five-year survival rates increased from 21% to 72% for children diagnosed ALL respectively in 1970-72 and 1985-87. Major improvements occurred up to the mid-seventies and again between cases diagnosed in the early and late eighties. Improvement in survival was statistically significant for children belonging to classes comprised between 2 and 10 years of age at diagnosis. Period of diagnosis was unrelated to probability of survival among the 13 cases diagnosed ALL at age 0. Survival was unrelated to sex, even in the early seventies and even after consideration of children dying more than 5 years after diagnosis. Between 1976-81 and 1982-87, an improvement in survival was found in all categories of WBC count at diagnosis: the ratio between the two estimates was somewhat higher for children with more than 50,000 WBC/mm3 at diagnosis than for other children. CONCLUSIONS: Present data are compared with those resulting from other population-based series: this exercise can be useful for an overall evaluation of delivery of cancer therapy at the population basis.


Subject(s)
Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality , Adolescent , Age Distribution , Child , Child, Preschool , Female , Humans , Infant , Italy/epidemiology , Leukemia/epidemiology , Male , Registries , Sex Distribution , Survival Analysis , Survival Rate/trends
9.
Drugs ; 43 Suppl 3: 6-10, 1992.
Article in English | MEDLINE | ID: mdl-1380432

ABSTRACT

The efficacy and tolerability of tropisetron in preventing cisplatin-induced nausea and vomiting was studied in 2 open trials and compared with the efficacy and tolerability of metoclopramide plus lorazepam in a randomised crossover trial. In the first study, tropisetron 10mg was administered intravenously over 15 minutes before the cisplatin infusion and a second 10mg dose was given after the 60-minute infusion of cisplatin (greater than 50 mg/m2) in 54 patients with advanced cancers, for a total of 165 courses. Good responses for nausea and vomiting were recorded in 83.0% and 87.9% of courses, respectively, with complete protection from nausea and vomiting in 44.8% and 66.1% of courses, respectively. In the second study in 25 patients whose characteristics and cisplatin schedule were comparable with those of the first study, very similar results were achieved in 104 courses of chemotherapy, despite a reduction in tropisetron dose to a single 5mg intravenous infusion 15 minutes before cisplatin. The efficacies of intravenous tropisetron 5mg and metoclopramide 2 mg/kg plus lorazepam administered 15 minutes before cisplatin in preventing acute and delayed nausea and vomiting were compared in a randomised crossover study involving 20 patients. Tropisetron was significantly superior (p less than 0.001) in controlling both acute and delayed (day 1) symptoms. In all studies, the tolerability of tropisetron was excellent. The most frequent side effect was mild to moderate headache, occurring in 5 to 7% of patients. In conclusion, our experience suggests that tropisetron is an effective and well tolerated antiemetic drug that improves the quality of life of cancer patients administered highly emetogenic chemotherapy regimens.


Subject(s)
Antiemetics/therapeutic use , Cisplatin/adverse effects , Indoles/therapeutic use , Nausea/drug therapy , Neoplasms/drug therapy , Vomiting/drug therapy , Adult , Aged , Cisplatin/therapeutic use , Female , Humans , Lorazepam/therapeutic use , Male , Metoclopramide/therapeutic use , Middle Aged , Nausea/chemically induced , Single-Blind Method , Tropisetron , Vomiting/chemically induced
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