90 research outputs found
Risk of urinary bladder cancer: a case-control analysis of industry and occupation
<p>Abstract</p> <p>Background</p> <p>Uncertainty remains about urinary bladder cancer (UBC) risk for many occupations. Here, we investigate the association between occupation, industry and UBC.</p> <p>Methods</p> <p>Lifetime occupational history was collected by in-person interview for 604 newly diagnosed UBC patients and 604 cancer-free controls. Each job title was assigned a two-digit industry code and a three-digit occupation code. Odds ratios (ORs) for UBC associated with ever being employed in an industry or occupation were calculated by unconditional logistic regression adjusting for age, gender and smoking status. We also examined UBC risk by duration of employment (>0 to <10, ≥10 years) in industry or occupation.</p> <p>Results</p> <p>Significantly increased risk of UBC was observed among waiters and bartenders (OR 2.87; 95% CI 1.05 to 7.72) and occupations related to medicine and health (OR 2.17; 95% CI 1.21 to 3.92), agricultural production, livestock and animal specialties (OR 1.90; 95% CI 1.03 to 3.49), electrical assembly, installation and repair (OR 1.69; 95% CI 1.07 to 2.65), communications (OR 1.74; 95% CI 1.00 to 3.01), and health services (OR 1.58; 95% CI 1.02 to 2.44). For these occupations we also observed a significant excess risk of UBC for long-term work (i.e. ≥10 years), with the exception of waiters and bartenders. Employment for 10 years or more was associated with increased risk of UBC in general farmers (OR 9.58; 95% CI 2.18 to 42.05), agricultural production of crops (OR 3.36; 95% CI 1.10 to 10.27), occupations related to bench working (OR 4.76; 95% CI 1.74 to 13.01), agricultural, fishery, forestry & related (OR 4.58; 95% CI 1.97 to 10.65), transportation equipment (OR 2.68; 95% CI 1.03 to 6.97), and structural work (OR 1.85; 95% CI 1.16 to 2.95).</p> <p>Conclusions</p> <p>This study provides evidence of increased risk of UBC for occupations that were previously reported as at-risk. Workers in several occupation and industry groups have a significantly higher risk of UBC, particularly when duration of employment is 10 years or more.</p
Mitochondrial dysfunction and biogenesis: do ICU patients die from mitochondrial failure?
Mitochondrial functions include production of energy, activation of programmed cell death, and a number of cell specific tasks, e.g., cell signaling, control of Ca2+ metabolism, and synthesis of a number of important biomolecules. As proper mitochondrial function is critical for normal performance and survival of cells, mitochondrial dysfunction often leads to pathological conditions resulting in various human diseases. Recently mitochondrial dysfunction has been linked to multiple organ failure (MOF) often leading to the death of critical care patients. However, there are two main reasons why this insight did not generate an adequate resonance in clinical settings. First, most data regarding mitochondrial dysfunction in organs susceptible to failure in critical care diseases (liver, kidney, heart, lung, intestine, brain) were collected using animal models. Second, there is no clear therapeutic strategy how acquired mitochondrial dysfunction can be improved. Only the benefit of such therapies will confirm the critical role of mitochondrial dysfunction in clinical settings. Here we summarized data on mitochondrial dysfunction obtained in diverse experimental systems, which are related to conditions seen in intensive care unit (ICU) patients. Particular attention is given to mechanisms that cause cell death and organ dysfunction and to prospective therapeutic strategies, directed to recover mitochondrial function. Collectively the data discussed in this review suggest that appropriate diagnosis and specific treatment of mitochondrial dysfunction in ICU patients may significantly improve the clinical outcome
Chronic obstructive pulmonary disease guidelines in Europe: a look into the future.
Clinical practice guidelines are ubiquitous and are developed to provide recommendations for the management of many diseases, including chronic obstructive pulmonary disease. The development of these guidelines is burdensome, demanding a significant investment of time and money. In Europe, the majority of countries develop their own national guidelines, despite the potential for overlap or duplication of effort. A concerted effort and consolidation of resources between countries may alleviate the resource-intensity of maintaining individual national guidelines. Despite significant resource investment into the development and maintenance of clinical practice guidelines, their implementation is suboptimal. Effective strategies of guideline dissemination must be given more consideration, to ensure adequate implementation and improved patient care management in the future.This article is freely available via Open Access. Click on the Additional Link above to access the full-text via the publisher's site
Critical analysis and validation of lymph node density as prognostic variable in urothelial carcinoma of bladder.
OBJECTIVE: To validate the prognostic relevance of lymph node density (LND) and
identify its optimal cut-points in a large international multicenter series of
patients treated with radical cystectomy (RC) for invasive bladder cancer.
METHODS: From 1993 to 2005, 4,430 bladder cancer patients who underwent RC
without neoadjuvant chemotherapy were reviewed; of these, 1,038 were pN+M0
disease and form the basis of this report. RESULTS: Median age of patients was 67
years with median follow-up in survivors of 33 months. Overall, 5-year DSS
estimate was 36%. Median number of lymph nodes removed was 18 (IQR, 11-32),
median number of positive lymph nodes was 2 (IQR, 1-5), and median LND was 14.3%
(IQR, 6.67-33.3%). LND as continuous variable was a stronger prognostic factor
for DSS in patients that underwent a more extensive PLND (P < 0.001). HR for
inverse association of LND with DSS increased incrementally with increasing LND
cut-points. Categorizing LND into quintiles revealed strong tertiary distribution
of risk based on LND 41% with cumulative 5-year DSS of 47%, 36%,
and 21%, respectively (P < 0.001). When patients were stratified by adjuvant
chemotherapy, LND remains independently prognostic in patients who received
adjuvant chemotherapy as well as those who did not. CONCLUSION: Lymph node
density is prognostic in bladder cancer patients who undergo a more extensive
PLND and remains prognostic even when adjuvant chemotherapy is used. Prognostic
value of LND is best represented as a continuum of risk and LND <6% represents
the best possible outcome in patients with nodal disease
The effectiveness of off-protocol adjuvant chemotherapy for patients with urothelial carcinoma of the urinary bladder.
PURPOSE: The role of adjuvant chemotherapy for patients with high-risk urothelial
carcinoma of the bladder (UCB) is not well defined. Here we address the value of
adjuvant chemotherapy in patients undergoing radical cystectomy for UCB in an
off-protocol routine clinical setting.
EXPERIMENTAL DESIGN: We collected and analyzed data from 11 centers contributing
retrospective cohorts of patients with UCB treated with radical cystectomy
without neoadjuvant chemotherapy. Patients were grouped into quintiles based on
their risk of disease progression using estimates from a fitted multivariable Cox
proportional hazards model. The association of adjuvant chemotherapy with
survival was explored across separate quintiles.
RESULTS: The cohort consisted of 3,947 patients, 932 (23.6%) of whom received
adjuvant chemotherapy. Adjuvant chemotherapy was independently associated with
improved survival (hazard ratio, 0.83; 95% confidence interval, 0.72-0.97%, P =
0.017). However, the effect of adjuvant chemotherapy was significantly modified
by the individual's risk of disease progression such that an increasing benefit
from adjuvant chemotherapy was seen across higher-risk subgroups (P < 0.001).
There was a significant improvement in survival between the treated and
nontreated patients in the highest-risk quintile (hazard ratio, 0.75; 95%
confidence interval, 0.62-0.90; P = 0.002). This group was characterized by an
estimated 32.8% 5-year probability of cancer-specific survival, with 86.6% of
patients having both advanced pathologic stage (> or =T(3)) and nodal
involvement.
CONCLUSION: Adjuvant chemotherapy is associated with a significant improvement in
survival for patients treated in an off-protocol clinical setting. Selective
administration in patients at the highest risk for disease progression, such as
those with advanced pathologic stage and nodal involvement, may optimize the
therapeutic benefit of adjuvant chemotherapy
International validation of the prognostic value of lymphovascular invasion in patients treated with radical cystectomy.
OBJECTIVE: To externally validate the prognostic value of lymphovascular invasion
(LVI) in a large international cohort of patients treated with radical cystectomy
(RC) for urothelial carcinoma of the bladder (UCB).
PATIENTS AND METHODS: We collected data from 4257 patients treated with RC and
pelvic lymphadenectomy for UCB, without neoadjuvant chemotherapy, at 12 centres.
LVI was defined as presence of nests of tumour cells within an endothelium-lined
space.
RESULTS: LVI was detected in 1407 patients (33.1%); the proportion of LVI
increased with advancing stage, higher grade, soft-tissue surgical margin
involvement, and lymph node metastasis (P < 0.001 for all). In standard
multivariate models, LVI was associated with both disease recurrence (hazard
ratio 1.43, P < 0.001) and cancer-specific mortality (1.45, P < 0.001). In the
entire cohort, adding LVI to a base model that included standard features
improved only minimally its predictive accuracy for both recurrence and
cancer-specific mortality (by 1.1% and 1.2%, respectively). In 3122 patients with
negative lymph nodes, LVI remained independently associated with and improved the
predictive accuracy of the standard predictors for recurrence (hazard ratio 1.68,
P < 0.001; +2.3%) and cancer-specific mortality (1.70, P < 0.001; +2.4%). By
contrast, in 1071 node-positive patients, LVI only marginally improved the
prediction of cancer-specific recurrence (hazard ratio 1.20, P < 0.001; +0.2%)
and survival (1.23, P < 0.001; +0.5%).
CONCLUSIONS: LVI is strongly associated with clinical outcome in node-negative
patients treated with RC. The assessment of LVI might help to identify patients
who could benefit from adjuvant therapy after RC. After confirmation in different
populations, LVI should be included in the staging of UCB
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