Central vein stenosis (CVS) has been associated with subclavian (SCV) catheter insertions. The prevalence of CVS in the current era with minimal use of SCV catheters is unknown. Furthermore, the prevalence of CVS in patients with access problems has not been previously described to our knowledge. We evaluated 235 prevalent patients on hemodialysis (HD), and, of these, 133 underwent venography for access related concerns over a 14 month period. Of these 133 patients, 55 (41%) had evidence of significant CVS on venogram. Patients with CVS had a longer duration on HD (43 +/- 12 months vs. 34 +/- 15 months, p = 0.018) and a history of a previous HD catheter insertion (52/55 patients vs. 59/78 patients, p = 0.0039). There were only 18 patients with a subclavian catheter insertion. In those with any history of previous HD catheter insertion, multivariate analysis demonstrated that number of catheters remains a significant factor (OR 2.69, p = 0.0004) even after excluding those subclavian insertions. This study demonstrates that CVS occurs in almost half of the patients with access problems undergoing venography. We confirm the important contribution of central vein cannulation to CVS and show that, despite minimizing subclavian catheter insertion, CVS remains a relatively common occurrence. Thus further studies should attempt to determine the true incidence of this problem and ultimately address the optimal treatment strategies.

AimsAnecdotal observations suggest that sub-clinical electrophysiological manifestations of arrhythmogenic right ventricular cardiomyopathy (ARVC) develop before detectable structural changes ensue on cardiac imaging. To test this hypothesis, we investigated a murine model with conditional cardiac genetic deletion of one desmoplakin allele (DSP ±) and compared the findings to patients with non-diagnostic features of ARVC who carried mutations in desmoplakin.Methods and resultsMurine: the DSP (±) mice underwent electrophysiological, echocardiographic, and immunohistochemical studies. They had normal echocardiograms but delayed conduction and inducible ventricular tachycardia associated with mislocalization and reduced intercalated disc expression of Cx43. Sodium current density and myocardial histology were normal at 2 months of age. Human: ten patients with heterozygous mutations in DSP without overt structural heart disease (DSP+) and 12 controls with supraventricular tachycardia were studied by high-density electrophysiological mapping of the right ventricle. Using a standard S1–S2 protocol, restitution curves of local conduction and repolarization parameters were constructed. Significantly greater mean increases in delay were identified particularly in the outflow tract vs. controls (P< 0.01) coupled with more uniform wavefront progression. The odds of a segment with a maximal activation–repolarization interval restitution slope >1 was 99% higher (95% CI: 13%; 351%, P= 0.017) in DSP+ vs. controls. Immunostaining revealed Cx43 mislocalization and variable Na channel distribution.ConclusionDesmoplakin disease causes connexin mislocalization in the mouse and man preceding any overt histological abnormalities resulting in significant alterations in conduction–repolarization kinetics prior to morphological changes detectable on conventional cardiac imaging. Haploinsufficiency of desmoplakin is sufficient to cause significant Cx43 mislocalization. Changes in sodium current density and histological abnormalities may contribute to a worsening phenotype or disease but are not necessary to generate an arrhythmogenic substrate. This has important implications for the earlier diagnosis of ARVC and risk stratification.

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Rationale: For developed countries there has been a significant, fast-paced rise in migrant populations. Society has a vested interest in these members of the population being aware of their risk of a communicable disease, and seeking health screening. Currently, screening interventions rely heavily upon socio-cognitive, majority-orientated theories that may not account for cultural factors differentially affecting migrant groups. Objective: To develop an inductive theory to explain processes underlying the readiness of migrants to engage in health screening. In understanding why some groups engage in screening more than others we examined the U.K. South Asian population, and screening for hepatitis B and C. Method: We conducted eight focus groups with first-generation South Asian migrants. Results were analysed using a three stage, process-orientated methodology based on the principles of grounded theory, with the explicit aim of developing new theory. Results: A theory of 'readiness to engage' is presented; embedded within participants' testimonies. The results highlight personal identity, family identity and the collective identity of the South Asian community; with family and community conceptualised as a singular force, acting to either silence or support. Identity issues and screening readiness were also strongly related to interactions with the healthcare-system, with participants often feeling misidentified, misunderstood, or under personal threat. 2 Conclusions: Our theoretical model takes account of the complex, interlocking relationship between the individual, the community, and healthcare system, and provides practical implications for healthcare providers of screening interventions. Airhihenbuwa, C. O. (1990). A conceptual model for culturally appropriate health education programs in developing countries.