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In particular, the change in distribution between implants and skin was, after the use of the drug, more dramatic. The use of non-drug therapies was responsible for this. The use of phosphate-based medications was associated with progressive renal failure with improved cardiac functionality (more than 90%), pulmonary inflammation (\> 70%), fibrosis (\> 50%), and alveolar lesions (compared to \<5% predicted). The use of specific drugs in procedures in recovery of function had a similar pattern as systemic infection with a peak incidence of infections occurring 48-84 hours after the administration of the therapeutic drugs \[see [Figure 6\].\]. However, there was no significant difference in mortality among the different intervention groups in terms of the administration pattern (\> 65-69 hours). Despite the major improvement, several large-scale studies were carried out to the use of phospho-selective agents, although neither the non-drug nor the phospho-drug therapy did significantly improve the outcomes or the risk of adverse reactions \[see [Figure 7\].\] As a result, the non-drug therapies were responsible for an average loss of 4 months. This increased safety was associated with a considerably higher percentage of patients to be taking other medications (48%, 37% and 21% after the use of the non-drug therapy respectively). In particular, two patients with systemic hemolysis in the prior week discontinued the non-drug therapy due to other complications.
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This might have led to improved outcomes. [Figure 7\]. DIAGNOSIS