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Outcomes complement

Even though outcome measures may fail to detect the intended effects, this does not automatically mean that regulation is ineffective it may be that this particular regulatory mechanism, although necessary, is unable to produce the intended outcomes alone. The challenge is to identify factors that will complement the regulatory mechanism in order to achieve the desired outcomes. [Pg.118]

With either type of dialysis, studies suggest that recovery of renal function is decreased in ARF patients who undergo dialysis compared with those not requiring dialysis. Decreased recovery of renal function may be due to hemodialysis-induced hypotension causing additional ischemic injury to the kidney. Also, exposure of a patient s blood to bioincompatible dialysis membranes (cuprophane or cellulose acetate) results in complement and leukocyte activation which can lead to neutrophil infiltration into the kidney and release of vasoconstrictive substances that can prolong renal dysfunction.26 Synthetic membranes composed of substances such as polysulfone, polyacrylonitrile, and polymethylmethacrylate are considered to be more biocompatible and would be less likely to activate complement. Synthetic membranes are generally more expensive than cellulose-based membranes. Several recent meta-analyses found no difference in mortality between biocompatible and bioincompatible membranes. Whether biocompatible membranes lead to better patient outcomes continues to be debated. [Pg.368]

Chiral a,/ -unsaturated A-acyloxazolidinones have been regarded as a complement for type I dienophile reagents. Evans et al.4 reported a Diels-Alder reaction promoted by dialkyl aluminum chloride. In this reaction, chiral a,/ -unsaturated A-acyloxazolidinones were used as highly reactive and diaster-eoselective dienophiles. The stereogenic outcome of the Diels-Alder adducts... [Pg.273]

Weng, W.K. and Levy, R., Expression of complement Inhibitors CD46, CD55, and CD59 on tumor cells does not predict clinical outcome after rituximab treatment in follicular non-Hodgkin lymphoma. Blood, 98, 1352-1357, 2001. [Pg.583]

During all phases of treatment, education, supportive therapy, and, at times, more specific types of psychotherapy are essential for a satisfactory outcome. For example, interpersonal therapy can complement adequate maintenance antidepressant treatment, possibly diminishing the frequency of episodes (see the section Role of Psychosocial Therapies in Chapter 7), and cognitive-behavioral techniques in combination with antiobsessive agents (e.g., clomipramine) can improve the quality of life for patients with obsessive-compulsive disorder, minimizing time spent on disabling rituals (see the section Obsessive-Compulsive Disorder in Chapter 13). [Pg.31]

Cynthia feels that health-related quality of life and patient satisfaction are important aspects of her clinic. She thinks that these outcomes can serve to complement the economic and clinical outcomes that she is reporting to the HMO and can further prove her case that the clinic is a valuable service to the heart failure patients. [Pg.481]

In the past, the outcome of a scientific debate depended to a large extent on the choice of decisive experiments, support by spectroscopic results, and the combination of many facts and details in an intricate puzzle. Nowadays, experimental observations are often complemented by data obtained from quantum chemical calculations. For example, it is now fully confirmed by... [Pg.231]

However, if D is slightly larger than D then A] < ii < A2 < 2 and Q is disconnected if either (a) A2 < S < 1x2 or (b) 1x2 < S hold. If (a) holds, then El and E2 are local attractors and the complement of the union of their basins of attraction has zero Lebesgue measure. In this case, the winner depends on how the chemostat is charged at / = 0 - that is, on the initial conditions. If (b) holds, then Eq,Ei,E2 are all local attractors and the complement of the union of their basins has zero Lebesgue measure. In this case, washout of all populations, competitive exclusion of X2 by Xi, and competitive exclusion of Xi by X2 are all possible outcomes, depending on the initial conditions. [Pg.40]

Our understanding of nature in general and polymers in particular is largely based on a combination of experience and models, Le. somehow simplified representations of reality. From experimentally derived experience we deduce models and from models we derive predictions about the outcomes of particular experiments, and so these two strands complement each other. Computer modelling is a relatively new third component which makes models less simplified and hence allows us to derive prediction for more complex situations, but also merges model and experience computer simulations are experienced as reality. [Pg.244]

Competition studies reported by Kuwajima, " which also complement the results of Nakai," illustrate the limitations of the 3-effect as a tool for predicting the outcome of vinylsilane-terminated cyclizations (Scheme 4). Acylium ion initiated cyclizations of (7a) and (7b) gave the expected cyclopentenones (8a) and (8b). However, compound (7c), upon treatment with titanium tetrachloride, gave exclusively the cyclopentenone proiduct (8c) arising fr the chemoselective addition on the 1,1-disubstituted alkene followed by protodesilylation of the vinylsilane. The reversal observed in the mode of addition may be a reflection of the relative stabilities of the carbocation intermediates. The internal competition experiments of Kuwajima indicate that secondary 3-silyl cations are generated in preference to secondary carbocations (compare Schemes 3 and 4), while tertiary carbocations appear to be more stable than secondary 3-silyl cari ations, as judged by the formation of compound (te). [Pg.584]

Figure 7-2 Control of the alternative complement pathway by activating surfaces. When complement component C3b binds to a surface, there exist two possible outcomes. Under normal conditions, when no activating surface is present (e g., if C3b has contacted normal tissue), sequential addition of blood cofactors H and I converts C3b into C3c, inactivating the complement protein. If an activating surface such as a microbe or damaged tissue is encountered, sequential addition of factors B and D drives the alternative pathway to the normal properdin (P) intermediate, and the complement cascade is triggered. The properdin-containing component (C3bBbP) feeds back to the beginning of the pathway, generating more C3. Figure 7-2 Control of the alternative complement pathway by activating surfaces. When complement component C3b binds to a surface, there exist two possible outcomes. Under normal conditions, when no activating surface is present (e g., if C3b has contacted normal tissue), sequential addition of blood cofactors H and I converts C3b into C3c, inactivating the complement protein. If an activating surface such as a microbe or damaged tissue is encountered, sequential addition of factors B and D drives the alternative pathway to the normal properdin (P) intermediate, and the complement cascade is triggered. The properdin-containing component (C3bBbP) feeds back to the beginning of the pathway, generating more C3.

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See also in sourсe #XX -- [ Pg.200 ]




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