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		<id>http://istoriya.soippo.edu.ua/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Selectpeen44</id>
		<title>HistoryPedia - Внесок користувача [uk]</title>
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		<updated>2026-04-22T17:43:47Z</updated>
		<subtitle>Внесок користувача</subtitle>
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	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Lu_W,_Nechuta_SJ,_Cadmus-Bertram_L,_Patterson_RE,_Sternfeld_B_et&amp;diff=281811</id>
		<title>Lu W, Nechuta SJ, Cadmus-Bertram L, Patterson RE, Sternfeld B et</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Lu_W,_Nechuta_SJ,_Cadmus-Bertram_L,_Patterson_RE,_Sternfeld_B_et&amp;diff=281811"/>
				<updated>2018-01-29T19:29:49Z</updated>
		
		<summary type="html">&lt;p&gt;Selectpeen44: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;2015;149(2):331?2. 25. Matthews CE, Wilcox S, Hanby CL, Der Ananian C, Heiney SP, Gebretsadik T, Shintani A. Evaluation of a 12-week home-based walking intervention for breast cancer survivors. Assistance Care Cancer. 2007;15(two):203?1. 26. Pinto BM, Rabin C, Dunsiger S.Lu W, Nechuta SJ, Cadmus-Bertram L, Patterson RE, Sternfeld B et al. Meeting the physical activity guidelines and survival soon after breast [https://dx.doi.org/10.1136/bcr-2013-202552 title= bcr-2013-202552] cancer: findings in the after breast cancer pooling project. Breast Cancer Res Treat. 2012;131(two):637?three. Chen X, Zheng Y, Zheng W, Gu K, Chen Z, Lu W, Shu XO. The impact of common physical exercise on quality of life among breast cancer survivors. Am J Epidemiol. 2009;170(7):854?two. Irwin ML, McTiernan A, Manson JE, Thomson CA, Sternfeld B, Stefanick ML, Wactawski-Wende J, Craft L, Lane D, Martin LW et al. Physical activity and survival in postmenopausal ladies with breast cancer: results in the women's health initiative. Cancer Prev Res (Phila). 2011;four(four):522?. Ballard-Barbash R, Friedenreich CM, Courneya KS, Siddiqi SM, McTiernan A, Alfano CM. Physical activity, biomarkers, and illness outcomes in cancer survivors: a systematic overview. J Natl Cancer Inst. 2012;104(11):815?0. Blanchard CM, Courneya KS, Stein K. Cancer survivors' adherence to life style behavior [http://ques2ans.gatentry.com/index.php?qa=135095&amp;amp;qa_1=illustrate-essential-nuances-optimism-efficiency-possibly Ses below illustrate some essential nuances to this optimism.Efficiency could] recommendations and associations with health-related good quality of life: final results in the American Cancer Society's SCS-II. J Clin Oncol. 2008; 26(13):2198?04. Lynch BM, Dunstan DW, Healy GN, Winkler E, Eakin E, Owen N. Objectively measured physical activity and sedentary time of breast cancer survivors, and associations with adiposity: findings from NHANES (2003?006). Cancer Causes Handle. 2010;21(two):283?. Littman AJ, Tang MT, Rossing MA. Longitudinal study of recreational physical activity in breast cancer survivors. J Cancer Surviv. 2014. Epub ahead of print. 24. Bluethmann SM, Vernon SW, Gabriel KP, Murphy CC, Bartholomew LK. Taking the next step: a systematic overview and meta-analysis of physical activity and behavior change interventions in recent [https://dx.doi.org/10.3389/fpsyg.2013.00735 title= fpsyg.2013.00735] post-treatment breast cancer survivors. Breast Cancer Res Treat. 2015;149(two):331?two. 25. Matthews CE, Wilcox S, Hanby CL, Der Ananian C, Heiney SP, Gebretsadik T, Shintani A. Evaluation of a 12-week home-based walking intervention for breast cancer survivors.Lu W, Nechuta SJ, Cadmus-Bertram L, Patterson RE, Sternfeld B et al. Meeting the physical activity recommendations and survival just after breast [https://dx.doi.org/10.1136/bcr-2013-202552 title= bcr-2013-202552] cancer: findings in the just after breast cancer pooling project. Breast Cancer Res Treat. 2012;131(two):637?three. Chen X, Zheng Y, Zheng W, Gu K, Chen Z, Lu W, Shu XO. The effect of common exercising on excellent of life among breast cancer survivors. Am J Epidemiol. 2009;170(7):854?2. Irwin ML, McTiernan A, Manson JE, Thomson CA, Sternfeld B, Stefanick ML, Wactawski-Wende J, Craft L, Lane D, Martin LW et al. Physical activity and survival in postmenopausal females with breast cancer: benefits from the women's well being initiative. Cancer Prev Res (Phila). 2011;4(4):522?. Ballard-Barbash R, Friedenreich CM, Courneya KS, Siddiqi SM, McTiernan A, Alfano CM. Physical activity, biomarkers, and illness outcomes in cancer survivors: a systematic review. J Natl Cancer Inst.&lt;/div&gt;</summary>
		<author><name>Selectpeen44</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Can_hinder_achievement_of_optimal_blood_concentrations_of_antiTB_drugs_in&amp;diff=280782</id>
		<title>Can hinder achievement of optimal blood concentrations of antiTB drugs in</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Can_hinder_achievement_of_optimal_blood_concentrations_of_antiTB_drugs_in&amp;diff=280782"/>
				<updated>2018-01-26T18:38:35Z</updated>
		
		<summary type="html">&lt;p&gt;Selectpeen44: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Important variations in adherence happen to be identified in a lot of RCTs.33 For that reason, pragmatic clinical trials, which are conducted inside a way that extra closely resembles common clinical practice, might be far more proper to get a far better estimate of [http://campuscrimes.tv/members/fiber97double/activity/685397/ Alder R, Lethbridge L, Tiny L. Eliminating the shortage of registered] remedy effectiveness.34,35 In the beginning of 2013, a systematic overview was published in Canada to evaluate the threat of therapy failure or illness relapse, acquired drug resistance, bacterial conversion immediately after two months of remedy, AEs, adherence, and remedy satisfaction connected with therapy of active TB making use of FDC or SD formulations.36 This study concluded that, although FDC formulations simplify TB therapy, the present evidence did not indicate that these formulations increase treatment outcomes amongst patients with active TB. Nonetheless, that systematic critique integrated research of both four-drug and [http://support.myyna.com/329460/surgical-patients-illustrate-particularly-undergoing-elective . Surgical sufferers properly illustrate this point, specifically these undergoing elective surgery] two-drug combinations and, hence, differs in the present one within the number of retrieved articles. These differences justify the need to get a revision to evaluate precisely the impact of 4-FDC versus SD [https://dx.doi.org/10.4103/2152-7806.162550 title= 2152-7806.162550] formulations. The World Health Organization has suggested 4-FDC treatment options given that 1999. Combined treatments stop drug choice by the patient (monotherapy) by providing all of the drugs in the same tablet.12,34,35,37 Resulting from their simplified and standardized nature, 4-FDC regimens facilitate dosage calculation and protect against prescription errors. Having said that, among by far the most relevant capabilities of 4-FDC formulations, the prevention of drug resistance, was not addressed in these research. Nevertheless, primarily based on their equivalent efficacies, user-friendliness, decrease charges, and operational and logistical positive aspects, generalized use of 4-FDC formulations really should continue to be advised. 1 limitation of this meta-analysis is that the incorporated research did not investigate adherence for the prescribed remedy.Can hinder achievement of optimal blood concentrations of antiTB drugs in patients co-infected with HIV.27 This observation suggests that 4-FDC therapy, by causing fewer gastrointestinal side effects, would advantage co-infected individuals. Some patientsSu (2002) Gravendeel (2003) Bartacek (2009) Lienhardt (2011)0.16 [ ?.02 , 1.34 ] 0.70 [ ?.82 , three.21 ] 1.63 [ ?.54 , 3.80 ] ?.20 [ ?.29 , ?.12 ]FE Model0.05 [ ?.82 , 0.92 ]?.?.two.Log Odds RatioFig. four ?Forest plot for default.b r a z i l i a n j o u r n a l o f m i c r o b i o l o g y four eight (2 0 1 7) 198?reported stopping medication since of AEs,28 whereas other folks indicated that they weren't informed about unwanted effects or what to do to counter them.29?1 No ophthalmic AEs (ocular toxic effects) were reported that may be connected using the new drug (EMB). Retrobulbar optic neuritis, the principle AE to EMB, is uncommon in the doses and exposure instances typically utilised for TB therapy.32 Regardless of the possible for providing the highest level of evidence in therapeutic intervention investigation, RCTs have been criticized simply because of their restricted generalizability. RCTs are typically performed below optimal health-related care and might underestimate the potential [https://dx.doi.org/10.1093/tropej/fmv055 title= tropej/fmv055] advantage of making use of 4-FDC formulations to improve adherence in settings exactly where malpractice or unmonitored therapies are frequent.&lt;/div&gt;</summary>
		<author><name>Selectpeen44</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=IngitisBartacek_et_al.,558/25/558_FDC,_15/564_SD6/344_FDC,_3/360_SD2/558_FDC_circumstances_of_hepatitisLienhardt&amp;diff=280089</id>
		<title>IngitisBartacek et al.,558/25/558 FDC, 15/564 SD6/344 FDC, 3/360 SD2/558 FDC circumstances of hepatitisLienhardt</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=IngitisBartacek_et_al.,558/25/558_FDC,_15/564_SD6/344_FDC,_3/360_SD2/558_FDC_circumstances_of_hepatitisLienhardt&amp;diff=280089"/>
				<updated>2018-01-25T01:21:35Z</updated>
		
		<summary type="html">&lt;p&gt;Selectpeen44: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;five ?Forest plot for quantity of [http://www.medchemexpress.com/IC261.html IC261 biological activity] patients with adverse effects.the authors of these studies. The majority of [https://dx.doi.org/10.1155/2013/480630 title= 2013/480630] the unwanted effects that were reported by the research within this review were not viewed as really serious and may be managed via symptomatic palliation in each groups of individuals (4-FDC and SD).IngitisBartacek et al.,558/25/558 FDC, 15/564 SD6/344 FDC, 3/360 SD2/558 FDC circumstances of hepatitisLienhardt et al.,798/40/798 FDC, 39/787 SD23/591 FDC, 19/579 SD4/591 FDC, 4/579 SDb r a z i l i a n j o u r n a l o f m i c r o b i o l o g y 4 8 (two 0 1 7) 198?Su (2002) Gravendeel (2003) Zaka (2009) Lienhardt (2011)?.04 [ ?.00 , 3.92 ] 0.01 [ ?.94 , 0.96 ]Zaka (2008) Bartacek (2009)0.90 [ 0.19 , 1.61 ] ?.14 [ ?.42 , 0.14 ] 0.17 [ ?.32 , 0.66 ]0.32 [ ?.75 , 1.38 ] 0.14 [ ?.36 , 0.63 ] Lienhardt (2011)FE Model0.14 [ ?.27 , 0.54 ] RE Model ?.00 0.00 Log Odds Ratio 4.00 ?.50 0.50 1.50 0.24 [ ?.32 , 0.79 ]Fig. three ?Forest plot for sputum conversion within the final phase of therapy.Log Odds RatioFig. 5 ?Forest plot for quantity of patients with adverse effects.the authors of these research. The random-effects model was selected for the reason that heterogeneity was identified (p = 0.0246 and I2 = 75.85 ). The null hypothesis was not rejected (p = 0.4091), suggesting that there was no statistical proof that the amount of individuals with AEs differed involving treatment groups. A forest plot (Fig. five) showed that the 95  CI range for the log OR contained zero (log OR: 0.24, 95  CI: -0.32 to 0.79), indicating that the OR among remedies was statistically equal to one particular. As a result, meta-analysis benefits didn't reveal a statistically important distinction involving 4-FDC and SD treatments when it comes to the amount of sufferers with AEs. For the evaluation of your number of individuals with gastrointestinal AEs, all 5 research collected associated information and were included in the evaluation. The fixed-effects model was selected due to the fact heterogeneity was not identified (p [https://dx.doi.org/10.5539/gjhs.v8n9p44 title= gjhs.v8n9p44] = 0.5656). The null hypothesis was rejected (p = 0.0006), suggesting that there was statistical proof that the likelihood of occurrence of gastrointestinal AEs differed in between therapy groups. A forest plot (Fig. six) showed that the 95  CI variety for the log OR did not contain zero (log OR: 0.50, 95  CI: 0.22?.79), indicating that the OR amongst treatment options was statistically diverse from 1. The meta-analytic measure (log OR) revealed that the SD remedy was related with a 1.65-fold [i.e., exp (0.5) = 1.65] higher likelihood of gastrointestinal AEs than the 4-FDC therapy.Su (2002) Gravendeel (2003) Zaka (2008) Bartacek (2009) Lienhardt (2011)two.65 [ ?.30 , five.61 ] 0.61 [ 0.18 , 1.03 ] 0.31 [ ?.50 , 1.12 ] 0.34 [ ?.17 [https://dx.doi.org/10.4103/2152-7806.162550 title= 2152-7806.162550] , 0.84 ] 0.63 [ ?.37 , 1.63 ]FE Model0.50 [ 0.22 , 0.79 ]?.00 0.2.four.six.Log Odds RatioFig. six ?Forest plot for quantity of individuals with gastrointestinal adverse effects.DiscussionOn the basis in the pooled benefits of the RCTs, 4-FDC therapy failed to show advantages more than the SD regimen in culture conversion following two or 6 months of therapy. Having said that, the outcomes didn't demonstrate total inferiority of FDC when compared with SD regimens when working with the strict definition applied in this critique. Except for one study that identified much better treatment satisfaction,22 none in the incorporated research identified improved patient adherence among TB patients treated with 4-FDC when compared with those treated with SD formulations. The majority of [https://dx.doi.org/10.1155/2013/480630 title= 2013/480630] the unwanted side effects that have been reported by the studies in this assessment were not thought of really serious and may very well be managed by way of symptomatic palliation in each groups of individuals (4-FDC and SD).&lt;/div&gt;</summary>
		<author><name>Selectpeen44</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Lu_W,_Nechuta_SJ,_Cadmus-Bertram_L,_Patterson_RE,_Sternfeld_B_et&amp;diff=279647</id>
		<title>Lu W, Nechuta SJ, Cadmus-Bertram L, Patterson RE, Sternfeld B et</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Lu_W,_Nechuta_SJ,_Cadmus-Bertram_L,_Patterson_RE,_Sternfeld_B_et&amp;diff=279647"/>
				<updated>2018-01-23T20:20:35Z</updated>
		
		<summary type="html">&lt;p&gt;Selectpeen44: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The effect of standard exercising on top quality of life among breast [http://campuscrimes.tv/members/canvashen7/activity/624491/ Ration line criteria of ?0   linear calibration with a weight of 1/x] cancer survivors. Chen X, Zheng Y, Zheng W, Gu K, Chen Z, Lu W, Shu XO. The impact of normal exercising on high quality of life among breast cancer survivors. Am J Epidemiol. 2009;170(7):854?2. Irwin ML, McTiernan A, Manson JE, Thomson CA, Sternfeld B, Stefanick ML, Wactawski-Wende J, Craft L, Lane D, Martin LW et al. Physical activity and survival in postmenopausal women with breast cancer: final results from the women's overall health initiative. Cancer Prev Res (Phila). 2011;four(4):522?. Ballard-Barbash R, Friedenreich CM, Courneya KS, Siddiqi SM, McTiernan A, Alfano CM. Physical activity, biomarkers, and disease outcomes in cancer survivors: a systematic overview. J Natl Cancer Inst. 2012;104(11):815?0. Blanchard CM, Courneya KS, Stein K. Cancer survivors' adherence to way of life behavior recommendations and associations with health-related good quality of life: final results from the American Cancer Society's SCS-II. J Clin Oncol. 2008; 26(13):2198?04. Lynch BM, Dunstan DW, Healy GN, Winkler E, Eakin E, Owen N. Objectively measured physical activity and sedentary time of breast cancer survivors, and associations with adiposity: findings from NHANES (2003?006). Cancer Causes Manage. 2010;21(2):283?. Littman AJ, Tang MT, Rossing MA. Longitudinal study of recreational physical activity in breast cancer survivors. J Cancer Surviv. 2010;four(2):119?7. Emery CF, Yang HC, Frierson GM, Peterson LJ, Suh S. Determinants of physical activity amongst women treated for breast cancer inside a 5-year longitudinal follow-up investigation. Psychooncology. 2009;18(4):377?6. Silber JH, [https://dx.doi.org/10.3121/cmr.2012.1100.ps1-07 title= cmr.2012.1100.ps1-07] Rosenbaum PR, Clark AS, Giantonio BJ, Ross RN, Teng Y, Wang M, Niknam BA, Ludwig JM, Wang W et al. Characteristics associated with variations in survival among black and white ladies with breast cancer. JAMA. 2013;310(4):389?7. Paxton RJ, Phillips KL, Jones LA, Chang S, Taylor WC, Courneya KS, Pierce JP. Associations amongst physical activity, physique mass index, and health-related high-quality of life by race/ethnicity inside a diverse sample of breast cancer survivors. Cancer. 2012;118(16):4024?1. Brawley OW. Overall health disparities in breast cancer. Obstet Gynecol Clin North Am. 2013;40(three):513?three. O'Neill SC, DeFrank JT, Vegella P, Richman AR, Henry LR, Carey LA, Brewer NT. Engaging in health behaviors to lower danger for breast cancer recurrence. Plos One particular. 2013;eight(1):e53607.23. Stacey FG, James EL, Chapman K, Courneya KS, Lubans DR. A systematic review and meta-analysis of social cognitive theory-based physical activity and/or nutrition behavior alter interventions for cancer survivors. J Cancer Surviv. 2014. Epub ahead of print. 24. Bluethmann SM, Vernon SW, Gabriel KP, Murphy CC, Bartholomew LK. Taking the next step: a systematic overview and meta-analysis of physical activity and behavior change interventions in recent [https://dx.doi.org/10.3389/fpsyg.2013.00735 title= fpsyg.2013.00735] post-treatment breast cancer survivors. Breast Cancer Res Treat. 2015;149(two):331?2. 25. Matthews CE, Wilcox S, Hanby CL, Der Ananian C, Heiney SP, Gebretsadik T, Shintani A. Evaluation of a 12-week home-based walking intervention for breast cancer survivors. Support Care Cancer. 2007;15(two):203?1.&lt;/div&gt;</summary>
		<author><name>Selectpeen44</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Can_hinder_achievement_of_optimal_blood_concentrations_of_antiTB_drugs_in&amp;diff=279234</id>
		<title>Can hinder achievement of optimal blood concentrations of antiTB drugs in</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Can_hinder_achievement_of_optimal_blood_concentrations_of_antiTB_drugs_in&amp;diff=279234"/>
				<updated>2018-01-22T18:15:34Z</updated>
		
		<summary type="html">&lt;p&gt;Selectpeen44: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Nonetheless, certainly one of essentially the most [http://www.tongji.org/members/eel36lead/activity/522400/ S, and attitudes have already been demonstrated to possess a important function] relevant characteristics of 4-FDC formulations, the prevention of drug resistance, was not addressed in those studies. One limitation of this meta-analysis is the fact that the incorporated studies did not investigate adherence for the prescribed treatment. Furthermore, the [https://dx.doi.org/10.1155/2013/480630 title= 2013/480630] effect on the Directly Observed Therapy Short-Course (DOTS) strategy on the outcomes of TB therapy was not assessed, which resulted in significantly less precise estimates.Can hinder achievement of optimal blood concentrations of antiTB drugs in sufferers co-infected with HIV.27 This observation suggests that 4-FDC therapy, by causing fewer gastrointestinal side effects, would benefit co-infected individuals. Some patientsSu (2002) Gravendeel (2003) Bartacek (2009) Lienhardt (2011)0.16 [ ?.02 , 1.34 ] 0.70 [ ?.82 , 3.21 ] 1.63 [ ?.54 , 3.80 ] ?.20 [ ?.29 , ?.12 ]FE Model0.05 [ ?.82 , 0.92 ]?.?.2.Log Odds RatioFig. 4 ?Forest plot for default.b r a z i l i a n j o u r n a l o f m i c r o b i o l o g y four 8 (two 0 1 7) 198?reported stopping medication for the reason that of AEs,28 whereas other people indicated that they were not informed about unwanted side effects or what to accomplish to counter them.29?1 No ophthalmic AEs (ocular toxic effects) were reported that may very well be connected with all the new drug (EMB). Retrobulbar optic neuritis, the main AE to EMB, is rare inside the doses and exposure instances frequently utilized for TB treatment.32 Despite the potential for supplying the highest amount of evidence in therapeutic intervention research, RCTs happen to be criticized because of their limited generalizability. RCTs are usually conducted under optimal medical care and may possibly underestimate the potential [https://dx.doi.org/10.1093/tropej/fmv055 title= tropej/fmv055] advantage of employing 4-FDC formulations to enhance adherence in settings where malpractice or unmonitored therapies are frequent. Essential differences in adherence happen to be identified in numerous RCTs.33 Consequently, pragmatic clinical trials, that are carried out inside a way that additional closely resembles standard clinical practice, could be extra suitable to receive a much better estimate of therapy effectiveness.34,35 At the beginning of 2013, a systematic review was published in Canada to evaluate the danger of therapy failure or illness relapse, acquired drug resistance, bacterial conversion right after two months of remedy, AEs, adherence, and remedy satisfaction linked with treatment of active TB utilizing FDC or SD formulations.36 This study concluded that, despite the fact that FDC formulations simplify TB therapy, the existing proof did not indicate that these formulations improve therapy outcomes amongst individuals with active TB. Even so, that systematic review included research of each four-drug and two-drug combinations and, as a result, differs from the present 1 within the number of retrieved articles. These differences justify the require for any revision to evaluate precisely the effect of 4-FDC versus SD [https://dx.doi.org/10.4103/2152-7806.162550 title= 2152-7806.162550] formulations. The Globe Well being Organization has advised 4-FDC remedies considering the fact that 1999. Combined remedies protect against drug choice by the patient (monotherapy) by delivering all of the drugs inside the identical tablet.12,34,35,37 As a result of their simplified and standardized nature, 4-FDC regimens facilitate dosage calculation and avert prescription errors.&lt;/div&gt;</summary>
		<author><name>Selectpeen44</name></author>	</entry>

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