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  1. Slide 1 (ppt file)

    effectivehealthcare.ahrq.gov/sites/default/files/module_iv1.ppt
    October 31, 2011 - Done effectively, facilitation is not a one-time event that occurs while someone leads a meeting or discussion … occur during scheduled meetings Module IV Quiz: Question 2: ANSWER Facilitation is: A one-time event … dynamics and processes A superfluous skill Module IV Quiz: Question 3: Facilitation is: A one-time event
  2. Layout 1 (pdf file)

    effectivehealthcare.ahrq.gov/sites/default/files/related_files/ace-inhibitor-arb-2007_executive.pdf
    January 01, 2007 - This may reflect low event rates among otherwise healthy patients and relatively few studies with extended
  3. effectivehealthcare.ahrq.gov/sites/default/files/related_files/vaccine-safety_executive.pdf
    January 01, 2020 - Case-control studies compare people who have a disease or adverse event (“cases”) with people who do … not have the disease or event (“controls”) and look back retrospectively to compare exposure to vaccine … in each group to determine the relationship between the vaccine and the disease/ event.13,14 aLevel … SCCSs compare outcome event rates during times when a person is exposed (postvaccination) with those … Odds ratios could be calculated for each event reported in each trial and postlicensure study and,
  4. effectivehealthcare.ahrq.gov/sites/default/files/related_files/renal-artery-stenosis_appendixes-2007.pdf
    January 01, 2007 - , blood pressure; CHF, congestive heart failure; CKD, chronic kidney disease; CVA, cerebrovascular event … treatment, or kidney function worsening (by GFR, SCr, or dialysis), or atherosclerotic cardiovascular event … unexpanded stent 0.8% Rocha- Singh 200565 208 (208) Angioplasty stent placement Major vascular event … In-hospital 2.4% Out of hospital up to 2 yr 2.9% Cerebrovascular accident 0% Major embolic event … 50% 100 Ostial: nd 3.5 yr 68% (3 yr) 59% (5 yr) C Retro 51 44% (100) 1984-2004 0-17 yr CKD event
  5. effectivehealthcare.ahrq.gov/sites/default/files/pdf/incident-user-design_research.pdf
    May 01, 2012 - , an intervention’s benefits may require an induction period of months or years to reduce clinical event … effectiveness evidence for another reason: accurate reflections of the induction period or time-to-event … incident use of an intervention and its alternative, investigators can compare cohorts’ times until event … than older drugs because their apparent rate would be lower; investigators would observe a higher event … Studies that opt for (event) risk scores instead of propensity scores to control confounding would also
  6. effectivehealthcare.ahrq.gov/sites/default/files/pdf/vaccine-safety_disposition-comments.pdf
    January 01, 2020 - TEP # 1 Introduction— Page 3 lines 11- 13 Change to “..the Vaccine Adverse Event Reporting System … It is also possible to have high or moderate strength of evidence for an extremely rare adverse event … Similarly, event severity was poorly described. … In many cases, the objective frequency of an event is described poorly, or not at all. … An understanding of the severity of an adverse event is necessary for decision-makers to determine
  7. effectivehealthcare.ahrq.gov/sites/default/files/related_files/vaccine-safety_disposition-comments.pdf
    January 01, 2020 - TEP # 1 Introduction— Page 3 lines 11- 13 Change to “..the Vaccine Adverse Event Reporting System … It is also possible to have high or moderate strength of evidence for an extremely rare adverse event … Similarly, event severity was poorly described. … In many cases, the objective frequency of an event is described poorly, or not at all. … An understanding of the severity of an adverse event is necessary for decision-makers to determine
  8. effectivehealthcare.ahrq.gov/products/coronary-stents-outcomes/research
    February 10, 2010 - resulted in release of two special FDA advisories in 2006, 7,8 as well as subsequent studies refining event … In the rare event that a single ACC-NCDR® record could be matched with multiple Medicare records using … Death was the only event defined both during the index PCI procedure (using ACC-NCDR® information) and … rate of repeat revascularization in our population (24%) may be due to not censoring patients after an event … Unadjusted and adjusted results from time-to-event analyses for prespecified endpoints.
  9. effectivehealthcare.ahrq.gov/sites/default/files/related_files/cer-257-antenatal-care-evidence-summary.pdf
    June 01, 2022 - supportive management, without which they expressed fears about repercussions from management in the event … of a rare adverse event associated with maternity care.
  10. effectivehealthcare.ahrq.gov/sites/default/files/pdf/ace-inhibitor-arb-2007_research-2007-1.pdf
    January 01, 2007 - • Safety (focusing on serious adverse event rates, overall adverse event rates, and withdrawals … Key Points • Cough was modestly more frequently observed as an adverse event in groups treated with … However, the nature of serious adverse event reporting was inconsistent, and rates of serious adverse … Depending on the definition used, adverse event rates ranged from 0 to 100 percent (median 32 percent … The one adverse event for which significant differential effects were apparent is cough.
  11. effectivehealthcare.ahrq.gov/sites/default/files/pdf/recombinant-factor-viia_clinician.pdf
    October 01, 2010 - In-Hospital, Off-Label Uses for rFVIIa1 Evidence on Benefits vs. Usual Care Evidence on Harms vs. Usual Care Spontaneous intracranial hemorrhage* No effect on mortality or functional status. ��� Attenuation of hematoma expansion. ��� Increased risk for arterial thromboembolic events, particularly at doses >40 …
  12. effectivehealthcare.ahrq.gov/products/asthma-immunotherapy/research-protocol
    September 14, 2016 - We will also review the FDA Adverse Event Reporting System (FAERS). … to judge the likelihood that the intervention was causally related to the observed serious adverse event … Summary of Protocol Amendments In the event of protocol amendments, the date of each amendment will … (McGraw Hill Concise Dictionary of Modern Medicine, 2002) An adverse event is any undesirable experience … (Food and Drug Administration, 2009) Serious adverse events (SAE): The event is serious and should
  13. effectivehealthcare.ahrq.gov/sites/default/files/vte-protocol-8-4-10.pdf
    February 01, 2008 - observational studies which compare pharmacologic VTE prophylaxis methods will be used to report VTE event … Baseline risk of bleeding will be summarized using event rates from trials or large observational studies … KQ 3 will be addressed by qualitatively reporting event rates of both asymptomatic and symptomatic … the change scores will be calculated using the method proposed by Follman and colleagues.10 In the event … Summary of Protocol Amendments In the event of protocol amendments, the date of each amendment will
  14. effectivehealthcare.ahrq.gov/sites/default/files/pdf/blood-clots-hip-knee-surgery_research-protocol.pdf
    February 01, 2008 - observational studies which compare pharmacologic VTE prophylaxis methods will be used to report VTE event … Baseline risk of bleeding will be summarized using event rates from trials or large observational studies … KQ 3 will be addressed by qualitatively reporting event rates of both asymptomatic and symptomatic … the change scores will be calculated using the method proposed by Follman and colleagues.10 In the event … Summary of Protocol Amendments In the event of protocol amendments, the date of each amendment will
  15. effectivehealthcare.ahrq.gov/sites/default/files/pdf/copd-anticholinergic-medicines_research.pdf
    December 01, 2009 - Because a medication switch may have been related to an event or an indicator of symptoms that may have … preceded this event, we did not want to attribute those events to exposure to the medications during … Specifically, an individual’s medication exposure was redefined each time there was an event during … Exposure was defined using the 180-day period prior to the day of the event. … controlling for propensity score, to examine the association between medication regimen exposure and risk of event
  16. effectivehealthcare.ahrq.gov/sites/default/files/pdf/asthma-immunotherapy_research-protocol.pdf
    September 14, 2016 - We will also review the FDA Adverse Event Reporting System (FAERS). … to judge the likelihood that the intervention was causally related to the observed serious adverse event … Summary of Protocol Amendments In the event of protocol amendments, the date of each amendment will … (McGraw Hill Concise Dictionary of Modern Medicine, 2002) b) An adverse event is any undesirable experience … http://www.fda.gov/Safety/MedWatch/HowToReport/ucm053087.htm ) c) Serious adverse events (SAE): The event
  17. effectivehealthcare.ahrq.gov/products/blood-clots-hip-knee-surgery/research-protocol
    August 06, 2010 - observational studies which compare pharmacologic VTE prophylaxis methods will be used to report VTE event … Baseline risk of bleeding will be summarized using event rates from trials or large observational studies … the change scores will be calculated using the method proposed by Follman and colleagues. 10 In the event … Eligibility criteria, demographics Population Events rates markedly different than in community Event … Venous thromboembolism WMD Weighted mean difference Summary of Protocol Amendments In the event
  18. effectivehealthcare.ahrq.gov/sites/default/files/related_files/rheumatoid-arthritis-medicine_executive.pdf
    April 01, 2012 - 1 Comparative Effectiveness Review Number 55 Drug Therapy for Rheumatoid Arthritis in Adults: An Update Executive Summary Background Rheumatoid arthritis (RA), which affects 1.3 million adult Americans, is an autoimmune disease that involves inflammation of the synovium (a thin layer of tissue lining a joint …
  19. effectivehealthcare.ahrq.gov/sites/default/files/pdf/acs-pci-adjunctive-devices_research-protocol.pdf
    July 01, 2010 - Eligibility criteria, demographics Population Events rates markedly different than in the community Event … Definition ACS acute coronary syndrome EPC Evidence-based Practice Center MACE major adverse cardiac event … Summary of Protocol Amendments In the event of protocol amendments, the date of each amendment will
  20. effectivehealthcare.ahrq.gov/products/calcineurin-inhibitor/research-protocol
    October 14, 2014 - from the time of transplant (de novo), or later post-transplant (elective) as a result of an adverse event … undertaken at any time post-transplant and is usually a result of an unacceptable CNI related adverse event … Definition Timing Minimization Lower dosage of CNI Planned de novo, or result of adverse event … of CNI dose until eliminated and replaced with other immunosuppressant Usually result of adverse event … CNI (CNI-minimization), conversion from CNI to another immunosuppression agent following an adverse event

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