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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
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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
-
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,
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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
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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
-
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
-
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
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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.
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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.
-
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.
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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 …
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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
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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
-
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
-
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
-
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
-
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
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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 …
-
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
-
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