| 
                    
                      
                          
                            
 
 | 
 
STATINS
Many Elders Don't Receive Primary Preventive Treatment for Cardiovascular Disease
Statins were unlikely to be prescribed for patients 75 or older. 
Previous
 research has shown that patients with known cardiovascular disease 
(CVD) are less likely to receive these drugs as they get older, and 
women are less likely than men to get these drugs. Whether the same is 
true for primary prevention of CVD is unclear. In this cross-sectional 
U.K. study, investigators assessed the effects of age and sex on primary
 prevention of CVD in 37,000 patients (age,   40). 
The proportion of patients who received antihypertensive drugs 
increased with age from 5% among the youngest patients (age range, 
40–44) to 57% among the oldest patients (age,   85).
 In fact, the likelihood of receiving an antihypertensive drug 
prescription increased significantly with each 5-year increment up to 
age 84 but not for age   85.
 The proportion of patients who received statins increased with age from
 3% among the youngest patients (age range, 40–44) to 29% among patients
 who were 70 to 74. The likelihood of receiving a statin drug 
prescription increased significantly with each 5-year increment up to 
age 74 but decreased significantly with each 5-year increment 
thereafter. Treatment of women and men did not differ.
 Comment: Increasing age increases risk for CVD, and many elders have high 10-year risk for CVD (  20%). For some elders (age,   75),
 primary prevention with antihypertensive and statin drugs can lower 
this risk. However, fewer randomized trial data exist for this age group
 (and especially for age   85)
 than for age <75 75.="75." and="and" be="be" call="call" clarification="clarification" clinical="clinical" considered="considered" drugs="drugs" effects="effects" elders="elders" especially="especially" expectancy="expectancy" for="for" guidelines="guidelines" in="in" life="life" of="of" older="older" overall="overall" p="p" polypharmacy="polypharmacy" populations.="populations." researchers="researchers" should="should" than="than" the="the" these="these" those="those" trials="trials" using="using">
 — Paul S. Mueller, MD, MPH, FACP
75>
 Published in Journal Watch General Medicine August 14, 2012
 
 |  
 
 | 
 
			  
			 
 
		 
			  
			  
statins primary prevention
Free 
                      Full-Text Article
Summary 
and Comment
Many Elders Don't Receive Primary Preventive Treatment for Cardiovascular 
Disease
Statins were unlikely to be prescribed for patients 75 or 
older.
Previous research has shown that patients with known 
cardiovascular disease (CVD) are less likely to receive these drugs as they
get older, and women are less likely than men to get these drugs. Whether 
the same is true for primary prevention of CVD is unclear. In this 
cross-sectional U.K. study, investigators assessed the effects of age and 
sex on primary prevention of CVD in 37,000 patients (age, 

40).
The proportion of patients who received antihypertensive drugs increased
with age from 5% among the youngest patients (age range, 40–44) to 
57% among the oldest patients (age, 

85). In fact, the likelihood of receiving an antihypertensive 
drug prescription increased significantly with each 5-year increment up to 
age 84 but not for age 

85. 
The proportion of patients who received statins increased with age from 3% 
among the youngest patients (age range, 40–44) to 29% among patients 
who were 70 to 74. The likelihood of receiving a statin drug prescription 
increased significantly with each 5-year increment up to age 74 but 
decreased significantly with each 5-year increment thereafter. Treatment of
women and men did not differ.
Comment: Increasing age increases risk for CVD, and many elders 
have high 10-year risk for CVD (

20%). For some elders (age, 

75), primary prevention with antihypertensive and statin drugs 
can lower this risk. However, fewer randomized trial data exist for this 
age group (and especially for age 

85) than for age <75 75.="75." and="and" be="be" call="call" clarification="clarification" clinical="clinical" considered="considered" drugs="drugs" effects="effects" elders="elders" especially="especially" expectancy="expectancy" for="for" guidelines="guidelines" in="in" life="life" of="of" older="older" overall="overall" p="p" polypharmacy="polypharmacy" populations.="populations." researchers="researchers" should="should" than="than" the="the" these="these" those="those" trials="trials" using="using">
— Paul
S. Mueller, MD, MPH, FACP
Published in Journal
Watch General Medicine August 14, 2012
75>
 
Citation(s):
  
Sheppard 
  JP et al. Impact of age and sex on primary preventive treatment for 
  cardiovascular disease in the West Midlands, UK: Cross sectional study. 
  
BMJ
    2012 Jul 12;  345:e4535. (
http://dx.doi.org/10.1136/bmj.e4535)
 
 
			  
			 
 
		 
		 
			  
 
statins 
Impact of age and sex on primary preventive treatment for cardiovascular disease in the West Midlands, UK: cross sectional study
 
    
      
      BMJ
      
    
    2012;
    345
    doi: 10.1136/bmj.e4535
    (Published 12 July 2012)
    
Cite this as:
      BMJ
       2012;345:e4535
     
 
 
 
More topics 

 
 
 
- J P Sheppard, research fellow1, 
 
- S Singh, clinical research fellow1, 
 
- K Fletcher, research fellow1, 
 
- R J McManus, professor2, 
 
- J Mant, professor3
 
- Correspondence to: R J McManus richard.mcmanus@phc.ox.ac.uk
 
 
Abstract
Objectives
 To establish the impact of age and sex on primary preventive treatment 
for cardiovascular disease in a typical primary care population.
Design Cross sectional study of anonymised patient records.
Participants
 All 41 250 records of patients aged ≥40 registered at 19 general 
practices in the West Midlands, United Kingdom, were extracted and 
analysed.
Main outcome measures 
Patients’ demographics, risk factors for cardiovascular disease (blood 
pressure, total cholesterol concentration), and prescriptions for 
primary preventive drugs were extracted from patients’ records. Patients
 were subdivided into five year age bands up to 85 (patients aged ≥85 
were analysed as one group) and prescribing trends across the population
 were assessed by estimating the proportion of patients prescribed with 
antihypertensive drug or statin drug, or both, in each group.
Results
 Of the 41 250 records screened in this study, 36 679 (89%) patients did
 not have a history of cardiovascular disease and therefore could be 
considered for primary preventive treatment. The proportion receiving 
antihypertensive drugs increased with age (from 5% (378/6978) aged 40-44
 to 57% (621/1092) aged ≥85) as did the proportion taking statins up to 
the age of 74 (from 3% (201/6978) aged 40-44 to 29% (675/2367) aged 
70-74). In those aged 75 and above, the odds of a receiving prescription
 for a statin (relative to the 40-44 age group) decreased with every 
five year increment in age (odds ratio 12.9 (95% confidence interval 
10.8 to 15.3) at age 75-79 to 5.7 (4.6 to 7.2) at age ≥85; P<0 .001=".001" by="by" consistent="consistent" differences="differences" in="in" no="no" p="p" prescribing="prescribing" sex.="sex." there="there" trends="trends" were="were">0>
Conclusions
 Previously described undertreatment of women in secondary prevention of
 cardiovascular disease was not observed for primary prevention. Low use
 of statins in older people highlights the need for a stronger evidence 
base and clearer guidelines for people aged over 75.
 
 
 
 
 
 
 
 
			  
			 
 
		 
			  
			  
dabigatran 
SUMMARY
  AND COMMENT
Within 12
  weeks of marketing approval, dabigatran was found to be responsible for 
  more adverse events than nearly all other medications.
Reviewing: 
  Radecki RP. Ann Intern Med 2012 Jul 3; 157:66
 
			  
			 
 
		 
			  
			  
                      
  
ACE-inhibitor 
  
  
Free 
                      Full-Text Article 
 | 
                    
                      
                        
                          
                            | 
 
Summary 
and Comment 
ACE Inhibitor Use Lowers Risks for Pneumonia
A meta-analysis showed that 
angiotensin-converting–enzyme inhibitors, but not 
angiotensin-receptor blockers, lowered risk. 
Many 
patients (as many as one third) who take 
angiotensin-converting–enzyme (ACE) inhibitors develop coughs. 
However, an enhanced cough reflex might lower risk for pneumonia. In this 
meta-analysis of 37 studies (18 randomized trials, 11 cohort studies, and 8
case-control studies), investigators evaluated the association between use 
of ACE inhibitors or angiotensin-receptor blockers (ARBs) and risk for 
pneumonia. 
Overall, use of ACE inhibitors was associated with a significant 34% 
lower risk for pneumonia compared with no use of ACE inhibitors and a 
significant 30% lower risk for pneumonia compared with ARB use. Subgroup 
analyses of patients with stroke or heart failure yielded similar results. 
Finally, use of ACE inhibitors compared with no use was associated with a 
significant 27% lower risk for pneumonia-related death.
 Comment: In this study, ACE inhibitor use was associated with 
attenuation of risks for pneumonia and pneumonia-related death. The authors
suggest that "patients taking ACE inhibitors who develop cough should, 
providing that cough is tolerable, persist with treatment." Although this 
suggestion is reasonable (especially because ACE inhibitors confer 
considerable cardiovascular benefit), many patients with ACE 
inhibitor–related cough find this side effect too annoying or 
disruptive to continue taking the drug.
 — Paul
S. Mueller, MD, MPH, FACP
Published in Journal
Watch General Medicine August 2, 2012
 
 |  
 
 | 
 
			  
			 
 
		 
			  
			  
 atrium fibrilleren  AF
   
 rate controle = hartfrequentie
 Rhythm controle = ritme
Detail van boezemfibrilleren met een snelle ventrikel-respons
 
 
Boezemfibrilleren is een ritmestoornis waarbij er sprake is van een 
chaotische depolarisatie van de atria. De sinusknoop wordt hierdoor als 
het ware overschreeuwd. De electrische acitiviteit in de boezems kan tot
 600 / min oplopen. Boezemfibrilleren ontstaat vaak rond eilandjes van 
cellen rond de inmonding van de longvenen in het linker atrium. 
Boezemfibrilleren is een van de meest voorkomende ritmestoornissen. Ongeveer 10% van de 70 jarige heeft boezemfibrilleren 
[1].
 De kans op boezemfibrilleren is verhoogd bij gedilateerde atria, 
atriale ischemie, hyperthyreoidie en alcoholgebruik. Er bestaan ook 
zeldzame erfelijke vormen van boezemfibrilleren.
De AV knoop is te traag om elk signaal uit de boezems door te 
geven. Willekeurig wordt er wel een signaal doorgegeven dat leidt tot 
kamercontractie. Door deze willekeur zijn de ventriculaire slagen 
onregelmatig en dat is meteen ook een van de belangrijkste ECG-kenmerken van boezemfibrilleren.
Soms is er sprake van grofslagig boezemfibrilleren dat zich uit 
in een onregelmatige basislijn, soms is de basislijn volledig vlak. 
Boezemfibrilleren wordt als volgt ingedeeld:
- Eerste geregistreerde episode: indien boezemfibrilleren voor het eerst geregistreerd wordt.
 
- Recidiverend boezemfibrilleren: na twee of meer episodes. 
 
- Paroxysmaal boezemfibrilleren: als recidiverend boezemfibrilleren telkens spontaan over gaat in sinusritme.
 
- Persisterend boezemfibrilleren: indien een episode van boezemfibrilleren langer dan 7 dagen aanhoudt.
 
- Permanent boezemfibrilleren: indien boezemfibrilleren aanhoudt ondanks een poging tot medicamenteuze of electrische cardioversie 
 
Lone AF is boezemfibrilleren in patienten jonger dan 60 jaar 
zonder klinische of electrocardiografische aanwijzingen voor hart- en of
 longziekte. Deze patiënten hebben een gunstigere prognose ten aanzien 
van trombo-embolische events.
Non-valvulair boezemfibrilleren is boezemfibrilleren 
zonder aanwijzingen voor rheumatische hartklepziekte of bij patienten 
zonder mechanische hartklep of hartklep reparatie. 
[2]
De behandeling van boezemfibrilleren kan door middel van 
ritme-controle (rhythm-control) of frequentie-controle (rate-control). 
Er is veel onderzoek gedaan naar de beste strategie. De verschillen op 
de lange termijn tussen beide strategieën verschillen in grote groepen 
patiënten weinig. 
[3]
-  Bij rhythm-control wordt er gestreefd naar sinusritme door met medicatie of electrische cardioversie het boezemfibrilleren te beëindigen.
 
-  Bij rate-conrol wordt het boezemfibrilleren 
geaccepteerd. Hierbij is de behandelig gericht op het voorkomen van hoge
 hartfrequenties door de AV knoop te onderdrukken met medicijnen. De 
streeffrequentie is onder de 100 slagen / min in rust en liefst nog iets
 lager.
 
 
			  
			 
 
		 
		 
			  
atrial fibrillation AF 
 
Rhythm vs. Rate Control in Older Atrial Fibrillation Patients
Rhythm control might be superior in the long term.
In a major trial published in 2002 (AFFIRM; 
JW Gen Med Dec 13 2002),
 investigators found no difference in outcome between rhythm and rate 
control during 5 years of follow-up in patients with atrial fibrillation
 (AF). However, many clinicians still favor rhythm control. In this 
retrospective cohort study, researchers used a Canadian database to 
identify 26,000 hospitalized patients (median age, 77) with incident AF 
who were treated with rhythm or rate control. Patient follow-up was 
available for as long as 9 years (median, 3.1 years); during that time, 
half of the patients died.
Analyses were adjusted for many demographic and clinical confounders.
 Compared with rate control, rhythm control was associated with 7% 
higher mortality at 6 months, equal mortality through 4 years, and 11% 
and 23% lower mortality at years 5 and 8, respectively.
Comment: Results from this population-based older cohort are 
similar to those of AFFIRM — no difference between rhythm and rate 
control for AF during short-term and intermediate-term follow-up. In the
 current analysis, however, rhythm control was superior during longer 
follow-up. Because potential unidentified confounders can't be ruled out
 in a retrospective study, a long-term randomized trial would be 
justified to confirm these findings.
— Thomas L. Schwenk, MD
Published in Journal Watch General Medicine July 26, 2012
Citation(s):
 
			  
			 
 
		 
			  
			  
PPI C. difficile
Summary 
and Comment
Proton-Pump Inhibitors Raise Risk for C. difficile Infections
In two 
meta-analyses, PPI use was associated with a 1.7-fold higher risk for 
Clostridium difficile infection.
In February 2012, the FDA 
issued a 
safety
alert regarding an association between proton-pump inhibitors (PPIs) 
and 
Clostridium difficile infection. In new meta-analyses, two 
groups of researchers used slightly different criteria to select studies in
which this association could be evaluated; all included studies (23 and 42,
respectively) were observational (cohort or case-control). Each 
meta-analysis involved roughly 300,000 patients.
In both meta-analyses, risk for 
C. difficile infection was 
significantly higher in PPI users than in nonusers (risk ratio, about 1.7).
Although results across individual studies were heterogeneous, nearly all 
trended toward higher risk. Most of the included studies were adjusted for 
confounding variables, including antibiotic use. Concomitant use of both 
PPIs and antibiotics — examined in one meta-analysis — was 
associated with greater risk for 
C. difficile infection than was use
of PPIs alone or antibiotics alone. Risk for 
C. difficile infection 
was higher with histamine (H)
2-receptor antagonists than with no
acid-suppressive therapy, but lower with H
2-receptor antagonists
than with PPIs.
Comment: The opportunity for residual confounding in these 
studies is substantial, because sicker patients are more likely both to 
receive PPIs and to be vulnerable to 
C. difficile infection. Still, 
these worrisome findings should remind clinicians to initiate PPIs only for
valid indications and to stop PPIs in patients who take them for unclear 
reasons.
— Allan
S. Brett, MD
Published in Journal
Watch General Medicine July 31, 2012
 
 
			  
			 
 
		 
			  
			  
statines 
SUMMARY
  AND COMMENT
An 
  observational study suggests that statin use before and during 
  hospitalization for stroke improves short-term outcomes.
Reviewing: 
  Flint AC et al. Neurology 2012 May 22; 78:1678