Osteoporosis Screening Update USPSTF 2011

Monday, January 24th, 2011

Screening for Osteoporosis: U.S. Preventive Services Task Force Recommendation Statement

From the U.S. Preventive Services Task Force, Rockville, Maryland.

Abstract

Description: Update of the 2002 U.S. Preventive Services Task Force (USPSTF) recommendation on screening for osteoporosis.

Methods: The USPSTF evaluated evidence on the diagnostic accuracy of risk assessment instruments for osteoporosis and fractures, the performance of dual-energy x-ray absorptiometry and peripheral bone measurement tests in predicting fractures, the harms of screening for osteoporosis, and the benefits and harms of drug therapy for osteoporosis in women and men.

Recommendations: The USPSTF recommends screening for osteoporosis in women aged 65 years or older and in younger women whose fracture risk is equal to or greater than that of a 65-year-old white woman who has no additional risk factors. (Grade B recommendation)

The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of screening for osteoporosis in men. (I statement)

Osteoporosis Screening Table USPSTF

Patient Population Under Consideration

This recommendation applies to older adults in the general U.S. population who do not have a history of an osteoporotic fracture, osteoporosis secondary to another condition, or other specific clinical indications for bone measurement testing. The USPSTF did not define a specific upper age limit for screening in women because the risk for fractures continues to increase with age and treatment harms remain no greater than small. Clinicians should take into account the patient’s remaining lifespan when deciding whether to screen patients with significant illness. In the Fracture Intervention Trial (1), the benefit of treatment emerged 18 to 24 months after initiation of treatment.

The quantity and quality of data on osteoporotic fracture risk other than hip fracture are much less for Asian, American Indian or Alaska Native, Hispanic, and black women than for white women. The USPSTF’s recommendation to screen women aged 65 years or older for osteoporosis applies to all racial and ethnic groups because the harms of the screening tests are no greater than small, the consequences of failing to identify and treat women who have low bone mineral density (BMD) are considerable, and the optimal alternative age at which to screen nonwhite women is uncertain.

Assessment of Risk

Multiple instruments to predict risk for low BMD and fractures have been developed and validated for use in postmenopausal women, but few have been validated for use in men. To predict fracture risk, the area under the receiver-operating characteristic curve ranges from 0.48 to 0.89 (2). Less complex instruments (that is, those with fewer variables) seem to perform as well as more complex ones (3). The USPSTF found no studies that assessed the effect on patient outcomes of using risk prediction instruments alone or in combination with bone measurement tests.

The USPSTF used the FRAX (Fracture Risk Assessment) tool (World Health Organization Collaborating Centre for Metabolic Bone Diseases, Sheffield, United Kingdom), available at www.shef.ac.uk/FRAX/, to estimate 10-year risks for fractures because this tool relies on easily obtainable clinical information, such as age, body mass index (BMI), parental fracture history, and tobacco and alcohol use; its development was supported by a broad international collaboration and extensively validated in 2 large U.S. cohorts; and it is freely accessible to clinicians and the public. The FRAX tool includes questions about previous DXA results but does not require this information to estimate fracture risk.

Based on the U.S. FRAX tool, a 65-year-old white woman with no other risk factors has a 9.3% 10-year risk for any osteoporotic fracture. White women between the ages of 50 and 64 years with equivalent or greater 10-year fracture risks based on specific risk factors include but are not limited to the following persons: 1) a 50-year-old current smoker with a BMI less than 21 kg/m2, daily alcohol use, and parental fracture history; 2) a 55-year-old woman with a parental fracture history; 3) a 60-year-old woman with a BMI less than 21 kg/m2 and daily alcohol use; and 4) a 60-year-old current smoker with daily alcohol use. The FRAX tool also predicts 10-year fracture risks for black, Asian, and Hispanic women in the United States. In general, estimated fracture risks in nonwhite women are lower than those for white women of the same age.

Although the USPSTF recommends using a 9.3% 10-year fracture risk threshold to screen women aged 50 to 64 years, clinicians also should consider each patient’s values and preferences and use clinical judgment when discussing screening with women in this age group. Menopausal status is one factor that may affect a decision about screening in this age group.

Considerations for Practice Regarding the I Statement

When deciding whether to screen men for osteoporosis, clinicians should consider the following factors.

Potential Preventable Burden

Bone measurement tests may potentially detect osteoporosis in a large number of men and prevent a substantial part of the burden of fractures and fracture-related illness in this population. The aging of the U.S. population is likely to increase this potentially preventable burden in future years.

Potential Harms

Potential harms of screening men are likely to be small and consist primarily of opportunity costs.

Current Practice

Routine screening of men currently is not a widespread practice.

Costs

Many additional DXA scanners may be required to screen sizeable populations of men for osteoporosis; DXA machines range in cost from $25 000 to $85 000.

Assuming that the relative benefits and harms of therapy in men are similar to those in women, the men most likely to benefit from screening would have 10-year risks for osteoporotic fracture equal to or greater than those of 65-year-old white women who have no additional risk factors. However, current evidence is insufficient to assess the balance of benefits and harms of screening for osteoporosis in men.

Screening Tests

The most commonly used bone measurement tests used to screen for osteoporosis are DXA of the hip and lumbar spine and quantitative ultrasonography of the calcaneus. Quantitative ultrasonography is less expensive and more portable than DXA and does not expose patients to ionizing radiation. Quantitative ultrasonography of the calcaneus predicts fractures of the femoral neck, hip, and spine as effectively as DXA. However, current diagnostic and treatment criteria for osteoporosis rely on DXA measurements only, and criteria based on quantitative ultrasonography or a combination of quantitative ultrasonography and DXA have not been defined.

Screening Intervals

The potential value of rescreening women whose initial screening test did not detect osteoporosis is to improve fracture risk prediction. A lack of evidence exists about optimal intervals for repeated screening and whether repeated screening is necessary in a woman with normal BMD. Because of limitations in the precision of testing, a minimum of 2 years may be needed to reliably measure a change in BMD; however, longer intervals may be necessary to improve fracture risk prediction. A prospective study of 4 124 women aged 65 years or older found that neither repeated BMD measurement nor the change in BMD after 8 years was more predictive of subsequent fracture risk than the original measurement (4).

Treatment

In addition to adequate calcium and vitamin D intake and weight-bearing exercise, multiple drug therapies are approved by the U.S. Food and Drug Administration to reduce fractures, including bisphosphonates, parathyroid hormone, raloxifene, and estrogen. The choice of therapy should be an individual one based on the patient’s clinical situation and the tradeoff between benefits and harms. Clinicians should provide patient education on how to use drug therapies to minimize adverse effects. For example, esophageal irritation from bisphosphonate therapy can be reduced by taking the medication with a full glass of water and by not lying down for at least 30 minutes afterward.

Other Approaches to Prevention

The USPSTF has updated its evidence review on falls prevention in older adults (2) and plans to issue an updated recommendation; in future months, the USPSTF also will issue a separate statement on the preventive effects of vitamin D and calcium supplements on osteoporotic fractures. When complete, these documents will be made available at www.uspreventiveservicestaskforce.org.

Useful Resources

The 10-year risk for osteoporotic fractures can be calculated for individuals by using the FRAX tool and could help to guide screening decisions for women younger than 65 years.

Summary guides for clinicians and patients on fracture prevention treatments for postmenopausal women who have osteoporosis are available from the Agency for Healthcare Research and Quality at http://effectivehealthcare.ahrq.gov. The recommendations in these guides may differ from those of the USPSTF because they were based on a systematic review that pooled data from trials that included women who had previous clinical fractures.

Other Considerations
Research Needs and Gaps

Given the absence of direct evidence that screening for osteoporosis reduces fracture-related morbidity or mortality, studies of long-term health outcomes of screened and nonscreened population groups are important. Research is needed to test the effectiveness of drug therapies for osteoporosis in men who do not have a history of fractures. The results of ongoing randomized trials of bisphosphonates for fracture prevention in men at high risk for fractures could help to assess whether these drugs are effective in men. Research to evaluate the outcome of screening women during periods of rapid bone loss (for example, during menopause) also should be supported.

Further research that would inform clinical decisions about screening for osteoporosis include studies to establish parameters for treatment using quantitative ultrasonography as a primary screening test for osteoporosis, studies that ascertain the true incidence of major osteoporotic fractures in nonwhite ethnic groups in the United States, studies clarifying optimal screening intervals, and studies of the effect of clinical and subclinical vertebral fractures on health-related quality of life.

Link to Full Article:
Ann Intern Med E-309published ahead of print January 17, 2011

Mid to Late-life Cholesterol and Dementia

Monday, January 24th, 2011

The 32-year relationship between cholesterol and dementia from midlife to late life. Neurology. November 23, 2010 75:1862-1863
Authors: Mielke, Zandi, Shao, et al

Methods:
The Prospective Population Study of Women, consisting of 1,462 women without dementia aged 38–60 years, was initiated in 1968–1969 in Gothenburg, Sweden. Follow-ups were conducted in 1974–1975, 1980–1981, 1992–1993, and 2000–2001. All-cause dementia was diagnosed according to DSM-III-R criteria and AD according to National Institute of Neurological and Communicative Disorders and Stroke–Alzheimer’s Disease and Related Disorders Association criteria. Cox proportional hazards regression examined baseline, time-dependent, and change in cholesterol levels in relation to incident dementia and AD among all participants. Analyses were repeated among participants who survived to the age of 70 years or older and participated in the 2000–2001 examination.

Results:
Higher cholesterol level in 1968 was not associated with an increased risk of AD (highest vs lowest quartile: hazard ratio [HR] 2.82, 95% confidence interval [CI] 0.94–8.43) among those who survived to and participated in the 2000–2001 examination. While there was no association between cholesterol level and dementia when considering all participants over 32 years, a time-dependent decrease in cholesterol over the follow-up was associated with an increased risk of dementia (HR 2.35, 95% CI 1.22–4.58).

Conclusion:

These data suggest that midlife cholesterol level is not associated with an increased risk of AD. However, there may be a slight risk among those surviving to an age at risk for dementia. Declining cholesterol levels from midlife to late life may better predict AD risk than levels obtained at one timepoint prior to dementia onset. Analytic strategies examining this and other risk factors across the lifespan may affect interpretation of results.

They pointed to animal and cell culture studies suggesting a causal link with high cholesterol leading to amyloid-beta deposition characteristic of Alzheimer’s disease. However, cholesterol declines in older age, “perhaps as a function of underlying subclinical pathology, sarcopenia, or change in appetite,” Haan explained. The study was also limited by loss of participants due to death or refusal, possible undiagnosed dementia, lack of genotyping for high-risk alleles, and unknown generalizability to men and populations outside of Sweden, the researchers noted.

Rivastigmine May Increase Mortality in Delirium among the Critically Ill

Sunday, November 28th, 2010

In the study “Effect of rivastigmine as an adjunct to usual care with haloperidol on duration of delirium and mortality in critically ill patients: a multicentre, double-blind, placebo-controlled randomised trial” , authors Maarten MJ, Roes, Honing et al concluded that Rivastigmine did not decrease duration of delirium and might have increased mortality.


The authors do not recommend use of rivastigmine to treat delirium in critically ill patients.

Delirium is frequently diagnosed in critically ill patients and is associated with adverse outcome. Impaired cholinergic neurotransmission seems to have an important role in the development of delirium. The study’s aim was to establish the effect of the cholinesterase inhibitor rivastigmine on the duration of delirium in critically ill.

Patients (aged ≥18 years) who were diagnosed with delirium were enrolled from six intensive care units in the Netherlands, and treated between November, 2008, and January, 2010. Patients were randomised (1:1 ratio) to receive an increasing dose of rivastigmine or placebo, starting at 0•75 mL (1•5 mg rivastigmine) twice daily and increasing in increments to 3 mL (6 mg rivastigmine) twice daily from day 10 onwards, as an adjunct to usual care based on haloperidol. The trial pharmacist generated the randomisation sequence by computer, and consecutively numbered bottles of the study drug according to this sequence to conceal allocation.

The primary outcome was the duration of delirium during hospital admission. Analysis was by intention to treat. Duration of delirium was censored for patients who died or were discharged from hospital while delirious. Patients, medical staff, and investigators were masked to treatment allocation. Members of the data safety and monitoring board (DSMB) were unmasked and did interim analyses every 3 months.

Findings
Although a sample size of 440 patients was planned, after inclusion of 104 patients with delirium who were eligible for the intention-to-treat analysis (n=54 on rivastigmine, n=50 on placebo), the DSMB recommended that the trial be halted because mortality in the rivastigmine group (n=12, 22%) was higher than in the placebo group (n=4, 8%; p=0•07). Median duration of delirium was longer in the rivastigmine group (5•0 days, IQR 2•7—14•2) than in the placebo group (3•0 days, IQR 1•0—9•3; p=0•06).

Interpretation
Rivastigmine did not decrease duration of delirium and might have increased mortality so we do not recommend use of rivastigmine to treat delirium in critically ill patients.

This trial is registered with ClinicalTrials.gov, number NCT00704301.

Funding
ZonMw, the Netherlands Brain Foundation, and Novartis.

Source
The Lancet, Volume 376, Issue 9755, Pages 1829 - 1837, 27 November 2010

Vaccinology Course November 18-19 2010

Sunday, November 7th, 2010

WHEN: November 18-19, 2010

WHERE:
San Lazaro Hospital Auditorium, Quiricada Street Sta. Cruz, Manila

The Vaccine Study Group, a research study group under the UP Manila – National Institutes of Health (NIH) has initiated and organized a Clinical Vaccinology Course for Health Care Providers, in cooperation of Philippine Foundation for Vaccination (PFV), Aging Study Group-NIH, San Lazaro Hospital and Society of Adolescent Medicine of the Philippines (SAMPI).


The main objective of the course is to give an overview and update in the field of vaccinology so that participants to the course will be confident to use vaccines both in clinical practice and as a public health intervention. The group believes that vaccination is the most effective control measure for diseases and would lead to an improvement of the health and economic status of communities and nations.


The course will be conducted by a group of distinguished professors, scientist and public health experts who have received basic and advanced vaccinology courses in France, Korea and other reputable vaccine institutions to enable them to give you what you would want to know most about vaccines.

HOW: Please contact the following to register (P2500.00 for two (2) days per registrant) or give a donation to our cause.

Dr Lulu C Bravo - Mobile No.: +6319189215998 or NIH 632-5254266 INTROP office: 5269167 PFV office: 567-2397.

Visit Link to Vaccinology Course Details

Call for Abstracts PSGM Asia Pacific Geriatric Conference Cebu 2011

Friday, October 29th, 2010

Philippine Society of Geriatric Medicine – Asia Pacific Geriatric Conference January 19-21, 2011, Cebu City, Philippines

The Organizing Committee through its Research Committee invites submission of abstracts in geriatrics and gerontology consistent with its theme, “Sharing and Integrating Best Practices in Geriatrics in the Asia Pacific Region.” These abstracts should be original and not be published elsewhere at the time of submission. A copy of the Institutional Review Board approval letter must be submitted for research abstracts.

Click here for Abstract submission detials

Cebu Asia-Pacific Geriatric Conference January 19-21 2011

Friday, October 15th, 2010

The Philippine Society of Geriatric Medicine will host the
4th Asia-Pacific Geriatric Network Conference, with the theme

“Sharing Best Practices in Geriatric Care in the Asia-Pacific Region”

Cebu CITY
January 19-21 2011

Click here to view the SCIENTIFIC PROGRAM and COMMITTEES

[caption id=”attachment_558″ align=”aligncenter” width=”231″ caption=”Convention Registration Fees 2011″]Convention Registration Fees 2011[/caption]

Convention Hotel: Marco Polo Cebu City

Registration and Housing Dates and Deadlines:

1. Registration and housing opens July 15, 2010
2. Early bird registration closes September 30, 2010
3. Last date to cancel registration and receive a refund minus an administrative fee of $75 or (peso equivalent) November 22, 2010.
4. Housing deadline to make a new reservation or change : November 30, 2010
5. On-site registration opens on January 18, 1:00 pm, Philippine time at the venue.

NOTE: Registration fee does not include housing or hotel accomodations!

For details, click this link to the Registration Page

Calcium May Increase Risk of Heart Attack

Sunday, September 19th, 2010

Calcium supplements are commonly prescribed to prevent and manage osteoporosis.

A few randomized trials on calcium supplements have shown an increased risk of cardiovascular adverse events in women taking calcium supplements. (Reid et al Am J Med 2006;119:777-85 and Bolland et al BMJ 2008;336:262-6)

[caption id=”attachment_523″ align=”aligncenter” width=”164″ caption=”osteoporotic hipfracture”]osteoporotic hipfracture[/caption]

A newly published meta analysis of clinical trials of calcium supplements (Bolland et al BMJ 2010 341 c3691) shows that calcium intake increases the risk of heart attacks (myocardial infarction) by 30%.

In this meta analysis, 15 trials were eligible for inclusion, five with
patient level data (8151 participants, median follow-up 3.6 years, interquartile range 2.7-4.3 years) and 11 with trial level data (11 921 participants, mean duration 4.0 years). The number of subjects in the analysis totalled 12,000 participants.

In the five studies contributing patient level data, 143 people allocated to calcium had a myocardial infarction compared with 111 allocated to placebo (hazard ratio 1.31, 95% confidence interval 1.02 to 1.67, P=0.035)

The authors conclude that calcium supplements (without co-administered vitamin D) are associated with an increased risk of myocardial infarction. As calcium supplements are widely used these modest increases in risk of cardiovascular disease might translate into a large burden of disease in the population.

Studies on Vitamin D with or without calcium are also warranted.

Paninigarilyo

Sunday, August 1st, 2010

From COMADD NIH Faculty Member Prof JD
March 13, 2010 2:00 pm

Nakapagtatakang di maunawaan.

Paninigarilyo’y di dapat simulan.

At kung nakaranas dapat ay tigilan.

Walang maidudulot kundi kasamaan.

Ito ay dahilan ng sakit na kanser.

Sakit din sa puso at iba pang klase.

Dahil ang panganib ay mas lumalaki.

Nikotinang sangkap siyang dumadale.

[caption id=”attachment_473″ align=”aligncenter” width=”96″ caption=”Cigarette-puffing Elderly”]Cigarette-puffing Elderly[/caption]

Isa pang masama’y amoy ng hininga.

Malayo ka pa lang simoy di maganda.

Kahit magsepilyo o maligo ka pa.

Amoy ng sigarilyo ay nakadikit na.

Maging perang laan para sa pagkain.

Kung nagsisigarilyo’y gutom titiisin.

Di ba naiisip ulcer ang aabutin.

O iba pang sakit kung iyong iisipin.

Batid nga ba ito ng nakararami?

O ang kabataa’y bulag nga o bingi?

Di nila makitang talagang posible.

Ang buhay na nila’y maigsi sa dati.

Kaya’t sana nama’y inyo ng isumpa.

Itong sigarilyong salot nga sa lupa.

Sinusunog nito ang pera at baga.

Dahil may adiksyong kadikit na sadya.

Dahil ang biktima’y lalong dumarami.

Kailangan pa bang sadyang makumbinsi.

Paninigarilyo ay hindi mabuti.

Baka mahuli na itong pagsisisi.

Centenarian Filipina Reveals Secrets to Longevity

Thursday, July 29th, 2010

Excerpt from Marjorie Gorospe, loQal.ph

115-year-old I-Apayao native Rufina Daluyon reflects the healthy lifestyle of the I-Apayao tribe and despite her age, the centenarian shows no signs of serious illness.

Apo Rufina can still talk and can still walk but she only speaks Ilocano. She shares her stories to willing listeners through her great granddaughter Susan.

1. Lifelong Physical Activity
The I-Apayao tribe is related to Isneg tribe and both tribes are known as good farmers.

2. Diet - mostly vegetables
Susan says being a member of the I-Apayao tribe, Apo Rufina is very fond of vegetables.

3. Good Genes
Apo Rufina’s husband lived for 126 years. Apo Rufina has three children, but only one among the three is still alive at a still remarkable age of 90.

4. Spirituality and Gratitude

5. Discipline
“Napakahigpit nya (Rufina) lalo pagdating sa pag-uwi ng maaga sa bahay at tamang pagkain. (She is very strict, particularly on curfews and eating the right food),” says Susan in jest.

[caption id=”attachment_453″ align=”aligncenter” width=”300″ caption=”Centenarian Northern Philippines”]Centenarian Northern Philippines[/caption]

“Minsan tinatanong na rin nya kung bakit di pa sya namamatay at mukha daw nalimutan na siya ni Lord sunduin. (She often wonders why she’s still alive and that the Lord probably has forgotten about her),” says Susan who often visits her great grandmother and gives her a shower.

For her part, Susan says she is thankful for the life that God has granted Apo Rufina.

But Susan admits that things are getting harder for Apo Rufina. Susan says all they can do is to give her the love that she deserves while she is still alive.

Folic Acid Does Not Prevent Memory Decline

Sunday, July 18th, 2010

The addition of folic acid to the list of vitamins and supplements for the prevention of memory decline is addressed in this meta-analysis. Wald et al conducted a meta-analysis of 9 randomized controlled trials on folic acid, with or without vitamin B and its effect on memory, speed of information processing, language and executive function (decision making). The median duration per study is 6 months and the median age of participants is 75 years.

The results showed no effect of folic acid in the prevention of cognitive decline (memory, speed of information processing, language and decision making) among individuals without preexisting dementia.

The pooled standardized mean difference
in cognitive function test scores was 0.01 (95% CI,
-0.08 to 0.10) after a median treatment of 6 months; an
increase of 1% of a standard deviation of a cognitive
function test score, with confidence intervals excluding
an improvement or a deterioration greater than 10% of 1
standard deviation.

Studies of longer duration are needed in order to address the role of folic acid in the prevention of cognitive decline.

Source: The American Journal of Medicine (2010) 123, 522-527