Every few years, a strain of bird flu becomes deadly to us. This year, the strain is H7N9 and it's already taking lives in China. Forgive my skepticism, but China may report only 13 deaths, but the true death toll could be higher. I suspect that it's higher.
So, what do we know about this bird flu?
I'd recommend the influenza A H7N9 resource page on the New England Journal of Medicine:
http://www.nejm.org/page/influenza
Of course, the CDC is also maintaining a page on Avian Flu.
This year, I suspect that social media monitoring/analytics may provide some valuable insights if this flu strain spreads globally.
Showing posts with label NEJM. Show all posts
Showing posts with label NEJM. Show all posts
Monday, April 15, 2013
Thursday, January 5, 2012
200 Years of the New England Journal of Medicine
It's amazing to see that the January 5th issue of the New England Journal of Medicine marks its 200th anniversary. The NEJM is doing quite a bit to promote this fact and they've published a series of very interesting articles to look back on the history of the journal. You can travel through time and see how medicine has evolved as technological advances have allowed physicians to cure diseases, fight illnesses, and discover new ailments. You can take a tour by visiting: http://nejm200.nejm.org/
Thursday, December 23, 2010
Can Congress Make You Buy Broccoli?
There's a fascinating editorial in the New England Journal of Medicine titled, "Can Congress Make You Buy Broccoli? And Why That’s a Hard Question." The authors are from the Department of Health Law, Bioethics, and Human Rights, Boston University School of Public Health, Boston. It was an interesting article, given that people are now debating the constitutionality of the Affordable Care Act (ACA). The authors point out four major reasons why the broccoli question is so difficult to answer. You can read the NEJM article here.
Wednesday, November 24, 2010
Which medical websites are physicians visiting?
What websites do physicians frequent? A company called comScore recently released some interesting data about professional medical websites. Here are some interesting stats from their report titled, "4 out of 5 U.S. Physicians Online Visited Health Care Professional Sites in Q1 2010":
% Reach of Physicians Online
Medscape.com 57.0%
NIH.gov 30.5%
Healthgrades.com 26.0%
Sermo.com 21.3%
NEJM.org 13.0%
I'm surprised they didn't list Wikipedia as an online website frequented by physicians. We know that many physicians are using Google to search for medical information and Wikipedia is often one of the top websites that appear on the search results.
% Reach of Physicians Online
Medscape.com 57.0%
NIH.gov 30.5%
Healthgrades.com 26.0%
Sermo.com 21.3%
NEJM.org 13.0%
I'm surprised they didn't list Wikipedia as an online website frequented by physicians. We know that many physicians are using Google to search for medical information and Wikipedia is often one of the top websites that appear on the search results.
Labels:
Medscape,
NEJM,
NIH,
online communities,
sermo,
social media
Wednesday, November 17, 2010
Telemonitoring in Patients with Heart Failure
Telemonitoring to Improve Heart Failure Outcomes (Tele-HF) was a multicenter, randomized, controlled trial designed to determine whether telemonitoring would reduce the combined end point of readmission or death from any cause among patients recently hospitalized for heart failure. What did you think about the findings published in the New England Journal of Medicine (NEJM)? The authors start by saying that "Small studies suggest that telemonitoring may improve heart-failure outcomes, but its effect in a large trial has not been established." Then, they conclude the paper with "Among patients recently hospitalized for heart failure, telemonitoring did not improve outcomes." Is this the final conclusion, or are we going to start over with the application and evaluation of newer telemonitoring technologies?
The authors definitely looked at a large sample of heart failure patients. 1653 patients were randomized to undergo either telemonitoring (826 patients) or usual care (827 patients). Telemonitoring was accomplished by means of a telephone-based interactive voice-response system that collected daily information about symptoms and weight that was reviewed by the patients' clinicians.
That type of telemonitoring technology sounds a bit archaic to me, but maybe it was considered "state of the art" for 2007. As we see advances in telemonitoring technology, what will we find in future studies?
The authors definitely looked at a large sample of heart failure patients. 1653 patients were randomized to undergo either telemonitoring (826 patients) or usual care (827 patients). Telemonitoring was accomplished by means of a telephone-based interactive voice-response system that collected daily information about symptoms and weight that was reviewed by the patients' clinicians.
That type of telemonitoring technology sounds a bit archaic to me, but maybe it was considered "state of the art" for 2007. As we see advances in telemonitoring technology, what will we find in future studies?
Monday, October 25, 2010
Cell Saver blood-recovery system (Haemonetics)
Haemonetics pioneered intraoperative cell salvage. Since its introduction in 1972 our Cell Saver® Autologous Blood Recovery system led the industry to become the standard of care.
The Cell Saver 5+ system is designed for surgeries like CABG, valve replacement, trauma, transplant, and other procedures where medium- to high-volume blood loss occurs. With the ability to deliver between 50-60% hematocrit and to remove nearly all traces of undesirable components such as free hemoglobin, the Cell Saver system is the standard of care and a critical tool to help avoid unnecessary allogeneic transfusions. And in a recent lab test, SmartSuction Harmony® surgical suction system significantly reduced hemolysis. Based on this finding, when a SmartSuction Harmony device is used with the Cell Saver system there may be an increase in the number of viable red blood cells reinfused to patients.
Labels:
hematology,
NEJM,
New England Journal of Medicine,
surgery
Wednesday, October 20, 2010
"Strategic napping" for medical and surgical residents?
How would you feel if your surgeon had just waken up from a "strategic nap" before operating on your brain? Here's a snippet from a recent New England Journal of Medicine commentary titled, "The ACGME’s Final Duty-Hour Standards — Special PGY-1 Limits and Strategic Napping." You'll see that I've highlighted the section on strategic napping:
On September 28, the Accreditation Council for Graduate Medical Education (ACGME) released new standards to which residency programs must adhere or risk losing their accreditation. Recognizing societal demands for improved patient safety, the task force that developed the standards has embraced stricter duty-hour limits and greater supervision for trainees in the first postgraduate year (PGY-1). The new standards reflect many of the recommendations made by the Institute of Medicine (IOM) in a 2008 report1 but differ from them on one critical issue — how graduate medical education (GME) programs can best prevent harmful medical errors committed by sleep-deprived residents. The IOM recommended that resident shifts longer than 16 hours include an uninterrupted 5-hour sleep period. The ACGME task force concluded that such a long sleep period was unworkable, instead recommending “strategic napping” during long shifts.
Are we kidding here? Do we really think that we're going to reduce medical errors by ensuring that our medical and surgical residents are taking "strategic naps?"
On September 28, the Accreditation Council for Graduate Medical Education (ACGME) released new standards to which residency programs must adhere or risk losing their accreditation. Recognizing societal demands for improved patient safety, the task force that developed the standards has embraced stricter duty-hour limits and greater supervision for trainees in the first postgraduate year (PGY-1). The new standards reflect many of the recommendations made by the Institute of Medicine (IOM) in a 2008 report1 but differ from them on one critical issue — how graduate medical education (GME) programs can best prevent harmful medical errors committed by sleep-deprived residents. The IOM recommended that resident shifts longer than 16 hours include an uninterrupted 5-hour sleep period. The ACGME task force concluded that such a long sleep period was unworkable, instead recommending “strategic napping” during long shifts.
Are we kidding here? Do we really think that we're going to reduce medical errors by ensuring that our medical and surgical residents are taking "strategic naps?"
Thursday, October 7, 2010
Accountable Care Organizations
What do you know about Accountable Care Organizations or ACOs? Is this the Silver Bullet that will fix the healthcare crisis?
Dr. Thomas Lee moderates a roundtable discussion addressing questions about the move toward ACOs under the Affordable Care Act. View the video of this NEJM roundtable discussion and contribute your comments.
Thomas H. Lee, M.D., Lawrence P. Casalino, M.D., Ph.D., Elliott S. Fisher, M.D., M.P.H., and Gail R. Wilensky, Ph.D.
N Engl J Med 2010; 363:e23October 7, 2010
Dr. Thomas Lee moderates a roundtable discussion addressing questions about the move toward ACOs under the Affordable Care Act. View the video of this NEJM roundtable discussion and contribute your comments.
Thomas H. Lee, M.D., Lawrence P. Casalino, M.D., Ph.D., Elliott S. Fisher, M.D., M.P.H., and Gail R. Wilensky, Ph.D.
N Engl J Med 2010; 363:e23October 7, 2010
Monday, July 26, 2010
The new NEJM.org
The New England Journal of Medicine (NEJM) website has been redesigned. Have you visited the "new" NEJM.org?
New features including Specialty Pages, the NEJM Archive, and My NEJM are among the new content and services highlighted.
New features including Specialty Pages, the NEJM Archive, and My NEJM are among the new content and services highlighted.
- The search function has improved and site navigation is much easier.
- The multimedia content is easier to navigate. If you're looking for an interactive medical case or a video, then you'll find it easily under the "multimedia" section under "articles."
- They've also added a social networking capability so that physicians and other clinicians can interact with other readers and have conversations about the content.
- Looking for an archived article? You can probably find it as a PDF on the new NEJM.org. I was reading an article published in 1833 (titled, "Fetid Abscesses — Remarks on the Fetid Abscesses Which Frequently Form in the Neighborhood of Mucous Membranes")
Labels:
multimedia,
NEJM,
New England Journal of Medicine
Wednesday, July 14, 2010
Thoughts about the final "meaningful use" rules
The final "meaningful use" rules came out yesterday. I'm still reading through the 800 page document and thinking about the amount of time it must have taken to come up with all these rules. The New England Journal of Medicine (NEJM) published a perspective article yesterday titled, "The “Meaningful Use” Regulation for Electronic Health Records." David Blumenthal, M.D., M.P.P., and Marilyn Tavenner, R.N., M.H.A. start the article with this paragraph:
Healthcare IT News is reporting that "Overall, AHA leaders said they remain concerned that the requirements may be out of reach for many hospitals. "Unfortunately, CMS continues to place some barriers in the way of achieving widespread IT adoption," AHA said in its statement."
The widespread use of electronic health records (EHRs) in the United States is inevitable. EHRs will improve caregivers’ decisions and patients’ outcomes. Once patients experience the benefits of this technology, they will demand nothing less from their providers. Hundreds of thousands of physicians have already seen these benefits in their clinical practice.They then remind the readers that:
Through HITECH, the federal government will commit unprecedented resources to supporting the adoption and use of EHRs. It will make available incentive payments totaling up to $27 billion over 10 years, or as much as $44,000 (through Medicare) and $63,750 (through Medicaid) per clinician. This funding will provide important support to achieve liftoff for the creation of a nationwide system of EHRs.That's a lot of money, but will it be adequate to ensure that hospitals and physicians are equipped with the support staff and the IT infrastructure to achieve "meaningful use" within their organizations?
Healthcare IT News is reporting that "Overall, AHA leaders said they remain concerned that the requirements may be out of reach for many hospitals. "Unfortunately, CMS continues to place some barriers in the way of achieving widespread IT adoption," AHA said in its statement."
Tuesday, July 6, 2010
Sensor-augmented insulin pump therapy for type 1 diabetes
We've seen some major advances in diabetes, insulin pumps, and glucose meters. I'm still waiting for the day when someone will announce that we have a fully functional artificial pancreas that doesn't require any user-input. Then, we'll have a truly closed-loop system that doesn't require any modifications from the user. A patient with type 1 diabetes could eat anything and this artificial pancreas would adjust the insulin dosages and regulate blood sugar like a real pancreas.
The New England Journal of Medicine (NEJM) recently published several articles about some technology advances in the care of patients with diabetes. Those articles are:
The New England Journal of Medicine (NEJM) recently published several articles about some technology advances in the care of patients with diabetes. Those articles are:
- Effectiveness of Sensor-Augmented Insulin-Pump Therapy in Type 1 Diabetes
- Continuous Glucose Monitoring — Coming of Age
We're probably going to see an increase in the use of continuous glucose monitors among patients with either type 1 or type 2 diabetes. Will this eventually become the "standard of care?" Right now, many people are unable to afford continuous glucose monitors and sensor-augmented pumps. How will this change over the next decade? Perhaps the biggest question is: who's going to pay for this expensive technology? If you're on the government-sponsored "public option" insurance plan, will you get coverage for this type of technology?
Monday, June 21, 2010
NEJM This Week on the iPhone or iPod touch
This app is a great example of a smartphone version of a medical journal. I'm sure we'll soon see every major medical journal offer smartphone apps so that busy health care professionals can access this content easily. Click here to access NEJM This Week
Thursday, June 3, 2010
Glomus tympanicum
Wouldn't you know it? It's glomus tympanicum. Sorry, but I don't remember learning about this in medical school. You won't find any information on Wikipedia either, so you'll have to do some traditional research to learn about it.
Friday, May 14, 2010
2 great medical technology articles in this week's NEJM
This week's New England Journal of Medicine (NEJM) has some great articles that focus on medical technology. The first is titled, "Robot-Assisted Therapy for Long-Term Upper-Limb Impairment after Stroke." In this study, the investigators found:
In patients with long-term upper-limb deficits after stroke, robot-assisted therapy did not significantly improve motor function at 12 weeks, as compared with usual care or intensive therapy. In secondary analyses, robot-assisted therapy improved outcomes over 36 weeks as compared with usual care but not with intensive therapy. (ClinicalTrials.gov number, NCT00372411 [ClinicalTrials.gov] .)The other fascinating article is titled, "An Entirely Subcutaneous Implantable Cardioverter–Defibrillator." We're not just talking about the body of the defibrillator. We're also talking about the leads. Can you imagine a defibrillator that doesn't require transvenous leads? Here's what the authors found:
In small, nonrandomized studies, an entirely subcutaneous ICD consistently detected and converted ventricular fibrillation induced during electrophysiological testing. The device also successfully detected and treated all 12 episodes of spontaneous, sustained ventricular tachyarrhythmia. (ClinicalTrials.gov numbers, NCT00399217 [ClinicalTrials.gov] and NCT00853645 [ClinicalTrials.gov] .)It's great to see how technology is changing the way we practice medicine. To read these articles, visit the NEJM (May 13, 2010 issue).
Labels:
cardiology,
NEJM,
New England Journal of Medicine,
robotics,
stroke
Monday, May 10, 2010
Effect of Bar-Code Technology on the Safety of Medication Administration
There's a great article in the The New England Journal of Medicine (NEJM) titled, "Effect of Bar-Code Technology on the Safety of Medication Administration." The use of technology in hospitals can significantly reduce medical errors.
Background: Serious medication errors are common in hospitals and often occur during order transcription or administration of medication. To help prevent such errors, technology has been developed to verify medications by incorporating bar-code verification technology within an electronic medication-administration system (bar-code eMAR).You can access the The New England Journal of Medicine (NEJM) abstract here: http://content.nejm.org/cgi/content/short/362/18/1698
Conclusions: Use of the bar-code eMAR substantially reduced the rate of errors in order transcription and in medication administration as well as potential adverse drug events, although it did not eliminate such errors. Our data show that the bar-code eMAR is an important intervention to improve medication safety. (ClinicalTrials.gov number, NCT00243373 [ClinicalTrials.gov] .)
Monday, April 19, 2010
Inhalers that use CFCs will be phased out
On April 13, 2010, the Food and Drug Administration (FDA) announced that seven metered dose inhalers that contain chlorofluorocarbons (CFCs) are being phased out in the United States.
- Tilade Inhaler (nedocromil), made by King Pharmaceuticals, last date for sale: June 14, 2010
- Alupent Inhalation Aerosol (metaproterenol), made by Boehringer Ingelheim Pharmaceuticals, last date for sale: June 14, 2010
- Azmacort Inhalation Aerosol (triamcinolone), made by Abbott Laboratories, last date for sale: Dec. 31, 2010
- Intal Inhaler (cromolyn), made by King Pharmaceuticals, last date for sale: Dec. 31, 2010
- Aerobid Inhaler System (flunisolide), made by Forest Laboratories, last date for sale: June 30, 2011
- Combivent Inhalation Aerosol (albuterol and ipratropium in combination), made by Boehringer Ingelheim Pharmaceuticals, last date for sale: Dec. 31, 2013
- Maxair Autohaler (pirbuterol), made by Graceway Pharmaceuticals, last date for sale: Dec. 31, 2013
You can learn more inhalers being phased out here.
Thursday, March 18, 2010
Social Media and Physicians on the NEJM
You don't see many articles on social media on the New England Journal of Medicine (NEJM). Here's one that may be of interest that starts with the following Editor’s Note:
“Social media has had a dramatic impact on the way the medical community communicates among its members and to the outside world. While it may be appropriate and safe to share deidentified cases or aggregate information with peers to ascertain the legitimacy of specific clinical approaches, research findings, policy issues, and professional needs or support, there are uses that pose potentially serious legal risks and consequences. These include the dissemination of information on specific patients, resulting in HIPAA violations, boundary breaches for “befriending” patients, and practicing medicine in jurisdictions where the clinician is not licensed. When using social media, physicians should ensure that they act responsibly and respect physician-patient confidentiality.”http://www.nejmjobs.org/career-resources/social-media-and-physicians.aspx
Labels:
NEJM,
New England Journal of Medicine,
social media
Do you remember what causes purple urine?
In medical school, we like to learn about zebras instead of horses. What I mean is that if you hear hoof beats, are you more likely to think about horses or zebras? We simply don't see rare diseases (zebras) because we tend to see more common diseases (horses). What's common is common. What's common is also more likely to present in an uncommon fashion.
So, what causes purple urine?
Here's the explanation from the NEJM (New England Journal of Medicine):
So, what causes purple urine?
Here's the explanation from the NEJM (New England Journal of Medicine):
Purple discoloration can occur in alkaline urine as a result of the degradation of indoxyl sulfate (indican), a metabolite of dietary tryptophan, into indigo (which is blue) and indirubin (which is red) by bacteria such as Providencia stuartii, Klebsiella pneumoniae, P. aeruginosa, Escherichia coli, and enterococcus species.When's the last time you saw any purple urine? To read more about purple urine on the NEJM, click here
Wednesday, March 17, 2010
More cardiology news from the ACC and the NEJM
Take a look at the list of recent NEJM publications:
Published Online March 15, 2010
- ORIGINAL ARTICLE -Lenient versus Strict Rate Control in Patients with Atrial Fibrillation
- EDITORIAL -Rate Control in Atrial Fibrillation
- ORIGINAL ARTICLE -Duration of Dual Antiplatelet Therapy after Implantation of Drug-Eluting Stents
- EDITORIAL -Optimal Duration of Clopidogrel Use after Implantation of Drug-Eluting Stents — Still in Doubt
- ORIGINAL ARTICLE -Effect of Nateglinide on the Incidence of Diabetes and Cardiovascular Events
- ORIGINAL ARTICLE -Effect of Valsartan on the Incidence of Diabetes and Cardiovascular Events
- EDITORIAL -Navigating the Choices for Diabetes Prevention
- ORIGINAL ARTICLE -Effects of Combination Lipid Therapy in Type 2 Diabetes Mellitus
- ORIGINAL ARTICLE -Effects of Intensive Blood-Pressure Control in Type 2 Diabetes Mellitus
- EDITORIAL -ACCORD and Risk-Factor Control in Type 2 Diabetes
Labels:
ACC,
cardiology,
cardiovascular,
NEJM,
New England Journal of Medicine
Sunday, March 14, 2010
ACCORD study data released at the ACC
In fact, there's an editorial in the NEJM titled, "ACCORD and Risk-Factor Control in Type 2 Diabetes." What's the bottom line?
- When it comes to lipid management in patients with type 2 diabetes: The combination of fenofibrate and simvastatin did not reduce the rate of fatal cardiovascular events, nonfatal myocardial infarction, or nonfatal stroke, as compared with simvastatin alone. The ACCORD study results do not support the routine use of combination therapy with fenofibrate and simvastatin to reduce cardiovascular risk in the majority of high-risk patients with type 2 diabetes.
- When it comes to blood pressure management: In patients with type 2 diabetes at high risk for cardiovascular events, targeting a systolic blood pressure of less than 120 mm Hg, as compared with less than 140 mm Hg, did not reduce the rate of a composite outcome of fatal and nonfatal major cardiovascular events.
So, many questions remain unanswered, but we know that aggressive lipid management with combination therapy may not be the best approach. We also know that in blood pressure management, "lower isn't always better." The medical management of diabetes needs to be individualized for each patient.
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