Sunday, February 26, 2012

Citrus Fruits May Lower Women's Stroke Risk

       oranges   Researchers have identified a compound found in oranges, grapefruits, and other citrus fruits that may lower a woman’s stroke risk.

           Previous studies suggest that eating fruits and vegetables helps protect against strokes, and many believe that antioxidant compounds known as flavonoids may explain why, because they have been shown to improve blood vessel function and they have anti-inflammatory effects.

       Among other things, flavonoids give fruits and veggies their vibrant colors. They are also found in chocolate and red wine. By some estimates there are more than 5,000 of them.

      In the newly published study, flavonoids abundant in citrus fruits known as flavanones appeared to give the most protection against stroke.

       Women whose diets included the highest amount of flavanones had a 19% lower risk of suffering a blood-clot-related stroke than women with the lowest intake of the compound.

      “Our study supports the conclusion that flavanones are associated with a modest reduction in stroke risk,” says researcher Kathryn M. Rexrode, MD, MPH, of Boston’s Harvard Medical School and Brigham and Women’s Hospital.

Source:http://www.webmd.com/stroke/news/20120223/citrus-fruits-may-lower-womens-stroke-risk

Saturday, February 25, 2012

FDA approves first Helicobacter pylori breath test for children

 

         Urea-breath-test  The first breath test for use in children ages 3 to 17 years to detect Helicobacter pylori (H. pylori) bacterial infections, responsible for chronic stomach inflammation (gastritis) and ulcers, was approved by the U.S. Food and Drug Administration (FDA) on Feb. 22, 2012.

              The FDA first cleared the BreathTek UBT test for adults in 1996. The U.S. Centers for Disease Control and Prevention (CDC) estimates that approximately two-thirds of the world’s population is infected with H. pylori. Most people with this infection never have any symptoms but have a two- to six-fold increased risk of developing gastric cancer and mucosal-associated-lymphoid-type lymphoma compared with uninfected people.

       “Results from this test, when considered with a physician’s assessment of the patient’s history, other risk factors, and professional guidelines, can quickly indicate infection, which allows a physician to initiate appropriate health measures in a timely manner,” said Alberto Gutierrez, Ph.D., director of the Office of In Vitro Diagnostic Device Evaluation and Safety in FDA’s Center for Devices and Radiological Health.

      The FDA based its approval of the BreathTek UBT test for children on a multi-center study of 176 patients, comparing its performance to a composite reference method and demonstrating 95.8 percent sensitivity and 99.2 percent specificity. An additional study was done at 1 to 6 months after therapy to support use for post-treatment monitoring of patients.  The sensitivity was 83.3 percent and the specificity was 100 percent. 

BreathTek UBT is manufactured by Otsuka America Pharmaceutical based in Rockville, Md.

Source: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm293278.htm

WHO takes India's name off polio endemic countries list

pulse  polio          WHO has taken India’s name off the list of polio endemic countries in view of the remarkable progress that India achieved by being polio free for the past one full year. The Union Minister for Health and Family Welfare Shri Ghulam Nabi Azad shared this important development today in the presence of Prime Minister of India Dr Manmohan Singh at the inaugural of the two day Polio Summit 2012 in New Delhi. The Polio Summit organised jointly by the Union Ministry of Health and Family Welfare and Rotary International also saw participation of Federal Minister for Interprovincial Coordination, Government of Pakistan, Mir Hazar Khan Bijrani; Minister of Health and Population, Government of Nepal Rajendra Mahato; Deputy Minister of Health, Government of Sri Lanka, Lalith Dissanayaka; Ministers of State for Health and Family Welfare, Shri Sudip Bandyopadhyay and Shri S Gandhiselvan, Secretary Health and Family Welfare Shri P K Pradhan, Rotary International President Mr. Kalyan Banerjee and The Rotary Foundation Chairman Mr. William Boyd as also subject experts from developing partners who have gathered at the Summit to renew and reinforce their commitment to eradicate polio in India.
        Reaffirming the commitment of India to achieve full immunization, Dr Manmohan Singh said “We must ensure that every Indian child, rich or poor, whether living in Ladakh or in Delhi has equal access to the best immunization. To this ambitious task I commit our government”. He noted that the coordinated efforts of the Government of India with close partnership of States Governments, international organizations and groups including the Rotary International, the World Health Organization and UNICEF and the 23 lakh volunteers as also supervisors, has helped to rid our country of the terrible scourge of Polio. The Prime Minister said “it is a matter of satisfaction that we have completed one year without any single new case of polio being reported from anywhere in the country. This gives us hope that we can finally eradicate polio not only from India but from the face of the entire mother earth. The success of our efforts shows that teamwork pays”.
        Dr Manmohan Singh also emphasized the need for nutritious food, safe drinking water, proper sanitation and education in addition to Universal access to safe vaccines. He said that we need to accelerate our efforts to achieve goal of providing universal access to health care at affordable cost for all our citizens. “The rising cost of health care is another key challenge. We are, therefore focusing our attention towards social security of the poor with regard to their health care. Public expenditure on health has increased from less than 1% of our GDP in 2006-07 to an estimated 1.4% of GDP by the end of the Eleventh Five year Plan. But we will need to work harder and do more if we have to reach our goal of increasing public expenditure on health to at least 2.5% of the GDP. Education and health will be the key priorities of the Twelfth Five Year Plan” he emphasized.
      Recalling India’s journey of combating Polio, the Union Minister for Health and Family Welfare Shri Ghulam Nabi Azad noted that the achievement of one full year without even a single polio case, which is being acclaimed worldwide, is the result of a strong political will at the highest levels making sure that there was never any shortage of resources or funds for the polio eradication initiative. He informed that 27 % of the global expenditure on polio eradication has come from India’s domestic resources. More than 99 percent coverage of children in the two remaining endemic states of Bihar and Uttar Pradesh is unprecedented, not witnessed anywhere else in the world on such a large scale, Shri Azad said. The aggressive mop up response against the polio virus has enabled us to stop further transmission of polio virus. He however added that we are highly mindful of the risks that persist not only on account of indigenous transmission but also importations from other endemic countries. “There is going to be zero tolerance for any new polio case and such a case will be declared as a public health emergency” he reiterated. All the states bordering the neighbouring countries have been alerted to strengthen surveillance for early detection of any imported polio virus. Special booths have been established in the bordering areas like Wagah border and Attari train station in Punjab and Munabo train station in Rajasthan, to ensure that all children under 5 years of age coming from across the border are given polio drops, the Minister added. The Polio Programme in India is the most shining example of strong and effective partnerships, Shri Azad noted. Shri Azad urged that we should re-dedicate ourselves and resolve that we will continue our efforts with the same vigour, so that India can be declared Polio Free by the year 2014
    

Source:http://pib.nic.in/newsite/erelease.aspx?relid=80530

Friday, February 24, 2012

Sequencing Human DNA in 15 mins- Revolution

    Nanopore_New_Images-26_copy-2  

          Oxford Nanopore, leading firm  in the field of mapping DNA, just announced two products that could dramatically change the field of DNA sequencing: a new DNA sequencer that may be able to handle a human genome in 15 minutes, and a USB thumb drive DNA sequencer that can read DNA directly from blood with no prep work.

     A nanopore is a ring of proteins, made by a bacterium, through which DNA can be threaded, like a string through a bead. In the method of DNA sequencing just debuted by Oxford Nanopore Technologies, long, intact strands of DNA are shunted through nanopores on a chip, and the electrical conductivity of each nucleic acid as it comes through the pore lets scientists tell which DNA “letter” it is—A, T, G, or C. A long strand of DNA analyzed this way, importantly, isn’t destroyed, so it can be reanalyzed, and errors introduced in processes that use chopping are also avoided. Using such basic physical laws to deduce a DNA sequence is a simple, elegant solution to a tough problem. That’s perhaps why nanopore sequencing methods have attracted some significant investment in recent years: the UN National Human Genome Research Institute had, by 2008, given $40 million to groups pursuing nanopore sequencing.

  Scientists are genuinely, if cautiously, excited by what they’ve seen of Oxford Nanopore’s work. I think it is all credible,” Chad Nusbaum, co-director of the Genome Sequencing and Analysis Program at the Broad Institute in Cambridge, Massachusetts, told Nature News. “I would bet they are even underplaying it because they don’t want to risk overpromising.” For scientists talking about biotech, that’s pretty hopeful phrasing.

Source:http://blogs.discovermagazine.com/80beats/2012/02/22/new-mini-dna-sequencer-size-of-a-usb-stick-is-fast-and-cheap/

          http://www.forbes.com/sites/matthewherper/2012/02/17/the-next-dna-disruptor/

FDA approves anorectic Qnexa

 

diet-pill-that-work         Qnexa was the first anti obesity drug approved by FDA in a decade. Last week expert advisory committee voted 20-2 in favour of Qnexa by Vivus as an antiobesity drug.This same drug was rejected by FDA in 2010 quoting the cardiac side effects and its teratogenic potential. But in a reversal it was accepted by majority of experts in the advisory committee.

    As the epidemic of obesity grows further the demand for approval of anti obesity drug was growing from all corners.In the last decade many antiobesity drugs were withdrawn from the market for their myriad no. of side effects. Even Qnexa had many issues.

      Qnexa is a combination of the anticonvulsant drug topiramate and the appetite suppressant phentermine.

    In a clinical trial involving 4,323 people, Qnexa  led to an average loss of about 10% of total body weight in the first year of use. Many users also saw improvements in blood pressure.
But the trials also found that that the drug caused a slight increase in heart rate, which can boost the odds of a heart attack or stroke. In addition, researchers detected an increased risk of birth defects — typically cleft lip — in women who became pregnant while taking the drug.

      Vivus Inc., the drug's manufacturer, addressed those concerns by proposing a tightly controlled system for prescribing Qnexa. To prevent birth defects, patients who take the drug will have to undergo monthly pregnancy testing and healthcare providers will get special training on the medication's risks and benefits. Vivus will also restrict distribution of the drug to registered pharmacies, among other measures.

Source:www.fda.gov/downloads/advisorycommittees/.../ucm218821.pdf

Thursday, February 23, 2012

Morbid obesity affects cognitive function?

        Morbid-Obesity Obesity is one of the important risk factors for Diabetes Mellitus , Cardiovascular diseases , microvasculopathy and many more diseases. But recently it has been found out that obesity also affects cognitive functions especially Memory.

      A research group  performed a prospective study total of 150 subjects (109 bariatric surgery patients enrolled in the Longitudinal Assessment of Bariatric Surgery project and 41 obese control subjects who had not undergone bariatric surgery). These 150 subjects completed a cognitive evaluation at baseline and at 12 weeks of follow-up. The demographic, medical, and psychosocial information was also collected to elucidate the possible mechanisms of change.

       The patients before bariatric surgery exhibited impaired performance at baseline.Same patients after 12 wks of bariatric surgery showed improved cognitive functions.The present results suggest that cognitive impairment is common in bariatric surgery patients, although these deficits might be at least partly reversible. Future studies are needed to clarify the underlying mechanisms, in particular, longitudinal studies using neuroimaging and blood markers.But this study adds one more dimension to the ill effects of obesity.

Gunstad, J., Strain, G., Devlin, M., Wing, R., Cohen, R., Paul, R., Crosby, R., & Mitchell, J. (2010). Improved memory function 12 weeks after bariatric surgery Surgery for Obesity and Related Diseases DOI: 10.1016/j.soard.2010.09.015

Source:http://www.sciencedirect.com/science/article/pii/S155072891000688X

Nilotinib as first-line therapy for chronic myeloid leukemia

        The history of treatment of chronic myeloid leukemia (CML) is divided into pre Tyrosine kinase inhibitor era and post Tyrosine kinase inhibitor era. The discovery of Imatinib revolutionized the treatment of CML and the mortality and morbidity associated with CML and chemotherapy have considerably decreased. There has been search for more tyrosine kinase (TKI)inhibitor for the treatment of CML as first line drugs. Dasatinib and Nilotinib have come up.

    It is considered that Nilotinib and Dasatinib can be used in Imatinib resistant CML. Nilotinib has been considered as 2nd line drug in the treatment till recent times. But latest trials have shown that Nilotinib is better than the legendary TKI Imatinib and Dasatinib in many aspects. It is safer,better tolerated and more efficacious drug than Imatinib and Dasatinib and clearly drug of choice in most patients with chronic phase CML.Recent article published in Indian Journal Of Cancer by Vaid A, Department of Medical Oncology,Cancer Institute,Medanta Hospital,Medicity,Gurgaon concludes that Nilotinib can be used as the first line therapy for chronic myeloid leukemia.

Source:http://www.indianjcancer.com/downloadpdf.asp?issn=0019-509X;year=2011;volume=48;issue=4;spage=438;epage=445;aulast=Vaid;type=2

Glucarpidase Approved to Lower Toxic Chemotherapy Levels in the Blood

 

          Last week, the Food and Drug Administration (FDA) approved glucarpidase (Voraxaze) to treat patients with toxic levels of the chemotherapy methotrexate (Abitrexate) in their blood.

       The kidneys usually eliminate methotrexate from the body, but patients receiving high doses of methotrexate can develop kidney failure. Glucarpidase is an enzyme that rapidly breaks down methotrexate into a nontoxic form that can be eliminated from the body more rapidly.

       “Prolonged exposure to high levels of methotrexate can result in kidney and liver damage, severe mouth sores, damage to the lining of the intestine, skin rashes, and death due to low blood counts,” explained Dr. Richard Pazdur, director of the Office of Hematology and Oncology Products in the FDA’s Center for Drug Evaluation and Research, in a news release.
Glucarpidase is designated an orphan drug, a designation given to therapies for diseases or conditions that affect fewer than 200,000 people in the United States.

        In a clinical study of 22 patients, treatment with intravenous glucarpidase was effective in 10 patients—that is, patients’ methotrexate levels fell below a critical level within 15 minutes and stayed below that level for 8 days. (Methotrexate levels were analyzed at NCI using a sensitive and specific test.) Although not all patients experienced this result, glucarpidase eliminated 95 percent of the methotrexate in all patients.

           A separate clinical study evaluated the safety of glucarpidase in 290 patients experiencing problems clearing methotrexate from their blood. The most common side effects observed in the study were low blood pressure, headache, nausea, vomiting, flushing, and abnormal skin sensation (paresthesia).

              Most of these patients were enrolled in a compassionate-use trial run by NCI’s Cancer Therapy Evaluation Program. The trial showed that glucarpidase was well tolerated and resulted in a rapid and profound decrease in methotrexate concentrations in the blood.

Source:http://www.cancer.gov/ncicancerbulletin/012412/page9

FDA approves Korlym for patients with endogenous Cushing’s syndrome

 

    On 17th Feb 2012, Korlym (mifepristone) was approved by the U.S. Food and Drug Administration to control high blood sugar levels (hyperglycemia) in adults with endogenous Cushing’s syndrome. This drug was approved for use in patients with endogenous Cushing’s syndrome who have type 2 diabetes or glucose intolerance and are not candidates for surgery or who have not responded to prior surgery. Korlym should never be used (contraindicated) by pregnant women.

   Prior to FDA’s approval of Korlym, there were no approved medical therapies for the treatment of endogenous Cushing’s syndrome.

  Endogenous Cushing’s syndrome is a serious, debilitating and rare multisystem disorder. It is caused by the overproduction of cortisol (a steroid hormone that increases blood sugar levels) by the adrenal glands. This syndrome most commonly affects adults between the ages of 25 and 40. About 5,000 patients will be eligible for Korlym treatment, which received an orphan drug designation by the FDA in 2007.

   Korlym blocks the binding of cortisol to its receptor. It does not decrease cortisol production but reduces the effects of excess cortisol, such as high blood sugar levels.

The safety and efficacy of Korlym in patients with endogenous Cushing’s syndrome was evaluated in a clinical trial with 50 patients. A separate open-label extension of this trial is ongoing. Additional evidence supporting the agency’s approval included several safety pharmacology studies, drug-drug interaction studies and published scientific literature. Patients experienced significant improvement in blood sugar control during Korlym treatment, including some patients who had marked reductions in their insulin requirements. Improvements in clinical signs and symptoms were reported by some patients.

   The most common side effects experienced by endogenous Cushing’s syndrome patients treated with Korlym in clinical trials were nausea, fatigue, headache, arthralgia, vomiting, swelling of the extremities, dizziness and decreased appetite. Other side effects of Korlym include adrenal insufficiency, low potassium levels, vaginal bleeding and a potential for heart conduction abnormalities. Certain drugs used in combination with Korlym may increase its drug level. Health care professionals must be aware of the potential for drug-drug interactions and adjust dosing or avoid using certain drugs with Korlym. 

    Korlym should never be used by pregnant women. Although pregnancy is an extremely rare occurrence in Cushing’s syndrome patients because of the suppressive effect of excess cortisol on female reproductive function, Korlym will carry a Boxed Warning advising health care professionals and patients that the therapy will terminate a pregnancy.

    The FDA has determined that a Risk Evaluation and Mitigation Strategy (REMS) is not necessary for Korlym to ensure that the benefits outweigh the risks for patients with endogenous Cushing’s syndrome. Several factors were considered in this determination including the following:

  • There are no other approved medical therapies for this debilitating form of Cushing’s syndrome and very sick patients would suffer if impediments to access were imposed.
  • The number of Cushing’s syndrome patients who will require treatment with Korlym is small, with an estimated 5,000 patients being eligible for treatment.
  • The number of health care professionals in the United States who would potentially prescribe Korlym is very small and highly specialized. They are familiar with the risks of Korlym treatment in the endogenous Cushing’s syndrome population and frequently monitor patient status.
  • The risks of Korlym treatment in the intended population can be managed through physician and patient labeling. The risks associated with Korlym will be outlined in a medication guide for patients.

The company has voluntarily proposed distributing Korlym through a central pharmacy to ensure the timely, convenient and appropriate delivery of the drug to Cushing’s patients or to the health care institutions where this therapy may be initiated. Most retail pharmacies are unlikely to keep adequate supplies of the drug for this rare condition and central distribution will give patients with Cushing’s syndrome better access to Korlym. 

Korlym is manufactured by Corcept Therapeutics of Menlo Park, Calif.

Source:http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm292462.htm

Wednesday, February 22, 2012

Post Graduate Diploma in Clinical Cardiology- An alternative to regular PG courses

      As the pool of non pg medical graduates is alarmingly increasing in India and the static development of medical facilities in medical colleges is creating a big vacuum in specialty medical sector.As many of medical graduates don’t wish to go to rural areas, they keep on trying for regular pg courses for years together.. And it is not wise to waste our precious years in mugging up silly mcq’s and trivia for years without serving the purpose of this education. As an alternative for regular pg courses, IGNOU has a cource pg diploma in clinical cardiology…

Post-Graduate Diploma in Clinical Cardiology (PGDCC)

Minimum Duration: 2 Years
Maximum Duration: 4 Years
Course Fee: Rs. 79,200
Minimum Age: No bar
Maximum Age: No bar
Eligibility:

MBBS (MCI recognised)

Note
Course Fees : Rs. 79,200 (Rs. 39,600/- per year. Student need to submit Rs. 39,600/- fee for the 1st Year fee during the admission. They need to submit the same amount as 2nd Year Fee before starting their 2nd Year Training.)

Click here for Study Centres

          While India has only about 150 positions for training Cardiologists (DM and DNB in Cardiology), less than hundred doctors eventually becomes specialists every year. There is wide gap between availability of cardiology expertise and load of cardiac morbidity in rural as well as urban area. Whatever cardiologists are trained, they are employed / practicing in metropolitan cities or large towns.

         This deprives the large population of our country from the cardiology expertise. In India , where 25 percent of the population are living below poverty line (2002) and more than 70 percent of them are living in rural area, most of the trained cardiologist are concentrated in the costly sophisticated tertiary care hospitals which are situated in the urban area. Since high tech hospitals are not only unaffordable but also non-accessible for most of the people of the country.

       This Programme will have a great social relevance. Indians are genetically three times more vulnerable for heart attack than Europeans. While the average age of heart attack victims in Europe is more than 60 years, the average age of Indians is between 40 to 50 making it a disease of breadwinner of the family causing major socio-economic upheavals.

       We are also genetically more vulnerable for diabetes at younger age , which again leads to premature atherosclerotic disease leading to heart attack. While in USA every fourth man develops heart attack before retirement in India it is every third man developing heart attack. One out of one thousand children in our country suffer from rheumatic valvular heart disease which if not treated early leads to major complications leading premature death. One out of hundred and forty children born anywhere in the world has heart disease. India produces the largest number of children in the world.

      So, for obvious reasons we produce the largest number of children with heart disease in the world. A country with over a billion population requires at least few thousands cardiologists to be produced every year to address the growing needs of the heart patients. If a doctor is trained as a Cardiologist after doing his MD in Medicine he obviously prefers to live in major city rather than migrating to smaller towns whereas if an MBBS doctor is given a course in Clinical Cardiology his chances of going to smaller towns ans semi-urban areas are bright.

OBJECTIVES

     To establish a core programme dedicated to train larger numbers of medical graduates in Clinical cardiology to deal effectively with the early recognition, management and prevention of common cardiovascular diseases (Non Invasive Cardiology) and associated diseases particularly Diabetes Mellitus.

Source:http://www.ignou.ac.in/ignou/aboutignou/school/sohs/programmes/detail/221/1

Spider naevi

pider naevi

Women with BRCA1 and BRCA2 mutations survive ovarian cancer at higher rates than those without mutations

 

      Results from a National Cancer Institute (NCI) sponsored multicenter study published in the Journal of the American Medical Association on January 25, 2012, provides strong evidence that BRCA1 and BRCA2 gene mutation carriers with ovarian cancer were more likely to survive in the five years following diagnosis than were women with ovarian cancer who do not have mutations in these genes. These findings expand on a 2011 abstract presentation of the results and also offer a contrast with a recent analysis of data from The Cancer Genome Atlas (TCGA) project, which reported an improved prognosis for only BRCA2 carriers. This new, larger study also found an improved prognosis for BRCA1 carriers, whereas the smaller TCGA data set suggested no difference between BRCA1 carriers and non-carriers.

         It is well known that rare mutations in the genes BRCA1 and BRCA2 confer high risks of both breast and ovarian cancer. While previous work suggested that ovarian cancer patients with a BRCA mutation have better survival than patients without these mutations, those studies were limited by small numbers and were not able to look at BRCA1 and BRCA2 mutations independently. In this study, NCI scientists further investigated the relationship between specific BRCA mutations and ovarian cancer survival. The investigators examined 1,213 cases of epithelial ovarian cancer, including 909 women with BRCA1 mutations, 304 with BRCA2 mutations, and 2,666 without mutations. They found that the BRCA2 mutation carriers had greater survival than BRCA1 mutation carriers. BRCA2 carriers showed a 52 percent survival rate at five years following diagnosis, while BRCA1 carriers showed a 44 percent survival rate. Women without the gene mutations had a survival rate of 36 percent. Previous work has suggested that the survival advantage of BRCA1 and BRCA2 mutation carriers may be due to a better response to platinum-based chemotherapy.

Source:http://www.cancer.gov/newscenter/pressreleases/2012/BRCAmutationsOvarianNewsNote/print

http://oncology-hematology.jwatch.org/

Disappointing News For Dapagliflozin

Matthew Mintz

As reported in the Wall Street Journal, the US FDA did not approve Astra Zenca and Bristol Myers Squib's pending drug dapagliflozin. According to the report, the companies stated that the FDA has requested additional clinical data "to allow for a better assessment of the benefit-risk profile for dapagliflozin." When the FDA requests "additional clinical data" this usually means there are unresolved safety concerns.  It also means there will certainly be a delay, as well as the possibility the drug never gets approved.  Concerns are likely due to higher than expected rates of breast and bladder cancer, as this was seen in some of the orginal studies submitted to the FDA.  Back in July, the FDA advisory panel voted against approving this drug, mainly for these safety concerns as well as some additional safety concerns regarding liver toxicity.

This is a major disappointment, as dapagliflozin was a novel diabetes agent.  It works by blocking SGLT2, which is important in the kidney's ability to reabsorb blood sugar. SGLT2 inhibitors like dapa prevent sugar reabsorption, and thus promote sugar excretion from the kidney.  Thus, diabetics taking this med literally lose sugar.  Though the efficacy of dapa is similar to the last generation of new drugs (TZD's, DPP4's), a significant side benefit is 1) by losing sugar you are losing calories and thus these medications promote weight loss and 2) when you lose sugar through the kidneys, you also lose fluid, which means dapa also works as a diuretic and can lower blood pressure.

Thus, as a diabetes pill that not only lowers blood sugar but also promotes weight loss and lower blood pressure, dapa and SGLT2 inhibitors are significant breakthroughs, making their delay all the more painful.

Source:http://boards.medscape.com/forums?128@96.Sz52ac2weTw@.2a2e9c87!comment=1

Cefpodoxime Flunks as a First-Line UTI Drug

 

Response rates were clearly inferior to those achieved with short-course ciprofloxacin.

Uncomplicated urinary tract infection (UTI) in women is easy to treat — so easy that guidelines advise reserving fluoroquinolones like ciprofloxacin for more-serious infections (Clin Infect Dis 2011; 52:e103). However, without the quinolones, the list of first-line drugs for a standard-issue Escherichia coli UTI is quite short.

In a recent, double-blind, randomized trial, researchers compared the oral fourth-generation cephalosporin cefpodoxime (Vantin) with ciprofloxacin in 300 young, healthy women with uncomplicated UTI. Treatment lasted for 3 days in each group.

Compared with women who received ciprofloxacin, those who received cefpodoxime were significantly less likely to sustain a microbiologic cure within 1 week after treatment (81% vs. 96%) and were also less likely to report complete clinical cure 1 month later (82% vs. 93%). Analyses of various subgroups (women with no prior UTI during the past year, women with strains susceptible to the study antibiotic) yielded similar results. Drug-related side effects were similar in both groups.

Comment: These results are sufficient to eliminate cefpodoxime from the list of first-line oral drugs for uncomplicated urinary tract infection. In fact, the official prescribing information for this drug acknowledges its "lower bacterial eradication rates" compared with those of other drug classes. Clinicians are left with trimethoprim-sulfamethoxazole, nitrofurantoin, fosfomycin, and — for those who choose to ignore rising concerns about drug resistance — the ever-tempting and convenient ciprofloxacin.

Abigail Zuger, MD

Published in Journal Watch General Medicine February 16, 2012

Fecal transplants: Natural treatment for IBD?

                Growing evidence for the effectiveness of fecal microbiota transplants as a treatment for patients with recurrent bouts of Clostridium difficile (C.difficile) associated diarrhea is presented in three studies -- including a long-term follow-up of colonoscopic fecal microbiota transplant (FMT) for recurrent C. difficile Infection that included 77 patients from five different states -- unveiled at the American College of Gastroenterology's (ACG) 76th Annual Scientific meeting in Washington, DC.

See Also:In a fourth study, investigators from the Centre for Digestive Diseases in Australia explored fecal bacterial transplantation as a treatment for Inflammatory Bowel Disease. While this is a new area of research, results of this study show success in treating IBD when the fecal transplant is done recurrently.

         The first study, "Long-term Follow-up of Colonoscopic Fecal Microbiota Transplant (FMT) for Recurrent C. difficile Infection (RCDI)," included 77 patients from five different states (RI, NY, OK, CA,WA) who previously had a colonoscopic fecal microbiota transplant at least three months ago for recurrent C. difficile infection, and found that FMT was successful in 70 out of 77 patients (91 percent) who were on average elderly, debilitated and had undergone multiple failed treatments, including antibiotic and probiotic therapies. Additionally, in six of the remaining seven patients, a single two-week course of vancomycin or a two-week vancomycin course plus one further FMT resulted in cure (98 percent).

      "Many of these patients we followed up with had been ill for a long time, but once they underwent the fecal microbiota transplant their response to the treatment was quick and their symptoms improved on average in about six days," said investigator Mark H. Mellow, MD, FACG, of INTERGRIS Baptist Medical Center in Oklahoma. The average duration of illness for these patients was 11 months, but after the procedure patients continued to improve and --without subsequent antibiotic treatment--did not have a recurrence of C. difficile infection during follow-up (on average , 17 months), according to Dr. Mellow and his team of co-investigators which included a leading pioneer of fecal microbiota transplantation, Lawrence J. Brandt, MD, MACG, of the Albert Einstein College of Medicine in New York.

      Results from a meta-analysis by researchers at the University of Toledo Medical Center were also unveiled, providing further evidence of the effectiveness of fecal microbiota transplantation. "Fecal Bacteriotherapy Works for Clostridium difficile Infection -A Meta-Analysis," reviewed the cases of 148 patients who had received fecal transplants for C. difficile infection. Follow-up ranged from 10 days to 62 months after the transplant, with an average follow-up of 1 year. Fecal transplant had an overall success rate of 85.4 percent, according to researchers, who also concluded that the procedure was a safe and effective treatment option for C. difficile infection.

          Clostridium difficile is a bacterium that causes infection leading to diarrhea and is most often related to antibiotic use during medical treatment. A major cause of morbidity and increasing health care costs among hospitalized patients, C. difficile infections have dramatically increased in recent years, with 500,000 cases in the United States annually and approximately 15,000 deaths each year, according to the U.S. Centers for Disease Control & Prevention. Up to 25 percent of patients will have a recurrence of C. difficile infection, and a proportion will be refractory to antibiotics. C. difficile is especially dangerous for patients with weakened immune systems such as the elderly and those with Inflammatory Bowel Disease (IBD). Therapies for this difficult-to-treat subpopulation include antibiotics, probiotics, toxin-binding medications, active vaccination, intravenous immunoglobon, and fecal microbiota transplant, for which the evidence has been mounting as an effective rescue for recurrent and refractory cases of C. difficile associated diarrhea.

       "While the concept of fecal transplantation may sound unpleasant to some, patient acceptance of this treatment is growing, especially when they have been suffering for months with recurrent C. difficile," said Dr. Mellow. "When we asked patients in our study about their choice of treatment if their infection recurred, 53 percent said fecal transplant would be their first choice for treatment."

          In a related study also unveiled at the ACG meeting, "Clostridium difficile Infection in Ulcerative Colitis: Increased Risk of Colectomy and Postoperative Infectious Complications," researchers from the University of Calgary found that patients with ulcerative colitis who were diagnosed with C. difficile were significantly less likely to respond to medical treatment and as a result require a colectomy when they diagnosed with C. difficile in the hospital or within 90 days of admission. In addition, patients with ulcerative colitis who had concomitant C. difficile, preoperatively were at a higher risk of infectious complications following a colectomy.

Researchers Find Fecal Microbiota Transplantation Effective For Treatment of IBD

   With the growing success of fecal transplantation for C.Difficile, researchers have started to explore the effectiveness of this procedure for other serious conditions, such as Inflammatory Bowel Disease (IBD). A second study, "Reversal of Inflammatory Bowel Disease (IBD) with Recurrent Fecal Microbiota Transplants (FMT)," reports successful treatment of severe mixed IBD using recurrent fecal microbiota transplants in three patient cases.

  • In Case 1, a 19-year old female with an 11-year history of severe IBD and who presented with worsening symptoms including bloody diarrhea and inflamed, ulcerated mucosa , and was considering a colectomy, experienced symptom improvement within several days after receiving FMT. She underwent FMT initially via colonoscopy in July 2009 then by seven daily rectal FMT and 26 weekly FMT's. Follow-up colonoscopy revealed no gross inflammation or edema, with the patient remaining clinically well.
  • In Case 2, a 23- year old male with a five-year history of steroid and anti-TNFα refractory ulcerative colitis presented with bloody diarrhea more than 20 times per day, anal fissures, severe abdominal pain and joint pain. Pre-FMT colonoscopy -- showed severe disease of the left colon with marked cecal inflammation. He underwent daily rectal FMT for the first month, followed by infusions of lessening frequency until he reached 1 FMT/6 weeks. He reported resolution of bleeding 1-2 weeks post-FMT, and formed stool at 1 month post-FMT, resumed work, study activities and regained weight. Colonoscopy at one year showed no histological inflammation but occasional pseudopolyps in the cecum and ascending colon.
  • In Case 3, a 57-year old female with a nine- year history of 5-ASA antibiotics, probiotics and immunosuppressant refractory ulcerative proctitis in spite of treatment. After training in our clinic, she performed 69, initially daily, then weekly rectal FMT with virtually immediate resolution of diarrhea, bleeding and mucus. Follow-up colonoscopy showed no visible or histological inflammation and she has remained off all therapy for the last four years.

      FMT may act as an antagonist to etiological infective agent(s) and aid in re-establishing depleted bacterial species, thereby reversing IBD, according to researchers from the Centre for Digestive Diseases in Australia.

   Commenting on the cases of FMT in IBD, lead researcher Thomas Borody, MD, PhD, FACG, said, "the rapid response of FMT and lack of adverse effects make FMT a viable option for treatment-refractory patients and is certainly an added option for those facing colectomy."

Source:http://www.sciencedaily.com/releases/2011/10/111031114945.htm

Introduction of Japanese Encephalitis Virus Genotype I, India

                  Seasonal outbreaks of fatal acute encephalitis syndrome (AES) occur regularly in several parts of India. Japanese encephalitis virus (JEV) has been the major and consistent cause of these outbreaks in the Gorakhpur region of Uttar Pradesh State, accounting for ≈10%–15% of total AES cases annually. In India, vaccinations against Japanese encephalitis (JE) are administered in areas where the disease is hyperendemic, including Gorakhpur, and AES cases are regularly investigated to clarify the effects of vaccination. Currently, >2,000 patients with AES are admitted each year to Baba Raghav Das Medical College, Gorakhpur.

            JEV is classified into 5 genotypes. Genotype III (GIII) is widely distributed in Asian countries, including Japan, South Korea, the People’s Republic of China, Taiwan, Vietnam, the Philippines, India, Nepal, and Sri Lanka . However, during the past decade, JEV GI has been introduced into South Korea, Thailand, and China and has replaced the GIII strains that had been circulating in Japan and Vietnam during the mid-1990s . Until 2007, all known JEV strains isolated in India belonged to GIII .

                The JE-endemic Gorakhpur region recorded a sudden increase in AES cases during September–November 2009. Clinical specimens collected from 694 hospitalized patients were examined for JEV infection by JEV-specific immunoglobulin M capture ELISA . Clinical specimens comprising 115 (16.6%) cerebrospinal fluid (CSF) specimens and 114 (16.4%) serum specimens showed recent JE infection among 158 (22.7%) of the case-patients.

                All CSF specimens were processed for JEV genome detection by diagnostic reverse transcription–PCR (RT-PCR), which amplified the nucleocapsid-premembrane genes. Additionally, envelope (E) gene–specific primers designed from Indian JEV isolate GP78 (GenBank accession no. AF075723) were used for E gene amplification.

The diagnostic RT-PCR detected JEV in 66 (9.5%) of 694 CSF specimens (GenBank accession nos. HM156543–HM156569, HM156573–HM156611). Among them, 27 sequences differed from the remaining 39, with only 86.2%–88.7% nt identity. The group of 27 sequences showed 99.2%–100% nt identity with each other and a high of 95.0% nt identity with Japanese GI swine JEV isolate (AB241119). The 39 sequences showed 94.2%–100.0% nt identity with each other and with other Indian GIII JEV strains. These findings indicate that both GI and GIII JEV strains circulate in the Gorakhpur region.

Figure

Thumbnail of Phylogenetic tree constructed by using a 1,381-nt Japanese encephalitis virus (JEV) envelope sequence directly amplified from cerebrospinal fluid specimens collected during the acute phase of illness from hospitalized acute encephalitis syndrome patients, India, September–November 2009. Multiple sequence alignment and phylogenetic analysis were conducted by using ClustalW software (www.ebi.ac.uk/Tools/clustalw2/index.html) and MEGA version 4 (www.megasoftware.net). The phylogenetic

Figure. Phylogenetic tree constructed by using a 1,381-nt Japanese encephalitis virus (JEV) envelope sequence directly amplified from cerebrospinal fluid specimens collected during the acute phase of illness from hospitalized acute encephalitis syndrome...

     The E gene sequence was amplified from 4/66 JEV-positive CSF samples (GenBank accession nos. HM156570–HM156572, HM156612). A comparison of E gene nucleotide sequences those of other JEV isolates from the region showed that 1 E gene sequence belonged to GIII and the other 3 to GI (Figure). The 3 GI E gene sequences were most similar (98.6%) with Japanese isolate 95–167/1995/swine (AY377579), followed by 98.5% similarity with Korean isolate K96A07/1996 (FJ938219). The single GIII E gene sequence showed 95.6%–99.8% nt identity with other Indian GIII isolates with the highest similarity (99.8% nt identity) with the 014178 (EF623987) JEV isolate from the 2001 Uttar Pradesh outbreak. Analysis of the E gene sequence amplified from 2 JEV isolates, obtained by injecting 29 CSF samples, positive by RT-PCR, into baby hamster kidney cells, showed 100.0% nt identity with sequences directly amplified from respective CSF specimens . Phylogenetic analysis of these E gene sequences, along with other 55 GenBank sequences, confirmed that 3 sequences belonged to JEV GI, and 1 belonged to GIII (Figure).

       The first JE outbreak in the Gorakhpur region was documented during 1978. Since then, JE epidemics have occurred regularly . This study demonstrated simultaneous detection and isolation of GI and GIII JEV strains from AES case-patients. Documented clinical symptoms among patients infected with the 2 strains were indistinguishable.

          GI JEV isolates from India share close genetic relationship with GI strains from Japan and Korea. In India, JEV neutralizing antibodies have been detected in 179 (34.8%) of 514 birds, including pond herons and cattle egrets, indicating a possible role in virus maintenance . Large perennial lakes, swamps, and rice fields provide a wintering and staging ground for several migratory waterfowl; such areas also favor breeding and survival of mosquitoes . Considering these conditions, GI JEV may have been introduced into India through migratory birds, as it has in other Asian countries . However, the exact mode of introduction of GI JEV into India is not known, and further studies are needed to determine the role of migratory birds in JE transmission.

        This study suggests the recent introduction of JEV GI strain in India. Simultaneous detection of GI and GIII strains indicates their co-circulation and association with human infections in Gorakhpur region. Because the live attenuated JE vaccine used in India is derived from GIII strain SA14–14–2, the efficacy of the vaccine to protect against GI JEV must be carefully evaluated. Thus, the genetic and antigenic variation among JEV strains circulating in India should be monitored to determine effects on JE epidemiology and ongoing vaccination efforts. Additionally, the expansion of GI JEV into other parts of India should be continuously tracked.

Pradip V. Fulmali, Gajanan N. Sapkal, Sulabha Athawale, Milind M. Gore, Akhilesh C. Mishra, and Vijay P. Bondre

Author affiliations: Author affiliations: National Institute of Virology, Pune, India (P. V. Fulmali, G.N. Sapkal, S. Athawale, A.C. Mishra, V.P. Bondre); National Institute of Virology, Gorakhpur, India (M.M. Gore)

Source:http://wwwnc.cdc.gov/eid/article/17/2/10-0815_article.htm

CDC Adult vaccination Recommendations 2012

 eCard: Adults need vaccines too!

                     Each year the U.S. recommended immunization schedule for adults is reviewed by scientific and medical experts who examine research on effective control of vaccine-preventable diseases. Changes in the 2012 recommendations reflect research that shows the best way to protect you and young, vulnerable children around you..

Take a look at the following updates; one or more may apply to you.

Hepatitis B Vaccination

Adults recently diagnosed with diabetes who are younger than 60 years old are now recommended to receive the hepatitis B vaccine as soon as possible.

HPV Vaccine

Males 22 through 26 years of age whose immune systems are weakened, who have sex with men, or who test positive for HIV, are now recommended to receive the HPV (human papillomavirus) vaccine. The HPV4 vaccine is also recommended for all boys at age 11 or 12 and catch-up vaccinations for males age 13 through 21 years.

Influenza Vaccine

A yearly flu vaccination is still recommended for everyone six months of age and older, but especially for seniors over 65, pregnant women, and those with health conditions like diabetes, asthma or heart disease. These groups are at high risk for serious flu-related complications.

Pneumoccocal Vaccine

The U.S. Food and Drug Administration (FDA) recently announced the approval of Prevnar 13, a pneumococcal vaccine, for use in adults age 50 years and older. Although CDC recommends that those age 65 and older and those age 19 through 64 with certain health conditions get another pneumococcal vaccine called Pneumovax, CDC has not issued any formal recommendation concerning Prevnar 13. Talk with your doctor if you have questions.

Tdap and Td Vaccine
  • The Tdap (tetanus, diphtheria, and pertussis) vaccine is now recommended for women in the third or late second trimester (20th week or more) of their pregnancy. 
  • Tdap is recommended for all those who are close contacts of infants younger than 12 months of age – for example, parents, guardians, grandparents, babysitters, nannies, teachers, and those who have not previously received the Tdap vaccine.
  • Other adults, who are not close contacts of children younger than 12 months of age, are still recommended to receive a one-time dose of the Tdap vaccine. After your initial dose of Tdap, you’ll need the Td booster every 10 years. But you don’t need to wait to get the Tdap vaccine if you have recently been vaccinated with the Td booster.
Zoster (Shingles) Vaccine

The FDA recently approved the use of zoster vaccine in those 50 years old; however, CDC continues to recommend that vaccination for shingles begin at age 60.

Source: http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6104a9.htm

Great guide for USMLE aspirants--Dr Conrad Fischer

  conrad fischer   The competition in this world is at its peak. Not all can fight and survive in this world. Few guys survive on their own but few need someone who can direct him towards right path. And the guiding force behind myriad no. of USMLE aspirants is Dr Conrad Fischer.

       Dr. Conrad Fischer is an award-winning medical educator, Associate Chief of Medicine for Educational and Academic Activities at SUNY Downstate School of Medicine, and Attending Physician at Kings County Hospital in Brooklyn NY, and a public health advocate.  He is the author of numerous USMLE test preparation guides and he teaches USMLE test preparation for Kaplan Medical.

           He is the author of Routine Miracles: Restoring Faith and Hope in Medicine, available from Kaplan Publishing wherever books are sold starting in September 2009.

The no. of students who were helped by his teaching is innumerable.. Students especially from South East Asian region are helped by his videos.

The changing scenario in Indian Medical Entrance is creating a necessity for teachers like Dr Conrad Fischer in India. There are few very good teachers in India for entrance preparation. To name a few Dr Thameem Saif, Dr Rajesh Kaushal, Dr Rajmurali Dr Shanmugapriya Dr Sunil..

Dr. Conrad Fischer’s blog http://seefisch.wordpress.com/

Follow him on facebook  https://www.facebook.com/pages/Conrad-Fischer-MD/121433839892?ref=ts

Twitter:https://twitter.com/#!/seefisch

Saturday, February 18, 2012

15 mins old gets pacemaker..

             Jaya Maharaj was 15 minutes old when she was sent to surgery at Lucile Packard Children’s Hospital and given a pacemaker that saved her life. The tiny girl — born nine weeks early, weighing 3.5 pounds, with a heart slightly bigger than a walnut — had been diagnosed before birth with congenital heart block. She is smaller than any pacemaker recipient ever reported in the medical literature.

Maharaj Baby

                    Jaya’s surgery is remarkable not just because of her small size but because many fetuses with her condition, congenital heart block, do not survive pregnancy. Research has shown that 20 to 50 percent of patients diagnosed prenatally die in utero or in the first weeks after birth. Yet premature delivery to implant a pacemaker carries its own hazards. When Leanne Maharaj, Jaya’s mom, was first referred to Packard Children’s from her hometown of Hayward, Calif., at 28 weeks pregnant, her doctors weighed the conflicting risks.

          “We knew that at any time the baby’s heart could give out,” said neonatologist Valerie Chock, MD, a member of the large, multidisciplinary team that planned Jaya’s birth and surgery. “We had to decide: At what point do we deliver to balance that risk against the risk of premature delivery?”

               Congenital heart block develops if, during pregnancy, the mother’s immune system mistakenly attacks nerve fibers that transmit heartbeat signals through the fetal heart muscle. When this happens, the fetal heart rate becomes dangerously slow. Congestive heart failure can develop, in which fluid backs up around the heart and lungs, and the body can’t get oxygen needed for growth. Even worse, the heart’s different chambers may beat in an uncoordinated way, and the heart can stop.

                    “So much was in the balance,” said Yasser El-Sayed, MD, the Packard Children’s high-risk obstetrician who oversaw Leanne’s care during pregnancy. “We just had to take it day by day, week by week.”

                    The threat to their eagerly awaited first baby was painful for Leanne and her husband, Kamneel, who relied on their extended family and their Hindu religion to cope. “Praying every day gave us faith and hope that something would help,” Kamneel recalled.

Norbert von der Groeben description of photo

                Jaya Maharaj received a pacemaker when her heart was the size of a walnut. Doctors say she can now expect to lead a normal life.

          Chock and El-Sayed worked with specialists in pediatric cardiology, cardiac electrophysiology, cardiac surgery, cardiovascular anesthesia, respiratory therapy and pharmacy to make sure every aspect of Jaya and Leanne’s complex case was addressed. Such collaborations are a regular occurrence in Packard Children’s Center for Fetal and Maternal Health, which coordinates care for high-risk pregnancies and has treated a few congenital heart block cases in the past.

                 The medical team checked Jaya twice a week before birth, monitoring her heart rate and growth, and looking for fluid around her heart and lungs. Leanne was given a steroid medication to minimize continued damage to Jaya’s heart. Because the baby was growing and not showing signs of heart failure, the team decided they could wait until 31 weeks’ gestation to deliver her.

          Early on Nov. 22, Leanne was wheeled into an operating room where about 25 clinicians waited to perform her cesarean and stabilize the newborn. In the adjacent operating room, another team prepared for Jaya’s surgery.

          The delivery went quickly. “When they took her out, she was crying, and my husband started crying,” Leanne remembered.

         Several clinicians set to work on Jaya: checking her heart rate, putting in a breathing tube and intravenous catheters for surgery, checking her oxygen levels, and administering medication for her premature lungs. Jaya’s 3.5-pound size, healthy for such a premature baby, confirmed that her heart defect had not hampered her growth in the womb. But her heart was beating only 45 beats per minute — far below a typical newborn’s rate of 120 to 150 beats per minute, and below the threshold of 55 beats per minute at which immediate artificial pacing is considered essential. The team had to begin her heart surgery as soon as possible.

       After the first flurry of activity, Leanne and Kamneel quickly greeted their baby. Then she was wheeled next door.

         The surgeon, Katsuhide Maeda, MD, had planned to give Jaya temporary pacing wires that would connect her heart to a device outside her body that generated a heartbeat signal. This approach has been used in tiny preemies before. It allows for a quick initial surgery but has the disadvantage of requiring the patient to go through a second chest surgery a few weeks later to implant a permanent pacemaker.

              In the operating room, Maeda revised his plan. “Jaya was in critical condition, but not so sick as to have needed chest compressions,” Maeda said. Though slow, Jaya’s heart rate was stable, so Maeda decided he could implant a permanent pacemaker and spare Jaya a second surgery a few weeks later.

               Still, Maeda proceeded cautiously. “Her heart muscle was so fragile that I had to be extra careful about putting stitches in,” he said. “The heart muscle on such a small baby is easily torn; that’s why people usually prefer just putting in temporary pacing wires.”

               With eight stitches total, Maeda connected two pacemaker leads to Jaya’s heart. He then implanted a pacemaker in her upper abdomen. The surgery was finished and Jaya’s heart rate had been raised to normal by the time she was two hours old.

After surgery, Jaya spent six weeks in the Neonatal Intensive Care Unit. With her heart pumping properly, she grew rapidly and was able to go home on Jan. 12. Her prognosis is excellent: Her pacemaker leads must be repositioned occasionally as she grows, and she will need new pacemaker batteries every five to seven years, but otherwise she will be able to lead a normal life.

Source:http://med.stanford.edu/ism/2012/february/pacemaker-0213.html

Friday, February 17, 2012

Renal Artery Stenting V/S Medical therapy in the treatment of Atherosclerotic Renal Artery Stenosis

          renal-stenting

         Atherosclerotic renal artery Stenosis (ARAS) is a far more common problem in India that thought.It is concluded that about 0.8% of Indian urban population has significant Atherosclerotic Renal artery stenosis.Its been long argued which therapeutic modality is the best for the treatment of ARAS.After few randomized trials its being concluded that Medical therapy(Renin Angiotensin Aldosterone System ) is the best therapy for the treatment of ARAS.

  Why renal artery stenting doesn't work in ARAS?
1.ARAS not only involves Renal artery but also intrarenal artery ,arterioles and peritubular capillaries. Stenting will not have any effect on Intrarenal  Atherosclerotic Renal Vascular Disease(ARVD)
2.ARAS protects the kidney from the ill effects of hypertension as the flow beyond the obstruction or stenosis is decreased. Stenting removes the stenosis or obstruction and kidney is exposed to high bp.
3.Stenting may cause distal atheroembolism,dissection of renal artery and cholesterol embolism that might accelerate the renal damage.

         In summary, published RCT provide no support for the notion that renal angioplasty with stenting improves blood pressure, preserves renal function or, reduces episodes of congestive heart failure in patients with ARAS. RA stenting is associated with procedure related morbidity and mortality. Agents that block RAAS improve outcomes and should be  a part of the medical regimen in ARAS.Medical therapy effectively controls ARVD at all levels of the vasculature and hence is the best therapy  for ARAS.

Source:http://www.indianjnephrol.org/downloadpdf.asp?issn=0971-4065;year=2012;volume=22;issue=1;spage=1;epage=4;aulast=Annigeri;type=2

Wednesday, February 15, 2012

Endocrine Society of India management guidelines for patients with thyroid nodules


Introduction
The term "thyroid nodule" refers to a distinct lesion within the thyroid gland that is palpably or radiologically distinct from the surrounding thyroid parenchyma. Thyroid nodules are common, seen in about 8.5% of the population. [1] They are more common among women. In India the prevalence of a palpable thyroid nodule in the community is about 12.2%, according to a recent study. [2] However, thyroid cancer is quite rare, and the incidence is 8.7 per 100000 people per year, though this seems to be increasing over the years. [3] Hence, whenever a patient presents with a thyroid swelling, the task of the clinician is to distinguish the benign nodule from the malignant one. This is a difficult task, and no test is perfect in this regard. However, a reasonable amount of success can be achieved by a good clinical evaluation and investigations.

Consensus Methods
The consensus committee reviewed three types of manuscripts: (1) Original Articles pertaining to the management of thyroid nodules published in the last 3 years (2) Consensus Statements published by various international societies and (3) Selected reviews and commentaries to assess expert opinion. Based on these three sources, the committee identified important clinical questions that needed to be answered. The answers to these questions were scored by the authors according to the modified United States Preventive Services Task Force (see http://consensus.nih.gov) used by the American Thyroid Association (henceforth referred to as the USPSTF-ATA) for grading its panelists' recommendations for managing thyroid nodules. [4] The grading is summarized below. It is important to note that only selected management points (and not all matter in the text) were subjected to consensus strength grading and the majority opinion was taken as the final score. The committee is aware that these guidelines will be used by thyroid specialists and non-specialists, and has tailored the recommendations to suit the management of thyroid nodules, which are very commonly encountered by doctors in the country [Table 1].


Table 1: Rating of panelists' evidence used for this consensus

Question 1. Which thyroid nodules need evaluation?
All thyroid nodules >1 cm need evaluation (recommendation strength: A). This includes both palpable and non-palpable nodules, the latter being radiologically distinct "incidentalomas" which are discovered by chance on imaging. Nodules that are below 1 cm need to be evaluated based on individual risk (see below).
The etiologies of thyroid nodules are important as these have an important link with nodule evaluation. Local or systemic features to suggest any of the ominous ones among these etiologies [Table 2] should provoke nodule evaluation, irrespective of the size. The etiology of thyroid nodules is diverse [Table 2]. Benign causes include the colloid nodule and the classical multinodular goiter. Occasionally, Hashimoto's thyroiditis and Graves' Disease may present with nodularity. Malignant causes include thyroid cancer, lymphoma as well as metastasis to the thyroid gland.


Table 2: Important causes of thyroid nodules

Question 2. What "clinical" features increase the risk of a thyroid nodule harboring malignancy?
Here, the term "clinical" evaluation refers to history and physical examination, a very important factor in the Indian setting, where state-of-the-art facilities may not be uniformly available (recommendation strength: C). The focus of clinical evaluation is to differentiate thyroid cancers from benign swellings. The following features are suspicious and should suggest a malignant thyroid swelling: family history of thyroid cancer or thyroid cancer syndrome (for e.g., multiple endocrine neoplasia), rapid nodule growth, a very firm/hard nodule, clinical signs of fixity to surrounding structures, vocal cord paralysis/hoarseness of voice, regional lymph node enlargement or the presence of another lesion (for e.g., a lung mass on respiratory examination) that suggests a distant metastases. While the above-mentioned features are classical features, it must be remembered that many patients do not come with these typical features, and the presence of the following factors in addition to the thyroid nodule should evoke further investigations: a history of radiation, male gender, extremes of age (<20 or >70 years), history of neck irradiation, nodule >4 cm in size or the presence of any pressure symptoms. [5]


Question 3. What investigations are appropriate for thyroid nodule management?
A serum TSH, an ultrasound evaluation and an fine needle aspiration cytology (FNAC) is appropriate for almost all thyroid nodules (recommendation strength A). These tests and their interpretation are described below. The role of nuclear scintigraphy is also discussed.
The Serum TSH
A TSH value that is < 0.2 mU/L indicates hyperthyroidism and a TSH that is >4 mU/L indicates hypothyroidism, and both are situations where medical therapy may be considered (recommendation strength: B). If the serum TSH is low, then a nuclear scan may be performed to look for a hot nodule. If the "hot" nodule corresponds to the radiologically discrete nodule (see below) then no further evaluation may be required (recommendation strength: B). It is important to note that a high TSH (particularly a slightly high TSH) does not exclude malignancy and when associated with thyroid nodule, a full evaluation including ultrasound/FNAC still needs to be performed. (recommendation strength: B)
Ultrasonography
All cases of suspected or confirmed thyroid nodules must be evaluated by ultrasound (recommendation rating A). This includes incidentalomas discovered on CT, MRI or PET scanning. The ultrasonography (USG) is the most cost-effective imaging procedure, and is highly sensitive in assessing nodule size and number. [6] Firstly, the USG can discern if the palpable abnormality is indeed a thyroid nodule. In addition other features of the nodule can be described: size, regional lymphadenopathy, location and the percentage of nodule volume that is cystic (the last 2 nodule features can help plan an FNAB). Combining the USG with a Doppler can result in a better estimation of malignant potential: risk of malignancy is lower when a nodule has an exclusively perinodular vascular pattern and the risk of malignancy may be higher when there is a purely central vascular pattern. In short, the following USG patterns suggest malignancy: irregular shape, ill-defined borders, hypoechogenecity, solidity, heterogenous internal echoes, microcalcifications, absence of a halo, an anteroposterior to transverse diameter ratio (A/T) greater than 1, infiltration into regional structures and suspicious regional lymph nodes. Of note, while multinodularity does not exclude malignancy, the absence of a truly dominant nodule in this setting may make cancer an unlikely possibility.
Fine needle aspiration biopsy
Every patient with a palpable thyroid nodule should undergo an FNAB (recommendation strength A). Every patient with a thyroid nodule that is >1cm must undergo FNAB (recommendation strength B). Hyperthyroid patients with "cold" nodules on scintigraphy as well as hypothyroid subjects with discrete nodules on ultrasound need FNAB. The FNAB is unarguably the best single test, and uses a 23-27-G needle to aspirate samples for cytological assessment. With experience, adequate samples can be obtained in >95% cases. USG-guided FNAB can lower the occurrence of non-diagnostic smears. [7] Degenerating and cystic nodules are problematic to aspirate. In this setting, the accuracy is improved by using ultrasound-guided aspirations from the appropriate solid zones. Overall all, a USG-guided FNAB with an onsite confirmation of adequate cellularity of the smear by a trained cytopathologist is the investigation with the highest sensitivity and specificity. In suspicious nodules, taking multiple aspirates will help to improve the sensitivity.
Palpation versus ultrasonography-guided fine needle aspiration biopsy
This is important from the Indian perspective, where treatment strategies are often guided by ground realities such as the patient's economic status. Palpation-guided FNAB is less expensive, can be performed by the practitioner, and has a reasonable level of accuracy (recommendation strength B). However, USG-guided FNAB is a very superior test (recommendation strength A). Although USG-guided FNAB is always preferable, palpation-guided FNA may still be carried out when a thyroid nodule >1 cm in maximum diameter is confirmed via USG examination. The USG is important here, as physical examination is inaccurate in assessing nodule size, its origin from the thyroid gland itself (as opposed to origin from adjacent tissues) and the degree of cystic change. In certain situations, the USG-guided FNAB becomes mandatory, and palpation-guided FNAB should never be used- this includes the following scenarios (recommendation strength: F): non-palpable nodules, nodules with >25% cystic change, previously FNAB-inconclusive nodules as well as suspicious nodules. These issues regarding FNAB, in addition to issue of training, technique, interpretation and consent have been described in detail and will not be covered here. [8],[9],[10]
Choosing the nodule for fine needle aspiration biopsy in multinodular goiter
In cases of multinodular goiter, the following criteria may be used to decide on the appropriate nodule for FNAB in the order listed: (1) nodules >1 cm in largest diameter with microcalcifications, (2) nodules >1.5 cm which is predominantly solid or has coarse calcifications, (3) nodules >2 cm which are mixed solid cystic or have undergone "substantial" growth since last ultrasound, (4) the largest nodule, in which the last criteria is controversial. It is questionable whether the USG-guided FNAB should choose nodules based on the size, or whether it must be based on nodule characteristics. For the present the consensus committee does not recommend for or against the last criteria (recommendation strength: F). The consensus panel also declines to define "substantial" USG-detected growth of the nodule over time (recommendation strength: F). A recent consensus has outlined the aforementioned characteristics, while also categorically stating that FNAB is not essential in "diffusely enlarged glands with multiple nodules of similar US appearance without intervening normal parenchyma". [11] This guideline also states that the first three aforementioned criteria be used in the decision for FNAB on solitary nodules. [11]
Radionuclide scanning
Nuclear scans use either one of the isotopes of iodine or technetium. These are handled differently by the follicular cells. Normal follicular cells take up both, but only radioiodine is organified and stored. Most benign and malignant neoplasms concentrate isotopes less avidly leading to a "cold' area on scanning. The rate of malignancy is about 10-15% in cold nodules, whereas malignancy is very unlikely in hot nodules. A hot nodule suggests hyperthyroidism-such nodules are usually not malignant. Nuclear scanning is a useful, but not an essential test in the routine evaluation of all thyroid nodules (recommendation strength I). This is in accordance with the well-accepted American Thyroid Association Guideline. [4]
Investigations to detect airway obstruction
Upper airways obstruction is rare in patients with goiter and is indicated by symptoms such as breathlessness and choking. There is a lack of correlation between the clinically assessed size of the goiter and the likelihood of upper airways obstruction. Plain radiography of the thoracic inlet and respiratory flow volume loops are specific means of identifying patients with functional tracheal compression who may need surgery (recommendation strength C). The better way to delineate deviation and compression of trachea is a spiral CT scan which could be done without contrast and is often required prior to operation.
Other tests
Anti-thyroid peroxidase antibodies are useful if Hashimoto's thyroiditis is suspected. However, thyroiditis can coexist with thyroid cancer and therefore a euthyroid patient with a nodule will still need evaluation despite antibodies being positive. The use of serum calcitonin measurements and serum thyroglobulin in the evaluation of thyroid nodules is controversial (recommendation strength F). [12]
Question 4. Is there a simple algorithm for thyroid nodule management?
It is often important to use a logical and step-wise approach in the management of thyroid nodules, and [Figure 1] lists such a strategy. However, the consensus committee strongly recommends against following any simple algorithm for all subjects (recommendation strength: F) and opines that therapies be individualized.


Figure 1: An algorithm for managing thyroid nodules. At any level, an intermediate result can justify the use of nuclear scintigraphy

Question 5. What are the indications for surgery?
Despite the many investigative options available to the clinician, the management of the nodule essentially depends on the FNAB result (recommendation strength: B). The possible reports from the cytopathologist are benign, malignant/suspicious, indeterminate and non-diagnostic.
The benign reports could either be colloid goiter, lymphocytic thyroiditis or a benign cyst. Subjects with a benign cytology are considered true negative if they are followed up for a period of at least 2 years - this will allow identification of those with changing symptoms for a repeat FNAB, and true negativity is confirmed if a diagnosis of thyroid neoplasia has not been made after a 2-year follow-up.
Surgery is required if malignant or suspicious cytology is reported. Rapid growth and increasing pressure effects (breathing difficulty) will signal the need for surgery. Some patients may undergo surgery for pressure effects like dysphagia, and other patients may opt for surgery because of cosmetic reasons due to the size of the goiter. It has been suggested that in subjects with a suspicious FNAB report, the rate of surgery may be reduced further by subjecting patients to radio nuclide scanning and performing surgery on those nodules that are cold or warm, and simply following up those with hot nodules without surgery as the risk of malignancy in these nodules is very low.
About 10-20% of cytological specimens may not have adequate material to enable an accurate interpretation and would be reported as non-diagnostic. A number of the non-diagnostic aspirates are due to cystic thyroid lesions. In cases where the report is persistently non-diagnostic, the USG results may be used to decide on the need for surgery (recommendation strength: C). In this category, if initial FNAC is non-diagnostic, it can be repeated under US guidance. If repeatedly non-diagnostic then based on clinical and US features and patient concern, a decision can be made for surgery or follow up. All the diagnostic procedures should be repeated in 6 months or earlier if the nodule enlarges.
A particular problem arises when the FNAB is indeterminate, i.e., when the FNAB is reported as follicular neoplasm and Hurthle neoplasms, as the differentiation between adenoma and carcinoma requires histological demonstration of vascular/capsular invasion. Surgery is generally advised.
In malignant/ suspicious cases, total thyroidectomy is the treatment of choice. The only exception could be a papillary microcarcinoma (<1 cm) carcinoma of the thyroid in the absence of local invasion. In this situation, the American Thyroid Association recommends hemithyroidectomy. [4] The choice of surgery (total or hemi- or subtotal thyroidectomy) in subjects with a benign cytology has often been a source of debate. In recent years, the consensus has veered toward total thyroidectomy, especially for bilateral benign multinodular goiters. [13] This is because of the chances of remnant hyperplasia or a histological surprise (a focus of malignancy in an otherwise classical multinodular goiter), may anyway necessitate completion thyroidectomy- and a second surgery.


Question 6. Is there an established role for non-surgical treatment ?
The use of levothyroxine suppression therapy to shrink non-malignant nodules is becoming less common, owing to its many disadvantages. [14] This treatment should be discouraged (recommendation strength: F) The advantages of this therapy are that it may slow nodule growth and prevent the appearance of new nodules. The disadvantages of suppressive levothyroxine therapy are modest efficacy, need for long term suppression, post-therapy regrowth, risk of atrial fibrillation/ cardiac arrhythmias and reduction in bone mineral density. I-131 therapy is an option in slightly enlarged, benign goiters, but benefits are limited by the very slow duration of action and need for contraception in female subjects. Ethanol injection into nodules (especially cystic ones) can reduce the goiter size by 45% at the end of 6 months, but has severe adverse effects: seepage of ethanol, hemorrhage into nodule, pain and even vocal cord paralysis. Laser therapy is still experimental, but it offers similar benefits as ethanol injection with lesser side effects. This is probably because of the higher degree of control and consequently lower risk of extra-nodular damage that this laser therapy entails.


Question 7. What is the optimal approach to a thyroid incidentaloma?
An impalpable thyroid nodule in a euthyroid patient detected incidentally by USG is termed a "thyroid incidentaloma". The prevalence of non-palpable thyroid nodules discovered on sonography in Asian adults is about 13%. [15] In the same study, the malignancy rate among these incidentaolmas was 28.8%. [15] These nodules are detected when sonography is performed for non-thyroid-related neck problems. It is important to perform a TSH estimation to look for a toxic nodule. A general management approach is to observe those nodules that are less than or equal to 1 cm in size and perform an FNAB under ultrasound guidance for nodules greater than 1 cm. [4] Routine FNAB for all nodules < 1-1.4cm is less desirable. [16] However, it is important to remember that the prevalence of malignancy in subjects with a non-palpable nodule is the same as that in a palpable nodule: hence, close follow-up is quintessential (recommendation strength: B). If 6-monthly ultrasounds document an increase in size, an attempt at USG-guided FNAB may be appropriate (recommendation strength: B). If other additional risk factors for malignancy exist (like family history or past radiation or typical USG features), then further evaluation of even nodules <1 cm is justified. With the increasing use of positron emission tomography (PET) scanning, many incidentalomas are being detected. [17] In India, PET Scan is expensive and available only at selected centers, and hence the committee did not decide that this topic requires a detailed recommendation at this point of time. Further evaluation of these PET-detected lesions must be based on clinical and USG-based assessment of malignant potential.


Question 8. What is the ideal management for cystic thyroid lesions?
Most cystic lesions are degenerating benign adenomas, which may be seen on USG within the cyst wall or adjacent to the nodule. A cyst that is encountered in the course of performing FNAB should be drained completely since many such lesions are adequately treated by aspiration alone. The cyst fluid may be sent for cytological evaluation. However, this is unlikely to provide much diagnostic information as the fluid usually contains only degenerative debris. The color of the cyst fluid can offer a clue: an amber colored fluid is indicative of a benign lesion and a crystal clear fluid may be seen in a parathyroid cyst. It is important to note that both benign and malignant cysts may yield a bloody fluid. Cysts that recur after aspiration are best operated upon. Solid-cystic thyroid nodules have a higher incidence of malignancy than the purely cystic lesions. USG can differentiate between a solid and cystic lesion, but 80% of thyroid nodules are solid/solid-cystic. Hence if the ultrasound report is the sole criteria to decide about surgery then 80% of patients will proceed to surgery. A better option is to perform an FNAB from the solid portion of the solid-cystic lesion using USG guidance, and then decide on therapy in all cystic thyroid lesions. [18] In cases of persistent, uncharacterized cystic lesions, surgery is the best option (recommendation strength: C).


Question 9. How should thyroid nodules be evaluated in children?
Children with thyroid nodules may be assessed using the adult guidelines. A detailed recommendation on thyroid nodules in children is beyond the scope of these guidelines. However, a few generalizations can be made: (a) Thyroid nodules are uncommon in children (<1.5%) (b) The management must be more aggressive than in adults as the prevalence of malignancy in these nodules is higher. It has been reported that among children who undergo surgery for thyroid nodules, the incidence of thyroid cancer is about 26%. [19] (c) in addition to the classical adult causes of thyroid nodules, certain etiologies are more common in childhood thyroid nodules-ectopic thyroid, hemiagenesis, dyshormonogenesis and thyroglossal duct cyst. (d) Children with a history of dyshormonogensis are at higher risk of developing follicular thyroid cancer. [19],[20] (e) Neck radiation in childhood increases the risk of future malignancies and finally (f) In general, children with thyroid nodules may be assessed using the adult guidelines (recommendation strength: C) i.e. TSH testing, USG and FNAB are the most important tests. [19]


Question 10. What is the management of thyroid nodules in pregnancy?
Pregnancy is associated with growth of pre-existing thyroid nodules as well as the growth of new nodules. [21] These are managed based on the stage of pregnancy at which it is detected and on the TSH level (recommendation strength: C). Detected in any trimester, no further evaluation is indicated for the nodule if the TSH is suppressed. Further testing, however, is necessary to rule out hyperthyroidism. Nodules detected during the third Trimester can safely be evaluated after completion of pregnancy as such delay is not expected to significantly affect the prognosis even if the nodule turns out to be malignant. When a nodule is detected in the first or second trimester and the TSH is normal or high, a FNAB is indicated. If it reports malignancy (DTC), the patient should be placed on suppressive therapy with levothyroxine (TSH to 0.1-1mU) and surgery considered in the second trimester (recommendation strength: B). [22] If the report is benign, no further evaluation is needed during pregnancy except levothyroxine to normalize the TSH. Evaluation after delivery may proceed in as indicated in the guidelines for the non-pregnant state. If FNAC is suspicious for malignancy, an US of the neck is recommended to look for suggestive sonographic features and for assessment of nodule size and for any suspicious lymph nodes. Even if the nodule appears benign by US, suppressive therapy with Thyroxine is recommended to maintain TSH in the range of 0.1 - 1.0 mU/L till completion of pregnancy.US may be repeated every Trimester for significant increase in dimensions. If there is no further enlargement, repeat FNAC need be performed only after delivery. If the nodule enlarges, a repeat FNAC/surgery may be considered. Alternatively, T4 suppression can be continued till pregnancy is completed and further evaluation planned as per guidelines. It has also been suggested that a distinction be made in suspicious lesions depending on whether they are of the "follicular neoplasm" type or the "papillary" type. It has been suggested from a small study that the former may be operated upon after delivery, while for the latter surgery may be considered in the 2 nd trimester itself (recommendation strength: B). [22]


Conclusions and future perspectives
These guidelines have been made for the Indian setting, and hence the committee has not recommended on the use of immunocytological studies (particularly with galectin-3 immunostaining) and molecular cytogenetic studies (BRAF, RAS, RET/PTC and PAX8/PPAR mutations) in predicting the risk of malignancy in thyroid nodules. However, the committee does predict their increasing use in future. Finally, a recent advancement in the management of thyroid nodules has been the use of recombinant TSH for amplifying the effect of I-131 in shrinking benign goiters. Recombinant TSH can increase the uptake of iodine by thyroid cells, and can thus augment the effect of I-131 on nodule size. Studies recently showed that recombinant TSH (rTSH) injections prior to I-131 therapy facilitated goiter shrinkage by an additional 50% as compared to I-131 alone. [23],[24] However, pain and compressive symptoms were more frequent with rTSH therapy. [23] In another study on very large multinodular goiters, rTSH-based I-131 therapy was shown to improve tracheal compression and improve inspiratory capacity. [25] Although r-TSH is now available in India, this therapy is costly, controversial and experimental. The committee does not recommend its routine use (recommendation strength: F).

Conclusion
The management of thyroid nodules requires a combination of clinical evaluation followed by appropriate investigations- an individualized approach, rather than a broad algorithm is increasingly becoming relevant. These consensus guidelines represent a summary of current medical evidence for thyroid nodule management, optimized for the clinical practice setting in India.

Source: http://www.ijem.in/downloadpdf.asp?issn=2230-8210;year=2011;volume=15;issue=1;spage=2;epage=8;aulast=Unnikrishnan;type=2