Archive for March 5th, 2008

OMNI Postings of 3/5/08

Aloxi is a new FDA-approved drug to treat the nausea of surgical patients.  Who knows?  It may find its way down to the ER like Zofran did.
http://omniphysicians.com/2008/03/04/new-drug-approved-for-nausea-aloxi/
What do you know about hydroxyurea in the treatment of sickle cell crises?  I don’t know much and so I am posting this article advocating its use.
http://omniphysicians.com/2008/03/04/hydroxyurea-and-sickle-cell-disease/
Niox Mino is a hand-held, point-of-care device to monitor airway inflammation in asthma.  I’m not sure if it’s applicable to Emergency Medicine, but it might be a neat way for asthmatics to monitor themselves and boost their steroid prophylaxis.
http://omniphysicians.com/2008/03/05/niox-mino-fda-approved/
Docs and lawyers get together to “break bread”  while trying to work out a solution to a patient’s complaint without going to a formal malpractice lawsuit.  It’s an experiment in Pennsylvania.  Will it work?  Ask the cobra and the mongoose.  Ask the wolf and the rabbit.  Ask Hillary and Barack.
http://omniphysicians.com/2008/03/04/lawyers-doctors-working-together/
A report on an interesting study in JAMA.  The subjects were given electric shocks and asked to rate their pain after taking the cheap or the expensive placebo. A $2.50 placebo made subjects feel better than 10 cent placebos.   The study’s venue was Guantanamo! 
http://omniphysicians.com/2008/03/05/better-placebo-effect-with-expensive-placebos/
Two dietary supplements have been recalled.  Aspire and Aspire Lite.  Seems that in some way in some fashion Viagra-like compounds found their way into the ingredients.  Imagine!  And you thought you felt more “vigorous” because of all the Vitamin E!
http://omniphysicians.com/2008/03/05/2-dietary-supplements-recalled/
Ciao!

Paul R.

553, 552, 551, 556, 557, 564.

Niox Mino FDA-approved

MedPage, 3/4/08:  The FDA has approved a handheld, point-of-care device to measure airway inflammation related to asthma, according to a statement from device maker, Aerocrine, Inc. 

 

The company said the Niox Mino is the first handheld device that provides “accurate, reproducible, and immediate measurement of fractional exhaled nitric oxide (FENO), a validated method for assessing asthma-related airway inflammation.” 

 

Although the device would not replace spirometry, which measures pulmonary function, Aerocrine claimed that FENO measurement can capture inflammatory changes following allergen exposure at an earlier stage than spirometry, “making it a more sensitive marker [for asthma].” 

 

“Niox Mino answers the need for a user-friendly, non-invasive, accurate, and cost-effective tool that enables any physician to monitor the underlying process of asthma-airway inflammation,” said Peter B. Boggs, M.D., of Louisiana State University in Shreveport, in a press release issued by Aerocrine. 

 

The device is already “used extensively” in Europe, the manufacturer said. 

Nuclear radiation and heart disease

Financial Times (3/5, Cookson) reports that there may be “an unexpectedly strong link between radiation exposure and heart disease,” according to a study published online by the International Journal of Epidemiology.

Scientists from Westlakes Consulting, a non-profit research organization in England, looked at “health records and radiation doses for 65,000 people employed at four nuclear sites…between 1946 and 2005.” The researchers “found a strong statistical association between increasing radiation and diseases of the heart and circulation, stronger than the better known link between occupational exposure and cancer.”loans payday banker americanindian loan interest 7-11 free125 ltv loansscore 437 credit loanstudent affinity loan directloan sba 504loans business alpha2007 needed loan asap Mapmovie thumbs xxxmovies sex horse freemovies hilton parisfetish moviesfree interracial movie free fucking moviesmovie next the girl doormovies porn hardcore freefree movies sex horse Map

Docs Need More Sleep

UPI (3/5) reports that the majority of “U.S. physicians report they aren’t getting the sleep they need to function at their best,” according to a survey conducted by the American College of Chest Physicians Sleep Institute.

        The poll included “all chest medicine disciplines, including pulmonology, cardiology, and…sleep medicine,” WebMD (3/4, Hitti) added. The results indicate that 93 percent of the 581 respondents “report caffeine use, compared with 82 percent of people who took part in the National Sleep Foundation poll.” Furthermore, about “30 percent of the doctors indicated that they don’t feel refreshed when they wake up, and 43 percent say their work schedule doesn’t let them get enough sleep.” Still, just “10 percent said sleepiness was a problem for them at least a few days per week, and 27 percent admitted dozing or napping at work sometime during the previous month.”

GAO to check FDA’s drug approval process

AP (3/5, Perrone) reports that Sen. Charles Grassley (R-Iowa) announced on Tuesday that “the Government Accountability Office (GAO) has agreed to study a much-debated method for approving drugs used to clear GlaxoSmithKline PLC’s diabetes pill Avandia (rosiglitazone) and Merck & Co., Inc. and Schering-Plough’s cholesterol drug Vytorin (ezetimibe/simvastatin).”

Sen. Grassley “requested the investigation after recent studies suggested the drugs may not lower the risk of heart attack and artery-clogging plaque, as assumed by millions of patients and doctors.” The main “issue now is whether [the] FDA should approve drugs based on biological measures, like cholesterol and blood sugar, without evidence they improve more meaningful measures like survival.” According to Robert Temple, M.D., the FDA’s Director for Medical Policy, “the agency has used several alternate study goals, often called surrogate endpoints, to approve drugs for decades.” Still, “[d]rug industry advocates favor shorter study goals because they involve smaller, less expensive and faster trials.”

FDA Medwatch: Tamiflu

3/4/08: Roche and FDA informed healthcare professionals of neuropsychiatric events associated with the use of Tamiflu, in patients with influenza. These symptoms, as described in post marketing reports mostly from Japan, include delirium and abnormal behavior leading to injury, and in some cases resulting in fatal outcomes.

These events were reported primarily among pediatric patients and often had an abrupt onset and rapid resolution. Patients with influenza should be closely monitored for signs of abnormal behavior. If neuropsychiatric symptoms occur, the risks and benefits of continuing treatment should be evaluated.

See the MedWatch 2008 safety summary, including links to the Dear Healthcare Professional letter and Tamiflu Prescribing Information, at:
http://www.fda.gov/medwatch/safety/2008/safety08.htm#Tamiflu

 

Case Report: Bilious Emesis in a 4-year-old

What Goes In Must Come Out!
Author:  Cindy L. Kerr, MSN, RN, CPNP-PC/AC 

J Pediatr Health Care.  2008;22(1):44-48.  ©2008 Mosby, Inc.

Posted 02/25/2008

Chief Complaint

In the emergency department, A.K.’s mother reports, “She has vomited twice today and it was green after lunch.”

History of Present Illness

A.K. is a 4-year-old African American girl with a one-day history of bilious emesis. Her mom reports that A.K. ate very little at lunch but that she often is a “picky eater.” A.K. was at home with her mom during the day and was playing in the house as usual. Her mom does report a brief episode of coughing in the morning that lasted just a few seconds. The first episode of vomiting occurred before lunch, and the second episode, which was described as green in color, occurred after lunch.

History

A.K.’s mom describes her as a healthy, active child who was a term infant born via spontaneous vaginal delivery. She has no known drug allergies, and her immunizations are up to date per mom’s verbal report. All developmental milestones have been achieved. A.K. was treated for “mild asthma” before her first birthday with intermittent albuterol (Proventil) delivered via a nebulizer, which was last dosed 1 year ago. For the past 2 years A.K. has been treated for gastroesophageal reflux with metoclopramide (Reglan), 3 mg by mouth three times per day. A.K. has never had any surgical procedures. The family history is noncontributory to the current symptoms. A.K. has always been a thin child described as a “very picky eater” who only eats small amounts at a time. Her mom denies any other symptoms of illness including fever, diarrhea, or abdominal pain.

Physical Examination in the Emergency Department

A.K.’s weight is 15 kg (25th percentile), and her height is 112 cm (90th percentile). Vital signs include an oral temperature of 36.9°, a heart rate of 116 beats per minute, a respiratory rate of 22 breaths per minute, and a blood pressure reading of 98/46 mm Hg. Her oxygen saturation in room air is 99%. The initial assessment of A.K. reveals a thin child, lying in bed. She appears alert but only answers questions with head nodding.

Examination of her head, eyes, nose, and throat reveal white sclera with pupils that are equal round and reactive to light. No rhinorrhea is noted, and her oral mucus membranes are intact and pink but tacky; she swallows without difficulty. Her neck is supple with full range of motion. A cardiovascular examination reveals no murmur and breath sounds that are clear and equal. A.K.’s abdomen is soft and flat; no tenderness is elicited with palpation, and hepatosplenomegaly is not appreciated. She moves all extremities equally, and motor strength is 5/5. Neurologic examination reveals an alert, quiet, but cooperative child with cranial nerves II-XII intact.

In the emergency department, intravenous fluids were started and blood work was done, including an electrolyte panel and complete blood cell count. The electrolyte panel, complete blood cell count, and liver function panel results were all within the expected range values.

An upright abdominal X-ray was obtained and revealed a radiopaque foreign body in the right upper quadrant of the abdomen. The remainder of the abdomen had expected findings of a nonspecific gas pattern. Upon return from her X-ray, A.K. had an additional episode of bilious emesis. To further assess the foreign body, a computerized axial tomography study of the abdomen was obtained. Findings confirmed a radiopaque foreign body within the small bowel, specifically in the first part of the duodenum. The object was described as a 2 by 3 cm ovoid radiopaque object.

Because of recurrent vomiting, a nasogastric tube was placed for decompression of the stomach and to prevent further vomiting. Nasogastric drainage was bilious in color.

Case Study Questions

  1. What is the significance of bilious emesis?
  2. What are the four most common locations within the gastrointestinal tract associated with foreign body obstruction?
  3. What are the treatment options in regard to foreign bodies within the gastrointestinal tract?
  4. Based on the recommendations for management of ingestions, what is the next step for this child?

Case Study Answers

1. What Is the Significance of Bilious Emesis?

The presence of bilious emesis is an indicator that surgical pathology may be the cause of symptoms. Bilious emesis can provide insight into where in the gastrointestinal tract the pathology may be occurring.

Bile is an alkaline, bitter-tasting, yellow-green fluid produced in the liver then concentrated and stored in the gallbladder. The gallbladder drains bile via the cystic duct into the common bile duct. The sphincter of Oddi controls bile flow through the common bile duct into the second part of the duodenum. When bowel obstruction occurs beyond the outlet of the common bile duct at the sphincter of Oddi, emesis will appear bilious. When the obstruction occurs proximal to this outlet, emesis more likely will not appear bilious.

When bilious emesis occurs after the neonatal period in patients with no previous surgical history or known gastrointestinal disorders, surgical pathology to consider include mid gut volvulus, intussusception, incarcerated inguinal hernia, and mechanical obstruction due to a foreign body.

Malrotation is a consequence of incomplete rotation of the gut during embryonic development. The result is a thin stalk of mesentery and blood supply that is predisposed to volvulus or twisting. Mid gut volvulus occurs when the bowel twists on this narrow base of mesentery, causing bowel obstruction and disruption of blood flow. Bowel necrosis can result and may injure large segments of the gastrointestinal tract. Mid gut volvulus has the highest incidence of manifestation in the first days of life, but it can occur at any age. One clinical hallmark of malrotation is bilious vomiting (Thapa & Sze, 2005). Other signs and symptoms include severe abdominal pain and signs of peritonitis not seen in the case of A.K.; therefore, this diagnosis was not included in the differential diagnosis list.

Intussusception is the telescoping of a segment of bowel into an adjacent segment. The result of this telescoping is compression of mesenteric vessels, causing venous congestion and venous stasis. Ultimately, this condition can lead to ischemia and bowel necrosis. Classic presentation of intussusception includes severe intermittent abdominal pain, vomiting, palpable abdominal mass, and currant-jelly stool (late sign). Intussusception occurs in all age groups, but most patients (75%) are younger than 2 years and rarely older than 5 years of age (Lam, 2000). Because A.K. denied complaint of abdominal pain and did not demonstrate any other signs and symptoms associated with intussusception, this surgical pathology was ruled out.

Incarcerated inguinal hernia results from entrapment of bowel or other viscera within the hernia sac. If the hernia is not reduced, strangulation of the contents may result. Incarceration occurs most commonly in the first 6 months of life and is relatively rare after the age of 5 years. Physical examination will reveal a firm red mass in the inguinal area, and the patient will be irritable and inconsolable. Bilious emesis results because of the obstruction of the bowel. Physical examination findings in the case of A.K. were not consistent with an incarcerated hernia.

Ingestion of foreign bodies is a common problem in children. Kay and Wyllie (2005) report that the incidence for all ages is 100,000 cases per year, with the majority occurring in children between the ages of 6 months to 3 years. Once in the stomach, 80% to 95% of all ingested foreign bodies pass safely and exit without difficulty (Brookes & Brind, 2003). Of the objects that do not pass, 10% to 20% percent require endoscopic removal, and less than 1% require surgical intervention (Kay & Wyllie). In the case of A.K., radiologic studies confirmed the presence of a foreign body.

2. What Are the Four Most Common Locations Within the Gastrointestinal Tract Associated with Foreign Body Obstruction?

In children without any underlying gastrointestinal tract pathology or history of abdominal surgery, four locations along the gastrointestinal tract are associated with foreign body obstruction. The most common location is the esophagus, which is the narrowest portion of the entire gastrointestinal tract. The second area is the gastric pylorus. Low and Killius (2000) point out that obstruction at this point is related to dimensions of the pylorus channel. When the pylorus muscle is thicker than 2 cm and longer than 5 cm, a narrow channel is created through which the foreign body must travel. An obstruction at this location would not produce bilious emesis because it is proximal to the outlet of bile at the sphincter of Oddi.

The third area of the gastrointestinal tract associated with obstruction is the duodenal sweep (Low & Killius, 2000). The duodenum is about 25 cm long and divided into four parts. The first portion is 5 cm long and extends from the pylorus to the superior duodenal flexure. At the superior duodenal flexure, the second portion begins and forms the first curve of the duodenal sweep. This sweep will take the duodenum completely around the head of the pancreas, forming the letter ‘C’ (Chaurasia, 1995). This sweep creates physiologic angulations that make passage of long or pointed objects troublesome.

The ileocecal valve in the right lower quadrant is the fourth area where foreign bodies typically produce mechanical obstruction (Low & Killius, 2000). Obstructions that occur beyond the second portion of the duodenal sweep and at the ileocecal valve will produce bilious emesis because they occur beyond the sphincter of Oddi.

3. What Are the Treatment Options in Regard to Foreign Bodies Within the Gastrointestinal Tract?

Beyond the esophagus, treatment decisions involving foreign bodies take into account several factors, including the object’s shape, size, chemical nature, duration of time it has been contained within the gastrointestinal tract, and patient symptoms.

In children, the most worrisome objects are long, sharp, and pointed. These objects have the highest risk (15%-35%) for causing perforation (Uyemura, 2005). When these types of objects are found before the duodenal sweep, endoscopic removal is recommended. If the sharp object cannot be removed, Uyemura recommends daily radiographs be obtained to follow progress of the object. If the foreign body does not progress over 3 days, surgical intervention should be considered.

In cases that involve blunt objects, location and size are key factors to consider. Most experts recommend endoscopic removal of items larger than 2 cm in diameter or 3 cm in length when they are past the stomach but proximal to the duodenal sweep in infants. For children older than 1 year, endoscopic removal is recommended for objects longer than 3 to 5 cm (Uyemura, 2005).

Metallic objects, magnets, and batteries are of concern because of their chemical nature; these objects can result in mucosal inflammation, ulceration, perforation, and lead toxicity (Low & Killius, 2000). In cases where the chemical nature of the object has higher risks associated with them, endoscopic retrieval is recommended (Prasad, Low, Tan, & Jacobsen, 2006). One also must consider the number of objects ingested, especially in cases involving magnets. Vijaysadan, Perez, and Kuo (2006) point out the concern when more than one magnet is ingested. The magnetic attraction between two or more objects can create a situation where the intestinal wall is compressed between them, leading to necrosis, intestinal perforation, or fistulae. When this compression involves mesenteric vessels, intraabdominal hemorrhage may result. Cases of ingestion involving more than one magnetic object regardless of location, shape, size, or patient symptoms the foreign bodies should be removed.

When the decision has been made to follow the progress of an object with serial abdominal radiographs, most experts agree that nontoxic, blunt objects can safely be monitored for up to 2 weeks when contained within the stomach and for 1 week when the object is contained within the duodenum (Prasad et al., 2006). Objects retained for prolonged periods may form a reactive fibrinous exudate leading to mucosal adherence, or the object may migrate outside of the intestinal lumen (Vijaysadan et al., 2006). In cases that cause symptoms such as abdominal pain, vomiting, fever, or rectal bleeding, immediate intervention is indicated, either with endoscopy or surgery.

4. Based on the Recommendations for Management of Ingestions, What is the Next Step for This Child?

The ovoid, 2 by 3 cm object is within the size range that is expected to pass freely through the gastrointestinal tract. Radiographs confirmed that the foreign body was within the first portion of the duodenum, a location that renders successful endoscopic removal likely.

Mom reported that A.K. had a coughing episode while playing in the house before lunchtime. This seemingly benign episode could be the time of ingestion. Many times ingestion is not a witnessed event. From a timing consideration, this object would fall into the category of watch and wait.

Adverse patient symptoms take precedence over other factors when considering treatment options. Because of persistent emesis, plans for endoscopic removal of the foreign body were made. A.K. was taken to the operating room for removal of a duodenal foreign body under general anesthesia using a fiberoptic endoscope.

Under general anesthesia, the endoscope was placed through the oral cavity and esophagus. The scope was advanced into the stomach, through the pylorus, and into the duodenum. As the scope was passed further into the duodenum, a glass object was identified, and the retrieval basket was advanced and placed around the object. The scope was removed along with the foreign body. The result was retrieval of a smooth glass disk, the type used for decorative purposes.

Further Assessment Indicated

Immediately following the endoscopic procedure, A.K. was given nothing by mouth until she fully recovered from the anesthesia, and then she was started on a clear liquid diet. She had no repeat episodes of vomiting. Her abdominal examination was benign, and she remained afebrile. By postoperative day 2 she was taking a full and regular diet and had a regular bowel movement.

To investigate why a small ovoid object would create an obstruction in this location of the bowel, an upper gastrointestinal study with small bowel follow-through was obtained. This study allows fluoroscopic visualization of the esophagus, stomach, and duodenum and would be specifically helpful in this case because lumen size of the organs would be obtained, allowing for detection of pathology such as fistula, diverticulum, web, or ring. If present, these abnormalities would explain the mechanical obstruction created by the round glass disk. Upper gastrointestinal findings included normal examination until there was delayed emptying of contrast into the second (descending) portion of the duodenum. The proximal portion of the second part of the duodenum appeared narrow with an irregular course. The mid and distal aspects of the second portion of the duodenum appeared normal. These findings are consistent with a stricture or stenosis in the proximal portion of the descending duodenum.

Case Conclusion

A.K. was taken back to the operating room for an exploratory laparotomy because of this duodenal stricture. Operative findings revealed the presence of an annular pancreas. Annular pancreas is a rare congenital anomaly occurring in 1 of every 12,000 to 15,000 live births (Lainakis et al., 2005).

An annular pancreas forms an incomplete or even full ring around the second segment of the duodenum. This ring causes various degrees of stenosis or atresia, which explains how the glass disk became trapped at this location. Some cases of annular pancreas remain asymptomatic throughout life, but the majority of cases present in the neonatal period as an intestinal obstruction producing bilious emesis (Lainakis et al., 2005). Whether symptoms present in the first days of life or in adulthood, surgery is required to repair the affected part of the duodenum when an annular pancreas is found.

Following her surgical intervention, A.K. recovered without complications. Postoperative care included a nasogastric tube for decompression of the stomach and to allow for bowel rest, pain management, and total parenteral nutrition. Over several days bowel function returned, as demonstrated by passing of flatus. The nasogastric tube was removed on postoperative day 3. Her diet was then advanced slowly. On postoperative day 5, she was ready for discharge home.

Primary Care Considerations

Postoperative care considerations for A.K. include monitoring growth parameters. Her height and weight dimensions, 25 percentile for weight and 95 percentile for height, may reflect the consequences of the delayed emptying seen during the upper gastrointestinal study. Delayed emptying can lead to feeling full longer and may be the reason she takes only small meals as described by her mother. The primary care provider also may see resolution of her gastroesophageal reflux symptoms.

Foreign body ingestion can be prevented. Pediatric nurse practitioners, through parental education and anticipatory guidance, can help parents prepare a safe environment for their child. Starting around 6 months of age, children begin to propel through their environment and explore by placing objects in their mouth. Parents who understand these developmental milestones and the risks associated with them can take pre-emptive action to create a safe environment to help prevent accidental ingestion.

References

  1. Brookes MJ, Brind AM. Coin ingestion, an unexpected finding at colonoscopy: Case report. Medscape General Medicine. 2003;5:8.
  2. Chaurasia BD. Intestines. In: Chaurasia BD editors. Human anatomy regional and applied. 3rd ed.. New Delhi, India: CBS Publishers; 1995;p. 212-226.
  3. Kay M, Wyllie R. Pediatric foreign bodies and their management. Current Gastroenterology Reports. 2005;7:212-218.
  4. Lainakis N, Antypas S, Panagidis A, Alexandrou I, Kambouri K, Kyriazis C. Annular pancreas in two consecutive siblings: An extremely rare case. European Journal of Pediatric Surgery. 2005;15:364-368.
  5. Lam VT. Intussusception. In: Arensman AM, Bambini DA, Almond PS editor. Pediatric surgery. Georgetown, Texas: Landes Bioscience; 2000;p. 89-93.
  6. Low VHS, Killius JS. Animal, vegetable, or mineral: A collection of abdominal and alimentary foreign bodies. Applied Radiology. 2000;29:23-30.
  7. Prasad STR, Low Y, Tan CE, Jacobsen AS. Swallowed foreign bodies in children: Report of four unusual cases. Annals Academy of Medicine. 2006;35:49-53.
  8. Thapa M, Sze R. Pediatric gastrointestinal emergencies. Applied Radiology. 2005;34:8-19.
  9. Uyemura MC. Foreign body ingestion in children. American Family Physician. 2005;72:287-291.
  10. Vijaysadan V, Perez M, Kuo D. Revisiting swallowed troubles: Intestinal complications caused by two magnets — A case report, review and proposed revision to the algorithm for the management of foreign body ingestion. Journal of American Board Family Medicine. 2006;19:511-516.

Direct Thrombin Inhibitors: Alternatives to Heparin

Author:  Leila Mureebe MD

Journal:    Vascular.  2007;15(6):372-375.

Abstract

After more than 70 years of effective clinical use, heparin remains the most common anticoagulant in use and one of the most commonly prescribed drugs to hospitalized patients. However, the biologic variability and immunogenicity limit its utility. With increasing volumes of vascular intervention and an aging population, an increase in the need for anticoagulation can be anticipated. This article reviews current viable options and barriers to the use of heparin.

Introduction

All elements of the Virchow triad are encountered during both vascular therapy and intrinsic vascular disease. Anticoagulation is routinely used during procedures to prevent thrombosis above the level of vessel occlusion (ie, angioplasty, aortic occlusion during endograft placement) and to prevent thrombus formation about a nidus such as a sheath or catheter. In addition, many patients requiring vascular disease management or therapy may have a hypercoagulable state. Up to 10% of patients undergoing peripheral vascular procedures have a hypercoagulable state,[1] and there is evidence that the platelets of patients with peripheral vascular disease are overactive.[2]

Heparin was introduced into clinical use in 1935 and remains the most common anticoagulant in use today. It is estimated that 30% of all patients admitted to a hospital receive some form of heparin. The most commonly prescribed form is unfractionated heparin (UFH), which is a mixture of polysaccharide chains. Heparin complexes with endogenous antithrombin and inactivates coagulation factors Xa, XIIa, Xia, and IXa. UFH is quickly available after intravenous administration (within 3 minutes), and its effect is easily assessed by way of the activated clotting time (ACT). The duration of action depends on the dose administered but is roughly 60 minutes. The activated partial thromboplastin time (aPTT) is used to monitor longer-term therapy. Heparin has an antidote in protamine, which complexes with heparin in a ratio of 1 mg protamine to 100 units of heparin and prevents the binding of heparin to AT. Heparin is ineffective against existing thrombus and has significant biologic variability owing to variable levels of plasma protein binding.[3] There are no firm recommendations regarding dosing of heparin for vascular interventions. High-risk interventions (brachiocephalic, small vessels) may benefit from administration of 75 to 100 units of heparin per kilogram of body mass during balloon angioplasty, whereas straightforward aortoiliac interventions may only require doses of 25 to 50 U/kg.[4] However, lower doses may be safe. One study demonstrates the safety and efficacy of roughly 50 U/kg for coronary interventions,[5] implying that lower doses may be sufficient even for small-vessel interventions.

Low-molecular-weight heparins (LMWHs) are shorter segments of depolymerized UFH. Several are available clinically, and they are differentiated by the specific fraction used in the preparation and slight differences in anticoagulant strength. LMWHs offer more anti-Xa activity than UFH and less anti-IIa activity. This theoretically leads to greater efficacy and lower bleeding complications. In addition, LMWHs are administered as a single subcutaneous injection and do not require monitoring to determine anticoagulant ability owing to more predictable biologic activity. This, however, is also their greatest weakness as there is no rapid method to assess anticoagulant adequacy. Several studies show both the efficacy and the safety of LMWH as the sole anticoagulant administered for the purpose of percutaneous coronary intervention (PCI).[6,7]

The indirect activity of heparin represents a major drawback to its use. In addition to variable biologic activity, the downfall of all heparins is their immunogenicity. Heparin-induced thrombocytopenia (HIT) syndrome occurs in roughly 1 to 3% of all patients who receive heparin. Heparin complexes with endogenous platelet factor 4 to form a unique epitope against which an antibody (most commonly immunoglobulin G) develops. In the presence of exogenous heparin, this antibody binds to platelets and leads to platelet cross-linking and generation of procoagulant microparticles and endothelial damage. The morbidity and mortality of HIT were recently assessed at 30% and 7%, respectively.[8] Therapy for HIT requires immediate cessation of all heparin, including flushes, and a decision regarding the need for further anticoagulation.[9] Although LMWH is historically associated with a lower rate of antibody formation, once heparin associated antiplatelet antibodies (HAAbs) are present, 20 to 60% of patients with HAAb owing to UFH will cross-react to LMWH.[10] Also, plasma from 34% of patients with HIT will aggregate platelets in the presence of LMWH. In addition to immunogenicity, UFH is associated with hemorrhagic complications. In a study evaluating patients treated with 59.1 ± 20.0 U/kg of heparin for peripheral vascular interventions, major bleeding occurred in 4.6%, and 7.6% required emergent repeat revascularization of the same target vessel.[11]

In contrast to the indirect inhibition of thrombin offered by heparin, direct thrombin inhibitors (DTIs) require no preceding interaction prior to their effect on thrombin (factor IIa). DTIs are more specific and have activity on both soluble and thrombus-bound thrombin. This is in stark contrast to heparin, which has no activity against thrombus-bound thrombin. In addition to these issues, several other factors may make DTIs more attractive pharmacologic agents for vascular patients. Thrombin itself has long been understood to have functions other than catalysis of fibrinogen to fibrin.[12] The “receptors” for thrombin, a family of molecules known as protease-activated receptors, are found on endothelial and vascular smooth muscle cells. Thrombin leads to proliferation of vascular smooth muscle cells and upregulates vascular endothelial growth factor expression. In addition to direct effects on vascular cells, thrombin also has a proinflammatory role. There is increasing evidence that inflammation is critically important in the development and progression of vascular disease.[13]

Given the central position of thrombin in vascular cell and platelet signaling, as well as inflammation, it is reasonable to hypothesize that DTIs would have beneficial effects on vascular physiology. There are multiple in vitro and in vivo studies of the effect of DTIs on vascular physiology.[12,14] In an in vivo study of blood from patients undergoing PCI, DTIs reduced platelet surface expression of P-selectin and decreased platelet-leukocyte aggregation compared with the blood from patients who had received heparin with a glycoprotein IIb-IIIa inhibitor. Furthermore, a reduction in leukocyte activation was also observed. This may translate into a reduction in progressive atherogenesis owing to platelet-leukocyte interactions.[15] The relationship between thrombosis and inflammation has been explored in the pulmonary bed, and inflammation was diminished through use of a DTI.[16] This inflammatory link is further supported by an experimental reduction in atherosclerotic lesion size after treatment with DTI.[17] Myocardial reperfusion injury has also been found to be moderated after DTI treatment.[18]

The first approved DTI was lepirudin (Refludan, Berlex Laboratories, Wayne, NJ). Lepirudin is a recombinant derivative of hirudin, the anticoagulant present in the saliva of the medicinal leech (Hirudo medicinalis). Lepirudin is a bivalent DTI, binding at both the catalytic site of thrombin (preventing the conversion of fibrinogen to fibrin) and the fibrinogen-binding site. Lepirudin is renally cleared, and its effect is markedly prolonged in patients with renal failure. There is no direct antidote for overdosage with lepirudin, but activated factor VII has been reported to be able to salvage coagulation after a failure to clear lepirudin.[19] The dose for patients with normal renal function is a bolus of 0.4 mg/kg followed by continuous infusion at 0.15 mg/kg/h, and the half-life is 80 minutes.

The US Food and Drug Administration (FDA) approved lepirudin for the treatment of HIT. The anticoagulant effect is monitored by the aPTT. It may also be monitored at point-of-care via the ecarin clotting time (ECT).[20] Caution is required when observing common laboratory measures of anticoagulation during treatment with lepirudin. The international normalized ratio is elevated out of proportion to the anticoagulant effect in patients receiving lepirudin.[21]Alternate testing is possible during dosing with lepirudin. A thromboelastograph, a common clinical coagulation instrument, has been successfully used to monitor the effects of hirudin in vitro, and additional tests are in development.[22] The inability to rapidly assess the effect of leipirudin limits its utility. As a point-of-care test, the ECT is not readily available at all institutions, and the aPTT does not provide the rapid response that is required during intervention.

Lepirudin is a safe and effective anticoagulant for patients with HAAb.[23] Although some patients form antibodies against hirudin, 23 patients were prospectively studied, and 56% developed antibodies against hirudin as detected by enzyme-linked immunosorbent assay. However, no patient demonstrated resistance or other effects attributable to the antihirudin antibodies. Any clinical significance of these antibodies is yet to be shown.[24]

Although it is approved for the treatment of HIT alone, lepirudin has been successfully used for anticoagulation during procedures in patients with HAAb. Lepirudin has been used for anticoagulation during renal replacement therapy with hemodialysis[25,26] and for anticoagulation during cardiopulmonary bypass.[19,20]

Argatroban (Glaxo SmithKline Pharmaceuticals, Research Triangle Park, NC) is a small (527 Da), synthetic direct thrombin inhibitor derived from l-arginine. Unlike lepirudin, argatroban binds reversibly to the catalytic domain of thrombin at only this single location as it is a univalent inhibitor. There is activity against both free and clot-bound thrombin, with no activity against factor Xa or plasmin.[27] In a study of anticoagulation for PCI using historical controls (HIT patients treated with heparin), argatroban resulted in improved clinical outcomes and no increase in hemorrhagic complications.[28] Standard dosing is 2 mg/kg/min intravenously, and the drug is titrated to achieve an aPTT of 1.5 to 3 times control and may be monitored at point-of-care via the ACT. Argatroban undergoes hepatic metabolism and excretion. It is a reversible inhibitor, with a half-life of 40 to 50 minutes, allowing rapid restoration of coagulation after infusion. Given that it is not renally cleared, it has a predictable effect in patients with renal insufficiency.[29] There is no specific antidote for argatroban, and administration should be discontinued if suspicion of overdosage or hemorrhagic complication exists. In the setting of PCI, argatroban is approved for use in patients with HIT and has been used at a dose of 25 µg/kg/min after a 350 µg/kg initial bolus and titrated to an ACT of 250 to 300 seconds. The results in these patients are comparable to those in historical heparin controls.[28]

Another direct thrombin inhibitor, bivalirudin, has been more extensively studied in PCI than the others but not in placebo-controlled trials. It has been evaluated as a safe and effective foundation anticoagulant for use in PCI.[30] Bivalirudin (Angiomax The Medicines Company, Parsippany, NJ; previous name hirulog) has been studied in subtherapeutic doses (Thrombin Inhibition in Myocardial Ischemia [TIMI] 7), and in heparin-controlled trials (Hirulog and Early Reperfusion or Occlusion [HERO]-2, TIMI 8) . In a large (5,674 patients) meta-analysis of six studies looking at outcomes after myocardial infarction, bivalirudin was associated with a significant reduction in the composite of death or infarction and in major hemorrhage.[31] The HERO-11 trial evaluated angiography in patients undergoing fibrinolysis, and the HERO-2 trial specifically evaluated bivalirudin in PCI. Compared with heparin, bivalirudin failed to reduce mortality but reduced the postprocedure myocardial reinfarction rate.[32] The Randomized Evaluation in PCI Linking Angiomax to Reduced Clinical Outcomes (REPLACE)-2 trial compared bivalirudin with provisional glycoprotein IIb-IIIa inhibition with heparin with glycoprotein IIb-IIIa inhibition during PCI. The dose of bivalirudin in this study was a 0.75 mg/kg bolus and a subsequent 1.75 mg/kg/h infusion. Only 7.2% of patients in the bivalirudin group received IIb-IIIa inhibitors, and there were similar 30-day outcomes in both groups.[33]

Warfarin sodium is the most commonly prescribed oral anticoagulant. Its use is complicated by a narrow therapeutic window and significant risk of hemorrhage at therapeutic concentrations. Dosing is difficult and requires frequent invasive monitoring. Alternatives to this oral option have been slow to come. Ximelagatran, an oral prodrug of the DTI melagatran, had shown efficacy in the prevention and treatment of venous thromboembolism, as well as stroke prevention in patients with atrial fibrillation.[34,35] Despite its efficacy and promise, ximelegatran has been withdrawn owing to hepatic toxicity.[36]

In summary, despite the safety profile and long history of heparin use, there are drawbacks that mandate that we continue to look for alternatives for our patients. Direct inhibition of thrombin may offer similar anticoagulant properties but also impact the underlying disease process. As we continue to gain experience and develop new DTIs, a new balance may be struck among cost, safety, and efficacy. Additional studies are still required to further our understanding of these important pharmacologic adjuncts.

References

  1. Donaldson MC, Weinberg DS, Belkin M, et al. Screening for hypercoagulable states in vascular surgical practice: a preliminary study J Vasc Surg 1990;11:825-31.
  2. Jagroop IA, Milionis HJ, Mikhailidis DP. Mechanism underlying increased platelet reactivity in patients with peripheral arterial disease Int Angiol 1999;18:348-51.
  3. Hirsh J. Heparin N Engl J Med 1991;324:1565-74.
  4. Schneider PA. , New York: Marcel Dekker; 2003. Endovascular skills: guidewire and catheter skills for endovascular surgery 2nd ed.
  5. Caussin C, Fsihi A, Ohanessian A, et al. Direct stenting with 3000 i.u. heparin Int J Cardiovasc Intervent 2003;5:206-10.
  6. Choussat R, Montalescot G, Collet JP, et al. A unique, low dose of intravenous enoxaparin in elective percutaneous coronary intervention J Am Coll Cardiol 2002;40:1943-50.
  7. Montalescot G, Cohen M. Low molecular weight heparins in the cardiac catheterization laboratory J Thromb Thrombolysis 1999;7:319-23.
  8. Shuster TA, Silliman WR, Coats RD, et al. Heparin-induced thrombocytopenia: twenty-nine years later J Vasc Surg 2003;38:1316-22.
  9. Mureebe L, Silver D. Heparin-induced thrombocytopenia: pathophysiology and management Vasc Endovasc Surg 2002;36:163-70.
  10. Kikta MJ, Keller MP, Humphrey PW, Silver D. Can low molecular weight heparins and heparinoids be safely given to patients with heparin-induced thrombocytopenia syndrome? Surgery 1993;114:705-10.
  11. Shammas NW, Lemke JH, Dippel EJ, et al. In-hospital complications of peripheral vascular interventions using unfractionated heparin as the primary anticoagulant J Invasive Cardiol 2003;15:242-6.
  12. Patterson C, Stouffer GA, Madamanchi N, Runge MS. New tricks for old dogs: nonthrombotic effects of thrombin in vessel wall biology Circ Res 2001;88:987-97.
  13. Libby P, Simon DI. Inflammation and thrombosis: the clot thickens Circulation 2001;103:1718-20.
  14. Mureebe L, Turnquist SE, Silver D. Inhibition of intimal hyperplasia by direct thrombin inhibitors in an animal vein bypass model Ann Vasc Surg 2004;18:147-50.
  15. Keating FK, Dauerman HL, Whitaker DA, et al. Increased expression of platelet P-selectin and formation of platelet-leukocyte aggregates in blood from patients treated with unfractionated heparin plus eptifibatide compared with bivalirudin Thromb Res 2006;118:361-9.
  16. Farivar AS, Delgado MF, McCourtie AS, et al. Crosstalk between thrombosis and inflammation in lung reperfusion injury Ann Thorac Surg 2006;81:1061-7.
  17. Bea F, Kreuzer J, Preusch M, et al. Melagatran reduces advanced atherosclerotic lesion size and may promote plaque stability in apolipoprotein E-deficient mice Arterioscler Thromb Vasc Biol 2006;26:2787-92.
  18. Mirabet M, Garcia-Dorado D, Ruiz-Meana M, et al. Thrombin increases cardiomyocyte acute cell death after ischemia and reperfusion J Mol Cell Cardiol 2005;39:277-83.
  19. Oh JJ, Akers WS, Lewis D, et al. Recombinant factor VIIa for refractory bleeding after cardiac surgery secondary to anticoagulation with the direct thrombin inhibitor lepirudin Pharmacotherapy 2006;26:569-77.
  20. Iqbal O, Tobu M, Aziz S, et al. Successful use of recombinant hirudin and its monitoring by ecarin clotting time in patients with heparin-induced thrombocytopenia undergoing off-pump coronary artery revascularization J Card Surg 2005;20:42-51.
  21. Stephens JL, Koerber JM, Mattson JC, Smythe MA. Effect of lepirudin on the international normalized ratio Ann Pharmacother 2005;39:28-31.
  22. Zakir RM, Hoffman W, Bhatt BA, Spillert CR. A functional clotting assay to monitor the hirudin dosage Blood Coagul Fibrinolysis 2007;18:119-23.
  23. Mudaliar JH, Liem TK, Nichols WK, et al. Lepirudin is a safe and effective anticoagulant for patients with heparin-associated antiplatelet antibodies J Vasc Surg 2001;34:17-20.
  24. Song X, Huhle G, Wang L, et al. Generation of anti-hirudin antibodies in heparin-induced thrombocytopenic patients treated with r-hirudin Circulation 1999;100:1528-32.
  25. Davenport A. Anticoagulation options for patients with heparin-induced thrombocytopenia requiring renal support in the intensive care unit Contrib Nephrol 2007;156:259-66.
  26. Gajra A, Vajpayee N, Smith A, et al. Lepirudin for anticoagulation in patients with heparin-induced thrombocytopenia treated with continuous renal replacement therapy Am J Hematol 2007;82:391-3.
  27. Lewis BE, Wallis DE, Berkowitz SD, et al. Argatroban anticoagulant therapy in patients with heparin-induced thrombocytopenia Circulation 2001;103:1838-43.
  28. Lewis BE, Matthai WH Jr, Cohen M, et al. Argatroban anticoagulation during percutaneous coronary intervention in patients with heparin-induced thrombocytopenia Catheter Cardiovasc Intervent 2002;57:177-84.
  29. McKeage K, Plosker GL. Argatroban Drugs 2001;61:515-22.
  30. Eres A. Use of bivalirudin as the foundation anticoagulant during percutaneous peripheral interventions J Invasive Cardiol 2006;18:125-8.
  31. Kong DF, Topol EJ, Bittl JA, et al. Clinical outcomes of bivalirudin for ischemic heart disease Circulation 1999;100:2049-53.
  32. White HD, Aylward PE, Frey MJ, et al. Randomized, double-blind comparison of hirulog versus heparin in patients receiving streptokinase and aspirin for acute myocardial infarction (HERO). Hirulog Early Reperfusion/Occlusion (HERO) Trial Investigators Circulation 1997;96:2155-61.
  33. Lincoff AM, Bittl JA, Harrington RA, et al. Bivalirudin and provisional glycoprotein IIb/IIIa blockade compared with heparin and planned glycoprotein IIb/IIIa blockade during percutaneous coronary intervention: REPLACE-2 randomized trial [published erratum appears in JAMA 2003;289:1638] JAMA 2003;289:853-63.
  34. Bauer KA. New anticoagulants: anti IIa vs anti Xa-is one better? J Thromb Thrombolysis 2006;21:67-72.
  35. Halperin JL. Ximelagatran: oral direct thrombin inhibition as anticoagulant therapy in atrial fibrillation J Am Coll Cardiol 2005;45:1-9.
  36. Boos CJ, Lip GYH. Ximelagatran: a eulogy Thromb Res 2006;118:301-4.

2 dietary supplements recalled

FDA Recall Alert, 3/4/08: Palo Alto Labs and FDA notified consumers and healthcare professionals of a voluntary nationwide recall of two dietary supplements, Aspire36 and Aspire Lite. The products were recalled because they were found to contain Aildenafil in trace amounts and Dimethyl sildenafil thione, an analog of Sildenafil, a drug used to treat erectile dysfunction. The presence of these ingredients in the dietary supplements may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers who have Aspire36 and Aspire Lite in their possession should stop using the products and return any unused product to the place of purchase.

Read the complete 2008 MedWatch Safety Summary, including a link to the manufacturer’s press release regarding this issue:

http://www.fda.gov/medwatch/safety/2008/safety08.htm#Aspire

Better Placebo Effect with Expensive Placebos

NY Times, 3/4/08: In marketing as in medicine, perception can be everything. A higher price can create the impression of higher value, just as a placebo pill can reduce pain.

Now researchers have combined the two effects. A $2.50 placebo, they have found, works better one that costs 10 cents.

The finding may explain the popularity of some high-cost drugs over cheaper alternatives, the authors conclude. It may also help account for patients’ reports that generic drugs are less effective than brand-name ones, though their active ingredients are identical.

The research is being published on Wednesday in The Journal of the American Medical Association.

The investigators had 82 men and women rate the pain caused by electric shocks applied to their wrist, before and after taking a pill. Half the participants had read that the pill, described as a newly approved prescription pain reliever, was regularly priced at $2.50 per dose. The other half read that it had been discounted to 10 cents. In fact, both were dummy pills.

The pills had a strong placebo effect in both groups. But 85 percent of those using the expensive pills reported significant pain relief, compared with 61 percent on the cheaper pills. The investigators corrected for each person’s individual level of pain tolerance.

“It’s a great finding,” said Guy H. Montgomery, an associate professor of cancer prevention at the Mount Sinai School of Medicine who was not involved in the research. “Their manipulation of price affected expectancies of drug benefit, and pain is the ultimate mind-body phenomenon.”

Previous studies have shown that pill size and color also affect people’s perceptions of effectiveness. In one, people rated black and red capsules as “strongest” and white ones as “weakest.” Other information like the country where the drugs were manufactured can also affect perceptions.

“It’s all about expectations,” said the lead researcher, Dan Ariely, a behavioral economist at Duke and the author of a new book, “Predictably Irrational: The Hidden Forces That Shape Our Decisions” (HarperCollins). His co-authors on the report were Rebecca Waber, Baba Shiv and Ziv Carmon.

“When you’re expecting pain relief, you’re secreting your own opioids,” Dr. Ariely added. “And when you get it on discount, you doubt it, and your body doesn’t react as well.”foreclosure alabama va loanguaranteed personal loans $5000payday 1 loan hour no faxingonline payday 21 15 application loan1995 loan default studentmortgage 50000 texas loan9 6 ga payday loanloan payday 6 online loan7 instant payday 10 loan texascheap payday loan 8 11 fax

Flat colonic lessions may be cancerous

NY Times, 3/5/08: 

An easily overlooked type of abnormality in the colon is the most likely type to turn cancerous, and is more common in this country than previously thought, researchers are reporting.

1

The findings come from a study of colonoscopy, in which a camera-tipped tube is used to examine the lining of the intestine. Generally, doctors search for polyps, abnormal growths that stick out from the lining and can turn into cancer. But another type of growth is much more dangerous, and harder to see because it is flat or depressed and similar in color to healthy tissue.

Japanese researchers became concerned about these flat lesions in the 1980s and ’90s, but studies here had mixed results and American doctors tended to think that flat growths were less common and less dangerous in the United States.

The new study, to be published Wednesday in the Journal of the American Medical Association, suggests otherwise.

Some doctors in this country were already alert to flat lesions, but the findings will pose a challenge to others, because it takes a trained and vigilant eye to see the growths and special techniques to remove them. The results also mean it is especially important that patients take the harsh laxatives that many dread in advance of the test. The flat lesions, hard to find even under the best conditions, will be impossible to see if any waste is left in the bowel.

Colon cancer is the second-leading cause of cancer death in the United States, after lung cancer, with about 154,000 new cases detected and 52,000 deaths a year. It is one of the few cancers that is totally preventable if precancerous growths are found and removed; it can also be cured with surgery alone if found early enough.

People who have just had a colonoscopy should not rush to schedule another one just to look for the flat growths, doctors said.

“I don’t think people have to panic that they’ve somehow been neglected and had poor care,” said Dr. David A. Rothenberger, deputy chairman of surgery at the University of Minnesota.

But he and other experts emphasized that people should see a doctor any time they have persisting symptoms that could indicate colon cancer, like rectal bleeding or a change in bowel habits — no matter how recently they had a colonoscopy. The test is highly reliable, but not perfect, doctors say.

Some doctors who perform colonoscopy just are not good at seeing flat lesions, but may improve with training and practice, said Dr. Douglas K. Rex, a gastroenterologist and professor of medicine at Indiana University.

“I think there are people who expect everything in there to be shaped like a golf ball,” he said. “It’s not.”

Dr. David Lieberman, chief of gastroenterology at Oregon Health and Science University, who wrote an editorial accompanying the study, said: “I think there will be some surprise. There has been in general some skepticism in the United States about how common flat and depressed lesions are and how important they are. So I think this study, coming from the United States and from a good group of investigators, will be a wake-up call to a lot of physicians and will prompt people to be looking for these lesions.”

The study, of 1,819 military veterans, mostly men, found that 9.35 percent had flat lesions, and those lesions were five times as likely as polyps to contain cancerous or precancerous tissue. Depressed or indented lesions were the least common but the most risky. Together, the flat or depressed lesions accounted for only 15 percent of the potentially cancerous growths found in the study, but were involved in half of the cancers. Once the doctors spotted the flat lesions, they sprayed a bluish dye on them to see their outlines better and remove them completely.

The first author of the study, Dr. Roy M. Soetikno of the Veterans Affairs Palo Alto Health Care System said, “The message for doctors is, Here is a large amount of data showing that these precursors of cancer, always believed to be a Japanese disease, are actually a disease here, and are important, because they are much more likely to be cancerous, and doctors need to spend the time to provide quality colonoscopy.”

The message to patients, Dr. Soetikno said, is that when preparing for colonoscopy, they must follow instructions to the letter and take the hated laxatives to make sure their bowels are empty so that doctors can see the lining.

If any waste remains, flat lesions will be buried by it. Studies have shown that in about a quarter of all colonoscopies, the bowel preparation is inadequate.

Dr. Rex said that male veterans tended to have more precancerous colon growths than other groups, so the rate of flat lesions in women or the general population might not be quite as high as those in the study.

Dr. Soetikno and his colleagues started an exchange program with doctors in Japan to learn their techniques for recognizing and removing the flat lesions.

American doctors should learn from overseas colleagues more often, Dr. Rothenberger said, adding, “We tend to get very smug about our abilities.”

The quality of colonoscopy has become a delicate issue, because an article in The New England Journal of Medicine in December 2006 found that some doctors were 10 times better than others at finding precancerous polyps. A major factor in their success was taking enough time to examine the colon thoroughly, as opposed to rushing through the procedure. Doctors who miss polyps would almost certainly miss flat lesions as well because they are harder to see. The new study underscores the need for careful examinations, because the flat lesions are more dangerous.

The study also raises doubts about whether “virtual colonoscopy,” performed by a CT scanner, will ever be able to take the place of the colonoscope inserted into the rectum, as many patients had hoped. The problem is that CT scans use X-rays to reveal shapes, and find polyps because they stick out. Flat lesions are unlikely to show up in such scans.

Studies show that from 0.3 percent to 0.9 percent of patients develop colon cancers within just a few years of having a colonoscopy and polyp removal — exactly what the procedure is supposed to prevent. Some doctors think that flat lesions, missed entirely during the colonoscopy or not fully removed, may account for some of these apparent failures.

Dr. Robert Smith, the director of screening for the American Cancer Society, said flat lesions were “a vexing issue” that had provoked a lot of arguments among doctors.

“This paper shows they’re more prevalent than we believed, and also quite serious with regard to the presence of features associated with an elevated risk of cancer,” Dr. Smith said.

The difficulty facing patients is how to be sure their doctors are doing a good job. Professional groups have issued guidelines about the best way to perform a colonoscopy, but they are recommendations, not rules. The groups also urge doctors to track their own success rates at finding precancerous growths to see how they measure up to standards, but even if they do keep track, the doctors do not have to share the data with anyone. And many people are loath to ask about it. The doctor wielding the scope is the last person most patients would want to offend.

“The patient really has no way to act as an informed consumer,” Dr. Smith said. “You can’t call up a facility and say, ‘By the way, is my doctor any good?’ or, ‘Tell me who the best one is.’ ”

He added: “For some physicians there is an expectation of trust, and it is offputting to have a patient request documentation of competence. However, some physicians know patients are hearing about these issues and are not offended by questions about performance and errors.”