Current Events

The NCAA likes to talk about culture.

In a news conference last July discussing the draconian penalties against Penn State in the Jerry Sandusky sexual abuse scandal, president Mark Emmert used the word eight times.

“Certainly, the lesson here is one of maintaining the appropriate balance of our values,” Emmert said. “Why do we play sports in the first place, and does that culture ever get to a point where it overwhelms the values of the academy, those things that we all hold dear?”

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While there are no regulations regarding how many operations an orthopedic surgeon can perform in a given day, multiple studies and articles show that a fatigued surgeon may put patients at risk.

One orthopedic surgeon is facing 261 medical malpractice lawsuits in state Supreme Court in Dutchess County. Plaintiffs’ attorneys have accused Dr. Spyros Panos of bouncing from operating room to operating room, and performing negligent or phantom procedures, resulting in harm to their clients.

Panos didn’t respond to Journal messages and has declined to comment previously. So has his law firm, Feldman, Kleidman & Coffey.

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Patient safety researchers at Johns Hopkins University estimate the occurrence of 80,000 'never events' between 1990 and 2010 in American hospitals.

Medical professionals universally agree that 'never events' should never happen during surgery.  These include leaving a foreign object inside a patient's body (estimated to happen 39 times a week nationwide), performing the wrong procedure (20 times a week), and operating on the wrong body part (20 times a week).  The researchers believe their estimates are actually low.  Foreign objects left in the body are discovered only when a patient experiences complications and doctors make an effort to find the cause; a number may go undetected.

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After raising questions last month about the deal, U.S. District Judge James Selna in Santa Ana, Calif., gave his final approval to a $1.6 billion settlement between Toyota Motor Corp. and consumers of its vehicles who alleged they suffered economic losses because of the sudden acceleration recalls.

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THURSDAY, July 18 (HealthDay News) -- Most malpractice claims against primary care doctors are the result of drug errors and missed diagnoses, particularly of cancer, heart attack and meningitis, a new review finds.

Researchers analyzed 34 studies published over the past two years, including 15 studies based in the United States.

In the United States, primary care doctors accounted for between 7.6 percent and 16 percent of all malpractice claims, according to the study published online July 18 in the journal BMJ Open. The number of claims brought against U.S. primary care doctors has remained fairly stable over the past two decades.

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THURSDAY, July 18 (HealthDay News) -- The children of women who take drugs to treat epilepsy during pregnancy may be at increased risk for physical and mental developmental delays early in life, a large, new study finds.

Epilepsy is fairly common among women of childbearing age, and the use of antiepileptic drugs by pregnant women ranges from 0.2 to 0.5 percent.

In this study, researchers recruited Norwegian mothers at 13 to 17 weeks of pregnancy. For more than 61,000 children, mothers provided details about motor development, language skills, social skills and autistic symptoms at age 18 months. At 36 months, mothers provided that information for more than 44,000 children.

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SAN FRANCISCO — A St. Louis-based drug maker will pay $3.5 million to settle allegations that it paid doctors to prescribe “outdated, third rate” antidepressants and sleep aids, the U.S. attorney’s office in San Francisco announced Thursday.

A former employee of Mallinckrodt LLC originally filed the lawsuit in 2008 under the federal False Claims Act. The employee alleged that between 2005 and 2010, the company paid doctors consulting and speaking fees and other inducements in exchange for prescribing drugs that otherwise would not have been prescribed.

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Talk about a family feud.

Park Avenue Medical Associates, which runs 120 health-care facilities across New York, Connecticut and Massachusetts, settled Medicare fraud allegations brought by the son of the chain’s chief medical officer and founding partner, The Post has learned.

The Manhattan US Attorney’s office, which picked up the whistleblower’s complaint in March, agreed to settle a probe and Park Avenue Medical agreed to pay a $1 million settlement, according to documents filed in Manhattan federal court Thursday.

In the settlement, Park Avenue Medical admits to instances of overbilling.

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An investigator probing the July 6 Asiana Airlines crash said Wednesday that lax monitoring of cockpit instruments and crewmates was the industry's "problem that never went away."

Speaking at an airline pilots' union safety conference, National Transportation Safety Board member Robert L. Sumwalt did not address the panel's review of the deadly July 6 crash. But he noted a 1994 NTSB report that found lapsed monitoring factored in 94 percent of aviation mishaps studied.

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ORLANDO, Fla -- U.S. Attorney General Eric Holder said Tuesday that it's time to question laws that expand self-defense - such as Florida's "stand your ground" law — in the wake of the George Zimmerman acquittal.

A day after he called Trayvon Martin's death "unnecessary," Holder told people at a national convention of the NAACP that such laws can be dangerous and that the federal government plans to do a thorough investigation into the Feb. 26, 2012, fatal shooting.

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Intuitive Surgical Inc. (ISRG), the maker of the da Vinci Surgical System robots, informed customers that 30 devices may not have been tested properly, according to the U.S. Food and Drug Administration.

The FDA, calling it a “class 2 recall,” said the action affects Intuitive’s da Vinci Si Vision System Cart, Si Surgeon Side Cart, Instrument Control Box and Dual Camera Controller, in notices posted on its website yesterday. Factory testing on the systems may not meet compliance standards, the regulator said. Intuitive sent the Urgent Device Correction notice to all affected customers on June 27, the FDA said.

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