An examination of cases raises questions about whether the #DEA is stopping threats or staging them.

Judge in Another Narco-terror Case Questions Proof

https://www.propublica.org/article/judge-in-another-narco-terror-case-questions-proof

A federal judge in Washington last week threw out the narco-terrorism conviction of an Afghan man whom U.S. authorities had touted as an example of the dangerous alliances between terrorists and drug traffickers. Haji Bagcho, in his mid–70s, was one of the first people prosecuted under a little-known section of the Patriot Act that made narco-terrorism a crime, even when none of the alleged activities occurred on American soil.

According to court documents, Bagcho had been under investigation by the Drug Enforcement Administration since 2006 and was eventually arrested in Pakistan in 2009. The DEA said an analysis of ledgers and other records seized from money exchange houses that did business with Bagcho suggested that the elderly heroin dealer was responsible for some 19 percent of the world’s supply of opium. And based almost entirely on the testimony of a single paid informant, who was identified during trial only as Qari, the agency alleged that Bagcho used the proceeds from his illegal narcotics business to support the Taliban.

The Narco-terror Trap

 

The DEA warns that drugs are funding terror. An examination of cases raises questions about whether the agency is stopping threats or staging them. Read the story.

“It is clear that the defendant’s illegal activities as a drug trafficker and supporter of terrorists constituted an extremely serious form of criminal conduct, particularly when, as in this case, the two activities were combined,” prosecutors argued. “His conduct directly threatened the lives of American service members, their NATO coalition partners and the Afghan public.”

It turns out, however, that Qari had previously been deemed a liar. According to court records, a different U.S. government agency had designated Qari a “fabricator and/or information peddler.” That agency, which was not identified publicly, had paid Qari $10,000 for information about terrorist activities, but then decided to cut off contact with him once it determined his information “seemed unrealistic and sensational.”

Court records indicate that in 2010, the unidentified agency conveyed its concerns about Qari to an agent in the DEA’s office in Kabul. But the DEA kept up its ties to Qari and paid him some $45,000 for his work as a confidential informant, at a time when the annual gross per capita income in Afghanistan was less than $600. Prosecutors in the Bagcho case said their check into Qari’s background failed to come up with the derogatory information “due to discrepancies in the spelling of Qari’s name.”

The first trial against Bagcho ended in a mistrial when jurors could not agree on a verdict. After a second trial, Bagcho was convicted on two counts of drug trafficking and one count of narco-terrorism. In a 24-page ruling, issued last Friday, Judge Ellen Segal Huvelle vacated the narco-terrorism count against Bagcho, saying “the government violated the defendant’s right to due process by failing to turn over favorable impeachment evidence.” She wrote, “Evidence that the DEA’s Kabul office was told that Qari had been deemed a liar by another government agency, yet it still elected to use him as a witness would serve to undermine the reliability of the government’s investigation and its sources.”

Earlier this month, a story by ProPublica and The New Yorker examined some 37 narco-terrorism cases highlighted by the DEA and found that a disturbing number of them also unraveled. In most of the cases, the only evidence of a link between drugs and terrorism entered into evidence was provided by the DEA, which used paid informants to lure targets into staged narco-terrorism conspiracies.

Shelli Peterson, a federal public defender who represented Bagcho at trial, said the ruling “vindicates our belief that Mr. Bagcho did not receive a fair trial.” She said, “This result should serve as a warning to prosecutors handling other cases involving national security to ensure that they follow the rules.”

Still, it remains unclear what affect the ruling will have on the life sentence Bagcho received as a result of the drug charges alone. A hearing is scheduled for the first week in January on whether Bagcho will get either a new trial or a new sentence.

They say that crime doesn’t pay.. unless you run a private prison

private prisons

What?!? Private prisons suing states for millions if they don’t stay full

Low crime rates bad for business for private prisons; they demand states keep them full

http://rollingout.com/2013/09/26/what-private-prisons-suing-states-for-millions-if-they-dont-stay-full/

The prison-industrial complex is so out of control that private prisons have the sheer audacity to order states to keep beds full or face their wrath with stiff financial penalties, according to reports. Private prisons in some states have language in their contracts that state if they fall below a certain percentage of capacity that the states must pay the private prisons millions of dollars, lest they face a lawsuit for millions more.

And guess what? The private prisons, which are holding cash-starved states hostage, are getting away with it, says advocacy group, In the Public Interest.

In the Public Interest has reviewed more than 60 contracts between private prison companies and state and local governments across the country, and found language mentioning “quotas” for prisoners in nearly two-thirds of those contracts reviewed. Those quotas can range from a mandatory occupancy of, for example, 70 percent occupancy in California to up to 100 percent in some prisons in Arizona.

It is very interesting and telling that so few major national news organization are willing to report on the monstrous, ravenous and criminal system that is devouring hundreds of thousands of black and brown boys. Even those who do not subscribe to conspiracy theories have looked askance at this shocking report.

Welcome to the greatest manifestation of modern-day slavery, ladies and gentlemen.

One of those private prisons, The Corrections Corporation of America, made an offer last year to the governors of 48 states to operate their prisons on 20-year contracts, according to In the Public Interest.

What makes these deals so odious and unscrupulous? Take a look:

1) The offer included a demand that those prisons remain 90 percent full for the duration of the operating agreement. You know what that means: if there are not enough prisoners then there will be an unspoken push for police to arrest more people and to have the courts send more to prison for petty, frivolous and nonviolent crimes. There will also be a “nudge” for judges to hand down longer or maximum sentences to satisfy this “quota.”

2) Private prison companies have also backed measures such as “three-strike” laws to maintain high prison occupancy.

3) When the crime rate drops so low that the occupancy requirements can’t be met, taxpayers are left footing the bill for unused facilities.

The report found that 41 of 62 contracts reviewed contained occupancy requirements, with the highest occupancy rates found in Arizona, Oklahoma and Virginia.

In Colorado, Democratic Gov. John Hinklooper agreed to close down five state-run prisons and instead send inmates to CCA’s three corrections facilities. That cost taxpayers at least $2 million to maintain the unused facilities.

It is getting more difficult to rationalize the societal cost of keeping prisons full just to satisfy private investors who treat prisoners as commodity and cattle .

Medical expert’s stupid ideas about opiate use/abuse continue to increase

Opioid Overdose Deaths Keep Rising

Prescription opioid and heroin overdose deaths hit record high

http://www.medpagetoday.com/PublicHealthPolicy/PublicHealth/55337?xid=nl_mpt_DHE_2015-12-19&eun=g578717d0r

Overdose deaths from opioids — both prescription opioids and heroin — reached an all-time high in 2014, according to the CDC.

Following a relative plateau around 16,000 deaths per year, prescription opioid overdose deaths shot up 16% in 1 year to 18,893 deaths in 2014, Rose Rudd, MSPH, of the CDC, and colleagues reported in Morbidity & Mortality Weekly Report.

Heroin deaths also continued to jump, reaching 10,574 that year, up from about 8,000 in 2013. The latest rate is nearly three times the heroin overdose rate in 2010, the CDC said.

HEROIN deaths increased 2574… all opiates increased 2893..  meaning prescription opiate overdoses increased 4%… Heroin increased 32%.. 56 % of all opiate deaths from ILLEGAL HEROIN

CDC director Tom Frieden, MD, MPH, said in a statement that the increase is “alarming,” and he called for greater prevention, treatment, and law enforcement efforts.

The largest increase in opioid overdose deaths involved synthetic opioids such as oxycodone and hydrocodone (methadone was excluded), Rudd and colleagues said. These drugs were involved in 5,500 deaths in 2014, nearly twice as many as the year before.

And many of these overdoses are believed to involve illicitly-made fentanyl, the agency said. While it’s hard to distinguish between prescription and illicit fentanyl, reports from states and drug seizure data have shown that a substantial proportion of the increase in synthetic opioid deaths is related to wider availability of this illicit fentanyl, the agency said.

Illicit fentanyl is also combined with heroin or sold as heroin, which might be contributing to the rise in overdose deaths from heroin as well, the researchers said.

The Office of National Drug Control Policy, which held its first of several community forums on opioid misuse this week, echoed the CDC’s concern that the rise in fentanyl-related deaths comes predominantly from increases in illicitly manufactured fentanyl.

Jane Ballantyne, MD, of the University of Washington, agreed that the increase in illicit fentanyl is a contributor, as is the price drop in other illicit opioids such as black-tar heroin from Mexico.

And as physicians and public health officials have succeeded in persuading doctors to prescribe fewer opioids, those who are seeking them — particularly those already dependent on opioids — may be turning to other, more dangerous sources, Ballantyne said.

Could that be CHRONIC PAIN PTS that are DEPENDENT on opiates to help maintain some quality of life ?

“Although efforts to reduce reliance on opioids for the treatment of chronic pain did reduce abuse and death initially, that reduction is probably overwhelmed by the thousands of people who have already become dependent on opioids through pain treatment,” Ballantyne said. “Their condition is likely to worsen as they age, they will need higher doses, and if they don’t get them from doctors they will turn to illicit sources which are even more dangerous.”

Ballantyne added that the medical community should continue to recognize that opioids aren’t the solution for chronic pain, and “recognize that those already dependent on opioids need help, which probably includes opioid maintenance.”

Overall drug overdose deaths rose to 47,055 from 43,982 the year before. The majority of these deaths (61%) involved an opioid, the CDC said, and misuse of prescription opioids is the greatest predictor of heroin misuse.

Both the CDC and ONDCP called for better prevention efforts and greater access to treatment for patients with addiction, particularly medication-assisted therapy, as well as stepped-up law enforcement efforts to curb use.

Both agencies also promoted greater use of the opioid overdose reversal agent naloxone, which is now available in many forms, including an auto-injector called Evzio and an official on-label nasal spray formulation, Narcan.

blocking the Justice Department and DEA from spending money to interfere with state medical marijuana laws or hemp research projects

Congress Blocks DEA Interference in Medical Marijuana States, Ends Needle Exchange Funding Freeze

The omnibus spending bill approved by Congress today includes important drug reform provisions, but not everything activists were looking for.

The omnibus spending bill approved by Congress this morning includes several drug reform provisions, although reformers didn’t get everything they wanted. The bill includes language blocking the Justice Department and DEA from spending money to interfere with state medical marijuana laws or hemp research projects and it also lifts a freeze on federal funding for needle exchange programs. 

But Congress failed to approve amendments to allow banks to provide financial services to marijuana businesses or to allow veterans to have access to medical marijuana, despite the Senate having approved both. And the Congress again included provisions that block Washington, DC, from taxing and regulating marijuana. 

The language blocking the Justice Department from going after medical marijuana where it is legal also came in the form of an amendment from Rep. Dana Rohrabacher (R-CA) and Rep. Sam Farr (D-CA), which was passed last year, but had to be renewed this year. In the Senate, Sen. Barbara Mikulski (D-MD) sponsored the amendment. 

Drug and criminal justice reformers welcomed the progress on Capitol Hill. 

“The renewal of this amendment should bring relief for medical marijuana patients and business owners,” said Michael Collins, Deputy Director of National Affairs for the Drug Policy Alliance. “For decades Congress has been responsible for passing disastrous drug laws. It’s encouraging to see them starting to roll back the war on drugs by allowing states to set their own medical marijuana policies.” 

“Patients who benefit from medical marijuana should not be treated like dangerous criminals, and the businesses that support them need to be protected from the old drug war mentality that still runs deep within the DEA,” said Maj. Neill Franklin (Ret.), executive director for Law Enforcement Against Prohibition (LEAP), a group of criminal justice professionals working to end the drug war. “It’s very encouraging to see such widespread support for protecting state’s rights and the rights of patients.” 

Reformers also cheered the removal of the ban on states and localities spending federal funds for needle exchange programs. The ban had been put in place in the midst of drug war and AIDS hysteria in 1988 and was repealed in 2009, when Democrats controlled both chambers, but reinstated by congressional Republicans after they regained control of the House in 2011. 

Since then, outbreaks of HIV and Hepatitis C in southwestern Indiana and the impact of rising heroin use in states like Kentucky and West Virginia have weakened Republican opposition to restoring the funding. 

“Syringe access programs are a sound public health intervention, rooted in science, and proven to drastically reduce the spread of HIV and hepatitis C,” said DPA’s Collins. “Lifting this archaic ban will save thousands of lives.” 

“Needle exchange is a public health and safety necessity,” said retired corrections officer, substance abuse counselor, and LEAP speaker, Patrick Heintz. “This new law will not only protect those who use drugs from disease, but it will help prevent other innocent victims who come into intimate contact with people who use IV drugs that have been forced for so long to share contaminated needles.” 

Needle exchange programs are proven to reduce the spread of HIV, Hep C, and other blood-borne diseases and are supported by every major medical and public health organization, including the American Medical Association, National Academy of Sciences, American Academy of Pediatrics, American Bar Association, and US Conference of Mayors, as well as UNICEF, the World Bank, and International Red Cross-Red Crescent Society.

One of 400,000 medical error deaths each year ?

Did Hospitals Kill Her Mom?

http://www.thedailybeast.com/articles/2015/12/18/did-hospitals-kill-her-mom.html

Paula Schulte couldn’t survive a cascade of medical mistakes. After that, her family couldn’t get answers—or accountability.

by Marshall Allen and Olga Pierce, ProPublica

Over the course of her lifetime, Paula Schulte survived painful scoliosis that contorted her spine, a head injury that left her in a coma for weeks, and cancer that cost her part of a lung.

What she couldn’t survive was 11 weeks in Florida hospitals.

Schulte, 64, was living an engaged life—staying in touch daily with her daughter, Stephanie Sinclair, a photojournalist, and taking afternoon drives with her husband, Joe. When she suffered an unexpected bout of seizures in August 2012, doctors said she would need only a short hospital stay until the drugs kicked in to remedy things.

Instead, her treatment triggered a cascade of medical mistakes.
Paula Schulte
Paula Schulte (Courtesy of Stephanie Sinclair)

A fall from bed broke her hip and wrist—injuries that went undiagnosed for days. A hip replacement became infected, requiring another surgery. A displaced IV pumped a caustic drug into her arm until it ballooned to the size of a melon.
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Schulte died as a rare syndrome, thought to be triggered by a reaction to medication, blistered her eyelids and attacked her internal organs. Doctors said it was the type of condition they had only read about in textbooks.

A close examination of Schulte’s care shows that for all the errors contributing to her decline, neither physicians nor hospitals were held accountable for any of them. Little was done to protect other patients from similar mistakes.

Strikingly, those involved with her treatment were unaware of the totality of the missteps that contributed to her death.
Salinas Valley Memorial Hospital nurses march in protest
KSBW – Salinas, CA

“There was no justice for my mother,” Sinclair said. “There was no consequence for any of this poor care on anybody’s part. I know that added to my father’s trauma, and I know that it added to mine.”

Schulte’s case illuminates how the health care system not only fails to protect patients but often compounds the harm by hiding the truth when patients or family members try to find out what went wrong.

Over the past three years, ProPublica has gathered the stories of more than 1,000 people from all 50 states who answered a detailed questionnaire about how they or a loved one was injured during medical care, including how the providers and regulators dealt with them after an error.
Archive photo of fine artist Paula Schulte holding her daughter Stephanie Sinclair when she was 11 months old. Courtesy of the Schulte family.
Archive photo of fine artist Paula Schulte holding her daughter Stephanie Sinclair when she was 11 months old. (Courtesy of Stephanie Sinclair)

Only 1 in 5 respondents said a provider or medical facility disclosed that harm had occurred—and in about half the cases, disclosure came only after pressure, such as a lawsuit or complaint. Getting an apology for a mistake or injury was even more rare: Just 1 in 8 reported receiving one.

“Everybody’s mom is great, but my mom was a gentle soul. To die such a violent death is what hurts my dad and I so much,” she said. “We knew my mom was sick, but never in our wildest dreams did we think she would die like that.”

Although ProPublica’s sample is not a statistical cross-section of the nation’s patients (participants are self-selected), the responses are consistent with what some experts call a gaping hole in U.S. health care. Again and again, patients say they are ignored or dismissed by providers who seem more interested in avoiding legal liability than in acknowledging what went wrong.

A recent study estimated that preventable harm in hospitals contributes to the deaths of between 210,000 and 440,000 patients each year. That would make medical injury the nation’s third-leading cause of death, just behind heart disease and cancer.

More than a decade ago, a landmark study by the Institutes of Medicine—“To Err Is Human”—called for a national registry to track medical harm and bring greater accountability.
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That hasn’t happened. Instead, it has been largely left to individual hospitals and practitioners to address and learn from incidents of patient harm.

Only 10 states require hospitals to disclose medical mistakes or unintended outcomes to patients. More than two-thirds of states have laws granting legal immunity for apologies by providers. But apologies aren’t required, and the laws on immunity often do not shield doctors from liability if they explain what went wrong.

Dr. Eric Thomas, a patient-safety expert from the University of Texas Medical School at Houston, said ProPublica’s questionnaire reflects a troubling reality that helps perpetuate harm. It is “unacceptable that such a small percentage of people are being told” about errors, Thomas argued, but doubly so because every undisclosed error is a lost chance to improve care.

ProPublica has gathered the stories of more than 1,000 people injuries during medical care. Only 1 in 5 respondents said a provider or medical facility disclosed that harm had occurred — and in about half the cases, disclosure came only after pressure, such as a lawsuit.

“Not only is it a matter of justice and professionalism,” he said, “but it is a matter of improving safety for future patients.”

A few hospitals have tried to break through barriers to disclosure with programs that invite patients and their lawyers to talk about errors and possible compensation before disputes escalate. Rick Boothman, who has instituted a more open approach as chief risk officer at the University of Michigan Health System, said the fear of lawsuits or professional discipline still remains a formidable obstacle.

“People can nod in agreement with the ethics of this,” he said. “And then a defense lawyer who gets paid by the hour will say, ‘Boothman is crazy. This will lead to catastrophe.’ That holds the well-meaning hospitals back.”

“We kissed her a million times in the last half hour of her life and surrounded her with love, but we could not protect her,” Sinclair said. “And who knew that the entity we were trying to protect her from was the health care system?”

In fact, data from Michigan and other similar programs show that taking responsibility for patient harm reduces lawsuits, Thomas said. “One of the main reasons that people sue,” he said, “is that they’re trying to find out what happened.”

In lieu of the courts, patients or their relatives can complain about poor care to an array of entities, from state regulatory agencies to The Joint Commission, the private, nonprofit organization that accredits most hospitals.

Schulte’s family turned to state regulators. They declined to investigate, saying the alleged errors didn’t pose an urgent threat to other patients. After Sinclair wrote to the Joint Commission, the group cleared the hospitals involved but said it couldn’t divulge any details.

“All anybody cared about was covering up for themselves,” Sinclair said.

***

Part I

On the morning of Aug. 12, 2012, Joe Schulte’s phone rang as he prepared to visit his wife at the hospital. The call delivered jarring news. Somehow, Paula Schulte had fallen out of her bed in the ICU. Staffers found her crumpled on the floor.

Joe rushed to Lawnwood Regional Medical Center, a 331-bed facility in Fort Pierce, just a few minutes from the couple’s house. He filled in Sinclair, who was on assignment photographing child brides in Ethiopia.

Over the years, the family had seen Paula through multiple hospital stays. Joe met Paula in the late 1970s, when he was a successful real estate broker with a house in a hip section of South Miami. Paula was artistic, funny and spontaneous. They married 18 months later, and Paula moved with her daughter, Stephanie, then 5, into Joe’s place.

Severe scoliosis had left Paula with metal rods in her spine. She experienced constant pain and felt insecure about growing up with a crooked back. When Stephanie was a small child, she recalled, her mom spent a year in a body cast after spinal surgery.

One night in 2001, while the rest of the family slept, Paula went to the kitchen, fell and slammed her head. Doctors had to perform brain surgery and medically induce a coma for two weeks. Staples closed 6-inch-long incisions on each side of Paula’s head.

The morning she was to awake, doctors warned that Paula might not be the same, perhaps even barely functional. Stephanie and Joe watched nervously as attendants removed her breathing tube. Would she even know them?

Paula looked around and smiled mischievously. “Well, this is a bitch,” she said to peals of laughter.

“Yep,” Stephanie said to Joe. “That’s her.”

In time, though, they did notice differences. Paula occasionally had trouble with vocabulary or thinking beyond the moment. Her talent for art, however—she had studied for years on a scholarship to the University of Miami—was undiminished. She continued to produce paintings of South Florida landscapes and other subjects in the vivid colors she favored.

When Schulte was admitted to Lawnwood that August, it was for a relatively minor problem—seizures that began after a doctor took her off the medication she’d been taking since the kitchen accident. The seizures left her disoriented and unable to speak. New medications were supposed to get her out of the hospital soon.

Joe rose each morning, made coffee and breakfast, then headed to Lawnwood for a 10-hour shift by his wife’s bedside. Mostly they watched Paula’s favorite TV shows while waiting for the medication to kick in.

With every shift change, Joe briefed the new nurses on the intricacies of his wife’s care. A private nurse Sinclair had hired to coordinate her mother’s care also checked in periodically.

It was on the fourth day that Joe got the call about her fall in the ICU. Falls are a common, preventable cause of injury to patients; Medicare now refuses to pay hospitals for additional treatment required when patients suffer serious falls in their care. Hospitals have become so attentive to fall prevention that employees sometimes sit with patients around the clock.

Still, about 1 million falls occur each year in hospitals, with about 11,000 of them contributing to the patient’s death.

Lawnwood doctors and nurses knew Paula was a fall risk because she was disoriented and her gait was unsteady. They noted the risk on her armband, her chart and the door of her room. To keep her safe, a bed alarm was ordered and bed rails were supposed to be raised.

Still, the bed alarm could be a nuisance, so it was often turned off, Joe recalled. The raised rails made it harder to tend to Paula, and at times they were lowered. Joe said the rails were down the night before the fall; he’d reminded a nurse to put them up.

After the fall, everyone at the hospital insisted Paula was fine. They had scanned her head and X-rayed her elbow and shoulder. Paula had discoloration and abrasions on her right arm, and it seemed to be hurting her, though she still was unable to speak. When hospital staff said there were no other injuries, Joe and Stephanie felt reassured.

Four days later, Paula was discharged to a nursing home, Emerald Health Care. By then she was able to communicate better. Nursing home records show that her right wrist was swollen and that she complained of pain. Joe noticed that her right foot twisted to the side.

Doctors ordered more X-rays and made a sickening realization: All this time, Schulte’s right hip and right wrist had been broken. Both would require surgery—an artificial hip and a metal plate and screws to repair her wrist.

Schulte’s primary care doctor tried to find out where the injuries had occurred. Nurses at Emerald told him Schulte hadn’t fallen at their facility and had arrived from Lawnwood with the fractures, he wrote in her medical records. The broken bones may have been missed because of Schulte’s inability to clearly communicate the source of her pain, he added.

Nurses’ notes from Lawnwood suggest the hospital may have missed clues. Schulte was “having pain with moving and turning,” and showed “generalized weakness” in her right leg, they say. She “became agitated” and “refused to complete” her range of motion exercises.

Rehabilitation notes say she needed help standing up and wasn’t able to step to the side.

When Sinclair heard about her mom’s hip, she immediately understood the situation was grave; many studies show that older people who break a hip have a significantly higher risk of dying.

Sinclair, then on a photo assignment in Ethiopia, sat in a restaurant and sobbed. She cut her work short and flew home.

***

Schulte’s family couldn’t imagine sending her back to Lawnwood after the fall. So they turned to St. Lucie Medical Center, a 229-bed facility nearby. She was admitted through the emergency room and assigned an orthopedic surgeon, Dr. Gerald Shute.

Shute declined to be interviewed or answer written questions about Schulte’s care. As with most surgeons, there is little public information about how his patients fare. ProPublica’s Surgeon Scorecard recently published complication rates and surgical volume for nearly 17,000 doctors who operated on Medicare patients. Shute’s volume of Medicare hip replacements is low.

On Aug. 24, 2012, the day before Schulte turned 65, Shute replaced her hip and affixed the plate in her broken wrist. She returned to Emerald Health Care five days later for physical therapy. Schulte was heavily medicated and at times agitated, according to nurses’ notes and Dr. Mark Pamer, who treated her at Emerald and provided a summary of her care to ProPublica.

Caregivers eventually noted swelling and yellow drainage from her hip incision, nurses’ notes from Emerald state. Eighteen days after he’d operated, Shute diagnosed two infections in the hip joint. Schulte returned to St. Lucie Medical Center, where Shute opened the wound, washed out the infection and deposited antibiotic beads.

Joe Schulte and Sinclair said they were told that infections “sometimes happen”—as if they are the product of random chance—a common explanation given to patients in such circumstances.

It’s true that infections are a frequent complication: The Centers for Disease Control and Prevention estimate that more than 700,000 patients a year get infections while hospitalized. Of those, about 75,000 die. Though it’s hard to pinpoint how infections are acquired, studies demonstrate that they can be prevented. The CDC, for instance, said increased vigilance led to a 19-percent drop in surgical-site infections for some procedures from 2008 through 2013.

As part of an extensive analysis of surgical complications published in July, Surgeon Scorecard reported that high-performing surgeons were able to operate on hundreds of patients with few or no infections.

To fight off Schulte’s infections, a port was installed in her chest to inject potent antibiotics. One of the drugs she was given, cefepime, can cause nonconvulsive seizures, which lack the violent irregular movements of a typical seizure but can do just as much damage to the brain.

The FDA had issued a warning that year about cefepime, saying it had caused seizures in some patients. Sinclair and Joe Schulte said they were not told about the risk.

For a third time, Paula Schulte found herself in a bed at Emerald Health Care. Sinclair said her mom was angry about the fall and infections and said every day that she just wanted to go home. While Sinclair returned to New York City, Joe spent his days with Paula, trying to cheer her up. The couple watched shows on Animal Planet.

Once again, her recovery didn’t go as expected. Nursing staff documented that Paula’s behavior became more erratic, that she had trouble expressing herself, acted confused and was hostile toward them and toward Joe, even when he tried to help her with physical therapy.

It became clear that something wasn’t right. Sinclair called Joe and heard her mother screaming in the background. Sometimes she would shout the same word over and over again, like “Hello! Hello! Hello!” or “Curtains! Curtains! Curtains!”

Pamer believed Schulte was delirious and prescribed two antipsychotic medications: Haldol, a potent drug sometimes used to sedate disruptive patients, and Zyprexa. The next day, though, a psychiatrist took her off the antipsychotics.

Pamer said Schulte’s symptoms were characteristic of several possible conditions, including delirium, brain disease or nonconvulsive seizures. Given the information at the time, he told ProPublica, there was no way to be sure about the cause. Pamer decided Schulte’s neurological condition was severe enough to send her back to the hospital.

When her ambulance arrived at St. Lucie Medical Center, records say she was disoriented, confused and agitated. Doctors admitted her with a diagnosis of “altered mental status.” Sinclair assumed her mother would go into intensive care and quickly see a neurologist. Instead, Paula’s room wasn’t in the ICU and was far from the nursing station.

That first night in the hospital, to correct low potassium levels, a nurse administered potassium chloride through an intravenous line in Schulte’s left arm.

Guidelines by the National Institutes of Health call for “extreme care” when giving potassium chloride. If the IV misses a vein or is dislodged and the drug infiltrates the arm, it can cause a chemical burn, killing tissue and causing the skin to peel away. Should an infiltration occur, the IV should be “discontinued at once,” the guidelines say.

At 4:30 a.m., a nurse noted in Paula’s record: “enlarging L FA infiltrate”—an infiltration in her left forearm. The charge nurse was called to the room, and a doctor was notified. “Will continue to monitor,” the nurse wrote. Medical records indicate the IV wasn’t pulled for 90 more minutes.

When Joe and Stephanie arrived in the morning, they were horrified. Paula was catatonic, eyes staring straight ahead. Her left arm was three times its normal size, blackened and taut like a balloon about to burst. Fluid seeped through the pores of her skin, which had partially detached from her hand in what doctors call “degloving.”

Staffers said the injury wasn’t a big deal; it happens sometimes and was treatable, Sinclair recalled being told.

Then the specialists took a look. Excess fluid had made pressure build up in Paula’s arm, choking off blood flow. They diagnosed compartment syndrome, a condition that can require amputation. Doctors did not go that far, but that evening, in the operating room, a surgeon carved long incisions in her arm down to the bone. Doctors drained a liter of fluid from the limb.

Caregivers and hospital officials didn’t offer an explanation for the injury, Sinclair and her stepfather said, and no one said it was the result of an error or a mistake. Sinclair said they called it an “unfortunate situation” and said the hospital would not bill Medicare for the treatment.

Paula lay unresponsive. In the chaos around the IV infiltration, the original reason she’d been admitted—her neurological symptoms—became secondary. Two days after being admitted, she still hadn’t seen a neurologist. Furious, Sinclair demanded that the hospital call one in.

She and Joe were present when the neurologist finally arrived. Paula’s eyes were open. The doctor moved his finger in front of her face. Nothing. He gave her several firm pinches with his fingers. She didn’t resist.

In consultation notes, the neurologist said it was “probable” Schulte had been experiencing nonconvulsive seizures. Treatment guidelines say such seizures must be addressed rapidly because they can quickly damage the brain and increase the risk of death. The neurologist prescribed an additional anti-seizure drug and said Paula needed to be closely watched, his notes state.

Sinclair blew up. She’d been asking for a neurologist for days. She stormed through the hospital, demanding a transfer. With the proper care, she believed Paula could come through. “She had survived so many things before,” Sinclair said. “We thought she could do it again.”

A helicopter ferried Paula to the University of Florida Health Shands Hospital, in Gainesville. Sinclair and Joe drove more than four hours to meet her. An infectious-disease specialist examined Paula, still unresponsive, and wrote in the medical record that her seizures likely were caused by the cefepime used to fight her hip infections. She was taken off the drug and given a new one.

About a day later, though, Joe noticed something curious: skin appeared to be peeling off Paula’s eyelids. He alerted doctors, who found patches on her back, too. The ominous symptoms were confirmed when a pathologist said Paula had a rare condition, Stevens-Johnson syndrome.

The ailment, nearly always caused by an unpredictable reaction to medication, starts with patches of blistered skin and can end with organ failure and death.

Paula had suffered seizures, a fall that resulted in undiagnosed hip and wrist fractures, two hospital-acquired infections and an IV infiltration that required her left arm to be slit open like a gutted fish. But nothing could have prepared her loved ones for what happened next.

The skin in Paula’s ears and mouth fell away. Her eyeballs became raw. Inside, doctors said, her organs were under attack.

Sinclair and Joe took stock of Paula’s suffering. They decided to let her go. At their instruction, doctors unplugged Paula from life-support. Twenty seven minutes later, she was dead.

“She squeezed my hand right before she died,” Sinclair said. “She knew what was happening.”

“Everybody’s mom is great, but my mom was a gentle soul. To die such a violent death is what hurts my dad and I so much,” she said. “We knew my mom was sick, but never in our wildest dreams did we think she would die like that.”

***

Part II

Charles Bosk, a sociologist at the University of Pennsylvania, has spent decades studying the way caregivers and health systems react when patients get hurt.

“When bad outcomes happen,” Bosk said, “patients first want an apology, second an explanation, and third reassurance that the hospital is taking steps to make sure no one is harmed in the same way again.”

Schulte’s loved ones say they never got a formal apology or explanation.

For weeks after Paula died, they were crippled by grief. They replayed Paula’s last two months, obsessed by the tumble of events.

They were about to confront a common scenario for patients and family members trying to come to grips with medical injuries. Bosk called it the “many hands” problem. With numerous doctors and nurses at different facilities involved in an episode of care, there is no overall responsibility.

The predicament is compounded by a prevailing ethic in health care: that patient safety is best served by a “no blame” environment. Harm is attributed to “system failures” rather than individuals. It’s as if medical providers don’t see themselves as part of the system, Bosk said.

At first, Sinclair thought an attorney could help. She assumed filing a malpractice lawsuit would be a simple matter. Despite what she regarded as the dramatic and well-documented nature of her mother’s injuries, the lawyers she contacted weren’t interested.

Malpractice cases can cost $50,000 or more to pursue. Attorneys usually take them on contingency, meaning they are paid if they win. The economics work only if potential damages are high, so a patient’s medical bills and lost future income can be more important than the merits of the case.

Sinclair met with an attorney who walked her through the math. Paula was older and didn’t have much income. “The most we could get is $50,000,” she recalls the attorney saying, “and we could spend that much on depositions and expert witnesses.”

Paula’s case also was complex, involving multiple facilities and many providers. More potential defendants could mean more expense. “We wish we could help everybody,” one lawyer wrote, declining the case. “Currently, we have no choice but to reject about 300 potential cases presented to us for every one case we can accept.”

Sinclair couldn’t believe it. “If you’re 65 years old and not bringing in a big income, they don’t value your life,” she said.

The malpractice door was shut. But Sinclair had obtained her mother’s medical records, a stack about 10 inches tall. She knew they held critical details and believed that if she could only convey the facts to the hospitals, they would see how errors had contributed to Paula’s death.

Early on, going through the records was just too hard. Sinclair was often forced to stop at details that were too painful or intimate. Eventually, she made slow progress. Her husband, Bryan, then in law school, helped her make a detailed timeline, listing events during Paula’s care down to the minute.

Not until February 2013, four months after her mother died, did Sinclair muster the courage to call Lawnwood Regional. The fall in the ICU had been the first domino to topple. She suspected that hospital officials might not know that it started Paula’s decline, or how things ended.

The hospital routed Sinclair to the risk management department. Patients who are harmed rarely meet anyone in risk management, but that department usually knows about them. Cases are often flagged for review before a patient is ever aware of it.

The traditional role of risk managers is to protect hospitals from lawsuits. In cases involving medical errors, they move to gather information and control what is disclosed. Critics call this approach “deny and defend”: Avoid acknowledging a mistake while aggressively protecting the institution.

When Sinclair called Lawnwood, she spoke to a person in the risk management department about Paula’s fall from bed and the undiagnosed hip and wrist fractures. To be explicit about the problems, she read directly from the medical records: that Lawnwood knew her mother was a fall risk, that she was unable to communicate clearly, that no one X-rayed the hip, and more.

A few weeks later, a letter from the interim risk manager arrived. It confirmed Paula’s fall and that her hip wasn’t X-rayed. “There were no complaints of hip pain,” the letter said.

“We are deeply sorry for the loss of your mother,” it continued. “We continue to strive to provide patient centered care and apologize if you feel our staff did not meet this goal.”

Sinclair wrote back, saying the hospital’s response left out key information. For one, her mother was speaking gibberish, so she couldn’t have complained about the broken hip. Precautions were supposed to prevent a fall in the first place, she wrote. Lawnwood’s response “answered none of our questions regarding the circumstances surrounding my mother’s care,” Sinclair said.

She added that her mother ended up dying after complications from the hip fracture, which “should give Lawnwood pause to perhaps handle such a request with compassion.” How would Lawnwood correct “this egregious and devastating wrong” and protect other families?

She never heard back.

In fact, subsequent incidents at Lawnwood suggest Sinclair was right to be worried about whether the hospital learned anything from Paula Schulte’s case. In late 2012, after Schulte died, another elderly patient fell in the hospital and suffered a hip fracture, Florida data shows.

As recently as March of this year, state inspectors cited Lawnwood after another patient fell and suffered a fracture. “There is no evidence the facility implemented measures developed to reduce re-occurrence or minimize risk of injury,” the inspectors’ statement of deficiencies said.

Officials at Lawnwood and St. Lucie Medical Center, both owned by Hospital Corporation of America, declined ProPublica’s interview requests. In an email, HCA spokeswoman Ronda Wilburn said Paula was “assessed and treated appropriately” at Lawnwood.

Wilburn said St. Lucie Medical Center had apologized for the “unfortunate IV incident” and had changed procedures after an internal review. She declined to specify what changes were made. Wilburn said the hip infections were diagnosed “several weeks” after Schulte left St. Lucie.

Sinclair considered the letter from Lawnwood’s risk manager a non-response. She felt gut-punched—too disheartened even to try asking questions about infections and the IV infiltration at St. Lucie, which she knew was run by the same corporation as Lawnwood.

Hospitals have broad leeway when it comes to deciding what to tell patients about medical errors. State laws aimed at encouraging disclosure are ambiguous or weak; hospital industry guidelines, though nominally promoting transparency, don’t require a detailed explanation.

Only 10 states require hospitals to tell patients about certain types of medical harm. None requires divulging how the harm happened, who was responsible or what steps hospitals are taking to make sure the harm doesn’t happen again. A national disclosure law, proposed by then-Sens. Barack Obama and Hillary Clinton in 2005 and modeled on the University of Michigan Health System’s program, never advanced out of committee.

The Joint Commission, the nation’s largest hospital accrediting agency, requires hospitals to inform patients about “sentinel events”—any injury that’s not related to the natural course of a patient’s illness that results in death, permanent harm or severe temporary harm.

Hospitals are also expected to conduct a “root cause analysis,” to reconstruct the event and determine how and why the harm occurred. But the hospital can “define and determine what information related to an adverse event or sentinel event should be disclosed… including whether the root cause should be disclosed,” a commission spokeswoman said in an email.

The American Hospital Association has guidelines that encourage open communication with patients, but they aren’t binding, either. Dr. John Combs, the AHA’s chief medical officer, would not comment specifically about Schulte’s case. However, he said that deflecting complaints from a family member would be out of step with today’s risk management standards.

Some hospitals are experimenting with new approaches.

Dr. David Mayer, vice president of quality and safety at MedStar Health, a Maryland-based hospital chain, is among a handful of federal grant recipients testing a program called Communications and Optimal Resolution—or CandOR—that “teaches people to be empathetic, and then, when apology is appropriate we take accountability,” he said.

“It’s not, ‘I’m sorry this happened to you,’ ” Mayer said, “It’s, ‘I’m sorry our care broke down and you were harmed by that care.’”

CandOR dictates that caregivers communicate immediately with patients after a bad outcome, even if it’s unclear why the harm occurred, or who was to blame. That contrasts with the more typical response in hospitals: to avoid talking to patients until any internal investigation is over, Mayer said. That can leave patients in the dark for months; if negligence isn’t determined, there may not be any communication with the patient, he said.

As in the Michigan health system’s program, financial compensation may be offered, or an explanation provided if no offer is made. Patients and their families are welcome to bring a lawyer to conversations with doctors or hospital officials, Mayer said.

Most hospitals still do things the old way; only about 100 of the country’s roughly 3,500 acute-care hospitals are trying approaches like CandOR, Mayer said.

***

After her mother’s funeral, when Sinclair saw the final death certificate, it set off a new round of frustrations and questions.

The document mentioned nothing about the fall that broke Schulte’s hip, the hospital-acquired injuries, missed diagnoses or infections. Though it listed several contributing factors, including Stevens-Johnson Syndrome, the certificate said the cause of death was epilepsy.

Yet Schulte’s discharge records from the Shands hospital showed—and doctors had asserted—that the seizures were resolved before she died.

Sinclair wrote the doctor at Shands who had completed the certificate. She asked to have it corrected to at least include the fall and the infections. “We just believe, out of respect for her, it should be accurate as to what actually transpired,” Sinclair wrote.

The accuracy of Schulte’s death certificate had a practical consequence. Schulte had life insurance that only paid out if her death were accidental—it was worth $100,000. Because the death certificate said she died of “natural” causes, Joe, who’d lost money in the 2008 financial crisis, didn’t have a claim.

There are numerous places where patients or their relatives can take such concerns, from state health agencies or nursing and medical professional boards to Medicare Quality Improvement Organizations. The Joint Commission also investigates complaints involving hospitals it accredits. Each agency has its own policies and jurisdictional limits.

About half of those who completed ProPublica’s questionnaire said they filed some sort of complaint. Many said they were disappointed with the outcomes, however. Some never heard back, while others reported getting generic responses asserting that the care was appropriate.

Sinclair didn’t fully understand, and struggled to navigate, the regulatory maze. Beset by grief, she didn’t file a complaint with the Florida Agency for Health Care Administration, which licenses hospitals, until June—more than two years after her mother died.

She took hours to prepare a three-page, single-spaced statement, including precise times and dates and quotes from the medical records. “As you can see, this is a very tragic series of events—rife with hospital error—resulting in devastating consequences for our family,” Sinclair wrote.

The next day, the agency sent a form letter. “Thank you for forwarding your concerns …” the letter began. While the agency “carefully reviewed” Sinclair’s complaint, it considers “current risks” to patients a higher priority, the letter said.

The agency would not be looking into the case.

About the same time, Sinclair sent letters about Lawnwood Regional and St. Lucie Medical Center to the Joint Commission. In October, four months later, two form letters arrived. They said the commission had contacted the hospitals and asked for responses concerning Paula Schulte’s care. The hospitals’ responses were found to be “acceptable,” the letters said.

“In line with our Public Information Policy, we cannot provide you with the organization’s response,” the form letters said. “This concludes our evaluation.”

Sinclair was outraged. How can the people most closely affected by the harm be entirely shut out of the conversation, she wondered.

Sinclair knew her mother wouldn’t live forever, but even photographing war and human rights abuses hadn’t prepared her for what happened in the end. The apathy she felt from medical providers and regulators only added insult to her mother’s many injuries, Sinclair said.

“We kissed her a million times in the last half hour of her life and surrounded her with love, but we could not protect her,” Sinclair said. “And who knew that the entity we were trying to protect her from was the health care system?”

 

Pt with mental health/substance abuse disorder more likely to commit suicide

Opioid-Benzo Combo Raises Deadly Drug Overdose Risk

http://www.pharmacytimes.com/news/Opioid-Benzo-Combo-Raises-Deadly-Drug-Overdose-Risk

Concurrently prescribed opioids and benzodiazepines increase the risk for deadly drug overdose in veterans.
 
A new study published in the British Medical Journal found 27% of US veterans who received opioids between 2004 and 2009 were taking benzodiazepines at the same time. Roughly half of the drug overdose deaths among that population occurred when the drugs were prescribed concurrently, and veterans’ risk of fatal drug overdose grew as their daily benzodiazepines doses increased.
 
Lead study author Tae Woo Park, MD, Msc, told Pharmacy Times in an exclusive interview how pharmacists can apply these alarming findings to their practice.
 
“Pharmacists can play an important role in helping prevent unintended consequences of combined benzodiazepine and opioid analgesic use,” explained Dr. Park, an assistant professor at the Warren Alpert Medical School of Brown University. “They can alert providers when patients are receiving high doses of these medications and possibly recommend naloxone distribution for these patients. They can also help identify multiple providers of these medications, possibly with help from prescription monitoring programs when available.”

The most commonly prescribed benzodiazepines in the study were on the Veterans Health Administration’s drug formulary, which includes alprazolam, chlordiazepoxide, clonazepam, diazepam, lorazepam, and temazepam. The opioids examined in the study were codeine, morphine, oxycodone, hydrocodone, oxymorphone, hydromorphone, fentanyl, propoxyphene, and methadone.
 
Veterans who received benzodiazepines were more likely to be women, middle-aged, white, and to live in wealthier areas. They were also more likely to have a history of mental health or substance abuse.
 
Of all fatal overdoses involving pharmaceuticals in 2010, 75% were tied to opioid analgesics, the researchers cited. In addition, 30% of drug overdose deaths involving opioids were related to the concomitant use of benzodiazepines.

“[D]rug overdoses are a leading cause of death in the United States, and prescribing benzodiazepines to patients taking opioids for pain is quite common,” said Dr. Park in a press release. “As we learn more about pharmaceuticals and how they interact with each other, we can try to reduce the risk of harm to patients.”

What you perceive is what you believe

mntmolejudicial

Opioid Abuse & The Missing Information

http://www.thehonestapothecary.com/2015/12/03/opioid-abuse-the-missing-information/

This is a post from a fellow Pharmacist blogger ( Jason Poquette) … I often talk about how the DEA/DOJ use vague and/or bulk numbers to get their point across about our “drug abuse epidemic”.  Jason looks at the issue of how data/information is being obfuscated to create a “false image” of the so called “epidemic”.

On any given morning I can open up my laptop and find probably half a dozen articles on our opioid abuse problem going on in the U.S.  The words in the headlines change, but the content and message are sadly always the same: Opioid and heroin addiction are rampant.

Sometimes the article is simply reporting the facts:

  • A pharmacy robbery in Oklahoma
  • A pain clinic closed in Tampa
  • A physician/pharmacist team exposed for pill mill prescribing
  • A grieving family over the loss of a loved one due to an overdose

Sometimes the article is trying to uncover solutions:

  • Focus on prescribers to solve the problem
  • Focus on pharmacies to solve the problem
  • Secure our borders to solve the problem
  • Open more recovery and treatment facilities to solve the problem
  • Educate the public to solve the problem        

Not only do we have lots of information describing the problem and proposing solutions, but we also have taken several steps to try and deal with the issue. 

For example:

  • Nationwide Prescription Monitoring Programs and Mandatory Reporting
  • Naloxone emergency kits
  • Abuse deterrent narcotic formulations
  • Rescheduling of Hydrocodone to CII status
  • Improved prescription security (tamper resistant prescriptions, mandatory electronic prescribing is coming soon)

But something about all this information and activity has always bothered me.  Something is missing in all our reporting about overdose deaths.  I feel like I’m trying to solve a puzzle with a missing piece. 

What is missing is data that traces the prescription medication involved in the death back to the source. 

In other words, to put it bluntly:  Where did the victim obtain the drug?  Who gave it to him/her?  That information is almost never revealed. 

We NEED to know where the drugs involved in DEATHS are coming from. The source is significant!  But everything we read online is typically general and non-specific.  We’re told we have a “diversion” problem and an “overprescribing” problem and that prescription opioids are being “stolen” and “sold.”  That’s not data.  That’s not research.  We have thousands of these terrible overdoses going on every year, but frankly we have NO reliable data upon which to design our strategy.

For example (this list is not comprehensive), did the medication involved in the overdose death come from…

A)  A legally obtained prescription for themselves by a doctor and pharmacy

B)  A stolen bottle of medications from an otherwise legally obtained prescription (e.g. from a friend or family member)

C)  An illegally purchased bottle of prescription medication on the street or from a pharmacy

D)  A fake or stolen prescription blank

E)  An emergency room prescription

F)  Pharmacy theft

G)  Unknown?

Can you see how the SOURCE of the offending substance should logically determine our strategy for correction?  But if you happen to have read the article this far (you are a hearty soul!), I warmly invite you to search online for this data.  Google it.  Look for studies.  Search for hard data, not “general” lists of possible sources for opioids that lead to addiction and death.  Actual numbers.  Percentages.  Figures.  Find the study that says “___% of overdose deaths came from prescription drugs obtained legally by the victim from his/her doctor, and ___% came from illegally purchased prescription drugs from an illicit source.”  Once you find that study, please send it to me.  I’m eager to see it.

Maybe you will have more success than I have had.  I can’t find that information.  Maybe I’m not that good at doing online research.  I will gladly concede that fact if someone can come up with answers and data that is verifiable. 

Maybe the sad reality is that the answer is unknown.  Maybe we have no idea where the drugs are coming from.  Maybe these awful deaths are made even more terrible by the deafening silence of information about how the poor victim obtained their lethal dose. 

If so, that breaks my heart.  And if that is the case, I’m not very optimistic about our efforts to combat this growing crisis.

Sugar Land-area CVS pharmacy gives woman wrong prescription — twice

Sugar Land-area CVS pharmacy gives woman wrong prescription — twice

http://abc13.com/news/local-pharmacy-gives-woman-wrong-prescription—-twice/1125404/

A Fort Bend County woman says she was given the wrong medication by a pharmacy, not once, but twice.

Wendy Flory says she picked up a prescription from the CVS pharmacy located on Crabb River Road near Sugar Land about two weeks ago. It was supposed to be a small pill used to treat her ongoing thyroid condition.

“Immediately, even before I opened the bottle I noticed that something was off. I was like, ‘Whoa, this is NOT the same pill,'” said Flory.

Instead she says she found a larger yellow pill with the letters “TVA19” on them. Searching the Internet she found the lettering generally indicates that the pills would be progesterone.

“Someone could be harmed from this type of error,” said Flory.

Several months ago she says she similarly noticed that the medication she received was something other than was prescribed. When she told officials at the CVS she says they apologized and offered her a $25 gift card.

This time she complained not just to the local store, but also to CVS corporate and the Texas State Board of Pharmacy.

A spokesperson for CVS says they are “actively looking into” this case. So far the company has had no further response.

A search of the state pharmacy board website produced record of a 2010 Agreed Board Order in which the pharmacy was fined $3,000 for allowing a pharmacy technician to work with an expired license. The pharmacy was also required to develop and implement policies to ensure all employees are properly licensed.

Flory says she posted details about her case on her neighborhood’s Facebook page. Since that posting she says at least 13 others have indicated they too have received either the wrong medication or a dosage that was not prescribed.

She hopes her case will serve as a reminder to others that you should always look closely at the medication you receive and make sure you have the correct prescription before you take it.

A CVS spokesperson would say only, “We sincerely apologize to ms. Flory. Our district pharmacy supervisor followed up with her as soon as we learned about this incident. The health and safety of our customers is our number one priority and we have comprehensive policies and procedures in place to ensure prescription safety.” that spokesperson calls prescription errors are rare occurrence.”

If you’d like to check out whether your pharmacy or pharmacist has faced disciplinary action, you can visit http://www.pharmacy.texas.gov.

 

You mean that wiretap warrants must be legal ?…but we’re the DEA !

DEA ignored prosecutor’s warning about illegal wiretap warrants, now it’s losing big

http://boingboing.net/2015/12/15/dea-ignored-prosecutors-parn.html

For years, the DEA relied on a Riverside, California magistrate judge, Helios Hernandez, to write illegal wiretap warrants, making Hernandez the national champion of wiretapping warrants, signing off on five times more than any other judge in America.

Despite warnings from their own prosecutors that the wiretap orders were illegal, the DEA persisted in using Henandez’s warrant-mill, rather than doing things the legal way. Hernandez’s warrants formed the basis for 2 million intercepted conversations involving 44,000 people.

 
 
 
 

Now, the DEA’s suspects are successfully challenging the evidence against them, and those cases are collapsing. Most recently, the suspects in a San Bernardino money laundering case prevailed despite the police having secretly intercepted couriers “carrying away boxes full of cash, sometimes stuffed with $100,000 or more.”

DEA spokespeople are furious — with the defendants, not with their own officers, whose corruption and unwillingness to follow the law blew their own cases.

The San Bernardino case was the first, but it will probably not be the last — many defendants and convicts across America had the cases against them built by the DEA with Henandez’s funny warrants.

Lawyers for Lay and the other suspects asked a judge in San Bernardino to throw out the wiretaps and all evidence tied to them. Prosecutors did not object; Deputy District Attorney Mallory Miller said during a hearing in October that they did “not have a legal position to oppose” the request.

Prosecutors dismissed the case.

Lay and others have taken the unusual step of asking a federal court in Los Angeles to return nearly $800,000 of the money DEA agents seized during the investigation. They started that fight before the criminal case was dismissed, but their case got considerably stronger after prosecutors in San Bernardino conceded that wiretap evidence was tainted. Justice Department lawyers have not indicated how they will respond to that request.

It is almost impossible to know how widely the DEA has used tainted wiretaps from Riverside County; many records related to the surveillance are sealed. State and federal court records show prosecutors have relied on Riverside County wires signed by Zellerbach’s assistants to make arrests in California, Kentucky, Oregon and Virginia.

After illegal wiretap, suspects go free and want a refund [Brad Heath and Brett Kelman/USA Today]

Justice officials fear nation’s biggest wiretap operation may not be legal [Brad Heath and Brett Kelman/USA Today]

Cody Berguson… #CVS BAD BOSS OF THE MONTH

Rx for Discrimination

http://badbossofthemonth.com/2015/10/rx-for-discrimination/

With a Backdated Firing, This Bad Boss Hit a New Low in Age Bias

Cody Berguson had laid the groundwork — he was ready to fire James King.

But Mr. King was unavailable: The 65-year-old pharmacist was caring for his wife, Trudy, who was hospitalized for surgery.

Mr. Berguson, a pharmacy supervisor for health giant CVS, waited a few days. Then he called in Mr. King and, in a two-minute meeting, terminated him.

The kicker: Mr. Berguson backdated the termination to before Trudy King’s surgery, which meant that CVS-supplied insurance no longer covered her hospitalization. The Kings had to pay their medical bills with credit cards.

Cody Berguson is our latest “Bad Boss of the Month.”

Earlier this year, a federal jury found CVS liable for age discrimination and awarded Mr. King more than $1 million in damages — then doubled it by finding that CVS “willfully” violated the Age Discrimination in Employment Act, for a final award of more than $2.1 million.

CVS is fighting the verdict.

At the time of his firing, Mr. King had worked at the CVS Pharmacy in Pell City, Ala., for more than seven years. Although he was 65, he had no intention of retiring: “I wanted to work until I died,” he said at trial, joking that his wife “didn’t want me around the house.”

In reality Mr. King enjoyed working and needed to pay for the education of his daughter, who was still in high school and planned to go to college.

Mr. Berguson, however, seemed to have a different plan.

Soon after Mr. King’s 65th birthday, the CVS supervisor started what Judge Virginia Emerson Hopkins characterized as a “retirement-related inquisition,” repeatedly asking Mr. King pointed questions like “Don’t you have enough money to buy an annuity and retire?”

Mr. Berguson also began what Mr. King called “a constant barrage of unjustified and petty criticisms,” writing up the pharmacist for sins including a “bad attitude.”

Before long, Mr. Berguson and another regional official called Mr. King into a meeting and told the pharmacist he was under investigation for allowing other employees to use his “manager card” for voiding transactions, among other things.

They also faulted him for taking too many smoke breaks — they had reviewed an entire day’s video and tracked his smoking to the minute — and for failing to properly document his purchase of two Diet Pepsis.

According to Mr. King, Mr. Berguson called him a “thief,” a “liar,” and “lazy” — and topped off the encounter by asking, “Now, what about retirement?”

Fearing the worst, Mr. King complained to Mr. Berguson’s boss and also called a company hotline to say he felt like a victim of age discrimination. But CVS did nothing — and things escalated.

One day when Mr. King was not working, a younger pharmacist filled a narcotic drug prescription via the store’s drive-through lane. It was for the wife of a local judge but, based on later investigation, was picked up by an unauthorized person.

A few days later, the irate judge — a longtime customer well-known to CVS staff — arrived at the pharmacy to get his wife’s pain medication. Seeking to make things right, Mr. King gave him replacement pills without forcing the judge to contact a doctor first.

In a prior incident of this type, CVS had sorted out details later. This time, however, Mr. Berguson told Mr. King he had violated state law and suspended the pharmacist without pay. CVS referred the incident to the Alabama State Board of Pharmacy — and reported it to local police.

A stunned Mr. King gave a statement to the pharmacy board investigator; he was told he’d be called for a hearing if the matter went any further. Neither the board nor the police ultimately took any action against him; Mr. King remains a pharmacist in good standing.

In the meantime, however, Mr. Berguson had sent an e-mail to CVS officials: “Considering … this latest issue, one month after meeting with him about the Pepsi issue … I would think it’s time to relieve Jim of his duties as an employee of CVS no matter what the state board decides to do with him.”

CVS approved the termination without waiting for further facts, and Mr. Berguson tried to implement it immediately — only to find Mr. King tending to his hospitalized wife.

As jurors heard, it wasn’t the first case of age discrimination involving Mr. Berguson. That’s “not coincidental,” Mr. King’s lawyers said: Under direction from CVS to hire a quota of newly-minted pharmacists, the supervisor had to create slots for cheaper, younger new hires across a 23-store territory from Auburn to Birmingham.

In a 2013 jury trial against CVS, veteran pharmacist Roger Harris won $800,000 on similar claims of Mr. Berguson’s prejudice.

Like Mr. King, Mr. Harris had been subjected to ageist heckling by Mr. Berguson; like Mr. King, he had received multiple write-ups over the six months before being fired; like Mr. King, he was terminated at age 65.

There was no sick wife in the case, but Mr. Harris suffered his own cruel flourish: Mr. Berguson fired him on his 65th birthday.