All from a fall

Not mine, but one like mine.

So I got the report on the MRI from my rowing-machine fall. Several new herniations, one of which is linked to the pain in my knees that just won’t go away. They want to know how people get hooked on painkillers? Make the co-pays for physical therapy too high for ordinary people to pay, and voila! Take a pill!

My only other option right now is to get cortisone injections in my spinal column, and I had really bad reactions the last two times I had cortisone shots. One ruptured a ligament in my ankle an hour after I got it, and the other one caused severe pain in my knee that never went away. So there you go.

And by “option,” I mean the one the lawsuit or my own insurance will pay for. A better option, at least for me, is prolotherapy for the ligaments supporting my spine, but that’s really expensive and insurance won’t cover it. Oh well.

They don’t actually want us to get well, in case you haven’t figured it out.

Maryland has few answers as opioid crisis reaches all-time high


While the entire country has been trying to fight the opioid crisis, Maryland seems to be losing the battle.

In 2017, the number of deaths due to alcohol and drugs climbed to 2,282 in the state. According to the Maryland Department of Health, that was an increase of 9 percent from 2016 and the majority of deaths, 2,009, were opioid-related overdoses. One of the biggest problems the state has had in reducing the numbers of deaths is that law enforcement has few ways to try and control the problem.

Unlike other states, it is not an issue of opioids being over-prescribed. Instead, it is largely due to the fact that fentanyl, an opioid much more powerful than heroin, is being added to heroin and cocaine that is being sold on Maryland’s streets. In most cases, it is added without the user’s knowledge.

Deaths due to fentanyl in Maryland increased by a staggering 42 percent in 2017 when compared with the year before. While there were 1,119 fentanyl-related deaths in 2016, that number climbed to 1,594 in 2017. Due to the fact that illicit fentanyl is mainly to blame for the problem, the best defense law enforcement currently has is trying to stop the sale of drugs on the street.

“The problem with that,” says Kush Arora of Price Benowitz, LLP, “is that it can be very difficult to determine who is actually selling the drugs. With numbers this high, law enforcement is feeling the pressure to make arrests, which could result in innocent people being accused of something they never did. There are other ways to fight this particular part of the problem.”

The state has deployed some of these other solutions, such as the stabilization center in Baltimore. The center is a place people can go if they are under the influence to get medical treatment and find resources for other social services. Access to naloxone, the drug that will reverse an overdose of opioids, has also been expanded.

However, more steps need to be taken. Many health officials have stated that even with the increasing numbers over the past seven years, the crisis in the state has still not peaked. More solutions need to be found, and quickly.

You snooze, you lose: insurers make the old adage literally true

Last March, Tony Schmidt discovered something unsettling about the machine that helps him breathe at night. Without his knowledge, it was spying on him.

From his bedside, the device was tracking when he was using it and sending the information not just to his doctor, but to the maker of the machine, to the medical supply company that provided it and to his health insurer.

Schmidt, an information technology specialist from Carrollton, Texas, was shocked. “I had no idea they were sending my information across the wire.”

Schmidt, 59, has sleep apnea, a disorder that causes worrisome breaks in his breathing at night. Like millions of people, he relies on a continuous positive airway pressure, or CPAP, machine that streams warm air into his nose while he sleeps, keeping his airway open. Without it, Schmidt would wake up hundreds of times a night; then, during the day, he’d nod off at work, sometimes while driving and even as he sat on the toilet.

“I couldn’t keep a job,” he said. “I couldn’t stay awake.” The CPAP, he said, saved his career, maybe even his life.

As many CPAP users discover, the life-altering device comes with caveats: Health insurance companies are often tracking whether patients use them. If they aren’t, the insurers might not cover the machines or the supplies that go with them.

In fact, faced with the popularity of CPAPs, which can cost $400 to $800, and their need for replacement filters, face masks and hoses, health insurers have deployed a host of tactics that can make the therapy more expensive or even price it out of reach.

Patients have been required to rent CPAPs at rates that total much more than the retail price of the devices, or they’ve discovered that the supplies would be substantially cheaper if they didn’t have insurance at all.

Experts who study health care costs say insurers’ CPAP strategies are part of the industry’s playbook of shifting the costs of widely used therapies, devices and tests to unsuspecting patients.

“The doctors and providers are not in control of medicine anymore,” said Harry Lawrence, owner of Advanced Oxy-Med Services, a New York company that provides CPAP supplies. “It’s strictly the insurance companies. They call the shots.”

Insurers say their concerns are legitimate. The masks and hoses can be cumbersome and noisy, and studies show that about third of patients don’t use their CPAPs as directed.

But the companies’ practices have spawned lawsuits and concerns by some doctors who say that policies that restrict access to the machines could have serious, or even deadly, consequences for patients with severe conditions. And privacy experts worry that data collected by insurers could be used to discriminate against patients or raise their costs.

Schmidt’s privacy concerns began the day after he registered his new CPAP unit with ResMed, its manufacturer. He opted out of receiving any further information. But he had barely wiped the sleep out of his eyes the next morning when a peppy email arrived in his inbox. It was ResMed, praising him for completing his first night of therapy. “Congratulations! You’ve earned yourself a badge!” the email said.

Then came this exchange with his supply company, Medigy: Schmidt had emailed the company to praise the “professional, kind, efficient and competent” technician who set up the device. A Medigy representative wrote back, thanking him, then adding that Schmidt’s machine “is doing a great job keeping your airway open.” A report detailing Schmidt’s usage was attached.

Alarmed, Schmidt complained to Medigy and learned his data was also being shared with his insurer, Blue Cross Blue Shield. He’d known his old machine had tracked his sleep because he’d taken its removable data card to his doctor. But this new invasion of privacy felt different. Was the data encrypted to protect his privacy as it was transmitted? What else were they doing with his personal information?

He filed complaints with the Better Business Bureau and the federal government to no avail. “My doctor is the ONLY one that has permission to have my data,” he wrote in one complaint.

In an email, a Blue Cross Blue Shield spokesperson said that it’s standard practice for insurers to monitor sleep apnea patients and deny payment if they aren’t using the machine. And privacy experts said that sharing the data with insurance companies is allowed under federal privacy laws. A ResMed representative said once patients have given consent, it may share the data it gathers, which is encrypted, with the patients’ doctors, insurers and supply companies.

Schmidt returned the new CPAP machine and went back to a model that allowed him to use a removable data card. His doctor can verify his compliance, he said.

Luke Petty, the operations manager for Medigy, said a lot of CPAP users direct their ire at companies like his. The complaints online number in the thousands. But insurance companies set the prices and make the rules, he said, and suppliers follow them, so they can get paid.

“Every year it’s a new hurdle, a new trick, a new game for the patients,” Petty said.

A Sleep Saving Machine Gets Popular

The American Sleep Apnea Association estimates about 22 million Americans have sleep apnea, although it’s often not diagnosed. The number of people seeking treatment has grown along with awareness of the disorder. It’s a potentially serious disorder that left untreated can lead to risks for heart disease, diabetes, cancer and cognitive disorders. CPAP is one of the only treatments that works for many patients.

Exact numbers are hard to come by, but ResMed, the leading device maker, said it’s monitoring the CPAP use of millions of patients.

Sleep apnea specialists and health care cost experts say insurers have countered the deluge by forcing patients to prove they’re using the treatment.

Medicare, the government insurance program for seniors and the disabled, began requiring CPAP “compliance” after a boom in demand. Because of the discomfort of wearing a mask, hooked up to a noisy machine, many patients struggle to adapt to nightly use. Between 2001 and 2009, Medicare payments for individual sleep studies almost quadrupled to $235 million. Many of those studies led to a CPAP prescription. Under Medicare rules, patients must use the CPAP for four hours a night for at least 70 percent of the nights in any 30-day period within three months of getting the device. Medicare requires doctors to document the adherence and effectiveness of the therapy.

Sleep apnea experts deemed Medicare’s requirements arbitrary. But private insurers soon adopted similar rules, verifying usage with data from patients’ machines — with or without their knowledge.

Kristine Grow, spokeswoman for the trade association America’s Health Insurance Plans, said monitoring CPAP use is important because if patients aren’t using the machines, a less expensive therapy might be a smarter option. Monitoring patients also helps insurance companies advise doctors about the best treatment for patients, she said. When asked why insurers don’t just rely on doctors to verify compliance, Grow said she didn’t know.

Many insurers also require patients to rack up monthly rental fees rather than simply pay for a CPAP.

Dr. Ofer Jacobowitz, a sleep apnea expert at ENT and Allergy Associates and assistant professor at The Mount Sinai Hospital in New York, said his patients often pay rental fees for a year or longer before meeting the prices insurers set for their CPAPs. But since patients’ deductibles — the amount they must pay before insurance kicks in — reset at the beginning of each year, they may end up covering the entire cost of the rental for much of that time, he said.

The rental fees can surpass the retail cost of the machine, patients and doctors say. Alan Levy, an attorney who lives in Rahway, New Jersey, bought an individual insurance plan through the now-defunct Health Republic Insurance of New Jersey in 2015. When his doctor prescribed a CPAP, the company that supplied his device, At Home Medical, told him he needed to rent the device for $104 a month for 15 months. The company told him the cost of the CPAP was $2,400.

Levy said he wouldn’t have worried about the cost if his insurance had paid it. But Levy’s plan required him to reach a $5,000 deductible before his insurance plan paid a dime. So Levy looked online and discovered the machine actually cost about $500.

Levy said he called At Home Medical to ask if he could avoid the rental fee and pay $500 up front for the machine, and a company representative said no. “I’m being overcharged simply because I have insurance,” Levy recalled protesting.

Levy refused to pay the rental fees. “At no point did I ever agree to enter into a monthly rental subscription,” he wrote in a letter disputing the charges. He asked for documentation supporting the cost. The company responded that he was being billed under the provisions of his insurance carrier.

Levy’s law practice focuses, ironically, on defending insurance companies in personal injury cases. So he sued At Home Medical, accusing the company of violating the New Jersey Consumer Fraud Act. Levy didn’t expect the case to go to trial. “I knew they were going to have to spend thousands of dollars on attorney’s fees to defend a claim worth hundreds of dollars,” he said.

Sure enough, At Home Medical, agreed to allow Levy to pay $600 — still more than the retail cost — for the machine.

The company declined to comment on the case. Suppliers said that Levy’s case is extreme, but acknowledged that patients’ rental fees often add up to more than the device is worth.

Levy said that he was happy to abide by the terms of his plan, but that didn’t mean the insurance company could charge him an unfair price. “If the machine’s worth $500, no matter what the plan says, or the medical device company says, they shouldn’t be charging many times that price,” he said.

Dr. Douglas Kirsch, president of the American Academy of Sleep Medicine, said high rental fees aren’t the only problem. Patients can also get better deals on CPAP filters, hoses, masks and other supplies when they don’t use insurance, he said.

Cigna, one of the largest health insurers in the country, currently faces a class-action suit in U.S. District Court in Connecticut over its billing practices, including for CPAP supplies. One of the plaintiffs, Jeffrey Neufeld, who lives in Connecticut, contends that Cigna directed him to order his supplies through a middleman who jacked up the prices.

Neufeld declined to comment for this story. But his attorney, Robert Izard, said Cigna contracted with a company called CareCentrix, which coordinates a network of suppliers for the insurer. Neufeld decided to contact his supplier directly to find out what it had been paid for his supplies and compare that to what he was being charged. He discovered that he was paying substantially more than the supplier said the products were worth. For instance, Neufeld owed $25.68 for a disposable filter under his Cigna plan, while the supplier was paid $7.50. He owed $147.78 for a face mask through his Cigna plan while the supplier was paid $95.

ProPublica found all the CPAP supplies billed to Neufeld online at even lower prices than those the supplier had been paid. Longtime CPAP users say it’s well known that supplies are cheaper when they are purchased without insurance.

Neufeld’s cost “should have been based on the lower amount charged by the actual provider, not the marked-up bill from the middleman,” Izard said. Patients covered by other insurance companies may have fallen victim to similar markups, he said.

Cigna would not comment on the case. But in documents filed in the suit, it denied misrepresenting costs or overcharging Neufeld. The supply company did not return calls for comment.

In a statement, Stephen Wogen, CareCentrix’s chief growth officer, said insurers may agree to pay higher prices for some services, while negotiating lower prices for others, to achieve better overall value. For this reason, he said, isolating select prices doesn’t reflect the overall value of the company’s services. CareCentrix declined to comment on Neufeld’s allegations.

Izard said Cigna and CareCentrix benefit from such behind-the-scenes deals by shifting the extra costs to patients, who often end up covering the marked-up prices out of their deductibles. And even once their insurance kicks in, the amount the patients must pay will be much higher.

The ubiquity of CPAP insurance concerns struck home during the reporting of this story, when a ProPublica colleague discovered how his insurer was using his data against him.

Sleep Aid or Surveillance Device?

Without his CPAP, Eric Umansky, a deputy managing editor at ProPublica, wakes up repeatedly through the night and snores so insufferably that he is banished to the living room couch. “My marriage depends on it.”

In September, his doctor prescribed a new mask and airflow setting for his machine. Advanced Oxy-Med Services, the medical supply company approved by his insurer, sent him a modem that he plugged into his machine, giving the company the ability to change the settings remotely if needed.

But when the mask hadn’t arrived a few days later, Umansky called Advanced Oxy-Med. That’s when he got a surprise: His insurance company might not pay for the mask, a customer service representative told him, because he hadn’t been using his machine enough. “On Tuesday night, you only used the mask for three-and-a-half hours,” the representative said. “And on Monday night, you only used it for three hours.”

“Wait — you guys are using this thing to track my sleep?” Umansky recalled saying. “And you are using it to deny me something my doctor says I need?”

Umansky’s new modem had been beaming his personal data from his Brooklyn bedroom to the Newburgh, New York-based supply company, which, in turn, forwarded the information to his insurance company, UnitedHealthcare.

Umansky was bewildered. He hadn’t been using the machine all night because he needed a new mask. But his insurance company wouldn’t pay for the new mask until he proved he was using the machine all night — even though, in his case, he, not the insurance company, is the owner of the device.

“You view it as a device that is yours and is serving you,” Umansky said. “And suddenly you realize it is a surveillance device being used by your health insurance company to limit your access to health care.”

Privacy experts said such concerns are likely to grow as a host of devices now gather data about patients, including insertable heart monitors and blood glucose meters, as well as Fitbits, Apple Watches and other lifestyle applications. Privacy laws have lagged behind this new technology, and patients may be surprised to learn how little control they have over how the data is used or with whom it is shared, said Pam Dixon, executive director of the World Privacy Forum.

“What if they find you only sleep a fitful five hours a night?” Dixon said. “That’s a big deal over time. Does that affect your health care prices?”

UnitedHealthcare said in a statement that it only uses the data from CPAPs to verify patients are using the machines.

Lawrence, the owner of Advanced Oxy-Med Services, conceded that his company should have told Umansky his CPAP use would be monitored for compliance, but it had to follow the insurers’ rules to get paid.

As for Umansky, it’s now been two months since his doctor prescribed him a new airflow setting for his CPAP machine. The supply company has been paying close attention to his usage, Umansky said, but it still hasn’t updated the setting.

The irony is not lost on Umansky: “I wish they would spend as much time providing me actual care as they do monitoring whether I’m ‘compliant.’”

ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox.

Federal government adds funds to Lyme disease fight

hd-are-your-flu-symptoms-lyme-disease-cover As someone who has suffered through decades with undiagnosed Lyme (because the tests have 50% false negatives), this is a subject near and dear to my heart:
New York has some of the highest instances of tick-borne infections in the United States.  The most well-known of those infections – Lyme Disease – poses serious and even deadly consequences for anyone that contracts it.  However, the Centers for Disease Control, the Federal agency responsible for dealing with the spread and containment of infectious diseases, only received $12 million in funding in 2017 to battle Lyme Disease.  Fortunately, the new Federal budget bumps that amount to $15 million – giving the agency more funds with which to attack the disease. “One of the most dangerous aspects of Lyme Disease is the manner in which it initially appears in a patient,” said John H. Fisher, an undiagnosed infectious disease attorney with the law firm of John H. Fisher, P.C. in Kingston, N.Y.  “The early symptoms of Lyme Disease are fever, body aches, headaches, and fatigue – symptoms that many people tend to ignore as nothing more than a cold.”  However, these symptoms mask the danger of the disease. Left untreated, Lyme Disease can lead to facial paralysis, short-term memory problems, inflammation of the brain and spinal cord, and arthritis – complications that could last for a lifetime. Not only does the disease present a challenge for individuals whose first inclination may be to try and shake off or ignore the symptoms; it can present problems for doctors or practitioners who are not regularly exposed to infectious diseases in attempting to diagnose the matter.  Primary care physicians or nurse practitioners may view the symptoms in a manner similar to the individual – that they are indications of a cold or other common bacterial or viral infection, and that a course of broad-spectrum antibiotics or rest and over-the-counter medications may be best.  However, failure to properly diagnose Lyme Disease can have long-term, serious consequences for the patient. If you or a loved one has been diagnosed with Lyme Disease, and have been told that the disease has been present for weeks or months, you may be in a situation where an examination of your case by an undiagnosed infectious disease attorney would be worth your time.  However, it is important to keep in mind the following: 1.) Was there a delay in diagnosis and treatment of the disease?  If there was, what was the reason for the delay? If the delay was because you or your loved one tried to “power through” the symptoms, there is no way to argue that the delay in diagnosis and treatment is the fault of a medical provider. 2.) If however, there was a delay in diagnosis and treatment of the illness even though the individual immediately sought medical care, the individual should then consider their current health and prognosis, and ask whether an earlier diagnosis would have changed the individual’s current health and prognosis. If these two questions are answered “yes”, then the person should consult with an undiagnosed infectious disease attorney for help in determining whether he or she has a possible claim for compensation against the practitioner responsible for the delay in diagnosis. Claims for damages related to an undiagnosed infectious disease are incredibly complex and require an in-depth understanding of the disease, the procedures for diagnosis, the treatments, and the outcomes.  Do not trust your claim to anyone other than an experienced undiagnosed infectious disease attorney.

About that flu shot…

What to Know About Getting a Flu Shot This Year, No Matter Who’s Paying

This was written by Ron K., our longtime reader and commenter.

It was a dark and stormy night . . except for the stormy part.

I’d been under the weather for two or three days. I was kicking myself for not having gotten a flu shot, but Christmas was less than a week away and I had stuff to do. After a day or so, I began to feel really crappy. The scary thing was my urine had turned red (kind of a rust color) and smelled really awful. I couldn’t sleep because every time I tried, I started coughing horribly. So I decided I’d better go to the urgent care.

I was there for about about 90 minutes before I was seen . . . about standard. I gave a sample for a urine test and waited another half hour or so.

Finally a doctor (maybe a nurse practitioner) came in. I had “nothing to worry about,” only “the flu” and a urinary tract infection. I was given a couple of prescriptions and sent on my way. I remember getting the medicine, and taking it. I remember it didn’t seem to help. I remember shivering and being unable to stop.

Next thing I remember was being in the desert and the light was a bright gold color, (yes I’m serious) but that’s a story for another day.

I was trying to open my eyes. I saw the face of my girlfriend but she was sideways and very close. She was saying something like, “He’s awake.” I started to ask, “What the hell is going on, where am I?” but I couldn’t talk. There was something over my mouth! Oh Dear God, not over my mouth, in my mouth. What the absolute fuck! I reached up to my face, but I couldn’t reach, my hands and arms were pinned, someone or something is holding me down. I tried to move and I couldn’t. No matter which way I rolled, I couldn’t move. Panic set in. I’ve always been terrified at the prospect of being unable to move, being trapped. (Tears fill my eyes and I can barely talk, just remembering.) I began to try to go all Incredible Hulk — pulling the bonds with all my might, twisting my arms, my shoulders, my wrists. Trying to push with my feet, with my legs, but all they did was flop around. No strength! Jesus Christ! What the fuck?! Fuck. Fuck! FUCK!

Then Denice’s face was back, telling me everything’s okay. “You’re in the hospital,” she said. “You’ve been really sick. You’ve been in a coma for 10 days. We’ve been worried sick.”

10 days? 10 days?! I would’ve screamed, except for that tube.

It was another 36 hours before they removed the tube and I could ask questions. It was almost New Year’s Eve, and there was a terrible winter storm across the South. It seems that I, indeed, had the flu, but I did not have a urinary tract infection. Instead, my flu had become pneumonia and the pneumonia caused my blood to turn septic. When I was admitted to the emergency room, I was coughing up a rust-colored foam. My heart rate was 160 beats per minute. Emergency room staff thought I was going into cardiac arrest. They told Denice two hours later would’ve been too late. They’d intubated me and hooked me up to dialysis. The coma was induced to keep me from unconsciously ripping the tube out of my mouth, like a too-real and very personal version of The Matrix. It took those 10 days to beat the pneumonia and clean my blood well enough to get my kidneys functioning on their own.

After leaving ICU, I spent a week learning how to eat and drink without choking, how to move my arms (to this day, my right arm doesn’t work as well as it once did.  I have extensive neuropathy — in my right arm from my shoulder to my fingertips).

I spent a month in a rehabilitation hospital, where they taught me how to walk again (albeit with a walker) and how to go to the bathroom, brush my teeth, cut my food, comb my hair . . . with only one functional hand.  The next four months, I had in-home rehabilitation that included tiny electric shocks to my quasi-dead arm. The neuropathy causes constant pain 24/7, like intermittent electric shocks or burns from my elbow to my fingertips. Although I haven’t been diagnosed, I swear I have PTSD. What do they call it, hypervigilant? Whatever it’s called, I jump at loud noises –not just jump, but come out ready to fight. When I go to the dentist and he tries to put in one of those foam block things to keep me from biting his fingers, I choke and cry and beg him to take it out.

And then I cry from shame when they do.

(If the text has been occasionally weird, that’s because I dictate to voice-to-text software now. One-handed typing doesn’t cut it.)

This has been my Christmas story — a cautionary tale, kids. I went from zero to dead in a handful of hours. Get that damn flu shot now! Because there is no tomorrow.

North Carolina grants public access to provider prescription habits

Photo by freestocks.org on Unsplash

North Carolina is hoping that opening up provider prescription histories, along with imposing new limitations on the prescription of opioids will work to hold more doctors accountable and decrease the number of opioid prescriptions issued in the state.

The law, called the NC STOP Act, put limitations on the number of opioid prescriptions that a medical provider can issue to an individual, based on many factors that any prescribing provider should analyze before to deciding whether to write a prescription. Currently, the state believes that 4,500 doctors exceed the prescription limitations across the state, and the number bay even higher. Blue Cross Blue Shield has begun to try and address the epidemic by blocking prescriptions for opioids that exceed seven days.

“On top of this, the state has created a searchable database for citizens who can type in the name of their doctor and find out whether he or she is a regular prescriber of opioids,” said Ben Whitley, a Winston-Salem Personal Injury Attorney with the Whitley Law Firm. The idea behind the database is that it will work to educate consumers about the approach their doctor takes toward prescribing opioids, while also creating accountability in doctors, knowing that their prescribing practices will be available for all to see.

For doctors that fail to comply with the Act by limiting the number of opioid prescriptions, the law authorizes the state licensing board to take action against the doctor by issuing notices of non-compliance and taking any other steps the board deems necessary to gain compliance.

From a legal standpoint, doctors that continually violate statutes like the NC STOP Act open themselves up to liability from a medical malpractice standpoint. If their improper prescribing of opioids leads to the death of a patient, and that doctor had been made aware of his or her violation of prescribing restrictions, it creates a much stronger case for any individual seeking compensation.

For the time being, however, consumers should utilize the database to inform themselves about the practices of their own doctor as well as any doctor they may be considering. Avoiding exposure to doctors with questionable prescribing practices may save heartache and trouble down the road.

Decline in vaccinations increases measles cases

Vaccine-refusing community drove outbreak that cost $395K, sickened babies

One thing I never thought I’d have to worry about as a grandmother is whether my grandchild’s going to get sick and dies from going to school with unvaccinated kids:

A downturn in the number of parents opting out of vaccinating their children against the measles virus has led to more regular occurrences of the public being exposed to the virus. The Missouri Department of Health and Human Services and the St. Louis County Department of Social Services are working to notify individuals that may have been exposed to the measles virus in two different locations in March.

The measles virus is highly infectious but preventable through vaccination. The virus’s frequency and spread had been greatly curtailed in the past decades in the United States thanks to vaccinations. However, a recent surge in the number of unvaccinated children due to disproven claims of a connection between vaccines and autism led to a corresponding surge in measles cases.

“Vaccination is an unquestioned ‘yes’ for many parents,” said Franklin County Personal Injury Attorney Gary Burger with Burger Law. “However, the parents who decide against vaccination run the risk that not only could their children become infected, but of unknowingly exposing others to the virus as well.”

What is a parent’s recourse if they have a child who is exposed to and contracts measles at an early age, prior to immunization?  Can they sue the other parents for failing to vaccinate their child? Under current law, says Burger, the answer is “probably not.” “Currently,” Burger said, “no state has a law requiring immunization. Many schools require proof of immunization before admission, but there are numerous waivers available to parents who do not want their kids vaccinated. Without a law requiring vaccination, there is no duty to vaccinate, and without a duty, it would be very difficult to prevail in any lawsuit.”

Until all parents can be totally satisfied as to the safety and efficacy of vaccines, there will continue to be unvaccinated children and until legislatures decide to require vaccinations, there will continue to be very little legal recourse for families whose children are exposed to viruses such as the measles.  

Changes to spinal fusion rules may lead to more time out of work

Spinal-Fusion-Surgery

Good. Far too many people get sent back to work before they’re ready:

Injured workers who are seeking to have certain back injuries covered by workers’ compensation insurance in Ohio will have to receive more non-surgical treatment prior to qualifying for surgical treatment under a new regulation.

Spinal lumbar fusion surgery has been used for decades to successfully treat injuries that cause severe pain with certain movements. The basic concept is that the weak part or parts of the spine are identified through evaluations and then fused together during surgery using bone grafts to create one larger, stronger bone. Like any operation, there are possible complications, but many times it is the only way to attempt to treat the pain.

The Ohio Bureau of Workers’ Compensation will now require that, prior to approval of lumbar fusion surgery, a worker must first receive conservative treatment, followed by at least two evaluations by the surgeon recommending the fusion, and a comprehensive evaluation. Additionally, the rule requires that the physician or operating surgeon follow the injured worked until he or she has “reached maximum medical improvement for the allowed lumbar conditions.”

There are certainly medical concerns related to lumbar fusion operations: the fact that this treatment is sometimes utilized inappropriately, or the fact that post-surgery pain medications can cause addiction.  A 2009 study from the National Institutes of Health, the US agency tasked with large amounts of medical research, found that spinal lumbar fusion surgeries had increased over the previous 10 years, but that reported patient improvements had not increased at the same rate. However, these new regulations will require a worker to be off of work for two months longer than usual in these situations, and the therapies, according to Daniel K. Resnick, MD, are less effective and “will not improve patient outcomes or cost-effectiveness.”

“The overall impact of this change in the regulations is hard to determine because they are so new, but it will almost certainly increase a worker’s time off the job due to injury,” said Charles Boyk, a partner with Charles E. Boyk Law Offices, LLC, a workers’ compensation law firm in Fremont, Ohio. “With this change, injured workers will need to ensure that they are adequately represented in any workers’ compensation hearing to ensure that their time off from work to comply with these new regulations will be fully compensated. I don’t want to see workers punished with loss of income if they aren’t aware of these new regulations.”