Health
As White House Presses for Booster Shots, Americans Are Slow to Get Them
BALTIMORE — The brand new coronavirus booster pictures have discovered a modest variety of takers at one in all this metropolis’s few remaining public vaccination websites, with 9 doses given on one latest day and 15 on one other.
Greater than a month after the retooled pictures have been rolled out, solely about 5 % of Baltimore residents have acquired one, a determine that displays the gradual uptake nationally. In a metropolis with stark well being disparities, native officers see a purpose to be nervous.
“The truth that we’ve been getting it so typically is making it uninteresting to individuals,” Rebecca Dineen, town’s Covid-19 vaccine coordinator, stated of the rounds of coronavirus pictures.
The anemic turnout underscores one more take a look at of the Biden administration’s pandemic technique, as federal and native officers cope with dwindling public endurance and diminishing funds for the virus response.
Solely about 15 million doses of the brand new pictures have been administered nationally since their introduction at first of September, representing lower than one in 10 people who find themselves eligible, and there are indicators that many People are unaware of or just tired of them. In a Kaiser Household Basis survey final month, half of adults stated that they had heard little or nothing in regards to the pictures.
As soon as outlined by provide shortages and mass vaccination websites, the nation’s ever-expanding inoculation marketing campaign has these days been characterised by apathy, with doubtlessly severe well being penalties for probably the most weak People ought to one other Covid wave sweep the nation this winter.
The tepid response to the pictures, public well being specialists say, is greater than only a advertising and marketing dilemma. Many People have just lately had a coronavirus an infection, drawing out the timeline for after they may search one other booster or inflicting them to skip one altogether. Others are cautious of continuous boosting or unintended effects that may maintain them from going to highschool or work.
The turnout for the brand new pictures, for which kids as younger as 5 grew to become eligible this week, may fall far in need of the response to the preliminary booster marketing campaign that the federal authorities undertook round a yr in the past, when administration officers say there was much less fatigue round vaccination and the pandemic extra broadly. Round 110 million individuals acquired a minimum of one dose of the unique booster formulation earlier than the brand new pictures have been approved on the finish of August.
Dr. Ashish Ok. Jha, the White Home Covid-19 coordinator, stated in an interview that the early turnout for the up to date boosters amounted to a “good begin” and that uptake was prone to steadily enhance this fall. Many People, he stated, have been treating the brand new vaccines like flu pictures, contemplating receiving one because the climate turned colder.
“We didn’t have an inside quantity in our heads, or a minimum of I didn’t have one in thoughts, of what we have been going to attain,” Dr. Jha stated. “My form of psychological mannequin was that it will actually begin ramping up as soon as we bought into October.”
Learn Extra on the Coronavirus Pandemic
Administration officers made an costly guess on the brand new marketing campaign at a fraught second in congressional funding negotiations, shopping for over 170 million doses with billions in repurposed funds — sufficient to vaccinate a lot of the roughly 225 million People who’ve had an preliminary spherical of vaccination.
One senior official stated the acquisition was modeled on how the federal authorities usually buys flu vaccines, with sufficient doses to achieve any American at tens of 1000’s of web sites whereas limiting what number of go to waste. Round 80 % of doses in latest weeks got at retail pharmacies, Dr. Jha stated, a rise from earlier Covid-19 vaccination campaigns.
Whereas many People nonetheless have substantial safety from previous vaccinations and infections, federal officers have pointed to analyses that present the brand new boosters may nonetheless save 1000’s of lives. Vaccine specialists say they anticipate the pictures to ship an preliminary burst of antibodies and a broadened immune response. The Covid vaccines have been redesigned to focus on Omicron subvariants on the belief that extra present formulations would offer higher and extra sturdy safety.
But researchers are nonetheless working to find out how properly the pictures shield individuals and the way lengthy these defenses final. The information that federal regulators gathered from the producers of the boosters, Pfizer-BioNTech and Moderna, continues to be preliminary, leaving specialists to invest in regards to the further advantages the brand new vaccines might provide, together with its affect on transmission or longer-lasting signs of Covid-19.
Federal officers will not be anticipated to have early knowledge from Pfizer and Moderna on what sort of short-term antibody responses the brand new vaccines induced in trial members till later this fall.
Well being officers and suppliers already know whom they should attain with the brand new pictures, as People over 75 have represented a majority of deaths from Covid-19 in latest months. Round half of these vaccinated with the brand new boosters to date are seniors, Dr. Jha stated.
White Home officers say they’ve tried to publicize the brand new pictures with federal advert campaigns, clinics at state and county gala’s and partnerships with native leaders. The administration is focusing on older People with outreach from the Facilities for Medicare and Medicaid Providers, whereas the White Home is working with CVS and Walgreens to extend booster consciousness, Dr. Jha stated.
“Once you stroll into CVS, you see indicators for the flu shot,” he stated, including, “We need to ensure that that’s getting tied into their outreach on Covid-19 vaccines as properly.”
Dr. Swati Gaur, the medical director for 2 long-term care services in Georgia, stated the problem had shifted from getting a provide of vaccine doses to waging a piecemeal persuasion marketing campaign to coax seniors into taking them.
In a single latest encounter, she stated, she spoke with a resident at one in all her services who had grown bored with getting vaccinated in opposition to the virus after 4 pictures and refused a fifth. She walked him by the potential advantages, and he agreed to get the shot.
Dr. Gaur stated it was essential that workers at long-term care services calling households and asking for consent to vaccinate knew find out how to have comparable conversations.
Biden administration officers have provided typically competing concepts of the urgency of the booster marketing campaign for youthful, more healthy individuals. Federal regulators scrambled to make the up to date pictures accessible forward of schedule late in the summertime, choosing that strategy as a substitute of providing second booster doses of the unique vaccine formulation to all adults. With case counts decrease, some prime officers have just lately provided a extra relaxed timeline, turning to an October theme.
Dr. Jha inspired People to get the brand new pictures by Halloween so their immunity can be bolstered by Thanksgiving. “What we’ve been making an attempt to do is give recommendation that simplifies it,” he stated, including, “The concept is that you simply don’t need to type of suppose too exhausting about are you eligible or are you not eligible.”
Some specialists have warned that makes an attempt to simplify messaging may backfire.
Dr. Walid F. Gellad, a drug security professional on the College of Pittsburgh, stated that efforts to achieve all age teams had diluted consideration to those that most want enhanced safety. When specialists over the previous yr have questioned whether or not youthful, more healthy People want boosting, he stated, “to these listening solely halfheartedly, it is going to simply sound like criticism of the booster, though it was criticism of the booster in these age teams.”
With the brand new pictures, extra People are making guesswork out of the timing. Performing on professional recommendation, a few of those that have just lately had the virus are ready three or extra months to get boosted, whereas others are timing the shot for the vacations or journey, or one other uptick in circumstances.
Amanda First, 32, a lawyer in New York, stated that after having a light case of Covid in July, she was not in a rush to get the following vaccine dose. However she bought one of many new boosters this month in order that she would have extra safety when spending time with household throughout the holidays.
“I’m cautiously optimistic it is going to present me safety,” she stated of the brand new shot. “However I wouldn’t be stunned if I’m reinfected.”
Munro Wooden, a 33-year-old net developer close to St. Louis, stated he acquired his first booster in June however had grown bored with the thought of standard Covid-19 pictures. He was nonetheless undecided on whether or not to get the brand new dose.
“Annual and even biannual boosters are uncomfortable sufficient that they don’t overcome the risk-reward threshold for me,” he stated, including, “If one other, a lot worse variant comes out and begins spreading as quickly because the preliminary Omicron wave, I’ll in all probability perk up and pay extra consideration.”
Baltimore’s preliminary vaccine rollout included intensive promoting and grass-roots work, and three-quarters of residents have now acquired a minimum of one vaccine dose.
Ms. Dineen, town’s Covid-19 vaccine coordinator, stated that metropolis officers have been nonetheless prioritizing getting first and second doses to weak individuals in poorly vaccinated neighborhoods, the place canvassers proceed to go door-to-door with the pictures.
These on the metropolis clinic in the future this month have been the vaccine-dedicated. “It’s one thing that wanted to be carried out,” Melvin Battle, a metropolis worker, stated, noting that “winter’s coming alongside.”
Paula Ladson-Gillis, one other metropolis worker, stated she knew a dose of one of many new vaccines may not forestall her from getting Covid-19, however it will a minimum of assist to maintain her from getting very ailing.
“I do know loads of individuals are relaxed — I’m not one in all them,” Ms. Ladson-Gillis stated. “And that even says extra to me why I need to get it, as a result of too many individuals will not be getting it.”
Health
How a Company Makes Millions Off a Hospital Program Meant to Help the Poor
Soon after being diagnosed with metastatic breast cancer, Virginia King sat in an outpatient clinic in Santa Fe, N.M, while a nurse injected her with a powerful drug to slow damage to her spine, where the disease had spread.
Even though the drug had a list price of about $2,700, the hospital that owned the cancer center billed Mrs. King’s insurance company $22,700. Her insurer paid $10,000, but the hospital wanted more.
She got a bill for over $2,500 — “more than half my take-home salary for a month,” said Mrs. King, 65.
She had unknowingly sought care from a hospital that participates in a federal program allowing it to buy drugs at a steep discount and charge patients and insurers a higher amount, keeping the difference.
The intention behind the program was for a small number of safety-net providers to have access to affordable drugs and be able to expand their care for needy patients. But instead, the program has exploded: Now, more than half of nonprofit hospitals in the United States take part. While some providers say it has helped keep their doors open, others — especially large nonprofit health systems — have been accused of maximizing payouts and swallowing the profits.
The program’s escalation has driven up health care costs for employers, patients and taxpayers, studies show.
In 2023, for instance, New York changed the way it administers drug benefits for Medicaid patients, in part because the state had discovered the cost of the federal program had increased by more than 200 percent over three years, said Amir Bassiri, the state’s Medicaid director.
“The numbers and the growth were staggering,” he said. “We all bear the cost.”
Along the way, one little-known middleman has been cashing in, The New York Times found.
The company, Apexus, has worked behind the scenes to supercharge the program, according to interviews with current and former employees and emails, internal reports and other documents.
Twenty years ago, the federal government chose Apexus to manage what was then a small program, negotiating with drug distributors and manufacturers to secure better prices and access to medications. But Apexus is allowed to collect a fee for almost every drug sold under the program, giving the company an incentive to help hospitals and clinics capture as many prescriptions as possible:
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Its “purchasing optimization team” shows hospitals how they can make more money by buying different drugs.
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A certification program and an Apexus-run “university” trains providers in boosting earnings.
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Apexus employees give advice that broadly interprets the rules of the program so hospitals can claim additional patients and drugs.
Apexus was on track to double its revenue from 2018 to 2022, projecting $227 million that year, according to a 2022 internal memo written for the directors of Apexus’ parent corporation and reviewed by The Times. The company costs relatively little to operate and has enjoyed profit margins above 80 percent, according to that memo and three former employees.
In a statement, Apexus said it simply executed its government contract and did not contribute to the growth of the program, called the 340B Drug Pricing Program. “The drivers of growth are multifaceted,” the statement said.
But in the 2022 memo, the president of Apexus, Chris Hatwig, posed a question: “Are there other areas for program expansion within 340B that we are not thinking about?”
Government officials have told Apexus to focus solely on administering the program and not to influence drug purchases. But Apexus leaders have sometimes ignored that request, according to two complaints filed with a government watchdog and six current and former employees, speaking on the condition of anonymity because they feared professional or legal retribution.
In its statement, Apexus said it was “fully transparent” with the Department of Health and Human Services and had never breached its contractual obligations.
The Health Resources and Services Administration, an agency within H.H.S. that oversees the program, declined to answer detailed questions from The Times. But in a statement, a spokeswoman said the agency “conducts rigorous oversight of all contracts,” and “to our knowledge, Apexus has not violated” its contract. Regulators and leaders of the company meet frequently to discuss the company’s work and prevent conflicts of interest, the spokeswoman said.
The growth of 340B has drawn criticism for years from Congress, drugmakers and employers, who say it has added to ballooning health care costs. But the role of Apexus has largely gone unexamined.
“They’ve got a license to hunt,” said Marsha Simon, who as a staff member of a congressional committee helped write the bill that authorized the program.
$66 Billion in Sales
Established in 1992, the 340B program essentially requires pharmaceutical manufacturers to offer discounts on outpatient drugs to hospitals and clinics that treat a greater share of low-income and uninsured patients.
The hospitals then can charge insurers and patients the standard price and keep the profits. Although the money is supposed to encourage care for impoverished patients, there are few rules to enforce that.
Patients rarely know they are part of this system. Their prescriptions can be counted as 340B when they get outpatient treatment at a hospital or clinic that qualifies for the program, regardless of the patients’ own income or insurance status. The provider can continue to make money off the patients’ future outpatient prescriptions, even if they get them somewhere else.
Apexus has had contracts to handle the program since the early 2000s. The government does not pay Apexus — instead, drugmakers and distributors pay the company a small percentage of sales.
Based in Irving, Texas, it is a subsidiary of Vizient, a private business owned by hospitals that negotiates a range of health care discounts. Apexus was established as a small nonprofit in 2007 but became a for-profit company in 2014.
Around the same time, 340B began to explode for a number of reasons. More hospitals qualified for the program after the Affordable Care Act expanded the number of people on Medicaid. Other health care systems qualified after acquiring hospitals and clinics in poor areas. Some, already eligible for 340B, bought up practices that used high-margin drugs, like oncology clinics. And a government rule change meant hospitals could make money from prescriptions filled at a greater number of pharmacies.
A decade ago, sales of 340B drugs were $12 billion. In 2023, they reached a high of $66 billion.
Fighting the program’s growth has become a top priority for drugmakers, as well as some employers and insurers.
In North Carolina, prescription drug spending for state employees jumped almost 50 percent from 2018 to 2022. A report in May from the state treasurer’s office found that 340B was partly to blame: Hospitals that participated in the program billed the state health plan far more than hospitals that did not — almost 85 percent more for certain cancer drugs. In one example, hospitals bought a drug commonly used to treat melanoma for an average of $8,000 but billed the state $21,512.
In some cases, costs are passed along to patients.
Mrs. King, the cancer patient in New Mexico, refused to pay her $2,500 bill, and the hospital, Christus St. Vincent, sent it to collections in July.
After The Times asked about the bill last month, a spokeswoman for Christus St. Vincent said the charge was “a misunderstanding and has been resolved,” adding that the drug program helped the hospital provide charity care and reinvest in cancer treatment and primary care.
Mrs. King switched to a free-standing oncology clinic that does not qualify for the federal drug program. That clinic billed her insurance $8,000 for the injection, about a third of what Christus St. Vincent had charged. Her responsibility was nothing.
An Ever-Growing Portfolio
Ms. Simon, who helped draft the legislation creating 340B, said the government chose an outside contractor like Apexus in order to negotiate with distributors and drugmakers on behalf of small hospitals and clinics without a lot of buying power.
But regulators and Apexus have expanded that role, allowing the company to build a highly profitable business off the program and the loosely written statute that authorized it. The company has been “aggressive” in helping health care facilities maximize their revenue from the program, said Shawn Gremminger, chief executive of the National Alliance of Healthcare Purchaser Coalitions, which represents employers who buy health insurance for more than 45 million people in the United States.
“This is a government contractor, and the goal of the government should not be, ‘How do we make more money for 340B providers?’” said Mr. Gremminger, whose organization has pushed for the program to be overhauled.
Over the past two decades, Apexus has adapted its business model to harness 340B’s tremendous growth. A 2022 PowerPoint presentation obtained by The Times showed that Apexus employees received bonuses if the company increased its revenue each year.
With exclusive access to sales data, Apexus’ “purchasing optimization team” will analyze a hospital system’s drug-buying habits and compare them with those of their competitors, according to four current and former employees. In some cases, Apexus will suggest that a hospital buy more 340B drugs or tweak its inventory in ways that can churn more cash.
Apexus declined to answer detailed questions about its optimization team, but said in a statement that the company “only provides technical assistance” in keeping with regulations.
Apexus also holds “340B University” events to help providers and others in the health care industry understand the program, and it fields questions through a national call center. But the rules governing the program are ambiguous, and Apexus offers broad interpretations, according to four current and former employees.
For instance, one of the thorniest issues is which patients can be claimed by hospitals for discounted drugs. The further a hospital casts its net, the more patients and drugs it can include under the program, and the more money it can make. Apexus has advised hospitals that they can mine records as far back as 36 months for eligible patients they may have missed, two of those employees said.
Similarly, Apexus employees have showed hospitals how to maximize the number of pharmacies they work with, boosting the number of prescriptions that can qualify for discounts, those employees said.
In its statement, Apexus said those examples were inaccurate but would not say how. It added that the company encouraged “conservative and responsible stewardship” of the 340B program, and that all information it provided was approved by regulators.
A spokeswoman for H.R.S.A. said it reviewed materials prepared by Apexus but declined to comment on that specific advice.
The company has developed other ventures that have brought in revenue:
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About eight years ago, Apexus began selling a $750 course for people to become “certified experts” in 340B.
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It started a business to give hospitals better access to specialty drugs — for conditions like cancer, H.I.V. and autoimmune diseases — which are major drivers of 340B’s growth. That company, Acentrus, helped hospitals and clinics provide data to manufacturers in exchange for deeper discounts and access to those drugs. It was sold last year.
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The company charges 3 percent in fees for a line of generic drugs that are managed and provided by drug distributors, according to former employees. Apexus simply provides access to the health systems.
For the last decade, Apexus has earned millions of dollars on drug purchases made outside the 340B program: Because not all outpatient drugs qualify for 340B discounts, hospitals must stock their pharmacies with medication purchased through different channels. Apexus acts as a middleman, making fees off those transactions.
That has frustrated drugmakers and competitors. In 2021, the drug manufacturer Baxter wanted to sell non-340B drugs to hospitals without going through Apexus, according to emails obtained under public-records laws. But government regulators would not allow it, a spokeswoman for Baxter said.
In early November, Premier, the main competitor to Apexus’s parent company, Vizient, sued the federal government over these sales. The setup, the suit argued, forces hospitals to pay higher prices for those non-340B drugs and drives revenue to drug manufacturers and Apexus.
In its statement, Apexus said its federal contract did not preclude it from developing other businesses, as long as they were not in conflict with the terms of the agreement.
Regulators were aware of these ventures, the company said, noting that its specialty drug business, Acentrus, was in “no way associated with” the 340B program. The 2022 company memo, however, said Acentrus “resulted in an additional $20 million” in revenue within the 340B program.
H.R.S.A. declined to comment on the scope of its authority over Apexus and whether it knew about all the company’s revenue-generating arms.
Criticized, but Pushing Ahead
About six years ago, Krista Pedley, then the director of the H.H.S. office in charge of 340B, reprimanded Apexus leaders in a Skype meeting, saying it was acting more like a sales-driven business than a program administrator. She reminded them that Apexus’ role was not to help 340B grow, according to five former or current employees familiar with the meeting.
For about a month afterward, regulators reviewed any communication Apexus had with health care facilities to make sure the company didn’t overstep, the employees said.
But that did not seem to dampen the company’s pursuits. (In an email, Ms. Pedley said she did not recall that meeting, and noted that her former office met regularly with Apexus.)
In 2021, an unnamed Apexus employee filed a complaint with H.H.S.’s Office of Inspector General, an internal watchdog, saying the company was “always trying to grow the program.” The company, the employee wrote, had hired “sales-type” staff to influence hospitals’ drug-purchasing decisions.
The complaint said that regulators did not understand Apexus’ business, and that employees had been told by company leaders to describe its work as “education.”
Another anonymous complaint, filed in 2022, echoed the allegation that Apexus had hired staff to help shape hospitals’ purchasing decisions, and said it was using “data in ways to drive revenue for itself, without asking (or asking and disregarding) the government’s opinion.”
Apexus declined to answer specific questions about the meeting with Ms. Pedley, but said The Times’s account was a “mischaracterization of our day-to-day, collaborative discussions” with the agency.
Apexus rejected the allegations in the anonymous complaints and said it had been unaware of them until The Times provided it with copies. The spokeswoman for H.R.S.A. said that it, too, had been unaware of the complaints.
In interviews, four current and former employees said that for years, Mr. Hatwig, Apexus’ president, acknowledged that regulators did not want the company to develop sales-focused arms of the business but encouraged his staff to do so anyway, saying that the government would not know.
Apexus denied that, saying that “everyone at Apexus understands the expectation that they conduct themselves and perform their work in an ethical and compliant manner.”
Julie Tate and Carson Kessler contributed research.
Health
3 signs your aging loved one may be ready for assisted living
As Mom and Dad grow older, the big question might be looming in the background: When is the right time to provide living support?
Dr. Macie P. Smith, a licensed social worker and gerontologist based in South Carolina, shared with Fox News Digital that there may be a few telltale signs that it’s time to make a move, whether it’s hiring an at-home aide or seeking out a living facility.
1. They’re at risk of harming themselves
Most importantly, Smith noted that if a senior is at risk of hurting themselves or getting into dangerous situations, it’s most likely time to call in help.
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Smith, who specializes in seniors living with Alzheimer’s disease and cognitive impairment, recommended starting with enlisting at-home aid before pulling a loved one out of their home.
“The last thing anybody wants to lose is their independence,” she said. “The last thing anybody wants is to live in a space with 50 other strangers.”
At-home support can help lower the risk of self-inflicted danger from incidents like leaving the stove on, or mobility issues that could lead to falls.
2. The person is having memory issues
As people age, their capacity to remember things begins to naturally slow down.
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Sometimes, this presents in the form of diseases like Alzheimer’s or dementia. The severity of memory loss in seniors dictates whether living support is necessary, according to experts.
Smith mentioned how forgetting familiar tasks and activities, like eating, can pose a danger to someone’s health.
“If their nutrition is poor, it may be because they are dealing with some pain that they are not expressing to anyone else,” she said. “They may be dealing with some depression and, frankly, they just don’t have the motivation.”
“Respect them enough to have the conversation, because they still have the ability to make decisions about their life.”
The expert advised watching out for signs of spoiled food in the refrigerator.
The person may also forget how to do simple tasks like making a bed, doing laundry, washing the dishes or following cooking instructions.
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“If they’re having trouble cognitively, they’re having trouble making decisions, and that’s going to ultimately impact … how they live independently,” Smith said.
3. They repeat themselves
Repetition of thoughts is also common in individuals living with Alzheimer’s disease and dementia.
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Smith noted that if your loved one is repeating themselves more frequently, it’s a good idea to bring in some support not only for help with day-to-day living, but also for attention and friendship.
“In some cases, it’s because they’re lonely,” she said. “It’s because they’re living by themselves, and they don’t have any type of engagement or motivation.”
‘Very difficult’ decision
Smith emphasized how difficult it can be to make the decision to place a loved one into care, especially if it means removing them from their home.
The senior should “always be a part of the conversation” when it comes to deciding the next steps, she urged.
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“The last thing you want to do is come in and uproot them from the place where they feel the most comfortable and safe, just because you feel they shouldn’t be there,” Smith said.
“Always include them in the conversation, even if they’re in the early stages of dementia,” she encouraged. “They still have a lucidity … to be able to participate in the decision-making process.”
Whether the decision is to bring in care or move somewhere new, Smith said the senior should never be made to feel unsafe or unfamiliar, as this can increase dangerous behaviors, cause agitation and lead to health decline.
The conversation also should not start with the assumption that the senior will not accommodate your request or suggestion.
“Don’t assume they’re not going to remember,” Smith said. “Don’t assume they’re going to be irritable and combative.”
“Respect them enough to have the conversation, because they still have the ability to make decisions about their life.”
Health
Cancer Remission Like Catherine’s Does Not Always Mean the Illness Is Cured
Princess Catherine, wife of Prince William, reported on Tuesday that her cancer was in remission. But what does it mean to be in remission from cancer?
Doctors discovered her cancer unexpectedly last March when she had abdominal surgery. She has not revealed the type of cancer she has, nor how advanced it was when it was discovered.
But she did say she had chemotherapy, which she said had been completed in September. She told the British news agency PA Media that she had a port, a small device that is implanted under the skin and attached to a catheter that goes into a large vein. It allows medicines like chemotherapy drugs to be delivered directly to veins in the chest, avoiding needle sticks.
Catherine told PA Media that chemotherapy was “really tough.”
“It is a relief to now be in remission and I remain focused on recovery,” she wrote on Instagram.
Her announcement “certainly is good news and is reassuring,” said Dr. Kimmie Ng, associate chief of the division of gastrointestinal oncology at the Dana-Farber Cancer Institute in Boston.
But cancer experts like Dr. Ng say that the meaning of remission in a patient can vary.
In general, when doctors and patients talk about remission, they mean there is no evidence of cancer in blood tests or scans.
The problem is that a complete remission does not mean the cancer is gone. Even when a cancer is “cured” — defined as no evidence of cancer for five years — it may not be vanquished.
That makes life emotionally difficult for patients, who have to have frequent visits with oncologists for physical exams, blood tests and imaging.
“It’s really scary,” Dr. Ng said. “The amount of uncertainty is very very hard,” she added.
But that ongoing surveillance is necessary, despite the toll it takes on patients.
“Different cancers have different propensities of returning or not returning,” said Dr. Elena Ratner, a gynecologic oncologist at the Yale Cancer Center.
As many as 75 to 80 percent of ovarian cancers, she noted, can come back in an average of 14 to 16 months after a remission, depending on the stage the cancer had reached when it was found and on the cancer’s biology.
“Once the cancer returns, it becomes a chronic disease,” Dr. Ratner said. She tells her patients: “You will live with this cancer. You will be on and off chemotherapy for the rest of your life.”
Dr. Ratner’s gynecological cancer patients have to come back every three months for CT scans to keep an eye out for evidence that the cancer has returned.
“The women live CT scan to CT scan,” she said. “They say that for two and a half months, they have a wonderful life, but then, in time for the next CT scan, the fear returns.”
“It costs them — it costs them a lot,” she said.
“It’s awful, yet I am amazed every day by their strength,” she said of her patients.
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