Dr. Cheryl Bettigole, a New Jersey-based family practitioner and a National Physician’s Alliance board member, has written an interesting editorial in the New England Journal of Medicine in which she states she is no longer surprised when laboratories charge her patients $1000 or more for a Pap smear.
According to Dr. Bettigole, the reason for the exorbitant charges are not the actual Pap smear itself (although she does mention the fact liquid-based preps are more expensive than conventional smears), but the tests that get added on, many of which she feels are unnecessary.
These additional tests include tests for HPV and STDs and “sophisticated laboratory tests for a variety of yeasts.” She does allow for the fact HPV testing is recommended for women between the ages of 30 and 64 every five years and routine STD testing is recommended for women between the ages of 15 and 25 who have signs/symptoms of infection.
She admits these often unnecessary tests get ordered by “a physician or nurse practitioner or the medical assistant processing the specimen”, but goes on to say laboratories must share in the blame for this problem. Her rationale for this is that labs have made it too easy for unnecessary tests to be ordered.
What used to require physicians to submit multiple collection vials and check multiple boxes on a requisition form now requires only one vial to be submitted and one box for a number of bundled tests to be checked. In addition, labs provide nothing “along the way” that alerts the physician or the patient to the tests’ cost or their clinical utility.
She also mentions the “savvy” marketing tactics employed by laboratory salespeople that mirror those in the pharmaceutical industry.
In the end, Dr. Bettigole worries these excessive lab costs may lead some women to forego cervical cancer screening simply because they cannot afford it.
Commentary
I completely agree with Dr. Bettigole that it would be an absolute travesty for any woman to not be screened for cervical cancer because of the expense.
And while I certainly applaud Dr. Bettigole for writing this editorial (and the NEJM for publishing it), I do have some additional thoughts.
I agree the responsibility lies with the clinician
I can do nothing but agree with Dr. Bettigole when she says, “…we physicians and our staff are responsible for ordering these unnecessary tests and hence responsible for the huge bills our patients are receiving.”
An exception to this exists in the world of surgical pathology, where additional immunohistochemistry, molecular tests, etc. may be necessary for final diagnosis, and the pathologist usually performs those sans an order from the clinician.
In my opinion, however, it matters not if a lab sends the slickest, best-dressed, and most knowledgeable and charming salesperson to the physician’s office, or if the lab uses an order form with only one box for all the tests it performs. The only tests that should be ordered are the ones that are necessary for that particular patient.
Laboratory medicine is in many ways a service industry, and clinicians (should) understand that. If the lab to which they send specimens regularly provides bad service by performing unnecessary or unwanted tests, or is somehow “tricking” the physician into ordering too many tests, then the physician should change labs.
That being said, there are many, many physicians out there who work for a hospital, or clinic, or some other entity that has a contract with a single lab, and they do not have a choice as to which lab they can use.
But if they do have a choice, then they are indeed responsible if a lab repeatedly provides bad patient care and they do nothing about it.
Now some of you may be wondering whether I believe it is the referring physician’s fault if a lab participates in outright fraudulent and illegal behavior (and unfortunately there are plenty of labs that do).
My answer to that is not the first time it happens, or the second, or even the third. But if it continues to happen with such frequency that the clinician is “no longer surprised” (to use Dr. Bettigole’s words), then yes, I believe it is.
Why is a medical assistant ordering tests?
As I highlighted above, Dr. Bettigole states some of the blame for this rests on the “medical assistant processing the specimen.” She further goes on to say (emphasis added):
It seems harmless, even possibly beneficial, to run these additional tests, and for our staff, it eliminates the risk of missing a test the doctor might have wanted to have run.
I guess I am curious as to why a medical assistant in her office is empowered to order tests she may not have even wanted.
Defensive medicine likely plays a role
Dr. Bettigole does not mention defensive medicine in her editorial, but I have to believe it is part of the problem.
It simply stands to reason that a physician’s chances of being sued decline dramatically if they don’t miss something significant. And the way to not miss something significant is to test for it.
I see this every day around the hospital in specialties other than pathology.
For some physicians, excessive lab charges are a feature, not a bug
And now for the cynical part.
As I have discussed numerous times in the past, 31 states allow physicians to client bill for pathology services. For those who do not know, this means referring physicians in those states can order an independent pathology lab to perform tests on samples from their patients and pay that lab (usually) far less than the usual and customary fee for those tests. The physician can then turn around and bill the patient up to and sometimes more than the full usual and customary fee, and pocket the difference as pure profit.
So for those physicians, a $1000 bill for gynecologic tests sounds like a really good idea, because probably at least $500 of that is going straight into their pockets, all for literally doing nothing.
I want to make clear I am in no way accusing Dr. Bettigole of doing this; I am merely mentioning it as a likely motivation for many clinicians out there.
In fact, New Jersey happens to be one of the 19 states that statutorily prohibits client billing for pathology services. So physicians there could not do this even if they wanted to. At least not legally.
Note: Many thanks to Ms. Naomi Kaufman Price, who alerted me to this editorial.








Although price competitive FDA-approved cytology and HPV cervical screening tests are available, non-FDA-approved Laboratory Developed Tests (LDT) may promote tesing for HPV strains not validated in clinical studies supporting FDA-approved tests, including testing for low risk HPV types. For a good example of this type of laboratory service, examine the following link:
http://mdnews.com/news/2013_06/05838-june13-a-more-complete-hpv-test.aspx
LDT may also promote testing for a wide variety of other infectious agents, some of which are of doubtful value at high cost.
It is legal to client bill a lot of the out of vial testing from liquid based paps. You can’t client bill the pap smear but you can client bill all those unnecessary tests is my understanding.
I wish you were correct that the physician cannot client bill for the Pap smear, but they can…at least in my state.
Sigh.
Even in states that have outlawed client billing for the actual pap test, I believe they CAN client bill all that other testing from the vial in those states. At least in my state they can. So they can client bill those 25+ tests that they run from the vial.
I wish the physician would have named the lab she was using. I bet money it was bio-reference labs. They are in new jersey and they are notorious for this.
A colleague of mine spoke to a gynecologist who said that he loved the fact that his pathologist called so many pap smears atypical (ASCUS) because then he got to do a lot of colposcopy which he billed for. The American medical system is broken.
I agree with Dr Cosell , the FDA has been tarred and feathered repeatedly in media for allowing profitable but dangerous products to be marketed . US News and World Report 2004 article : http://health.usnews.com/usnews/health/articles/041213/13fda_2.htm
title – Is The FDA A Sick Agency In Need Of A Cure ?
Cytotechs have complained for years about perceived fraud in pap smears . In particular , liquid based paps , while a beneficial product , appear to be falsely advertised ; computer assisted microscopes , the performance of which , should be an issue of consternation . It seems as though profiteering is givin precedence to safety . Please see this article I wrote :
http://meshmedicaldevicenewsdesk.com/featured-articles/pap-smears-a-technican-speaks-out-about-problems-and-profits/ .
this is why the cuts in routine pathology are happening because of the overutilization in molecular pathology. ordering thousands of $$$ of molecular on STDs that a routine $12.00 culture could accomplish. what ever happened to looking for signs and symptoms and getting a history before you order tests. it is the behemoth labs fault for putting these designer tests on their requisitions. what a dopey clinician to have her medical assistants ordering her tests for her. and she admitted this in the NEJM. you should not give your doctor licensed duties to an MA to do. are they doing her Pap smears for her too? if thats the case take away her license to practice. there is no reason she shouldn’t be cost conscious when ordering lab tests. she is the one ordering the tests and no one is twisting her arm. why doesn’t the insurance company and medicare require preauthorization for these expensive tests. no wonder the behemoth labs are making so much off this molecular overutilization. so now the pathologists have to suffer who are using their two eyeballs and their brain and who went through tens of thousands of hours of training as they cut our codes to smithereens.