Max's Mommy kindly emailed this paper to me in full PDF version(1). And I kind of liked it. Since there's been a lot of discussion lately, I wanted to tell you how I came to this conclusion, and what I think this study means for a patient like you. Take it with a grain of salt. My ability to interpret these things is limited by my rather stunted ability to care about statistics. Either the rest is good, or someone will call me out in the comments(2). In any case, I hope it'll be worth a read.

So let me start with the question I always ask when I pick up a scientific paper: why should I care?

The truth is, no-one reads these things for fun. To find out whether you should care about this study, you need to know what the researchers are trying to ask. A well-designed study doesn't ask much - the more you ask at once, the more confused your answers become. IVF with PGS (Mastenbroek et al) asks what happens to pregnancy and live birth rates when you do PGD using laser-assisted biopsy of three-day-old embryos for no apparent reason on IVF patients between the ages of 35 and 41. If you are looking for an answer to any other question, you are reading the wrong publication.

Examples of Questions Not Addressed By This Article:

  • What happens when you do PGD for a very good reason on a young patient (one with a balanced translocation, for example)?
  • What is the rate of live, healthy births from IVF with PGD, as opposed to IVF without(3)?
  • What happens when you do PGD using a different technique(4)?
  • What happens when you do PGD on a woman with a history of recurrent pregnancy loss, or PCOS, or a pistaccio icecream addiction?
  • Can PGD help predict this season's celebrity shoe fashions?

The list is endless. You can probably think of a few of your own.

Having established what the study is asking, you need to decide if the question is important, and if it's relevant to you. In the case of this study, a lot of people will be nodding "yes" to both. There are an awful lot of patients starting IVF at age 35 or above, who have been through the standard infertility workup, and have no special reason for doing PGD. And the PGD technique described is widely enough used(4).

You could study a different PGD technique, but you'd be asking a different question, and patients and clinicians in the field have to know how to apply the tools they've got. Likewise, if you're a member of a special patient group - keep walking, sister. The question you're interested in is just not here.

One of the big reasons to care about this paper is their length of followup(5). Followup can be difficult, and/or researchers get lazy, so a lot of IVF studies get sketchy after six or seven weeks' gestation. Thing is, as a patient, I actually don't give a fuck about pregnancy rates - even clinical pregnancy rates. I care about having a live baby, and getting to take him home.

There's a subtle distinction to be made here between bad science and irrelevant science. Highly rigorous studies can ask questions very few people are interested in, and a paper on the very thing you want to know can leave you without answers due to ill-thought-out methodology. Relevance is also relative - don't get angry with the researchers because you want to know about the effect of pistaccio icecream addiction on embryo implantation rates, and they've decided to study fruits of the forest. Fruits of the forest eaters are people too(6).

To sum up: when Aunt Jane (or your friendly newspaper health science reporter) brings you IVF with PGS (Mastenbroek et al), don't forget to ask that all-important question: why should I care? What are the researchers asking, and is it relevant to me? If there's no reason to take an interest, you've got more important things to do with your time(7).

(Part Two, in which we actually read the paper, coming soon.)

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(1)If you're interested - either in PGD or following my train of thought - email me. (Back)

(2)That's an invitation. I know there are scientists out there - don't pull your punches. I can take it. This blog category is not the place for unconditional support. (Back)

(3)Is this a more important question? Perhaps. The researchers tell us they are in the process of collecting this data. I know I'm not the only one who would be interested in these results. (Back)

(4)A lot of clinics prefer to biopsy older/bigger embryos. Personally, I'd be more interested in seeing the same study repeated using a different technique, but the one described here seems widely-used enough to make this paper important to clinical practice. See also the paragraph about bad science vs relevant science. (Back)

(5)Technically, they based their analysis primarily on the ongoing pregnancy rate rather than the live birth rate, but apparently the latter mirrored the former. Truth be told, I would care more if they'd focussed on the latter. At least they reported live birth rates, which is more than I can say for many studies. (Back)

(6)Lesser people, in many ways, but still. (Back)

(7)This may seem like a very basic step. I think that's why so many people forget to perform it. Newspaper reporters, in particular, have an incentive to try and make the article seem as widely relevant as possible - at least until you read beyond the headline and first few paragraphs. And Aunt Jane, as you know, is just an idiot.

To bring it back to this study, I've decided through these questions that I don't personally care too much. The fact I'm not in the right agegroup doesn't worry me a lot - genetic abnormalities and implantation failures occur in my agegroup too - although I should keep this factor in mind. I'm in a special patient group, though, having suffered three chemical pregnancies and a miscarriage at nine weeks, and the article says nothing about whether PGD helps this group specifically (although that's been investigated elsewhere).

A proper analysis of the live, healthy, take-home baby rates from each group would be more important to me. Hopefully, this is coming. Interestingly, the rates of miscarriage due to foetal abnormalities appear to be about the same in each group from the data reported, although they weren't looking into that very rigorously at all. Arguably, too many questions. The other reason for my ambivalence is I think my clinic uses a different PGD technique.

This is me, though - you might have decided the article is exactly what you are looking for, and it might still answer your question well. We'll have to read it to find out. (Back)



I surged. I tried to book a flight. Not only have the airbus people not come through on time with some airline thing they were supposed to do, but the entire population of the northern hemisphere is on holidays for summer, and contrary to millions of years' worth of carefully-honed seasonal migratory patterns, they're all flying south for it. There are a fucking lot of people in the northern hemisphere.

After much googling, several phone calls to different travel agents, and the invocation of my frequent flyer status*, I broke down and wept on the phone to Qantas who - bless that woman's concerned customer service and soothing voice** and damn me for not getting her name - managed to dig me up an airfare which will have me in town at the right time.

It leaves tomorrow night***.

"It's been a really horrible couple of years," I found myself sobbing at one point, "and every time I turn around someone's thrown one more obstacle in my way. I just thought booking flights was the least of my worries."

Half an hour and a few deep breaths later, I guess it still is****.

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*Bronze...

**She suspects I won't have quite the same problem next time. Sure, the airbus situation isn't going to be fixed in a hurry, but the summer holidays will end (although she did warn me about the Rugby World Cup in September/October - at least I'll be prepared). And I have great faith that the market will work to fill any medium or long-term gaps. That is, of course, if there has to be a next time (smack!).

***Fuck! That means I have to go NOW to return those library books.

****Still have to get Mr Bea there, of course - that is, if we want to use fresh, new, vitamin-enriched sperm. Thankyou, September 06 Bea for having the foresight to freeze twelve straws of semen, even though that meant having to collect the last lot en route to the airport in the half-hour gap between the clinic opening and Mr Bea departing indefinitely for foreign shores. They said you were crazy. You were, kid. Just crazy enough.

____Update____

Mr Bea now safely booked. Must remember not to collapse in tears quite so easily in future. I think I may be feeling a little on edge.


The OPK gave me teaser lines, but I did not actually surge. My test results did not come through. I was not impelled to have another flip-out over the possible outcome!

The world at large did not concede that, since I've been waiting quite a while, it's my turn to be pregnant next and not some woman who only just had a son eighteen months ago.

But I did not let this spoil my lunch.

My sister did not fail her very important exam. Neither did she get the job she wanted.

I did not hear back about a course I've applied for.

I did not expect the Fifty Good Deeds fund to be up to $73.58 already.

And the Aerosmith version of "Give Peace A Chance" from the Amnesty International Album did not sound the way I thought it would. But it was still cool.




First, I have to be honest and say this entry is no-where near as exciting as the one I just posted over at the International Infertility Film Festival site. So please, if you have to choose - go there. I'm secretly hoping you'll come back after you've finished, but I understand if that can't be the case as I know your time is valuable, especially with film festival deadlines looming. I'll make things short, if that helps.

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It's been two weeks since my blood tests and biopsy, and I think I've held up pretty well so far. The results are now due sometime within the next week, and I just wanted to say, "Holy fuck, what if they find something really fucking terribly wrong and it all goes to shit and this is the end or maybe which in some ways might be worse they say it's bad news but not quite the end because if you just keep trying statistically speaking after thirty-seven cycles of IVF you'll probably but of course no guarantees manage to make it to term and oh good fucking grief what will we do if it's bad news?"

Thankyou. I'm planning to flip out briefly again tomorrow at six. Join me!


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