C (4:19)
So that's the question that we're gonna cover, is that the case, is MVP better or is AFI or does it just doesn't matter. Let's figure it out when we come back. This is Dr. Chapas obgyn no spin podcast. So what's neat about being in the OB community is it really is a small world. We talked about SMFM console series number 46, which we will touch on in this episode, which has to do with the management of polyhydramnios. But one of the authors was. Is Jodi Dash. So Jody was an MFM fellow when I was still a resident in the lands. That's parkland and phenomenal. She's just great. She's just a great person. But I remember when she first started first year as a fellow and then it went on to do look amazing, great things. So great job, Jody. But that was console series number 46. That was in 2018. But our main focus is this new BJOG publication from January 2026. Now, let me just. We're going to cover lots of things, but it's going to be fast. But what I really want to cover is the main finding of this January 2026 piece from Vince et al. Which we'll, we'll cover this. But more importantly, what it is and what it is not. What it is is a great attempt to an question that we just don't have the data for. And so hopefully this was going to figure it out because as it says in the intro, which methodology AFI versus MVP has a stronger association with adverse perinatal outcomes is uncertain. In other words, while we know that MVP is better for oligo, we've already said that because that's a better predictor of adverse things happening. We don't really know if it's AFI or MVP for poly. So we're going to figure it out. So this was a systematic review of the literature. Phenomenal. So we're like, yes, it's going to fill a gap. So let me just tell you very briefly what it is. What this paper is, is a great attempt to answer that question that we just stated. What it isn't is a good answer. Because they're like, man, we had these high hopes and we had 133 studies that we screened. We're like, yeah. And then they found, quote, well, there's no real RCTs comparing the outcomes using MVP, AFI or both. And while there are five non RCT studies that were assessed for eligibility, they had 5,319 patients. That's good. However, only one retrospective study reported neonatal outcomes, end quote. So like, well, we had high hopes for this, but we have, there just really isn't high quality RCTs to tell us which one's better. So again, what it is is a great attempt to answer a question. What it isn't is a real solid answer. But I'm gonna tell you what they found. Should we do MVP or AFI for poly? Because it's kind of disappointing. All right, so in their final statement here, before I tell you which one is better, AFI or MVP, quote, there's an urgent need for RCTs comparing different ultrasound methodologies for the diagnosis of poly in terms of adverse perinatal outcomes so that we can have a solid evidence based management of polygon poly in everyday clinical practice, end quote. So they're like, hey, look, I'm gonna tell you what I found. I'm gonna tell you which one is better or if it really doesn't matter at all. But we really need much better, higher quality data to guide us here. Okay? So what it is is a valiant attempt to answer a question while we know that MVP is better. For oligo. Is that the same for poly? What it isn't is a real, firm, solid, high quality data answer, because we just don't have that. So it's like. In other words, I'm going to give you an answer, but it's kind of crappy data because we need lots better randomized clinical trials to answer this. Okay, anyway, so let me just go back for a minute. Before we get into the Pauli thing, let me just remind all of us about the oligo issue in ACOG's practice bulletin number 229. That's one on endopartum fetal surveillance, and it says, determination of the amniotic fluid volume by a deepest vertical pocket greater than 2 cm is considered evidence of adequate amniotic fluid, although oligohydramniose. I'm reading directly here from the practice bulletin. Although oligohydramnios has been commonly defined as a single deepest vertical pocket fluid of two or less. Again, not contained in umbilical cord of fetal extremities or an AFI of 5cm or less, available data from randomized controlled trials supports the use of the deepest vertical pocket for the diagnosis of oligo. End quote. All right, so again, a single deepest vertical pocket of 2 centimeters or less is oligo. So it's inclusive of the two. All right, so every. Everybody good. Remember, normal fluid is greater than 2. So if it's 2.1, technically you dodged it by 0.1. Still normal, right? Now, if you really have to do a 2.1, I mean, please make sure you're not missing oligo. All right, but the point is it is greater than 2. So oligo is defined as a fluid Maxwell vertical pocket of 2cm. So 2.0 or less, it has to be greater than 2. 2 is still considered low. So we get that RCT support that. So for all ago, we've got solid evidence. Rather than AFI of 5, please use an MVP of 2. That is what ACOG and SMFM say for surveillance. Okay, now just so we remind ourselves of the definitions of polyhydramnios and their different categories. Mild, moderate or severe. Let's go back to console series number 46, where Jody Dash was part of that authorship. Okay, so remember that a deepest vertical pocket of 8cm or more is considered poly. Or if you're going to use an AFI, it's 24cm or more. But these are further subdivided. Mild, moderate or severe. So let's do. First, the Deepest vertical pocket, 8 to 11 is considered mild, 12 to 15 is considered moderate. More than 16 is considered severe. All right, so deepest vertical pocket, 8 to 11, 12 to 15, and then greater than 16 for AFI, 24 to 30 is mild, 30 to 35 is moderate, and then more than 35 is severe. Okay, now I am going to touch on that consult series, the management of poly. I'm just going to read one right after the other. Boom, boom, boom, boom. We're just going to go rapid fire. There's six recommendations on how to manage poly, which we've covered in the past, but it's going to tie in nicely to this new publication from bjog. Okay. Okay. So we get it for oligo. And if you're going to do endopartic fetal surveillance, I'm a big fan of modified biophysical profile. Just getting the deepest vertical pocket and NST as the acute and chronic marker. Acute is the nst, chronic is the masculine fluid pocket, maximum vertical pocket, because that is the same risk of stillbirth as a full. You need to know how to do a full biophysical in case the modified is not conclusive. In other words, if one of the values is off, if it's two out of four, you need to do the full to get more information. Unless you're missing that minus two is for fluid. Then you got to figure out why there's low fluid. Is she ruptured? Is it really amniotic fluid as a result of placental insufficiency? And remember, the ACOG says persistent oligo over 36 weeks is a standalone indication for. For induction because of the potential. The potential of umbilical cord compression. So I'm a big fan of modifieds, getting the NST and the maximum vertical pocket. And if it's four out of four, you're done. So the point is, if you're going to do surveillance, ACOG and SMFM prefer the maximum vertical pocket. For the diagnosis of normal fluid, which is greater than 2, 2 or less is considered oligo. And remember, we covered this in the past. Also, what gets you the two on a biophysical profile, either the full or the modified, is if the fluid is greater than 2. So even if it's poly, you still get a 2. But it should be a biophysical profile score of this with an asterisk. It says, hey, even though we gave two points for fluid which is above two, you got to know that the fluid is still not normal because it's poly. So it's not. If the fluid is within the normal range, the only thing that counts is that it's greater than 2. For a maximum or vertical pocket to be considered normal or greater than 5 on an AFI to say normal fluid, you get a checkbox. All right, so polyhydramniose. There's no specific caveat that would take away the points on the either a full or modified biophysical profile that still gets a 2 determination because it's greater than 2 centimeters or 5 centimeters on the A5. Okay, so very quickly, let me just. Let me just kill this fast, because it's going to be relatively fast, because this research letter, by the way, I love the way BJOG does research letters, y'. All. It's like three pages long. I mean, it's like, hey, here's what we found. Boom, boom, boom. Here's the results, and here's what you need to know. Very nice. Okay, now, some studies are amenable to research letters, others aren't. But this one definitely was because there was very little data to look at. The short of it was in this publication, whether you use an MVP or an afi, knowing, of course, that the data was very limited, it didn't matter. Both of them were linked to adverse perinatal outcomes. Now, as it says, quote, this is interesting, and in contrast with the literature regarding oligo, where oligo seems to have a much better prediction of morbidity mortality based on maximal vertical pocket. But in this case, the same is not true for poly. So whether you call poly mild, moderate, or severe by deepest vertical pocket or by afi, it doesn't matter. Both of them seem to be predictive against adverse perinatal issues. So remember, guys, that we worry about core compression with oligo. We get that. But poly also is linked with some adverse perinatal outcomes. So poly isn't good either. That's got its own set of issues. Okay, so oligo is not good for perinatal outcomes, and poly is not good for perinatal outcomes. Both of these are associated with adverse issues. And on the poly side, unlike for oligo, it really doesn't matter if you use the AFI or if you use the maximum vertical pocket. The morbidities were reflected in either determination method.