What Every Midwife Should Know About ACOG and VBAC: Critique
of ACOG Practice Bulletin No. 5, July 1999, “Vaginal Birth After Previous Cesarean
Section”
by Marsden Wagner, MD, MSPH
[Editor's Note: To order copies of this practice bulletin (ISSN 1099-3630), contact:
The American College of Obstetricians and Gynecologists
409 12th Street, SW
P.O. Box 96920
Washington, DC 20090-6920]
Problems With Final Recommendations
Problems With the First Recommendation in Level C: “Because
uterine rupture may be catastrophic, VBAC [vaginal birth after cesarean] should be attempted in institutions equipped
to respond to emergencies with physicians immediately available to provide emergency
care.”
The first problem with this recommendation is that of the eight final recommendations,
it is this one which has the largest impact on maternity care in the United States.
Yet by the American College of Obstetricians and Gynecologists' (ACOG) own admission, there is no evidence to back up this recommendation.
This is of course the reason this recommendation has been placed in Level C, thus making it
ACOG's confession that since there are no data, ACOG will simply have to go
on the basis of “expert opinion.” This is a sad regression to the days
of “Trust me, I'm a doctor”—in spite of the new direction of medical care
to evidence-based practice.
This is not the first time ACOG has been willing to make recommendations without
any evidence base. For example, ACOG's written statement that homebirth is not safe
also doesn't try to reference any data and flies in the face of overwhelming scientific
evidence that planned homebirth and planned birth in an out-of-hospital freestanding
birth center are perfectly safe options for the great majority of pregnant women.
So this recommendation—“VBAC should be attempted in institutions
equipped to respond to emergencies with physicians immediately available”—
has no data to support it, no studies showing improvements in maternal mortality or
perinatal mortality related to the characteristics of institutions or availability
of physicians. What ACOG doesn't say is that one study included in their reference
list in their document compared VBAC and repeat cesarean section in three types of
hospitals—community, regional and tertiary care—and while community and regional
hospitals had more repeat cesarean sections and more failed VBAC, no difference in
mortality rates for these two procedures by type of institution is reported1. This
study suggests the ACOG recommendation is scientifically unfounded.
The second problem with the recommendation “VBAC should
be attempted in institutions…” is that it is based on an unproven
assumption: Cesarean section can be accomplished faster if the labor takes place
at a tertiary care hospital. ACOG presents no data in support of this assumption.
On the other hand, out-of-hospital birth has been shown scientifically to be safe
when attended by midwives who, when necessary, can be in close contact with a hospital
capable of emergency cesarean section. This is why homebirth and freestanding birth
centers have been proved safe in those places in the United States with good communication
and respect between home and hospital. The midwife can telephone the hospital and
describe the emergency, and while the woman is in transport, the hospital staff is
preparing, scrubbing in, etc.
How long does it take to do a cesarean section if the labor is in a tertiary care
hospital in the United States? While ACOG has recommended in the past that the "decision
to incision" time be no more than 30 minutes, in one study at a university hospital
in the United States2, 52 percent of the emergency cesarean sections for fetal
distress had a decision to incision time that exceeded 30 minutes.
One reason for this delay is that in the United States it is not the laboring
woman who is in transport, it is the absent doctor who is in transport, the doctor
who has been trying to monitor the labor in the hospital by telephone. The ACOG recommendation
“to have a physician immediately available” is
in reality a criticism of the U.S. system, in which the laboring woman's doctor is
usually not available and must be called to come in.
The elegant solution is not to take away valid choices for childbirth from the
woman and her family but to change the system. Rather than insisting that the woman
having a VBAC be transported at the beginning of labor to a big hospital that is
away from her primary caregiver, her family, her friends and familiar community,
instead do what is done in the other highly industrialized countries with maternal
and perinatal mortality rates lower than ours: Develop a system in the United States
in which there is close communication during childbirth between primary care in the
community—home, birth center, small hospital—and the big hospital so that when the
woman in labor needs to be transported, the decision to incision time is no greater
than if the same woman were laboring in the big hospital and needed to be transported
from the delivery suite to the surgical suite for a cesarean section.
A third problem with the recommendation “VBAC should be
attempted in institutions…” is that it is aimed entirely at the
treatment of uterine rupture and not at the prevention of uterine rupture. The increasing
rate of uterine rupture in the United States during the past decade has been alarming,
which rightly concerns ACOG. But ACOG's solution is analogous to responding to an
increasing rate of drowning at a summer camp by placing some life rings out in the
lake rather than teaching children how to swim better.
Attempts have been made to identify risk factors for uterine rupture, but the
focus has been on maternal factors such as number and type of uterine scars. There
has been insufficient attention in the obstetric literature or by ACOG to any relationship
between the management of the VBAC and uterine rupture. The key issue here is pharmacological
induction of labor with VBAC, which leads us to look at another final recommendation.
Problems With the Second Recommendation in Level B: “Use
of oxytocin or prostaglandin gel for VBAC requires close patient monitoring.”
After delaying for years while Cytotec induction spread like wildfire in the United
States—resulting in thousands of VBAC Cytotec inductions, which led to hundreds of
uterine ruptures and dozens of dead newborns—ACOG finally closed the barn door on
Cytotec induction of VBAC, but only after research showed a rate of uterine rupture
with Cytotec induction of VBAC 28 times higher than the rate of VBAC uterine rupture
without Cytotec induction3.
But the ACOG recommendation on VBAC under review here does not shut the barn door
on the use of other pharmacological agents to induce VBAC, as this recommendation
(under Level B, meaning based on limited or inconsistent scientific evidence) states:
“Use of oxytocin or prostaglandin gel for VBAC requires close
patient monitoring.” Take note that this means it is OK to use it as long as
you closely monitor.
Read carefully the paragraph titled “Induction” in this ACOG document.
It is an example of trying to torture the data until they confess to what you
want them to say.
Induction or augmentation with oxytocin has been suspected as
a factor responsible for uterine rupture. A meta-analysis found no relationship
between the use of oxytocin and rupture of the uterine scar. However, other studies
indicate that high infusion rates of oxytocin place women at greater risk. Although
there are studies that suggest that prostaglandin gel applied to the cervix or vagina
appears to be safe, there are occasional reports of uterine rupture with prostaglandin
preparations.
The statement “A meta-analysis found no relationship between the
use of oxytocin and rupture of the uterine scar” is false.
The meta-analysis they are referring to—by Rosen et al.—found a uterine rupture
rate of 2.3 percent with oxytocin induction of VBAC, compared with 1.5 percent with
no oxytocin induction of VBAC4. So there is a relationship, but it does not reach
a level of statistical significance. It would take a larger sample size to reach
statistical significance because uterine rupture is an unusual event. But it is what
scientists call a "trend," and this trend is consistent with a relationship
found in other studies. As ACOG states in this same paragraph: “However,
other studies indicate that high infusion rates of oxytocin place women at greater
risk [of uterine rupture].”
So the evidence, while not totally conclusive, strongly suggests that using oxytocin
with VBAC increases the chance for uterine rupture. Yet ACOG does not recommend
against oxytocin VBAC induction. Why? If the evidence is inconclusive, the cautious,
conservative approach would be to follow the basic rule of medical practice: “First
do no harm.” But induction is extremely obstetrician friendly, as it allows
the practitioner some control of a busy practice through scheduling the induction
at a convenient time rather than waiting for spontaneous labor, which is 24/7.
Proof? Data from the Centers for Disease Control (CDC) show induction of labor
in the United States ruing the past 10 years doubled, to 20 percent of all births from 10 percent. The same CDC data also show an increasing trend throughout the last decade
for more births Monday through Friday5. This is the same decade in which uterine
rupture also increased. The CDC data strongly support the possibility that the increase
in uterine rupture the past 10 years is due to increased induction of labor, including
induction of VBAC.
ACOG's Process for Making These Recommendations
Who Made These Recommendations?
In the practice bulletin's summary it says Level C recommendations are based “primarily
on consensus and expert opinion.” Who was involved in the consensus, and
who are the experts? There is an urgent need for transparency here. I contacted ACOG,
but they were unwilling to say who was in the group making this practice bulletin.
Since the first recommendation in Level C—“Because uterine
rupture may be catastrophic, VBAC should be attempted in institutions equipped to
respond to emergencies with physicians immediately available to provide emergency
care”—affects the care of a large group of pregnant women at the time
of giving birth, consensus needs to include not only obstetricians but also midwives, nurses,
family physicians, perinatal epidemiologists and consumers. Were any of these groups
represented, or were only obstetricians? This is particularly important when a recommendation,
such as this one, is of the “you need more of us” variety. Since this recommendation
is friendly (an advantage) to obstetricians and unfriendly (a disadvantage) to family
physicians, midwives and many women, the recommendation easily could be seen as self-aggrandizing
for obstetricians.
Here, an editorial from The Lancet, January 8,
2000, is instructive:
Advocacy guidelines developed by a single-specialty
group in isolation may be counterproductive, because those disciplines and professions
that were not involved in the development of the guidelines but may be required to
implement the recommendations mount their attacks and lodge their disclaimers. Some
of the guidelines may be of the Good Old Boys Sat at Table (GOBSAT) variety, based
on received wisdom rather than current scientific evidence, and may be biased by
undeclared conflicts of interests.…Studies have shown that the balance of disciplines
within a guideline-development group has considerable influence on the guideline
recommendations. Widespread multidisciplinary participation is essential not only
to ensure that the guideline is valid, but also that it is valued by all the members
of the multidisciplinary team, in order to be incorporated successfully into practice.6
Inappropriate Influence of Non-Medical Factors
Near the beginning of the document, mention is made of ACOG's fear of litigation:
“Physicians in the United States, facing increased medical-legal
pressures…” Furthermore, in this document, ACOG’s fear of litigation
focuses on fear of VBAC litigation: “Increasingly, these adverse
events during trial of labor have led to malpractice suits.” ACOG’s fear
of VBAC itself is revealed in the Figure 1 algorithm, which includes the need to
“counsel patient regarding benefits and risks of VBAC”
but does not include a similar need to counsel patient regarding benefits
and risks of the woman's other choice: cesarean section. To what extent do ACOG’s
fear of VBAC and fear of litigation influence the recommendations in this document?
To understand the importance of this question, it is necessary to understand ACOG.
ACOG is not a college in the sense of an institution of higher learning, nor is
it a scientific body. It is a “professional organization” that in reality
is one kind of trade union. Like every trade union, ACOG has two goals: promote the
interests of its members, and promote a better product (in this case, well-being
of women). But if there is conflict between these two goals, the interests of obstetricians
come first.
Proof that ACOG puts members’ interests first? In September 1998 ACOG published
Committee Opinion No. 207, “Liability Implications of Recording Procedures or
Treatments,” which includes the statement: “Recording solely for the purpose
of patient memorabilia or marketing is not without liability.…The Committee
strongly discourages any recording of medical and surgical procedures for patient
memorabilia.” In other words, ACOG recommends that doctors and hospitals refuse
permission for women and families to make a videotape of their baby’s hospital birth.
Fear of litigation against their members has higher priority for ACOG than women’s
rights and family values—the need of the family to record one of the most important
events in their lives. This is why ACOG recommendations cannot always be considered
the gospel and the recommendations in this document are suspect. Should the United
Auto Workers have the final say on standards of auto safety?
Impact of Recommendations
The first Level C recommendation, “VBAC should be attempted
in institutions equipped to respond to emergencies with physicians immediately available
to provide emergency care,” has a huge impact on the system of maternity
care in the United States that goes far beyond obstetric practice. If this policy is followed, it drastically reduces or
eliminates several options available to women with previous cesarean section, including
having their birth at home, in a freestanding birth center or in a small community
hospital. Because of all the unnecessary cesarean section in the past, American women
with a scarred uterus are a significant minority of pregnant women—in the neighborhood
of 15 percent. If the nearest large hospital is at some distance, it makes a family-centered birth
difficult or impossible and is likely to eliminate continuity of care throughout
pregnancy and birth. Scientific data show such continuity of care significantly improves
birth outcomes.
In addition to this impact on women and families and birth outcomes, this recommendation
also has a major impact on community-based midwives, family physicians, birth centers
and small hospitals.
Conclusions
Two of the eight recommendations are without scientific justification. One recommendation—VBAC
only with surgeons right there—has a tragic, unnecessary, negative impact on maternity
care and maternity care providers in the United States. The second—oxytocin and prostaglandin
induction is OK during VBAC—is quite likely dangerous for birthing women.
We see a double standard in ACOG recommendations depending on whether or not
they are doctor friendly (are of benefit to ACOG members). If a recommendation has
no evidence to support it but is of benefit to obstetricians—VBAC only in hospitals
with surgeons standing by—ACOG will make the recommendation. Other solutions to the
same problem that are not obstetrician friendly—facilitation of communication, collaboration
and transport between primary and tertiary birth care—will not be recommended even
though they would benefit many women. As a second example of this double standard,
if there is inconsistent evidence on an issue—oxytocin or prostaglandin induction
for VBAC—ACOG will make the doctor-friendly recommendation, approving its use even
though the data show a trend that is likely to put some women at risk. ACOG recommendations
consistently put the needs of ACOG members before the needs of women unless there
is overwhelming evidence that may finally force an ACOG recommendation which is not
doctor friendly—no Cytotec induction for VBAC.
We also see little evidence that ACOG is trying to find out why there is increasing
uterine rupture so that it can be prevented in the future. ACOG should be making
every effort to promote research on the management of those labors during the past 10 years
that ended with uterine ruptures, including the percent of ruptures associated with
VBAC and the percent associated with the use of Cytotec, oxytocin or prostaglandin
gels. There is also an urgent need for far more research on the relationship between
characteristics of places of birth (home, birth centers, community hospitals, regional
hospitals, tertiary care hospitals) and uterine rupture. Armed with this kind of
data, ACOG could make evidence-based recommendations, be they doctor friendly or
not.
ACOG's primary allegiance to the needs of its members over the needs of women
and families requires their recommendations to be suspect unless confirmed by overwhelming
scientific evidence. As ACOG recommendations come from a single-specialty organization,
they always must be carefully evaluated as to bias and should never be the sole basis,
nor even the most important justification, for maternity care policy in the United
States.
Marsden Wagner, MD, is a neonatologist and perinatal epidemiologist.
He was responsible for maternal and child health in the European Regional Office
of the World Health Organization for 14 years. Now living in Washington, D.C., he
travels the world talking about appropriate uses of technology in birth and utilizing
midwives for the best outcome.
References
- McMahon, M. (1996). Comparison of a trial of labor with an elective second cesarean
section. New Eng J Med 335 (10): 689-695.
- Chauhan, S., et al. (1997). J Reprod Med 42
(6): 347-352.
- Plaut, M., et al. (1999). Uterine rupture associated with the use of misoprostol
(Cytotec) in the gravid patient with a previous cesarean section. Amer
J Obstet Gynecol 180 (6): 1535-1542.
- Rosen, M., et al. (1991). Vaginal birth after cesarean: a meta-analysis of morbidity
and mortality. Obstet Gynecol 77 (3): 465-470.
- www.cdc.gov/nchs/birth
- Editorial. (2000). Development of practice guidelines. The
Lancet 355: 82-83.
Learn more about cesarean prevention and VBAC in Midwifery
Today Issue 57. In "Choosing Cesarean Section" Marsden Wagner tells us that
the risk/benefit factors of c-sections depend on the reason for doing them: "Where
the baby is not in trouble, the risks to the baby still exist, meaning that the woman
who chooses CS puts her baby in unnecessary danger."
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