OPINION OF THE COURT
This is our first opportunity to confront the Emergency Medical Treatment and Active Labor Act (“EMTALA” or the “Act”). 42 U.S.C. § 1395dd, et seq. Among other things, the Act forbids hospitals from refusing to treat individuals with emergency conditions, a practice often referred to as “patient dumping.”
Appellants Christopher and Honey Torretti’s son, Christopher, was born with severe brain damage after Mrs. Torretti’s high-risk pregnancy went awry. On the morning of the birth, Mrs. Torretti went to her routine outpatient fetal monitoring ap
I. Background
This case, like most cases brought under EMTALA, is tragic. This was Mrs. Torretti’s second pregnancy. Her first child was born healthy. Both pregnancies were high-risk because she is an insulin-dependent diabetic. Her primary obstetrician was Dr. Patricia McConnell, a member of the Peden Group, an obstetrics practice group based out of Lankenau Hospital (“Lankenau”). Lankenau is рart of the Main Line Health system and located in Wynnewood, Pennsylvania.
Because of Mrs. Torretti’s diabetic condition (which can present complications during a pregnancy), Dr. McConnell referred her to the Paoli Hospital Perinatal Testing Center (“Paoli”), located in Paoli, Pennsylvania, for monitoring throughout both pregnancies. Paoli is a center for fetal monitoring and consultation only, and is located in a medical building adjacent to Paoli Hospital. It is also owned by Main Line Health. The two hospitals are approximately twenty miles apart.
In Mrs. Torretti’s third trimester, she began to have complications, primarily involving premature contractions. During this period, the Peden Group incrеased Mrs. Torretti’s monitoring appointments at Paoli to twice per week from once per month. The Peden Group also monitored her as an outpatient at Lankenau on one occasion in mid-April 2005. Two weeks later, when she went to Paoli for routine monitoring on April 30, the Paoli medical staff detected that she was experiencing pre-term labor and directed her to Lankenau where she was hospitalized for three days. On that occasion, she drove herself from Paoli to Lankenau.
Near the end of Mrs. Torretti’s pregnancy, in her 34th week, she had a routine monitoring appointment scheduled at Paoli on Monday, May 23. Two days before the appointment, she called Dr. MсConnell twice. First, she complained of contractions. Dr. McConnell told her to put her feet up and relax. The second time Mrs. Torretti called, the contractions had lessened, but she explained that she was very uncomfortable because of her large size and had noticed a decrease in fetal movement. She asked about the possibility of receiving a therapeutic amniocentesis, a treatment to reduce her discomfort by removing some of the excess amniotic fluid. Dr. McConnell advised her to drink a glass of ice water to try and stir the baby; thereafter, for whatever reason, Mrs. Torretti detected increased movement. The doctor also told her that she could сome to Lankenau if she preferred, but that nothing could be done until Monday. Mrs. Torretti chose not to go the hospital that weekend and did not believe that her condition was emergent. 2
Dr. Gerson sat Mrs. Torretti in a chair and began the non-stress test. Over a 28-minute period, the test did not show expected fetal heart rate variability — -normal accelerations and decelerations. Lack of variability in a non-stress test could be explained by a normal variant, such as a prolonged sleep cycle, or could be the sign of a problem. About the same time Mrs. Torretti began the non-stress test, her contractions returned. She indicated the “pain was so bad” that she was “grasping either the arm of the chair or both arms of the chair at once, and either almost grunting or to a degree yelling.” The non-stress test indicated that she had 16 contractions in the 28 minutes of fetal monitoring — her contractions lasted approximately 50 to 70 seconds and were lié to 2\ minutes apart.
Dr. Gerson was aware of Mrs. Torretti’s diabetic condition. He noted in her medical documents that her abdominal circumference was large- — “off the charts.” The fetus weighed approximately eleven pounds. Also, the ultrasound test indicated that she had excess amniotic fluid, but that the fetus “was moving its limbs and body.”
Based on these preliminary test results and Mrs. Torretti’s diabetic condition, Dr. Gerson terminated the non-stress test and sent her to Lankenau for longer-term monitoring of the baby. 5 In directing Mrs. Torretti to Lankenau, he also consulted with her regular doctor, Dr. McConnell, by telephone. Dr. Gerson testified that this plan appeared to be “perfectly safe” based on the “best information we had.” He further testified that, even though she was having contractions, which had been commonplace throughout her third trimester, “delivery wasn’t necessarily going to be imminent or need to be imminent and [ ] it was appropriate for her to go to Lankenau Hospital.” 6 The nurse assisting Dr. Ger-son commented to Mrs. Torretti that she believed Mrs. Torretti might deliver the baby sometime that day, but gave no indication of an emergency or imminency.
Mrs. Torretti testified that, while at Paoli, nothing in the statements or demeanor of anyone on Paoli’s staff, including Dr. Gerson, indicated to her that her condition was emergent. For example, Mrs. Torretti stated that “[t]here was no
As is customary, Dr. Gerson sent an explanatory letter to the Lankenau medical personnel along with the Torrettis. When Mrs. Torretti arrived, she had to wait approximately 15 to 20 minutes for a room. She stated that when she was first connected to the monitor, her condition seemed to be about the same as it had been at Paoli, but then “it worsened very quickly.” Shortly thereafter, another doctor with the Peden Group checked on her. When he looked at the preliminary results, he exclaimed “oh shit!” The doctors immediately rushed Mrs. Torretti into surgery and she gave birth via caesarean section. The baby, Christopher Torretti, was born with severe brain damage.
Defendants moved for summary judgment on the EMTALA claim. The District Court ruled that the Torrettis did not offer sufficient evidence to raise a reasonable inference that defendants, specifically Dr. Gerson, knew Mrs. Torretti presented a medical emergency, and thus failed to sustain their burden under EMTALA.
Torretti v. Paoli Mem. Hosp.,
No. 06-3003,
II. Standard of Review
When the District Court grants a motion for summary judgment, our review is plenary.
See Elsmere Park Club, L.P. v. Town of Elsmere,
III. EMTALA Background
EMTALA requires hospitals to give certain types of medical care to individuals presented for emergency treatment: (a) appropriate medical screening, (b) stabilization of known emergency medical conditions and labor, and (c) restrictions on transfer of unstabilized individuals to outside hospital facilities. 42 U.S.C. § 1395dd(a)-(c)
7
;
see Urban v. King,
43
Congress enacted EMTALA in the mid-1980s based on concerns that, due to economic constraints, hospitals either were refusing to treat certain emergency room patients or transferring them to other institutions.
See
68 F.R. 53,222, 53,223 (Sept. 9, 2003);
see also
H.R.Rep. No. 99-241, pt.3, at 27 (July 31,1985),
reprinted in
1986 U.S.C.C.A.N. 579, 605 (indicating that Congress was “greatly concerned about the increasing number of reports that hospital emergency rooms are refusing to accept or treat patients with emergency conditions if the patient does not have medical insurance”). As noted abovе, this practice is known as “patient dumping.”
Power v. Arlington Hosp. Ass’n,
There is no general common-law duty for hospitals to accept and treat all individuals. Under EMTALA, however, any individual who suffers personal harm as a direct result of a hospital’s violation of the statute may bring a private civil action for damages. 42 U.S.C. § 1395dd(d). While an EMTALA action usually will be brought in conjunction with a state statutory claim or common-law medical malpractice or negligence action arising out of the same events, it does not create a federal cause of action for malpractice.
See,
IV. Outpatients Do Not Trigger EMTALA Coverage
In analyzing an EMTALA claim, the Act does not stand alоne. The Department of Health and Human Services’ Centers for Medicare and Medicaid Services (CMS) promulgated a Federal Regulation, 42 C.F.R. § 489.24(a)-(b),
9
and Final Rule, 68 F.R. 53,222 (Sept. 9, 2003),
10
clarifying the reach of EMTALA.
See
Brian Kamoie,
EMTALA: Dedicating an Emergency Department Near You,
37 J. Health L. 41, at 55-56 (2004) (explaining that because of confusion in the interpretation and application of EMTALA, CMS set up a “Regulatory Reform Task Force” to recommend clarifications to the statute). Generally, we defer to a government agency’s administrative interpretation of a statute unless it is contrary to clear congressional intent.
See Chevron USA Inc. v. Natural Res. Defense Council, Inc.,
CMS has the congressional authority to promulgate rules and regulations interpreting and implementing Medicare-related statutes such as EMTALA. See generally 42 U.S.C. §§ 1302, 1395hh; 5 U.S.C. § 551, et seq. Among the 2003 clarifications, the Regulation and Final Rule address where and when EMTALA applies. CMS solicited public comments and took into account a range of objections to the proposed Regulation, providing a lengthy discussion responding to the comments and its reasons for its interpretation in the Final Rule. The Regulation was not raised by the parties or the District Court. Nevertheless, it is instructive to answer the question before us: whether Mrs. Torretti fits within EMTALA’s scope — a patient antidumping statute. CMS has concluded that EMTALA does not apply to patients (and outpatients), which interpretation precludes the Torrettis’ EMTALA claim in the first instance because Mrs. Torretti was an outpatient who came to Paoli for a scheduled appointment.
CMS exрlains that EMTALA does not apply to outpatients, even if during an outpatient encounter “they are later found to have an emergency medical condition ... [and] are transported to the hospital’s dedicated emergency department.”
The Torrettis argue that EMTALA is triggered because Mrs. Torretti came to Paoli for “what was, from the inception, a potential ‘emergency medical condition’ ” because “EMTALA protects people who present ‘for what may be an emergency medical condition.’ ” Appellants’ Supp. Br. at 2 (quoting 68 F.R. 53,222) (emphasis added). This is not supported in the record. Mrs. Torretti came to Paoli for her scheduled bi-weekly appointment involving routine monitoring of her high-risk pregnancy and did not present as an emergency to the Paoli medical staff. 15 In fact, she testified that, because of her complications throughout her third trimester, she did not believe she was in an emergent state until after she began the monitoring at Lankenau and her condition quickly changed. Her other actions and testimony, as well as the testimony of her husband and the medical personnel, are consistent with this view.
The Torrettis also imply that, regardless of whether Mrs. Torretti was a “patient,” because she had a high-risk pregnancy, each scheduled visit to Paoli during her pregnancy would qualify as a presentment of an emergency medical condition to trigger EMTALA coverage. Appellants’ Supp. Br. at 3 (“Mrs. Torretti came to [Paoli] for what was, from the inception, a potential ‘emergency medical condition.’ As the fetus of a woman who has been an insulin-dependent diabetic since infancy, her baby was at serious risk of stillbirth or fetal death.”) (citation omitted). This is an unreasonable interpretation of the Act that broadens its scope beyond Congress’s intent. To illustrate this point, individuals in equivalent situations to Mrs. Torretti would be hospital outpatients who have routinely scheduled weekly or monthly appointments to receive dialysis or chemotherapy for treatment of kidney disease and cancer, respectively. We believe it is clear that Congrеss did not intend EMTALA to cover these individuals every time they come to the hospital for their appointments, even though they suffer from serious medical conditions that risk becoming emergent.
Given this context, we believe CMS’s more restrictive interpretation on this issue is consistent with EMTALA, and is in accord with the Act’s intent. Congress passed EMTALA to curb the problem of patient dumping by creating a statutory duty for hospitals to examine and treat individuals who come to them for emergency care. 42 U.S.C. § 1395dd. Accordingly, this interpretation is entitled to
Chevron
deference.
See Chevron,
One final note on this issue is that in supplemental briefing the Torrettis point to a Ninth Circuit Court case,
Arrington v. Wong,
In this circumstance, the Torrettis will have to pursue legal avenues other than EMTALA because the statute does not apply here. Moreover, claims of negligence or malpractice more accurately reflect the relief the Torrettis seek.
Y. Summary Judgment
Although we have concluded that Mrs. Torretti’s circumstances are not those contemplated by EMTALA coverage, we would be remiss if we did not address the substance of the claim for future guidance. The Torrettis alleged a “stabilization” claim — that defendants violated EMTALA because they did not stabilize her emergency condition and inappropriately transferred her. Under this theory, EMTALA requires that Mrs. Torretti (1) had “an emergency medical condition; (2) the hospital actually knew of that condition; [and] (3) the patient was not stabilized before being transferred.”
Baber v. Hosp. Corp. of Am.,
As the District Court concluded, the requirement of actual knowledge is the key to this issue. We adopt this
mens rea
condition precedent, which conforms with all our sister circuit courts of appeals that have addressed this issue under EMTALA.
See, e.g., Vickers,
The District Court concluded that the Torrettis’ evidence was not sufficient to raise a disputed issue, and we agree with that conclusion. As we outlined above in the fact section, there is no evidence that any of the hospital staff at Paoli, and specifically Dr. Gerson, actually knew that Mrs. Torretti’s condition was an emergency before directing her to Lankenau for further monitoring. The medical personnel at Paoli knew her pregnancy was high-risk because of her diabetic condition, which was indicated in her medical charts and the Paoli testing results from that day, and she had a recent history of treatment for pre-term labor and contractions similar to those exhibited at Paoli (and approximately three weeks prior to the May 23 appointment, mеdical personnel at Paoli sent her to
Lankenau
for further monitoring). She arrived for a routine appointment and did not present herself as an emergency patient, neither she nor Dr. McConnell believed her situation was emergent over the weekend preceding the Paoli appointment, she did not believe her condition was emergent until
after
she arrived at
Lankenau
and her condition changed quickly, Dr. Gerson did not indicate that he believed her condition was emergent
{e.g.,
before Mrs. Torretti left Paoli, he expressly stated to the contrary when asked about transporting her to
% sfc sj: %
In this context, we affirm the District Court’s grant of summary judgment.
Notes
. The District Court had subject matter jurisdiction over this EMTALA action pursuant to 42 U.S.C. § 1395dd, ef seq., and supplemental jurisdiction over the state claims pursuant to 28 U.S.C. § 1367. We have appellate jurisdiction under 28 U.S.C. § 1291.
. See App. 97 (Question: "Did you feel your condition was emergent on the 21st?” Mrs. Torretti’s answer: "No.”).
. A non-stress test is a non-invasive test that measures fetal heart rate and contractions. Dr. Andrew Gerson, a perinatologist, explained that the test can last anywhere from 20 minutes tо more than two hours, depending on the person.
. See App. 101a (Question: "Did you feel your condition was emergent that day [at Paoli]?” Mrs. Torretti's answer: "No.”).
. Dr. Gerson stated that “one of the other concerns was [that Mrs. Torretti] be evaluated for her own sugar status and diabetes status, which, again, was one of the factors that made me realize that I thought she was going to [a] need more prolonged period of monitoring than what we could provide for her.”
. Dr. McConnell confirmed this view in testifying that Dr. Gerson told her that Mrs. Torretti would need prolonged monitoring, but that he did not anticipate a delivery that day.
. The statute states in pertinent part:
(a) Medical screening requirement In the case of a hospital that has a hospital emergency department, if any individual (whether or not eligible for benefits under this subchapter) comes to the emergency department and a request is made on the individual's behalf for examination or treatment for a medical condition, the hospital must provide for an appropriate medical screening examination within the capability of the hospital's emergency department, including ancillary services routinely available to the emergency department, to determine whether or not an emergency medical condition (within the meaning of subsection (e)(1) of this section) exists.
(b) Necessary stabilizing treatment for emergency medical conditions and labor
(1) In general[:] If any individual ... comes to a hospital and the hospital determines that the individual has an emergency medical condition, the hospital must provide either — •
(A) within the staff and facilities available at the hospital, for such further medical examination and such treatment as may be required to stabilize the medical condition, or
(B) for transfer of the individual to another medical facility in accordance with subsection (c) of this section.
(c) Restricting transfers until individual stabilized
(1) Rule[:] If an individual at a hospital has an emergency medical condition which has not been stabilized (within the meaning of subsection (e)(3)(B) of this section), the hospital may not transfer the individual unless .... [considerations not applicable to this case.]
. Hospitals that voluntarily participate in the Medicare or Medicaid programs and have effective provider agreements
must comply
with EMTALA.
In re Univ. Med. Ctr.,
. Titled "Special responsibilities of Medicare hospitals in emergency cases.”
. Titled "Medicare Program; Clarifying Policies Related to the Responsibilities of Medicare-Participating Hospitals in Treating Individuals with Emergency Medical Conditions.”
.
Cf. Lopez-Soto v. Hawayek, 175
F.3d 170, 173-76 (1st Cir.1999) (explaining that subsections (a) (screening) and (b) (stablilization) of EMTALA should be read in the disjunctive because (a) uses the term "emergency department” and (b) uses the term "hospital,” and concluding thаt transferring an infant born in the maternity ward with an emergent condition to another hospital with specialized care without stabilization would qualify as a claim under EMTALA). We note that this case came before CMS's 2003 clarifying Regulation and Final Rule. We do not attempt to speculate at how the First Circuit Court of Appeals would view this question in light of the revised Regulation, but in the Court's analysis it noted that the EMTALA "provisions create distinct obligations and apply to different classes of individuals.”
Id.
at 175. We also note that a "labor and delivery department,” where the baby in
Lopez-Soto
was born and transferred from, is considered to be a "dedicated emergency department” under the Regulation and Final Rule and thus falls under EMTALA, whereas Paoli's Perinatal Testing Center is for outpatient fetal monitoring and consulting only.
See
As was the Lopez-Soto Court's focus, CMS pointed out that the nomenclature discrepancies in the statute have led to confusion and the uneven application of EMTALA. See68 F.R. at 53,227-228 ; see also Kamoie,37 J. Health L. at 46-47, 51-52 . By focusing EMTALA obligations across methods of classification, such as by distinguishing between hospital patients and other individuals who come to the hospital, CMS attempted to clarify the statute. See68 F.R. at 53,224 ("We proposed to clarify the extent to which EMTALA applies to inpatients and outpatients. We believe these clarifications will enhance understanding for hospitals as to what their obligations are under EMTALA, so that they more clearly understand to whom they are obligated under this provision of the statute, and whose care will be governed by the Medicare hospital [conditions of participation].”).
. The pertinent part of subsection (a) of the Regulation states:
(a) Applicability of provisions of this section.
(1) In the case of a hospital that has an emergency department, if an individual (whether or not eligible for Medicare benefits and regardless of ability to pay) “comes to the emergency department,” as defined in paragraph (b) of this section, the hospital must—
(i) Provide an appropriate medical scrеening examination within the capability of the hospital's emergency department, including ancillary services routinely available to the emergency department, to determine whether or not an emergency medical condition exists. The examination must be conducted by an individual(s) who is determined qualified by hospital bylaws or rules and regulations and who meets the requirements of § 482.55 of this chapter concerning emergency services personnel and direction; and
(ii) If an emergency medical condition is determined to exist, provide any necessary stabilizing treatment, as defined in paragraph (d) of this section, or an appropriate transfer as defined in paragraph (e) of this section. If the hospital admits the individual as an inpatient for further treatment, the hospital's obligation under this section ends, as specified in paragraph (d)(2) of this section. 42 C.F.R. § 489.24(a).
. "Outpatient means a person who has not been admitted as an inpatient but who is registered on the hospital or CAH [critical access hospital] records as an outpatient and receives services (rather than supplies alone) directly from the hospital or CAH.” 42 C.F.R. § 410.2.
. The pertinent part of the CMS Final Rule states:
EMTALA does not apply to any individual who, before the individual presents to the hospital for examination or treatment for an emergency medical condition, has begun to receive outpatient services as part of an encounter.... Such individuals would bе included under this policy, regardless of whether or not they began the nonemergency encounter in order to keep a previously scheduled appointment or under orders of a physician or other medical practitioner.... [W]e believe it is inappropriate to consider such individuals, who are hospital outpatients who have protections under the [Medicare Conditions of Participation], to have "come to the hospital” for purposes of EMTALA as well, even if they subsequently experience an emergency medical condition.
. We note, however, that EMTALA could be triggered in a circumstance where an individual comes to the hospital requesting treatment fоr an emergent condition, despite having a pre-scheduled appointment within the hospital for a related or unrelated reason.
See
. Mrs. Torretti's testimony that, near the end of her ultrasound, she heard Dr. Gerson state that "it had a sсore of two,” is not enough to raise a disputed issue of material fact. She believed the number referred to her biophysical profile score, though she did not state any reasons for this belief. That profile measures the health of the baby using both an ultrasound and a non-stress test. The corresponding score ranges from 0, which is very problematic, to 10, which is the best score.
Dr. Gerson testified that he was not able to conduct a formal biophysical profile, but that the ultrasound showed
both gross body movements and limb movements, as well as [excess] fluid around the baby[, which] allowed me to come to the conclusion that the baby had a biophysical profile score of 6, which is a profile score thаt allows one to draw a conclusion that delivery wasn’t necessarily going to be imminent or need to be imminent and that it was appropriate for her to go to Lankenau.
This number is corroborated in Mrs. Torretti’s medical report, which states that the biophysical profile score is 6. It is also consistent with Dr. Gerson’s actions in sending Mrs. Torretti to Lankenau for further monitoring. Moreover, the letter Dr. Gerson sent to Lankenau indicated that, based on her ultrasound, "the placenta was found in the Posterior position and noted to be grade 2.” This information is consistent with the statement Mrs. Torretti overheard Dr. Gerson make during the ultrasound. As the District Court concluded, Mrs. Torretti’s speculation alone, without more, is insufficient to survive summary judgment.
