Ebola hemorrhagic fever, or Ebola virus disease (EVD), has emerged in the last year as a global threat and humanitarian disaster for the affected countries of West Africa and has also come to the United States (US) and Europe.
The treatment of the first and three subsequent US patients outside of Africa at Emory University provided a number of challenges, as well as strategic and tactical lessons that included detailed planning and team work across multiple academic and health care units, emphasizing biosafety, the importance of institutional communications, addressing unanticipated challenges such as waste management, and the logistics of working closely with governmental agencies and outside collaborators.
In providing effective care for individuals, the value of mobilizing a diverse health and academic community to work collaboratively to addressing a global threat is emphasized. This includes dissemination of best practice information; providing education and training about EVD; expansion of new knowledge about the clinical course, complications, and pathogenesis of EVD; the creation of new institutional forums, and engagement in the broader policy and equity issues of contagious health threats.
Ebola hemorrhagic fever, or Ebola virus disease (EVD), is caused by a highly contagious group of enveloped, single-stranded, negative-sense RNA viruses of the family Filoviridae. The disease has historically carried 53%–88% mortality [1–3]. In December 2013, what has now become the largest and most devastating Ebola outbreak ever recorded, caused by a new strain of the Zaire species (Zaire ebolavirus), began in Meliandou, Guinea, West Africa and soon enveloped neighboring Sierra Leone and Liberia, with cases also in Nigeria, Senegal, and Mali [1–5]. WHO (World Health Organization)/CDC (United States Centers for Disease Control and Prevention) reports 27,550 cases and 11,235 deaths in the three principal countries as of June 28, 2015 , which may be an underestimation of at least a factor of 2.
On August 2 and 5, 2014, two medical missionaries who developed EVD in late July while working at Eternal Love Winning Africa (ELWA) hospital in Liberia were evacuated from Monrovia by a specially designed air ambulance to Emory University Hospital (EUH) . Until August 2, 2014, EVD had not been seen or treated in humans outside of Africa. The initial call for help for these missionaries came to our institution on July 30 and would mobilize multiple resources at Emory University, in particular those of the academic medical center, EUH, Emory Healthcare, and the Robert W. Woodruff Health Sciences Center, the faculty, nurses, staff, and leadership of these units, and our communications and other Emory University support teams. The successful treatment and discharge of these first two patients by August 21, 2014, was only the first chapter of the impact of this outbreak on Emory, the US, Europe, and the global community. At least 25 individuals have now been treated outside of Africa (US: 11, Europe: 14, with five deaths). The US, Europe, and the rest of the world can expect to continue to be touched by this epidemic and by future communicable disease outbreaks.
The strategic and tactical lessons and challenges presented by providing care for the first and subsequent US EVD patients at Emory University provide an opportunity to share lessons that may help others. Specific clinical and immunological features and diagnostic and detailed management issues of the patients at Emory are reported separately [7–11]. It is very important to acknowledge the tremendous inequity between EVD care available in our academic medical center versus sites in West Africa. This disparity, illustrated by this outbreak, will require much future work to address.
EUH is the flagship clinical care facility for Emory Healthcare, staffed by 1,221 Emory School of Medicine faculty physicians, with over 3,600 employees, 25,300 admissions, and 157,000 outpatient visits annually. The hospital has one of the highest case-mix indexes (a measure of complexity of illness treated) among the University Healthsystem Consortium (UHC)-ranked facilities. Emory had established strong programs in health care delivery, quality, infectious diseases (ID), infection control and biosafety, immunology, vaccines, and public health that were important to its ability to respond to this series of events.
The Serious Communicable Diseases Unit (SCDU) (Fig 1, Box 1) of EUH is a special isolation unit. This unit was designed and constructed in 2002 following the 2001 anthrax bioterrorism event but was also created, given the global connectivity of Atlanta and its institutions, to address naturally acquired, highly communicable emerging infectious diseases such as EVD. The unit was built and set up in close collaboration with and with financial support from the adjacent CDC to provide care for CDC scientists and staff who have contracted highly communicable infectious diseases in laboratory settings or while traveling abroad.
Box 1. The SCDU
The SCDU was designed (Fig 1) to provide an extraordinarily high level of clinical isolation with more enhanced capacities than are normally provided to isolate patients in many hospital settings. The unit has a special outside entrance for emergency use and is separated from patient care areas in order to not impact other clinical services. It was the first of three such high-level civilian facilities in the US.
The SCDU was constructed (purposely to provide rapid isolation, security, flexibility, and access to special resources) within the EUH clinical research unit. The clinical research unit has been in existence for some 60 years and supports clinical research through the National Institutes of Health (NIH)-funded Clinical and Translational Science Awards (CTSA) program. The SCDU offers on-call, highly trained staff operating under standardized, ready-to-go protocols for providing care for patients infected with highly communicable contagious diseases.
While not necessary for treatment of EVD, the isolation rooms feature negative pressure air handling, 20 air changes per hour, with laminar flow and high-efficiency particulate air (HEPA)-filtering completed before the air is 100% exhausted outside of the hospital (no recirculation). General and intensive care can be provided. The SCDU was activated on two previous occasions. The first was in 2003 for a CDC worker with concern for having been infected with severe acute respiratory syndrome (SARS) in Hong Kong, China. The second was in 2005 for a CDC employee in Angola with potential Marburg virus hemorrhagic fever. While unit activation has been infrequent, intensive training in this unit to maintain a state of readiness has been continuous for well over a decade, including detailed preparation for transport of patients and the training of nurses and physicians.
A virtual tour of the SCDU and videos addressing many of the most frequently asked questions, together with access to all SCDU policies and standard operating procedures (SOPs), are available on the Emory education web site: www.emoryhealthcare.org/ebolaprep .
The ID program at EUH was built to provide expertise in hospital epidemiology, antimicrobial management, transplant infectious diseases, and clinical microbiology. For over a decade, Emory University was an active member of the NIH Research Centers of Excellence (RCE) in Biodefense and was the site for the biosafety training program for select pathogens of the Southeast Regional Center of Excellence for Emerging Infections and Biodefense (SERCEB) RCE. This particular program provided invaluable expertise, equipment, and support for the EVD effort. Emory ID and Emory Healthcare (EHC) also created the TravelWell clinic, an outpatient clinic available for assessment and evaluation of pre- and post-travelers and supporting major Atlanta corporations and the CDC. Emory’s TravelWell is part of a 57-site worldwide travel network (GeoSentinel) with a 10-year database of 3,000 entries of those who either had returned ill following travel to Liberia, Sierra Leone, Guinea, or Nigeria or had just emigrated from one of those countries.
The Decision to Accept EVD Patients into the SCDU
The request for medical care for the initial patients came from the missionary organizations Samaritan’s Purse and Serving in Mission (SIM) USA and from the patients themselves. The decision was coordinated through the US State Department and the CDC. EUH and EHC leadership made the decision to accept the patients—a decision made quickly but not lightly. The decision was based on the need, confidence in the overall preparedness of EUH, and the more than a decade plus of training and preparation to address highly communicable diseases at EUH (Box 2 and Box 3). Importantly, as an academic medical center and research institution, the decisions were also based upon what we might learn in treating these patients (e.g., advancing knowledge about human health) and how such knowledge could be applied to the current outbreak.
Box 2. SCDU Preparation and Operations
The SCDU medical team is led by the SCDU director, an ID trained physician who has spearheaded for over a decade efforts in establishing the protocols, training, education, and operations of the unit in conjunction with the CDC. Three other faculty members of the Department of Medicine, four additional ID physicians, two pathologists, five medical technologists, and 21 critical care nurses also support the unit.
An SCDU unit director, clinical nurse specialist, and team coordinator handle logistics, organize training sessions, determine supply needs, and establish nursing schedules. Nurses provide care in 4-hour stretches to minimize donning and doffing of personal protective equipment. The overall effort has directly involved over 125 staff and support personnel.
During the care and treatment of EVD patients, there were daily communications between the SCDU medical team and the CDC’s Division of High-Consequence Pathogens and Pathology (DHCPP), the Division of Healthcare Quality Promotion, and the Emergency Operations Center for Ebola established at CDC, and with the US Food and Drug Administration (FDA) and other US federal agencies, as well as frequent communications with other academic units, industry, and providers in West Africa.
The primary focus of training was on biosafety for all individuals who provided direct care or handled body fluids. All of these individuals received mandatory education and training, followed by strict competency verification before medical or nursing staffs were permitted to provide care for these patients.
Effective and assertive communication was central to the safety of the SCDU team. Use of the buddy system was an essential element of the focus on individual and colleague safety. Because communication was so important, the team developed rules to govern direct patient care communication as well as within daily team huddles. These rules were reviewed each morning during the daily huddle and served as a platform to empower all members of the team, regardless of role, to facilitate communication and to maintain strict SOPs.
Box 3. The SCDU Support Teams
The hospital support team was led by the CEO of EUH. The chief medical and nursing officers of EHC and EUH, and in particular the vice president of operations of EUH, were also heavily involved in leading the support efforts. During the care and treatment of the EVD patients, an operations team of key administrators and nursing and physician leadership met twice a day. Despite the extensive preplanning, opportunities to refine and improve both clinical and operations were noted, and all aspects of the hospital services were involved. Pharmacy, environmental services, engineering/facilities support, and pastoral care/counseling were especially important.
Other ID faculty, including a pediatric ID specialist with experience in EVD, provided support for the frontline medical team. Periodic conference calls focused on support, therapeutic options in treating patients, and issues of postexposure prophylaxis, vaccines, surge planning, protocol development, and discussions of research as it related to EVD. To facilitate the necessary availability of SCDU dedicated ID providers, alternate faculty were recruited to cover the regular duties of the SCDU physicians. ID support also included contacting key national and international research leaders in EVD; evaluating, contacting, and obtaining, through outside groups, experimental vaccines and new drugs for Ebola; and communicating with the CDC, FDA, NIH, and other federal agencies, other university partners, and biotech/industry contacts, all of which were essential in the effort.
The Emory Environmental Health and Safety Office (EHSO) was engaged immediately after the call for ongoing support. While clinical care settings are very different from those of labs, EHSO staff included individuals with expertise in training on Biosafety Level BSL 3 and 4 laboratory safety, which was helpful in translating to our clinical care situation. Conversations were conducted by EHSO with other national biosafety leaders in EVD. (See “Biosafety.”)
The SCDU team was also supported by the Department of Emergency Medicine and the Emory Office of Critical Event Preparedness and Response focusing on the complexity of patient transport and emergency care. They worked closely before and during the event with Phoenix Air Group, the air ambulance transport service, and the Grady Hospital Ambulance service. Critical Care established a 24/7 Medical Intensive Care Unit (MICU) attending coverage for critical care management issues including airway management and line placement issues. Other subspecialties, such as renal medicine, were required on a case-by-case basis. The location of the SCDU away from other patient care units of EUH significantly reduced the impact on our other health care delivery and patient operations. DHCPP at CDC provided critical help to the unit for viral loads, specialized assays, and other support.
Special Challenges of Addressing EVD
Different outside perspectives and guidance were initially provided about the level of biosafety needed for EVD. Ebola viruses have a very low infectious dose, 1–10 aerosolized organisms, in nonhuman primate models  and can reach extremely high levels in blood (up to 1010 RNA copies per ml of serum ), stool, sweat, and other body secretions. Exposure of health care workers to infected body fluids via emesis, sweat, urine, saliva, diarrhea, or blood is a significant concern. There was also initial concern that this strain was not behaving epidemiologically as expected and the personal protective equipment (PPE) guidelines in Africa were not fully effective in prevention of transmission. Further, we had to demonstrate our ability to safely manage these patients.
To achieve the lowest risk to health care personnel, the highest level of biosafety was initially employed. This included MAXAIR powered air-purifying respirators (PAPRs), fluid-resistant body suits along with cover aprons, double gloves and shoe covers, and wiping down all surfaces with US Environmental Protection Agency (EPA)-registered disinfectants (no spraying) when doffing PPE. Other key biosafety SOPs developed were autoclaving within the unit for waste management, followed by disposal of regulated medical waste off-site after it had been autoclaved; decontamination; and handling of laboratory samples and waste. The consequences of transmission stressed the need for the highest level of biosafety.
The importance of the EHSO office in reinforcing the prior training of personnel and monitoring the clinical staff for consistency and adherence to biosafety from training sessions to practices in real-time clinical care cannot be overemphasized. This included how to “don and doff” impermeable fluid-resistant body suits, proper use of PAPRs, coordination of the disposal of waste, and the handling and transport of lab samples. EHSO also helped prepare and support the team psychologically, challenging them with spills and other incidents to practice remaining calm in the face of potential unexpected occurrences. Team engagement demonstrated the importance of melding the philosophies of clinical treatment/practice and biocontainment/biosafety. Feedback from frontline physicians, nurses, and hospital staff highlighted the contributions of EHSO to the effort and the value of the EHSO biodefense education and training expertise.
Waste management for EVD is a significant hurdle. EVD results in copious amounts of vomit and diarrhea with up to 10 liters of fluid lost by patients each day. Up to 40 large “bags” per day of regulated medical waste were generated by our first two patients. A large-capacity autoclave was mobilized, with postautoclaved waste stored in 32-gallon leak-proof rubber waste containers in the SCDU until removal and incineration. All waste in toilets was disinfected with an EPA-registered disinfectant before flushing. Importantly, no traces of Ebola RNA on "high-touch surfaces" such as beds and bathrooms were detected during active care or after patient discharge prior to terminal decontamination with vaporized hydrogen peroxide.
Guiding principles for communications included consistent messaging and protecting patient privacy while educating the public. Internal communications with a focus on transparency and education, within the bounds of confidentiality of medical information and protecting our patients’ privacy, were vital. These included meetings with EUH hospital leadership and staff to address concerns, frequent emails and other communications with all faculty and staff at EHC and Emory, making sure instructions/checklists were in place, and facilitating the dissemination of protocols. To avoid unauthorized access to electronic medical records, a chart-warning flag was implemented. Confidentiality of medical information regulations were repeatedly stressed to all medical staff, residents, and fellows.
In external communications and interface with the media, the Emory communications teams tirelessly addressed media logistics, developed web and social media material, worked closely with governmental and nongovernmental external groups, developed talking points, and prepared the hospital and SCDU teams for communications venues. To maximize our preparedness and to address national concerns, press conferences and media interviews were conducted, and an EVD Questions and Answers document was developed and posted. The story exploded in broadcast print and social media. Over 84,000 media stories have been written linking Emory and Ebola. Emory communications created an Emory Healthcare Ebola Preparedness Protocols website (www.emoryhealthcare.org/ebolaprep)  to make our clinical and biosafety protocols and other information widely available to the public. To date, 20,267 registrants have downloaded these educational materials.
Addressing a Surge of Cases of Possible Ebola
The admissions heightened Ebola and other bio-threat concerns both locally and nationally. Questions about potential EVD patients began to occur immediately in our health care system and throughout the US. We developed and disseminated flow diagrams, algorithms, and SOPs  for evaluating patients in emergency rooms and other health care provider settings where EVD was a consideration. CDC guidelines as they became available and current EVD articles were also disseminated. Our teams engaged local, regional, state, and national health care groups, and guidance was provided to questions about travelers from the region coming to Emory, to airlines flying to West Africa, and to multinational corporations based in West Africa. Travelers’ diarrhea with fever and malaria are the problems most commonly encountered by travellers to West Africa. However, yellow fever along with Lassa fever, endemic in West Africa as well, can cause similar symptoms to those of Ebola. Typhoid and less frequently diseases such as dengue and other viral syndromes can cause such signs/symptoms, though not usually as severe. The intersection of the seasonal influenza epidemic with returning CDC workers from West Africa further amplified the evaluations of febrile episodes. Timely initial screening—with establishment of contact and droplet precautions early while the risk assessment, including an extensive travel history and the evaluation of exposure risk and symptoms, was continued—was emphasized. Policies and procedures for the continuing care of our discharged patients were also developed .
Disseminating Knowledge: Education and Training
As noted, a highly trained group of faculty, nurses, biosafety support, and other providers staff the EUH SCDU. While no trainees (e.g., fellows, residents, or students) served on the direct care team, trainees benefitted from the experience of the unit and clinical experience with EVD through conferences and other education venues (e.g., Public Health Grand Rounds and ID seminars). An EVD “Micro Vignette” and other educational materials were developed for resident and fellow education. Further, ID and other specialty fellows have been integrated into the management planning for EVD patients, educated on the broader policies and procedures of the unit, are involved with the development of protocols for the management of Ebola patients who present to the Emergency Department (ED) or other clinical settings, and are educated about the collective experiences in treating the patients. In addition, a Massive Open Online Course (MOOC) “Ebola at Emory: Patients to Populations” has been launched , an EBOLA Academic Learning Community was established, and other efforts to educate and support graduate and undergraduate student activities were undertaken. Emory faculty and staff also actively participate in national education and training efforts, including multiple presentations at national meetings, engagement in training forums sponsored by the CDC and the US Department of Health and Human Services (HHS), writing publications and communications, and conducting press conferences. Fifty-five US hospitals, including many in academic medical centers, have now been designated as Ebola treatment centers.
Generating New Knowledge
Work was initiated to better understand EVD pathogenesis and therapeutic options [7–11,15–19], including optimal patient management, fluid and electrolyte replacement, and dialysis [7–8]; evaluation of concomitant infections (e.g., malaria or Lassa fever); levels of EVD viremia, monitoring viral RNA in body sites  and environmental samples; tracking EVD specific immune responses ; evaluation of available investigational drugs and their safety, risks, and benefits; options for immune therapy (monoclonal antibodies [mAbs], convalescent sera) and available supplies; available investigational vaccines [2,18], best practices in clinical operational management; and postexposure prophylaxis. In addition, the generation of new knowledge about EVD biosafety, infection control, and waste management has resulted from this event. These activities have now expanded as a broader institutional effort that includes new drug discovery for EVD, generation of human Ebola mAbs, expanded study of EVD glycobiology, focus on biomarkers as correlates of clinical EVD outcome, work on the ecology and the emergence of EVD and other tropical-associated zoonoses, clinical trials of Ebola vaccine, and modeling the spread and control of EVD in West Africa. This work required close coordination with and the support of the Emory Institutional Review Board (IRB), collaboration with the FDA, establishment of emergency investigational new drugs (INDs), and work with drug and biologic manufacturers and with multiple other governmental agencies. These and other EVD research and scholarly projects generated by the decision continue at Emory.
The event also led to broad faculty engagement across all parts of the institution through the creation of an Emory Ebola Task Force and Ebola Faculty and Community Discussion Forum . The Task Force includes leaders from across the campus and is directed at facilitating cross-cutting institutional initiatives such as EVD research, education and training activities, input into public policy issues around EVD, development of an institutional travel policy to West Africa, establishing procedures for trainee involvement in Ebola care, and the support of the humanitarian, research and control efforts in West Africa.
EVD has arrived in North America and Europe and impacted us globally. Academic medical centers can be expected to be at the frontline to address EVD and other highly communicable infectious agents in the future. Our experience (Box 4) with EVD emphasized prepared infrastructure and coordination of clinical care, hospital and emergency operations, transportation, infection control, biocontainment, communications, and education and training initiatives. Unanticipated major challenges can be expected. The importance of detailed planning, preparedness, and team work across multiple academic and health care units, the emphasis on biosafety, key partnerships with environmental health and safety and institutional communications, and working closely with governmental agencies and outside collaborators to manage these threats is highlighted.
Box 4. Key Lessons and Recommendations
Communicable infectious diseases will continue to be global threats to human health and have the potential to cause repeated humanitarian disasters.
Our experience as an academic health center with EVD emphasized the importance of preparation, communications, and implementation:
Coordination, detailed planning, and teamwork across governmental, nongovernmental, academic, and health care units
Preparedness in training, biosafety, surveillance, and communications
Environmental Health and Safety as a key support team member
Evaluation of provider competency in biosafety
Donning and doffing of PPE
Waste management protocols
Decontamination and containment protocols
Specimen handling for diagnostic testing
An organizational structure to solve unanticipated challenges and the logistics of working closely together
The rapid dissemination of best practice information
Providing education forums and frequent educational communications (both internal and external) around disease transmission and risk
Consistent messaging and protecting patient privacy while educating the public
Expanding new knowledge about the clinical course, complications and pathogenesis, diagnosis, treatment, and prevention
Engagement in the broader policy issues of global health care inequities
The institutional experience, while providing the opportunity to effectively care for these individuals, has led to best practice information and the education and training of others, created key academic, governmental, and community partnerships, expanded research programs in EVD, and resulted in the development and communication of new knowledge about this emerging disease. Mobilizing our diverse academic community to work collaboratively on this global problem is also an important long-term outcome.
2. WHO Ebola Outbreak. http://www.who.int/csr/disease/ebola/en/
3. Baize S, Pannetier D, Oestereich L, et al. Emergence of Zaire Ebola virus disease in Guinea. N Engl J Med 2014; 371:1418–1425. doi: 10.1056/NEJMoa1404505 24738640
4. Meltzer MI, Atkins CY, Santibanez S, Knust B, Petersen BW, Ervin ED, Nichol, ST, et al. Estimating the Future Number of Cases in the Ebola Epidemic—Liberia and Sierra Leone, 2014–2015. MMWR September 26, 2014; Supplement 1–14.
5. WHO Ebola Response Team. Ebola Virus Disease in West Africa—The First 9 Months of the Epidemic and Forward Projections. N Engl J Med 2014; 371:1481–1495. doi: 10.1056/NEJMoa1411100 25244186
6. Centers for Disease Control and Prevention. CDC Ebola Outbreak in West Africa—Case Counts. http://www.cdc.gov/vhf/ebola/outbreaks/2014-west-africa/case-counts.html
7. Lyon GM, Mehta AK, Varkey JB, Brantly K, Plyler L, McElroy AK, et al. Clinical Care of Two Patients with Ebola Virus Disease in the United States. N Engl J Med 2014; 371(25):2402–2409. doi: 10.1056/NEJMoa1409838 25390460
8. Connor MJ Jr, Kraft C, Mehta AK, Varkey JB, Lyon GM, Crozier I, et al. Successful Delivery of RRT in Ebola Virus Disease. J Am Soc Nephrol 2014 26:31–37. doi: 10.1681/ASN.2014111057 25398785
9. Hill CE, Burd EM, Kraft CS, Ryan EL, Duncan A, Winkler AM, et al. Laboratory test support for ebola patients within a high-containment facility. Lab Med 2014; 45(3):e109–11. doi: 10.1309/LMTMW3VVN20HIFS 25184220
10. Smith EL, Rice KL, Feistritzer NR, Hill C, Vanairsdale S, Gentry J. Care of patients with ebola virus disease. J Contin Educ Nurs 2014 Nov; 45(11):479–81. doi: 10.3928/00220124-20141027-12 25365183
11. Fox J, Bornstein B, Grant S (2015) Emory Healthcare Ebola Preparedness Protocols. www.emoryhealthcare.org/ebolaprep
12. Franz DR, Jahrling PB, Friedlander AM, McClain DJ, Hoover DL, Bryne WR, et al. Clinical recognition and management of patients exposed to biological warfare agents. JAMA 1997; 278(5), 399–411. 9244332
13. Towner JS, Rollin PE, Bausch DG, Sanchez A, Crary SM, Vincent M, et al. Rapid Diagnosis of Ebola Hemorrhagic Fever by Reverse Transcription-PCR in an Outbreak Setting and Assessment of Patient Viral Load as a Predictor of Outcome. J. Virol 2004; 78: 4330–4341. 15047846
14. Evans DP, del Rio C (2015) Ebola Virus Disease: An Evolving Epidemic. https://www.coursera.org/course/ebola
15. Kraft CS, Hewlett AL, Koepsell S, Winkler AM, Kratochvil CJ et al. The Use of TKM-100802 and convalescent plasma in 2 patients with Ebola virus disease in the United States. Clin Infect Dis. 2015 Apr 22. pii: civ334. Epub ahead of print.
16. Moreno CC, Kraft CS, Vanairsdale S, Kandiah P, Klopman MA et al. Performance of Bedside Diagnostic Ultrasound in an Ebola Isolation Unit: The Emory University Hospital Experience. Am J Roentgenol 2015; 204: 1157–1159.
17. McElroy AK, Akondy RS, Davis CW, Ellebedy AH, Mehta AK, et al. Human Ebola Virus Infection Results in Substantial Immune Activation. Proc Natl Acad Sci USA 2015; 112: 4719–4724. doi: 10.1073/pnas.1502619112 25775592
18. Lai L, Davey R, Beck A, Xu Y, Suffredini AF et al. Emergency Postexposure Vaccination with Vesicular Stomatitis Virus-vectored Ebola Vaccine after Needlestick. JAMA 2015; 313: 1249–55. doi: 10.1001/jama.2015.1995 25742465
19. Varkey JB, Shantha JG, Crozier I, Kraft CS, Lyon GM al. Persistence of Ebola Virus in Ocular Fluid during Convalescence N Engl J Med 2015; 372: 2423–2427.
20. Emory University (2015) Ebola Faculty and Community Discussion Forum. http://www.idn.emory.edu/resources/events/eboladiscussion.html