lunes, 20 de octubre de 2014

Ahead of Print -Health Care Response to CCHF in US Soldier and Nosocomial Transmission to Health Care Providers, Germany, 2009 - Volume 21, Number 1—January 2015 - Emerging Infectious Disease journal - CDC

Ahead of Print -Health Care Response to CCHF in US Soldier and Nosocomial Transmission to Health Care Providers, Germany, 2009 - Volume 21, Number 1—January 2015 - Emerging Infectious Disease journal - CDC

CDC. Centers for Disease Control and Prevention. CDC 24/7: Saving Lives. Protecting People.

Volume 21, Number 1—January 2015


Health Care Response to CCHF in US Soldier and Nosocomial Transmission to Health Care Providers, Germany, 2009

Nicholas G. CongerComments to Author , Kristopher M. Paolino, Erik C. Osborn, Janice M. Rusnak, Stephan Günther, Jane Pool, Pierre E. Rollin, Patrick F. Allan, Jonas Schmidt-Chanasit, Toni Rieger, and Mark G. Kortepeter1
Author affiliations: Landstuhl Regional Medical Center, Landstuhl, Germany (N.G. Conger, E.C. Osborn, J. Pool, P.F. Allan)Walter Reed Army Institute of Research, Silver Spring, Maryland, USA (K.M. Paolino)Force Health Protection, Fort Detrick, Maryland, USA (J.M. Rusnak)Bernard Nocht Institute, Hamburg, Germany (S. Günther, J. Schmidt-Chanasit, T. Rieger)Centers for Disease Control and Prevention, Atlanta, Georgia, USA (P. Rollin);Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA (M.G. Kortepeter)


In 2009, a lethal case of Crimean–Congo hemorrhagic fever (CCHF), acquired by a US soldier in Afghanistan, was treated at a medical center in Germany and resulted in nosocomial transmission to 2 healthcare providers (HCPs). After his arrival at the medical center (day 6 of illness) by aeromedical evacuation, the patient required repetitive bronchoscopies to control severe pulmonary hemorrhage and renal and hepatic dialysis for hepatorenal failure. After showing clinical improvement, the patient died suddenly on day 11 of illness from cerebellar tonsil herniation caused by cerebral/cerebellar edema. The 2 infected HCPs were among 16 HCPs who received ribavirin postexposure prophylaxis. The infected HCPs had mild or no CCHF symptoms. Transmission may have occurred during bag-valve-mask ventilation, breaches in personal protective equipment during resuscitations, or bronchoscopies generating infectious aerosols. This case highlights the critical care and infection control challenges presented by severe CCHF cases, including the need for experience with ribavirin treatment and postexposure prophylaxis.
Crimean–Congo hemorrhagic fever (CCHF) is a life-threatening viral illness endemic to areas of Africa, southeastern Europe, Russia, China, India, and the Middle East. CCHF is caused by infection with a tickborne virus (family Bunyaviridae, genus Nairovirus), and is generally acquired through the bite of an infected tick or contact with blood or body fluids of infected animals (13). The disease is characterized by the abrupt onset of a febrile illness usually 2–7 d (range 2–14) after exposure to the virus and by subsequent severe changes in mental status, hemorrhagic manifestations, and hepatorenal failure (1,4). Case-fatality rates vary by region but are 30%–50% (range 1%–73%) in most regions; death generally occurs 5–14 d after symptom onset and is most commonly due to multi-organ failure, shock, severe anemia, cerebral hemorrhage, and/or pulmonary edema (1,5).
We report a fatal case of CCHF in a US soldier deployed to Afghanistan, who was aero-evacuated to Germany for treatment, and the documented nosocomial infection of 2 health care providers (HCPs) who were at risk for exposure and had received ribavirin postexposure prophylaxis (PEP). We also review infection control interventions and contact surveillance, both of which were required because of the patient’s severe bleeding and the risk for aerosol production. Research on human subjects was conducted in compliance with US Department of Defense, federal, and state statutes and regulations relating to the protection of human subjects and adheres to the principles identified in the Belmont Report (1979;

The Case

On 8 September 2009, a 22-year-old male US soldier who worked in field operations outside Kandahar City, Afghanistan, sought care at a military medical clinic for a 4-d history of nonbloody diarrhea, abdominal pain, bloody emesis, and fever (39.2°C). The patient reported frequent outdoor activities, tick bites, and exposure to undercooked goat meat and blood the week before the onset of illness. Ciprofloxacin was prescribed for probable gastroenteritis. The patient did not improve by the next day and returned to the clinic, reporting somnolence and lethargy. He was transferred to a Combat Support Hospital at Kandahar Air Base.
Admission laboratory values demonstrated anemia, thrombocytopenia, acute renal insufficiency, and elevated levels of hepatic transaminases. Within a few hours of admission, the patient had worsening lethargy; bloody diarrhea; gingival bleeding; hypoxia requiring intubation; and a hypotensive episode after intubation, which required vasopressor therapy for 24 h. The patient was treated with intravenous levofloxacin (replaced ciprofloxacin), meropenem, fresh-frozen plasma (6 U), platelets (2 U), packed erythrocytes (2 U), and infusions of furosemide and pantoprazole.
On September 10, the patient was emergently aero-evacuated to Landstuhl Regional Medical Center (LRMC; Landstuhl, Germany). During the flight, his respiratory status deteriorated (requiring 100% FiO2) and he continued to bleed from multiple sites (nares, gingiva, gastrointestinal, and venipuncture sites). Treatment on route included fresh-frozen plasma (6 U), packed erythrocytes (1 U), and cold-water lavage to decrease upper gastrointestinal bleeding.
The patient arrived at LRMC on September 11 (day 6 of illness); he was in multiorgan, failure and large amounts of bright red blood were in the endotracheal tube. During the initial physical examination, he exhibited respiratory compromise, temperature of 37.3°C, blood pressure of 147/74 mm Hg (reference values for clinical/laboratory values are in Table 1), pulse rate of 118 beats/min, and 90% saturation on 100% oxygen. Significant findings included edematous conjunctivae with mild hemorrhage; nasopharyngeal bleeding; coarse breath sounds; large ecchymoses at venipuncture sites; scattered petechiae on the trunk, arms, and upper thighs; extensive edema of the extremities and scrotum; and melena on rectal examination. Emergent bronchoscopy revealed diffuse bleeding in the airways. Admission laboratory and radiography results (Table 1) supported a presumptive diagnosis of CCHF, and infection control measures for possible viral hemorrhagic fever (VHF) were implemented (9).
On day 7 of illness, reverse transcription PCR (RT-PCR) of a serum sample obtained at admission showed a CCHF viral load of 1.2 × 109 copies/mL (CCHF virus was later isolated from blood and urine samples obtained on day 6 of illness; CCHF IgM and IgG serologic results were negative on day 6 of illness) (Table 1). Oral and then intravenous ribavirin therapy were initiated; the intravenous ribavirin was administered within 24 h of admission and under an Investigational New Drug protocol after the patient’s family gave consent (Table 1) (3,10). Treatment with the broad-spectrum antibiotics was discontinued. Repetitive emergency bronchoscopy was required to control severe pulmonary hemorrhage.
On day 8 of illness, the patient’s pulmonary status continued to deteriorate: development of adult respiratory distress syndrome required placement of bilateral chest tubes to drain bloody pleural effusions, administration of nitric oxide, and use of advanced inverse ratio bilevel mechanical ventilation. The severe adult respiratory distress syndrome was complicated by massive pulmonary hemorrhaging that required multiple bronchoscopies and infusion of blood products (packed erythrocytes [32 U], fresh frozen plasma [80 U], platelets [34 packs], factor VII [4 U], and cryoprecipitate [3 U]). Tris (hydroxymethyl) amino methane and continuous hemodialysis were initiated for progressive renal failure and severe acidosis (serum creatinine 8.2 mg/dL, bicarbonate 12 mmol/L), and multiple boluses of glucose were given for recurrent hypoglycemia.
On day 9 of illness, the patient’s oxygenation and blood product transfusion requirements lessened, but hypoglycemia and acidosis persisted; a bicarbonate drip was initiated. Because fulminant hepatic failure occurred (aspartate aminotransferase 9,628 U/L, alanine aminotransferase 2,151 U/L, total bilirubin 8.1 mg/dL), liver dialysis was initiated by using a liver albumin dialysis machine. Early on day 11 of illness, liver dialysis was discontinued because the patient's condition appeared to be stabilizing (serum viral load and hepatic transaminases were decreasing, and less ventilatory support and fewer blood product transfusions were required). However, neurologic examination later that morning showed bilateral fixed and dilated pupils, and before brain imaging was possible, the patient suffered a cardiorespiratory arrest. A postmortem computer tomographic scan image demonstrated diffuse cerebral and cerebellar edema, a small right frontal parenchymal hemorrhage, and bilateral cerebellar tonsil herniation.

Hospital Infection Control

Because a CCHF diagnosis was not considered likely at the time of the initial 2 emergency bronchoscopies, standard precautions for infection control were used. The 2 bronchoscopists wore a gown, gloves, eye protection, and surgical masks; other persons in the room wore N95 respirators or surgical masks. More stringent infection control measures for VHFs, including airborne precautions, were implemented once a diagnosis of CCHF was considered (5) (Table 2). The patient was placed in an airborne-infection isolation room with an anteroom, which had restricted visitation and intensive care unit (ICU) entry. Sign-in sheets tracked who entered the patient’s room; those entering were required to wear a fluid-resistant gown, gloves, N95 respirator, eye protection/face shield, and shoe coverings. Biohazard suits (Tyvek; DuPont, Richmond VA, USA) with powered air-purifying respirators were worn during subsequent bronchoscopies and chest tube placement. Infection prevention and control staff provided refresher training on the proper donning and doffing of personal protective equipment (PPE) and oversaw the decontamination of bronchoscopes and ventilators. The procedures for disposing of medical wastes were in accordance with German regulations for handling infectious biohazardous materials (Table 2).
Laboratory interventions involved limiting blood draws and analyses to the most critical samples and to a single laboratory technician. Laboratory personnel wore gowns, gloves, and N95 respirators. Centrifugation of specimens was performed within a Class II biosafety cabinet. Laboratory equipment was decontaminated immediately after use and all nonreusable equipment was autoclaved before disposal. Blood and urine samples were pretreated with polyethylene glycol (to reduce viral load) before being shipped to Bernard Nocht Institute (Hamburg, Germany) for CCHF diagnostic testing. The cadaver was placed in 2 sealed body bags; the outside of each bag was decontaminated with a 10% bleach solution. RT-PCR analysis of deep cadaver tissue samples was performed after embalming and confirmed to be negative. Bleach (10%) or standard hospital-grade disinfectants were used for terminal cleaning of the patient’s room and all surfaces and equipment in the airplane used to aero-evacuate the patient to Germany.

Outbreak Investigation

Contact tracing commenced immediately after diagnosis and included a wide group of persons who may have been at risk for exposure to the patient’s blood/body fluids: personnel in the patient’s deployed unit, persons at the Combat Support Hospital in Kandahar, the medical evacuation team, and persons at LRMC (HCPs, laboratory workers, and transport, housekeeping, and volunteer staff). Among these contacts, 18 HCPs were identified as having been at risk for exposure and were offered oral ribavirin PEP (off-label use); 16 of the 18 accepted treatment (Table 3). Most of the 18 HCPs were present during bronchoscopies or ventilation procedures that used a bag-valve-mask device and had reported blood splashes on their gowns. Although there were no known percutaneous exposures, 2 HCPs reported blood on intact skin. Also, some HCPs wore only a surgical mask as PPE during the initial bronchoscopies and/or were unsure if they had always maintained a properly fitted N95 respirator during subsequent bronchoscopies. The group of 16 HCPs who accepted ribavirin PEP included a medic in Kandahar who had a blood exposure on his ungloved hand during an emergency intravenous catheter insertion and a physician in Kandahar who emergently intubated the patient without wearing an N95 respirator. The group also included an LRMC ICU nurse and respiratory therapist, both of whom had met the patient on arrival at LRMC and manually ventilated him during transport to the ICU without wearing a mask or eye protection; during the transport, the patient was actively bleeding from intravenous catheter sites and coughing blood into the endotracheal tube. These 2 HCPs (and others) were also present during the initial 2 bronchoscopies, during which they may not have worn surgical masks at all times (and no eye protection) and their gowns had been soaked from blood exposures. In addition, the respiratory therapist’s face shield dislodged immediately after being sprayed with blood while she was manually ventilating the patient using a bag-valve-mask device during a life-threatening hypoxic event. The ICU nurse also had blood contact on her skin (wrist) during resuscitation, when her gown sleeve slipped from the glove. The respiratory therapist and ICU nurse were also among the HCPs, aside from a few physicians, who spent the most time directly caring for the patient. The remaining 72 personnel had unlikely/no identifiable exposure risk and were instructed to have their temperatures taken twice daily for 15 d and to contact the infectious diseases physician for any febrile illness within this same time period (Table 3).
An oral ribavirin PEP regimen of 600 mg twice daily for 7 d was recommended initially; this dosage was based on drug availability, drug tolerance, and dosage regimens reported in the literature (3). Seventy-two hours later, a more oral ribavirin became available, and the 16 HCPs were offered a 4-times-daily dosing regimen (600 mg/dose) and/or extension of PEP from 7 to 14 d. Because of the drug’s side effects, all HPCs chose to remain on a twice-daily dosing regimen; only 2 HCPs accepted an extension of PEP to 14 d. Side effects (mainly fatigue, dyspepsia, nausea, and headache) were reported by all 16 HCPs. Of the 12 HCPs compliant with blood draws, 10 showed an increase in total bilirubin (range 1.2–5.7 mg/dL) and 2 had mild anemia (nadir hemoglobin 11.9 g) attributed to hemolysis caused by ribavirin. Leukopenia was observed in 1 HCP (leukocyte count 2,800 cells/mm3).
To assess possible seroconversion in the patient’s contacts, initial and follow-up (4–6 wk) blood samples were obtained from personnel in the patient’s deployment unit (n = 62), persons at the Combat Support Hospital in Kandahar (n = 55), and persons at LRMC (n = 74) and sent for serologic testing at the Centers for Disease Control and Prevention (Atlanta, GA, USA) (11). Although baseline serologic testing was not done, results of serologic testing done at 8 weeks for 2 HCPs who received oral ribavirin PEP (the ICU nurse and the respiratory therapist at LRMC) were consistent with acute CCHF seroconversion: CCHF virus–specific IgM and IgG titers were >6,400, and over the next 2 mo, IgM titers declined (Table 3). These 2 HCPs were the most symptomatic of the 16 persons who received ribavirin PEP, and the only persons to seek medical attention for their symptoms. Symptoms were initially noted 4–5 d after exposure (day 4 of ribavirin PEP). The ICU nurse had moderate abdominal discomfort and jaundice (total bilirubin of 5.7 mg/dL; direct bilirubin 0.2 mg/dL; reference values for alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, leukocytes, and platelets). The respiratory therapist experienced fatigue, myalgias, and chills (no documented fever). She had a reference bilirubin level and mild leukopenia (leukocytes decreased from 4,200 cells/mm3 to 2,800 cells/mm3), and she missed 3 d of work because of her symptoms. For both HCPs, the symptoms and laboratory abnormalities were initially attributed to side effects of ribavirin therapy (particularly the elevated bilirubin level and gastrointestinal discomfort); in retrospect, the respiratory therapist’s symptoms most likely represented CCHF symptoms ameliorated by ribavirin PEP. Ameliorated CCHF as a cause of symptoms in the ICU nurse could not be excluded.


This fatal case of CCHF in a US soldier illustrates several issues regarding clinical management, infection control measures, epidemiologic investigation, and ribavirin PEP in CCHF infection. Early recognition and diagnosis of CCHF is paramount, so that medical care and appropriate infection control measures can be implemented in the initial phase of illness and, thereby, improve survival and prevent nosocomial transmission. Delayed diagnosis and implementation of infection control measures can result in the need for extensive public health resources to evaluate and follow up on exposed HCPs and contacts (1217).
The greatest risk for nosocomial transmission of the CCHF virus has been from percutaneous exposure with contaminated needles. Blood exposure on intact skin is a much lower risk, but sporadic transmission has been reported after skin or mucosal exposures to infectious blood. Nosocomial infection has also been reported without a clear source of virus transmission, and possible droplet (patient-to-patient) transmission has been reported (3).
Bronchoscopies and other procedures producing infectious aerosols were potential sources of CCHF virus transmission to the 2 HCPs reported here; however, no other HCPs who were present during the initial 2 bronchoscopies showed seroconversion. Thus, it is probable that virus transmission resulted from exposure to infectious blood during initial transport of the patient to the ICU, when neither HCP wore proper PPE (surgical mask/N95 respirator) while manually ventilating the patient or from a breach in PPE (particularly, for 1 HCP when her face shield dislodged during a resuscitation procedure). Of concern, both HCPs were unaware of their PPE breaches/exposures during resuscitation efforts; they were noted by other HCPs. The PPE breaches and potential blood/body fluid exposure risks led to the use of biohazard suits and powered air-purifying respirators during subsequent bronchoscopies and chest-tube placements. Compared with face shields, powered air-purifying respirators are less likely to become dislodged. The 2005 Centers for Disease Control and Prevention’s modified PPE guidelines for suspected VHFs at US hospitals note that extenuating circumstances (i.e., procedures generating aerosols, severe pulmonary involvement, or copious bleeding) may necessitate an increase in PPE (i.e., plastic aprons, leg/shoe coverings) or airborne precautions (9).
The processing of serum specimens with high viral loads in analyzers outside the Class II biosafety cabinet in a non–negative-pressure laboratory was a concern. Pretreatment of specimens to reduce viral load (i.e., with heat inactivation or polyethylene glycol) will be recommended in future cases, even though such treatment may affect laboratory results (9,18). Also, the CCHF virus has been detected in urine by RT-PCR as late as day 36 after illness onset; however, infectivity has been unclear because the virus had not been previously cultured from urine (19,20). The culture of the CCHF virus in patient samples obtained on day 6 of illness indicates that a positive RT-PCR result for urine may represent viable virus and the potential for late transmission of virus by patients who have recovered from CCHF.
Ribavirin, a synthetic purine nucleoside analog, has demonstrated in vitro activity against CCHF virus and decreased death rates in infected suckling mice (3). Ribavirin efficacy in humans has not been evaluated in placebo-controlled trials against CCHF because of ethical concerns. However, retrospective analyses of ribavirin-treated CHHF virus–infected cohorts (compared with untreated historical controls) often report a decrease in CCHF-associated death if given within 72 h after the onset of symptoms (3). Anecdotal reports of ribavirin PEP in CCHF cases are limited, but they also suggest a possible benefit in preventing or ameliorating disease in most HCPs (2,3). However, the optimal dosage and duration of oral ribavirin for CCHF prophylaxis is unknown. PEP regimens in the literature range from 200 mg twice daily to as high as 4 g daily for 5–14 d; the most common regimen is 500 mg 3–4 times/d for 7-10 d. A 2-g loading dose is recommended in some regimens, particularly when treatment initiation is delayed (3,21). Drug side effects (mainly gastrointestinal intolerance and fatigue) often limit the dosage and duration of ribavirin PEP (3).
CCHF virus IgM and IgG titers in the 2 seropositive HCPs corresponded to acute infection from nosocomial transmission because these persons had no other risk factors for recent exposure to the virus. The mild/absent CCHF symptoms in these 2 HCPS who received a lower dose and duration of ribavirin PEP (600 mg twice daily for 7 d) may provide further insight regarding the potential benefit and dosage regimen for oral ribavirin PEP. The estimation of 88% of CCHF cases in Turkey being subclinical in a recent seroprevalence study would likely necessitate a controlled clinical trial to assess the efficacy and dose for ribavirin PEP (22).
On arrival at LRMC (day 6 of illness), the patient had a poor prognosis for survival: ribavirin treatment had been delayed >4 d after symptom onset; he was somnolent; and he had severe bleeding and coagulopathy, significantly elevated levels of hepatic transaminases, a platelet count of <20,000/mm3, and a serum viral load of >1 × 108 copies/mL (4,2328). However, with supportive care, the patient showed clinical improvement (i.e., improved respiratory status, decreased bleeding and blood product requirements, and improved end-organ function). Continuous renal replacement therapy was particularly helpful in controlling the patient’s life-threatening metabolic derangements; hepatic replacement therapy was of uncertain benefit and interfered with the optimal use of continuous renal replacement therapy. On day 10 of illness, the patient was able to follow commands, his serum viral load was declining, and CCHF-specific IgG was present.
There were multiple possible reasons for the fatal brain herniation on day 11 of illness. CCHF infection can cause endothelial cell dysfunction (with increased vascular permeability) through the induction of cytokines (tumor necrosis factor-α, interleukin-6, interleukin-10, interferon [IFN]-γ), which can result in cerebral edema (28,29). Increase in these cytokines and markers for increased endothelial cell permeability (i.e., vascular endothelial growth factor [VEGF]-A and soluble VEGF receptor 1) have been correlated with increased serum viral load and increased risk of death and/or severe CCHF disease (Table 2) (3036). In a similar VHF case (Marburg virus disease) with elevated levels of cytokine and soluble VEGF receptor 1 in which brain herniation occurred, the patient had cerebral edema that was not controlled with renal and hepatic dialysis, mannitol, and hypotonic saline (37). Other contributing factors for cerebral edema include possible direct effects of the virus in the brain and the combination of hepatic failure, persistent acidosis, and large osmotic shifts caused by dialysis; frontal lobe hemorrhage was not a significant factor because of its small size and location.
Severe CCHF has been attributed to a delayed IFN-α response in infected persons and to insensitivity of infected cells to the effects of the response (i.e., down-regulation of the host’s innate immune response) (38,39). The failure of ribavirin to prevent death in mice lacking type I IFN-α receptors (serum viral load was reduced, only delaying death), its poor ability to cross the blood–brain barrier, and its delayed initiation in this soldier, suggest a minimized effect of ribavirin against CCHF virus in this fatal case (3,40). However, a newer antiviral drug, favipiravir (a nucleoside analog also known as T-705), may offer promise as a future treatment option for CCHF. Mice lacking type I IFN-α receptors had no detectable CCHF-specific antibody if given favipiravir within 2 d of CCHF virus challenge, and all mice treated within 3 d of challenge survived with no detectable virus in the blood or organs (40).
This case of a soldier who died from CCHF illustrates the need to maintain an index of suspicion for CCHF and other VHFs in febrile travelers returning from VHF-endemic areas so that supportive care and appropriate infection control measures can be implemented early in the course of illness. This case highlights the critical care challenges in caring for a patient with severe CCHF and describes nosocomial CCHF virus infection in 2 HCPs who were receiving oral ribavirin PEP (600 mg twice daily). The 2 nosocomial infections stress the need for infection control policies that educate HCPs to use contact and droplet precautions (minimal requirements) when caring for patients presenting with fever and hemorrhage. In tertiary-care medical settings, procedures and emergency resuscitations performed on VHF patients with severe hemorrhage may pose risks for HCPs that are different from those in smaller hospitals in developing countries, where such procedures may not be available. Because the risk for aerosol production, splashing blood, and breaches in PPE (i.e., dislodged face shields, face masks, sleeve separation from gloves) is highest during resuscitative efforts, in this VHF case with severe hemorrhage, Tyvek suits with powered air-purifying respirators were indicated for the HCPs at highest risk for possible exposure to infectious materials (i.e., bronchoscopists). Although in this case, the potential antiviral effect of ribavirin may have been decreased because of late initiation of the drug and poor penetration of the blood–brain barrier, ribavirin may have contributed (along with CCHF IgG) to the patient’s improved clinical condition and decreased serum viral load. In addition, the probable CCHF virus seroconversion of 2 HCPs who had ameliorated or no symptoms after receiving ribavirin PEP may contribute further to the experience with and dosing regimen for ribavirin PEP in HCPs exposed to CCHF virus.
Dr. Conger is an active-duty officer in the US Air Force and board certified in infectious diseases and internal medicine. He is currently working as a master clinician at Wright-Patterson Medical Center, Wright-Patterson Air Force Base, and is the US Air Force's infectious diseases consultant.


We thank LCDR Stephan Olschlager and Petra Emmerich for assistance with virological diagnostics; the Force Health Protection Division, United States Army Medical Materiel Development Activity, Fort Detrick, Maryland, USA, for help with the investigational new drug treatment protocol for intravenous ribavirin; and Nancy Tang for her professional translation of the Chinese literature regarding hemorrhagic fevers.


  1. Bente DAForrester NLWatts DMMcAuley AJWhitehouse CACrimean–Congo hemorrhagic fever: history, epidemiology, pathogenesis, clinical syndrome and genetic diversity. Antiviral Res2013;100:15989DOIPubMed
  2. Erby A. Crimean–Congo hemorrhagic fever virus. In: Dongyou Liu, editor. Manual of security sensitive microbes and toxins. Boca Raton (FL): CRC Press; 2014. p. 37–52.
  3. Rusnak JM. Experience with ribavirin for treatment and postexposure prophylaxis of hemorrhagic fever viruses: Crimean Congo hemorrhagic fever, Lassa fever, and hantavirus [cited 2014 Sep 15].
  4. Swanepoel RGill DEShepherd AJLeman PAMynhardt JHHarvey SThe clinical pathology of Crimean–Congo hemorrhagic fever. Rev Infect Dis.1989;11:S794800DOIPubMed
  5. Karti SSOdabasi ZKorten VYilmaz MSonmez MCaylan RCrimean–Congo hemorrhagic fever in Turkey. Emerg Infect Dis2004;10:137984.DOIPubMed
  6. Wölfel RPaweska JTPetersen NGrobbelaar AALeman PAHewson RVirus detection and monitoring of viral load in Crimean–Congo hemorrhagic fever virus patients. Emerg Infect Dis2007;13:1097100DOIPubMed
  7. Lambert AJLanciotti RSConsensus amplification and novel multiplex sequencing method for S segment species identification of 47 viruses of theOrthobunyavirus, Phlebovirus, and Nairovirus genera of the family Bunyaviridae. J Clin Microbiol2009;47:2398404DOIPubMed
  8. Olschläger SGabriel MSchmidt-Chanasit JMeyer MOsborn EConger NGComplete sequence and phylogenetic characterisation of Crimean-Congo hemorrhagic fever virus from Afghanistan. J Clin Virol2011;50:902DOIPubMed
  9. Centers for Disease Control and Prevention (CDC). Interim guidance for managing patients with suspected viral hemorrhagic fever in US Hospitals;2005 19 May [cited 2014 Sept 11].
  10. World Health Organization. Application for inclusion of ribavirin in the WHO model list of essential medicines [2010 Sep 15].
  11. Khan ASMaupin GORollin PENoor AMShurie HHMShalabi AGAAn outbreak of Crimean–Congo hemorrhagic fever in the United Arab Emirates, 1994–1995. Am J Trop Med Hyg1997;57:51925 .PubMed
  12. Burney MIGhafoor ASaleen MWebb PACasals JNosocomial outbreak of viral hemorrhagic fever caused by Crimean hemorrhagic fever–Congo virus in Pakistan, January 1976. Am J Trop Med Hyg1980;29:9417 .PubMed
  13. Amorosa VMacNeil AMcConnell RPatel ADillon KEHamilton KImported Lassa fever, Pennsylvania, USA, 2010. Emerg Infect Dis.2010;16:1598600DOIPubMed
  14. Jauréguiberry STattevin PTarantola ALegay FTall ANabeth PImported Crimean–Congo hemorrhagic fever. J Clin Microbiol2005;43:49057.DOIPubMed
  15. Barry MRussi MArmstrong LGeller DTesh RDembry LTreatment of a laboratory-acquired Sabia virus infection. N Engl J Med.1995;333:2946DOIPubMed
  16. Timen AKoopmans MPVossen ACvan Doornum GJGunther Svan den Berkmortel FResponse to imported case of Marburg hemorrhagic fever, the Netherlands. Emerg Infect Dis2009;15:11715DOIPubMed
  17. World Health Organization. Global alert and response (GAR). Ebola virus disease, West – update. 2014 Jul 27[cited 4 Aug 2014].
  18. Bhagat CILewer MPrins ABeilby JPEffects of heating plasma at 56 degrees C for 30 min and at 60 degrees C for 60 min on routine biochemistry analytes. Ann Clin Biochem2000;37:8024DOIPubMed
  19. Bodur HAkinci EOnguru PCarhan AUyar YTanrici ADetection of Crimean–Congo hemorrhagic fever virus genome in saliva and urine. Int J Infect Dis2010;14:e2479DOIPubMed
  20. Thomas SThomson GDowall SBruce CCook NEasterbrook LReview of Crimean Congo hemorrhagic fever infection in Kosova in 2008 and 2009: prolonged viremias and virus detected in urine by PCR. Vector Borne Zoonotic Dis2012;12:8004DOIPubMed
  21. Keshtkar-Jahromi MSajadi MMAnsari HMardani MHolakouie-Naieni KCrimean–Congo hemorrhagic fever in Iran. Antiviral Res.2013;100:208DOIPubMed
  22. Bodur HAkinci EAscioglu SOnguru PUyar YSubclinical infection with Crimean–Congo hemorrhagic fever virus, Turkey. Emerg Infect Dis.2012;18:6402DOIPubMed
  23. Ozturk BTutuncu EKuscu FGurbuz YSencan ITuzun HEvaluation of factors predictive of the prognosis in Crimean–Congo hemorrhagic fever: new suggestions. Int J Infect Dis2012;16:e8993DOIPubMed
  24. Hatipoglu CABulut CYetkin MAErtem GTErdinc FSKilic EIEvaluation of clinical and laboratory predictors of fatality in patients with Crimean–Congo haemorrhagic fever in a tertiary care hospital in Turkey. Scand J Infect Dis2010;42:51621DOIPubMed
  25. Çevik MAErbay ABodur HGulderen EBastug AKubar AClinical and laboratory features of Crimean–Congo hemorrhagic fever: predictors of fatality. Int J Infect Dis2008;12:3749DOIPubMed
  26. Ozbey SBKader CErbay AErgonul OEarly use of ribavirin is beneficial in Crimean–Congo hemorrhagic fever. Vector Borne Zoonotic Dis.2014;14:3002DOIPubMed
  27. Onguru PDagdas SBodur HYilmaz MAkinci EEren SCoagulopathy parameters in patients with Crimean–Congo hemorrhagic fever and its relation with mortality. J Clin Lab Anal2010;24:1636DOIPubMed
  28. Saksida ADuh DWraber BDedushaj IAhmeti SAvsic-Zupanc TInteracting roles of immune mechanisms and viral load in the pathogenesis of Crimean–Congo hemorrhagic fever. Clin Vaccine Immunol2010;17:108693DOIPubMed
  29. Connolly-Andersen AMMoll GAndersson CAkerström SKarlberg HDouagi ICrimean–Congo hemorrhagic fever virus activates endothelial cells. J Virol2011;85:776674DOIPubMed
  30. Weber FMirazimi AInterferon and cytokine responses to Crimean Congo hemorrhagic fever virus; an emerging and neglected viral zoonosis.Cytokine Growth Factor Rev2008;19:395404DOIPubMed
  31. Ergonul OTuncbilek SBaykam NCelikbas ADokuzoguz BEvaluation of serum levels of interleukin (IL)-6, IL-10 and tumor necrosis factor-α in patients with Crimean–Congo hemorrhagic fever. J Infect Dis2006;193:9414DOIPubMed
  32. Papa ABino SVelo EHarxhi AKota MAntoniadis ACytokine levels in Crimean–Congo hemorrhagic fever. J Clin Virol2006;36:2726.DOIPubMed
  33. Ozturk BKuscu FTutuncu ESencan IGurbuz YTuzan HEvaluation of the association of serum levels of hyaluronic acid, sICAM-1, sVCAM-1, and VEGF-A with mortality and prognosis in patients with Crimean–Congo hemorrhagic fever. J Clin Virol2010;47:1159DOIPubMed
  34. Peyrefitte CNPerret MGarcia SRodriguez RBagnaud ALacote SDifferential activation profiles of Crimean–Congo hemorrhagic fever virus– and Dugbe virus–infected antigen-presenting cells. J Gen Virol2010;91:18998DOIPubMed
  35. Bodur HAkinci EOnguru PUyar YBasturk BGozel MGEvidence of vascular endothelial damage in Crimean–Congo hemorrhagic fever. Int J Infect Dis2010;14:e7047DOIPubMed
  36. Bakir MBakir SSari ICelik VKGozel MGEngin AEvaluation of the relationship between serum levels of VEGF and sVEGFR1 with mortality and prognosis in patients with Crimean–Congo hemorrhagic fever. J Med Virol2013;85:1794801DOIPubMed
  37. van Paassen JBauer MPArbous MSVisser LGSchmidt-Chanasit JSchilling SAcute liver failure, multiorgan failure, cerebral oedema, and activation of proangiogenic and antiangiogenic factors in a case of Marburg haemorrhagic fever. Lancet Infect Dis2012;12:63542.DOIPubMed
  38. Andersson ILundkvist AHaller OMirazimi AType I interferon inhibits Crimean–Congo hemorrhagic fever virus in human target cells. J Med Virol.2006;78:21622DOIPubMed
  39. Andersson IKarlberg HMousari-Jazi MMartinez-Sobrido LWever FMirazimi ACrimean–Congo hemorrhagic fever virus delays activation of the innate immune response. J Med Virol2008;80:1397404DOIPubMed
  40. Oestereich LRieger TNeumann MBernreuther CLehmann MKrasemann SEvaluation of antiviral efficacy of ribavirin, arbidol, and T-705 (favipiravir) in a mouse model for Crimean–Congo hemorrhagic fever. PLoS Negl Trop Dis2014;8:e2804DOIPubMed


Suggested citation for this article: Conger NG, Paolino KM, Osborn EC, Rusnak JM, Günther S, Pool J, et al. Health care response to CCHF in US soldier and investigation of nosocomial transmission to health care providers, Germany, 2009. Emerg Infect Dis. 2015 Jan [date cited].
DOI: 10.3201/eid2101.141413

1Preliminary results from this study were presented at the 1) Annual Meeting of the Armed Forces Infectious Disease Society; May 23, 2010, San Antonio, Texas, USA; 2) NATO Biomedical Advisory Committee; May 27, 2010, Munich, Germany; and 3) Asian Pacific Military Medicine Conference; May 3, 2011, Sydney, New South Wales, Australia.

No hay comentarios:

Publicar un comentario