TY - JOUR
T1 - Management and outcomes after multiple corneal and solid organ transplantations from a donor infected with rabies virus
AU - Maier, T.
AU - Schwarting, A.
AU - Mauer, D.
AU - Ross, R. S.
AU - Martens, A.
AU - Kliem, V.
AU - Wahl, J.
AU - Panning, M.
AU - Baumgarte, S.
AU - Müller, T.
AU - Pfefferle, S.
AU - Ebel, H.
AU - Schmidt, J.
AU - Tenner-Racz, K.
AU - Racz, P.
AU - Schmid, M.
AU - Strüber, M.
AU - Wolters, B.
AU - Gotthardt, D.
AU - Bitz, F.
AU - Frisch, L.
AU - Pfeiffer, N.
AU - Fickenscher, H.
AU - Sauer, P.
AU - Rupprecht, C. E.
AU - Roggendorf, M.
AU - Haverich, A.
AU - Galle, P.
AU - Hoyer, J.
AU - Drosten, C.
PY - 2010/4/15
Y1 - 2010/4/15
N2 - Background. This article describes multiple transmissions of rabies via transplanted solid organ from a single infected donor. The empirical Milwaukee treatment regimen was used in the recipients. Methods. Symptomatic patients were treated by deep sedation (ketamine, midazolam, and phenobarbital), ribavirin, interferon, and active and passive vaccination. Viral loads and antibodies were continuously monitored. Results. Recipients of both cornea and liver transplants developed no symptoms. The recipient of the liver transplant had been vaccinated ∼ 20 years before transplantation. Two recipients of kidney and lung transplants developed rabies and died within days of symptomatic disease. Another kidney recipient was treated 7 weeks before he died. The cerebrospinal fluid viral load remained at constant low levels (<10,000 copies/mL) for ∼5 weeks; it increased suddenly by almost 5 orders of magnitude thereafter. After death, no virus was found in peripheral compartments (nerve tissue, heart, liver, or the small intestine) in this patient, in contrast to in patients in the same cohort who died early. Conclusions. Our report includes, to our knowledge, the longest documented treatment course of symptomatic rabies and the first time that the virus concentration was measured over time and in different body compartments. The postmortem virus concentration in the periphery was low, but there was no evidence of a reduction of virus in the brain.
AB - Background. This article describes multiple transmissions of rabies via transplanted solid organ from a single infected donor. The empirical Milwaukee treatment regimen was used in the recipients. Methods. Symptomatic patients were treated by deep sedation (ketamine, midazolam, and phenobarbital), ribavirin, interferon, and active and passive vaccination. Viral loads and antibodies were continuously monitored. Results. Recipients of both cornea and liver transplants developed no symptoms. The recipient of the liver transplant had been vaccinated ∼ 20 years before transplantation. Two recipients of kidney and lung transplants developed rabies and died within days of symptomatic disease. Another kidney recipient was treated 7 weeks before he died. The cerebrospinal fluid viral load remained at constant low levels (<10,000 copies/mL) for ∼5 weeks; it increased suddenly by almost 5 orders of magnitude thereafter. After death, no virus was found in peripheral compartments (nerve tissue, heart, liver, or the small intestine) in this patient, in contrast to in patients in the same cohort who died early. Conclusions. Our report includes, to our knowledge, the longest documented treatment course of symptomatic rabies and the first time that the virus concentration was measured over time and in different body compartments. The postmortem virus concentration in the periphery was low, but there was no evidence of a reduction of virus in the brain.
UR - http://www.scopus.com/inward/record.url?scp=77950279991&partnerID=8YFLogxK
U2 - 10.1086/651267
DO - 10.1086/651267
M3 - Article
C2 - 20205588
AN - SCOPUS:77950279991
SN - 1058-4838
VL - 50
SP - 1112
EP - 1119
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 8
ER -