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1. Age- and Sex-Related Differences in Patients With Wild-Type Transthyretin Amyloidosis: Insights From THAOS

Author

Emdin, Michele, Hanna, Mazen, Azevedo, Olga, Lino Cirami, Calogero, Gonzalez Costello, Jose, Slosky, David, Moelgaard, Henning, Nativi Nicolau, Jose, Hummel, Scott, Jeon, Eun-Seok, Fine, Nowell, Murali, Srinivas, Miller, Edward, Shah, Sanjiv, Witteles, Ronald, Waddington-Cruz, Marcia, Lenihan, Daniel, Sekijima, Yoshiki, Van Cleemput, Johan, Correia, Edileide de Barros, Cariou, Eve, Quan, Dianna, Freimer, Miriam, Steidley, David, Hüsing-Kabar, Anna, Plante-Bordeneuve, Violaine, Nienhuis, Hans, Wixner, Jonas, Ralph, Jeffrey, Ventura, Hector, Zivkovic, Sasa, Delgado, Diego, Fernandéz Torrón, Roberto, Gottlieb, Stephen, Cotts, William, Tallaj, Jose, Brunkhorst, Robert, Polydefkis, Michael, Mueller, Christopher, Tschoepe, Carsten, Gonzalez Moreno, Juan, Sarswat, Nitasha, Luo, Jin, Tauras, James, Warner, Alberta, Mora-Ayestaran, Nerea, Dispenzieri, Angela, Kristen, Arnt V., Maurer, Mathew S., Diemberger, Igor, Drachman, Brian M., Grogan, Martha, Gupta, Pritam, Glass, Oliver, Amass, Leslie, and Garcia-Pavia, Pablo

Published
2024
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2. Temporal Trends of Wild-Type Transthyretin Amyloid Cardiomyopathy in the Transthyretin Amyloidosis Outcomes Survey

Author

Barroso, Fabio Adrian, Van Cleemput, Johan, Fine, Nowell, Schmidt, Hartmut, Gess, Burkhard, Moelgaard, Henning, Planté-Bordeneuve, Violaine, Adams, David, Inamo, Jocelyn, Vita, Giuseppe, Cirami, Calogero Lino, Luigetti, Marco, Emdin, Michele, Sekijima, Yoshiki, Yamashita, Taro, Jeon, Eun-Seok, Gonzalez Duarte Briseno, Maria Alejandra, Nienhuis, Hans, Azevedo, Olga, Campistol Plana, Josep Maria, Moreno, Juan Gonzalez, Costello, Jose Gonzalez, Wixner, Jonas, Parman, Yesim, Shah, Sanjiv, Quan, Dianna, Marburger, Tessa, Polydefkis, Michael, Gottlieb, Stephen, Ralph, Jeffrey, Sarswat, Nitasha, Luo, Jin, Murali, Srinivas, Cotts, William, Drachman, Brian, Steidley, David, Hummel, Scott, Slosky, David, Ventura, Hector, Jacoby, Daniel, Hoffman, James, Tauras, James, Zivkovic, Sasa, Tallaj, Jose, Lenihan, Daniel, Mueller, Christopher, Nativi-Nicolau, Jose, Siu, Alfonso, Dispenzieri, Angela, Maurer, Mathew S., Rapezzi, Claudio, Kristen, Arnt V., Garcia-Pavia, Pablo, LoRusso, Samantha, Waddington-Cruz, Márcia, Lairez, Olivier, Witteles, Ronald, Chapman, Doug, Amass, Leslie, and Grogan, Martha

Published
2021
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3. Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis: Insights From THAOS

Author

van Cleemput, Johan, Waddington-Cruz, Marcia, Schmidt, Hartmut, Dillmann, Klaus-Ulrich, Mølgaard, Henning, Moreno, Juan Gonzalez, Costello, Jose Gonzalez, Beamud, Francisco Munoz, Davila, Lucia Galan, Adams, David, Inamo, Jocelyn, Lairez, Olivier, Vita, Giuseppe, Merlini, Giampaolo, Cirami, Calogero Lino, Luigetti, Marco, Emdin, Michele, Sekijima, Yoshiki, Jeon, Eun-Seok, Oh, Jeeyoung, Gonzalez Duarte Briseno, Maria Alejandra, Nienhuis, Hans, Coelho, Teresa, Conceicao, Isabel, Azevedo, Olga, Badelita, Sorina, Press, Rayomand, Parman, Yesim, Shah, Sanjiv, Quan, Dianna, Marburger, Tessa, Polydefkis, Michael, Witteles, Ronald, Gottlieb, Stephen, Sarswat, Nitasha, Drachman, Brian, Steidley, David, Hummel, Scott, Slosky, David, Jacoby, Daniel, Nativi-Nicolau, Jose, Tauras, James, Zivkovic, Sasa, Tallaj, Jose, Lenihan, Daniel, Caponetti, Angelo Giuseppe, Rapezzi, Claudio, Gagliardi, Christian, Milandri, Agnese, Dispenzieri, Angela, Kristen, Arnt V., Wixner, Jonas, Maurer, Mathew S., Garcia-Pavia, Pablo, Tournev, Ivailo, Planté-Bordeneuve, Violaine, Chapman, Douglass, and Amass, Leslie

Published
2021
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4. Management and Outcomes of Cardiogenic Shock in Cardiac ICUs With Versus Without Shock Teams

Author

Papolos, Alexander I., Kenigsberg, Benjamin B., Berg, David D., Alviar, Carlos L., Bohula, Erin, Burke, James A., Carnicelli, Anthony P., Chaudhry, Sunit-Preet, Drakos, Stavros, Gerber, Daniel A., Guo, Jianping, Horowitz, James M., Katz, Jason N., Keeley, Ellen C., Metkus, Thomas S., Nativi-Nicolau, Jose, Snell, Jeffrey R., Sinha, Shashank S., Tymchak, Wayne J., Van Diepen, Sean, Morrow, David A., and Barnett, Christopher F.

Published
2021
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10. ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable

Author

Brannagan, III, Thomas H., Auer-Grumbach, Michaela, Berk, John L., Briani, Chiara, Bril, Vera, Coelho, Teresa, Damy, Thibaud, Dispenzieri, Angela, Drachman, Brian M., Fine, Nowell, Gaggin, Hanna K., Gertz, Morie, Gillmore, Julian D., Gonzalez, Esther, Hanna, Mazen, Hurwitz, David R., Khella, Sami L., Maurer, Mathew S., Nativi-Nicolau, Jose, Olugemo, Kemi, Quintana, Luis F., Rosen, Andrew M., Schmidt, Hartmut H., Shehata, Jacqueline, Waddington-Cruz, Marcia, Whelan, Carol, and Ruberg, Frederick L.

Published
2021
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12. Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner

Author

Gertz, Morie, Adams, David, Ando, Yukio, Beirão, João Melo, Bokhari, Sabahat, Coelho, Teresa, Comenzo, Raymond L., Damy, Thibaud, Dorbala, Sharmila, Drachman, Brian M., Fontana, Marianna, Gillmore, Julian D., Grogan, Martha, Hawkins, Philip N., Lousada, Isabelle, Kristen, Arnt V., Ruberg, Frederick L., Suhr, Ole B., Maurer, Mathew S., Nativi-Nicolau, Jose, Quarta, Candida Cristina, Rapezzi, Claudio, Witteles, Ronald, and Merlini, Giampaolo

Published
2020
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18. Clinical Practice Patterns in Temporary Mechanical Circulatory Support for Shock in the Critical Care Cardiology Trials Network (CCCTN) Registry

Author

Berg, David D., Barnett, Christopher F., Kenigsberg, Benjamin B., Papolos, Alexander, Alviar, Carlos L., Baird-Zars, Vivian M., Barsness, Gregory W., Bohula, Erin A., Brennan, Joseph, Burke, James A., Carnicelli, Anthony P., Chaudhry, Sunit-Preet, Cremer, Paul C., Daniels, Lori B., DeFilippis, Andrew P., Gerber, Daniel A., Granger, Christopher B., Hollenberg, Steven, Horowitz, James M., Gladden, James D., Katz, Jason N., Keeley, Ellen C., Keller, Norma, Kontos, Michael C., Lawler, Patrick R., Menon, Venu, Metkus, Thomas S., Miller, P. Elliott, Nativi-Nicolau, Jose, Newby, L. Kristin, Park, Jeong-Gun, Phreaner, Nicholas, Roswell, Robert O., Schulman, Steven P., Sinha, Shashank S., Snell, R. Jeffrey, Solomon, Michael A., Teuteberg, Jeffrey J., Tymchak, Wayne, van Diepen, Sean, and Morrow, David A.

Published
2019
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21. 2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis

Author

Kittleson, Michelle M., primary, Ruberg, Frederick L., additional, Ambardekar, Amrut V., additional, Brannagan, Thomas H., additional, Cheng, Richard K., additional, Clarke, John O., additional, Dember, Laura M., additional, Frantz, Janell Grazzini, additional, Hershberger, Ray E., additional, Maurer, Mathew S., additional, Nativi-Nicolau, Jose, additional, Sanchorawala, Vaishali, additional, and Sheikh, Farooq H., additional

Published
2023
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24. Microvascular Loss and Diastolic Dysfunction in Severe Symptomatic Cardiac Allograft Vasculopathy

Author

Daud, Anees, Xu, David, Revelo, Monica P., Shah, Zubair, Drakos, Stavros G., Dranow, Elizabeth, Stoddard, Gregory, Kfoury, Abdallah G., Hammond, M. Elizabeth H., Nativi-Nicolau, Jose, Alharethi, Rami, Miller, Dylan V., Gilbert, Edward M., Wever-Pinzon, Omar, McKellar, Stephen H., Afshar, Kia, Khan, Farman, Fang, James C., Selzman, Craig H., and Stehlik, Josef

Published
2018
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26. Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS) : 14-year update

Author

Dispenzieri, Angela, Coelho, Teresa, Conceição, Isabel, Waddington-Cruz, Márcia, Wixner, Jonas, Kristen, Arnt V., Rapezzi, Claudio, Planté-Bordeneuve, Violaine, Gonzalez-Moreno, Juan, Maurer, Mathew S., Grogan, Martha, Chapman, Doug, Amass, Leslie, Pavia, Pablo Garcia, Tarnev, Ivaylo, Costello, Jose Gonzalez, Briseno, Maria Alejandra Gonzalez Duarte, Schmidt, Hartmut, Drachman, Brian, Barroso, Fabio Adrian, Yamashita, Taro, Lairez, Olivier, Sekijima, Yoshiki, Vita, Giuseppe, Jeon, Eun-Seok, Hanna, Mazen, Slosky, David, Luigetti, Marco, LoRusso, Samantha, Beamud, Francisco Munoz, Adams, David, Moelgaard, Henning, Press, Rayomand, Cirami, Calogero Lino, Nienhuis, Hans, Plana, Josep Maria Campistol, Inamo, Jocelyn, Jacoby, Daniel, Emdin, Michele, Quan, Dianna, Hummel, Scott, Witteles, Ronald, Dori, Amir, Shah, Sanjiv, Lenihan, Daniel, Azevedo, Olga, Murali, Srinivas, Zivkovic, Sasa, Low, Soon Chai, Nativi-Nicolau, Jose, Fine, Nowell, Tallaj, Jose, Tschoepe, Carsten, Torrón, Roberto Fernandéz, Polydefkis, Michael, Merlini, Giampaolo, Badelita, Sorina, Gottlieb, Stephen, Tauras, James, Correia, Edileide Barros, Ventura, Hector, Gess, Burkhard, Darstein, Felix, Oh, Jeeyoung, Marburger, Tessa, Van Cleemput, Johan, Salutto, Valeria Lujan, Parman, Yesim, Chao, Chi-Chao, Sarswat, Nitasha, Mueller, Christopher, Steidley, David, Ralph, Jeffrey, Warner, Alberta, Cotts, William, Hoffman, James, Rugiero, Marcelo, Misawa, Sonoko, Blanco, Jose Luis Munoz, Davila, Lucia Galan, Sadeh, Menachem, Luo, Jin, Kyriakides, Theodoros, Wang, Annabel, Kaufmann, Horacio, Dispenzieri, Angela, Coelho, Teresa, Conceição, Isabel, Waddington-Cruz, Márcia, Wixner, Jonas, Kristen, Arnt V., Rapezzi, Claudio, Planté-Bordeneuve, Violaine, Gonzalez-Moreno, Juan, Maurer, Mathew S., Grogan, Martha, Chapman, Doug, Amass, Leslie, Pavia, Pablo Garcia, Tarnev, Ivaylo, Costello, Jose Gonzalez, Briseno, Maria Alejandra Gonzalez Duarte, Schmidt, Hartmut, Drachman, Brian, Barroso, Fabio Adrian, Yamashita, Taro, Lairez, Olivier, Sekijima, Yoshiki, Vita, Giuseppe, Jeon, Eun-Seok, Hanna, Mazen, Slosky, David, Luigetti, Marco, LoRusso, Samantha, Beamud, Francisco Munoz, Adams, David, Moelgaard, Henning, Press, Rayomand, Cirami, Calogero Lino, Nienhuis, Hans, Plana, Josep Maria Campistol, Inamo, Jocelyn, Jacoby, Daniel, Emdin, Michele, Quan, Dianna, Hummel, Scott, Witteles, Ronald, Dori, Amir, Shah, Sanjiv, Lenihan, Daniel, Azevedo, Olga, Murali, Srinivas, Zivkovic, Sasa, Low, Soon Chai, Nativi-Nicolau, Jose, Fine, Nowell, Tallaj, Jose, Tschoepe, Carsten, Torrón, Roberto Fernandéz, Polydefkis, Michael, Merlini, Giampaolo, Badelita, Sorina, Gottlieb, Stephen, Tauras, James, Correia, Edileide Barros, Ventura, Hector, Gess, Burkhard, Darstein, Felix, Oh, Jeeyoung, Marburger, Tessa, Van Cleemput, Johan, Salutto, Valeria Lujan, Parman, Yesim, Chao, Chi-Chao, Sarswat, Nitasha, Mueller, Christopher, Steidley, David, Ralph, Jeffrey, Warner, Alberta, Cotts, William, Hoffman, James, Rugiero, Marcelo, Misawa, Sonoko, Blanco, Jose Luis Munoz, Davila, Lucia Galan, Sadeh, Menachem, Luo, Jin, Kyriakides, Theodoros, Wang, Annabel, and Kaufmann, Horacio

Abstract

Background: Transthyretin amyloidosis (ATTR amyloidosis) is a rare, life-threatening disease caused by the accumulation of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in the heart, peripheral nerves, and other tissues and organs. Methods: Established in 2007, the Transthyretin Amyloidosis Outcomes Survey (THAOS) is the largest ongoing, global, longitudinal observational study of patients with ATTR amyloidosis, including both inherited and wild-type disease, and asymptomatic carriers of pathogenic TTR mutations. This descriptive analysis examines baseline characteristics of symptomatic patients and asymptomatic gene carriers enrolled in THAOS since its inception in 2007 (data cutoff: August 1, 2021). Results: This analysis included 3779 symptomatic patients and 1830 asymptomatic gene carriers. Symptomatic patients were predominantly male (71.4%) and had a mean (standard deviation [SD]) age of symptom onset of 56.3 (17.8) years. Val30Met was the most common genotype in symptomatic patients in South America (80.9%), Europe (55.4%), and Asia (50.5%), and more patients had early- versus late-onset disease in these regions. The majority of symptomatic patients in North America (58.8%) had ATTRwt amyloidosis. The overall distribution of phenotypes in symptomatic patients was predominantly cardiac (40.7%), predominantly neurologic (40.1%), mixed (16.6%), and no phenotype (2.5%). In asymptomatic gene carriers, mean (SD) age at enrollment was 42.4 (15.7) years, 42.4% were male, and 73.2% carried the Val30Met mutation. Conclusions: This 14-year global overview of THAOS in over 5000 patients represents the largest analysis of ATTR amyloidosis to date and highlights the genotypic and phenotypic heterogeneity of the disease. ClinicalTrials.gov Identifier: NCT00628745.

Published
2022
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30. Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS)

Author

Dispenzieri, Angela, Coelho, Teresa, Conceição, Isabel, Waddington-Cruz, Márcia, Wixner, Jonas, Kristen, Arnt V., Rapezzi, Claudio, Planté-Bordeneuve, Violaine, Gonzalez-Moreno, Juan, Maurer, Mathew S., Grogan, Martha, Chapman, Doug, Amass, Leslie, Pavia, Pablo Garcia, Tarnev, Ivaylo, Costello, Jose Gonzalez, Briseno, Maria Alejandra Gonzalez Duarte, Schmidt, Hartmut, Drachman, Brian, Barroso, Fabio Adrian, Yamashita, Taro, Lairez, Olivier, Sekijima, Yoshiki, Vita, Giuseppe, Jeon, Eun-Seok, Hanna, Mazen, Slosky, David, Luigetti, Marco, LoRusso, Samantha, Beamud, Francisco Munoz, Adams, David, Moelgaard, Henning, Press, Rayomand, Cirami, Calogero Lino, Nienhuis, Hans, Plana, Josep Maria Campistol, Inamo, Jocelyn, Jacoby, Daniel, Emdin, Michele, Quan, Dianna, Hummel, Scott, Witteles, Ronald, Dori, Amir, Shah, Sanjiv, Lenihan, Daniel, Azevedo, Olga, Murali, Srinivas, Zivkovic, Sasa, Low, Soon Chai, Nativi-Nicolau, Jose, Fine, Nowell, Tallaj, Jose, Tschoepe, Carsten, Torrón, Roberto Fernandéz, Polydefkis, Michael, Merlini, Giampaolo, Badelita, Sorina, Gottlieb, Stephen, Tauras, James, Correia, Edileide Barros, Ventura, Hector, Gess, Burkhard, Darstein, Felix, Oh, Jeeyoung, Marburger, Tessa, Van Cleemput, Johan, Salutto, Valeria Lujan, Parman, Yesim, Chao, Chi-Chao, Sarswat, Nitasha, Mueller, Christopher, Steidley, David, Ralph, Jeffrey, Warner, Alberta, Cotts, William, Hoffman, James, Rugiero, Marcelo, Misawa, Sonoko, Blanco, Jose Luis Munoz, Davila, Lucia Galan, Sadeh, Menachem, Luo, Jin, Kyriakides, Theodoros, Wang, Annabel, and Kaufmann, Horacio

Subjects
Male, Amyloid Neuropathies, Familial, Registry, Neurologi, Cardiomyopathy, General Medicine, Amyloidosis, Genetic Profile, Amyloid Neuropathies, Transthyretin, Phenotype, Familial, Neurology, Surveys and Questionnaires, Polyneuropathy, Humans, Prealbumin, Pharmacology (medical), Female, Genetics (clinical)
Abstract

Background Transthyretin amyloidosis (ATTR amyloidosis) is a rare, life-threatening disease caused by the accumulation of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in the heart, peripheral nerves, and other tissues and organs. Methods Established in 2007, the Transthyretin Amyloidosis Outcomes Survey (THAOS) is the largest ongoing, global, longitudinal observational study of patients with ATTR amyloidosis, including both inherited and wild-type disease, and asymptomatic carriers of pathogenic TTR mutations. This descriptive analysis examines baseline characteristics of symptomatic patients and asymptomatic gene carriers enrolled in THAOS since its inception in 2007 (data cutoff: August 1, 2021). Results This analysis included 3779 symptomatic patients and 1830 asymptomatic gene carriers. Symptomatic patients were predominantly male (71.4%) and had a mean (standard deviation [SD]) age of symptom onset of 56.3 (17.8) years. Val30Met was the most common genotype in symptomatic patients in South America (80.9%), Europe (55.4%), and Asia (50.5%), and more patients had early- versus late-onset disease in these regions. The majority of symptomatic patients in North America (58.8%) had ATTRwt amyloidosis. The overall distribution of phenotypes in symptomatic patients was predominantly cardiac (40.7%), predominantly neurologic (40.1%), mixed (16.6%), and no phenotype (2.5%). In asymptomatic gene carriers, mean (SD) age at enrollment was 42.4 (15.7) years, 42.4% were male, and 73.2% carried the Val30Met mutation. Conclusions This 14-year global overview of THAOS in over 5000 patients represents the largest analysis of ATTR amyloidosis to date and highlights the genotypic and phenotypic heterogeneity of the disease. ClinicalTrials.gov Identifier: NCT00628745.

Published
2022

31. Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis

Author

Caponetti, Angelo Giuseppe, primary, Rapezzi, Claudio, additional, Gagliardi, Christian, additional, Milandri, Agnese, additional, Dispenzieri, Angela, additional, Kristen, Arnt V., additional, Wixner, Jonas, additional, Maurer, Mathew S., additional, Garcia-Pavia, Pablo, additional, Tournev, Ivailo, additional, Planté-Bordeneuve, Violaine, additional, Chapman, Douglass, additional, Amass, Leslie, additional, van Cleemput, Johan, additional, Waddington-Cruz, Marcia, additional, Schmidt, Hartmut, additional, Dillmann, Klaus-Ulrich, additional, Mølgaard, Henning, additional, Moreno, Juan Gonzalez, additional, Costello, Jose Gonzalez, additional, Beamud, Francisco Munoz, additional, Davila, Lucia Galan, additional, Adams, David, additional, Inamo, Jocelyn, additional, Lairez, Olivier, additional, Vita, Giuseppe, additional, Merlini, Giampaolo, additional, Cirami, Calogero Lino, additional, Luigetti, Marco, additional, Emdin, Michele, additional, Sekijima, Yoshiki, additional, Jeon, Eun-Seok, additional, Oh, Jeeyoung, additional, Gonzalez Duarte Briseno, Maria Alejandra, additional, Nienhuis, Hans, additional, Coelho, Teresa, additional, Conceicao, Isabel, additional, Azevedo, Olga, additional, Badelita, Sorina, additional, Press, Rayomand, additional, Parman, Yesim, additional, Shah, Sanjiv, additional, Quan, Dianna, additional, Marburger, Tessa, additional, Polydefkis, Michael, additional, Witteles, Ronald, additional, Gottlieb, Stephen, additional, Sarswat, Nitasha, additional, Drachman, Brian, additional, Steidley, David, additional, Hummel, Scott, additional, Slosky, David, additional, Jacoby, Daniel, additional, Nativi-Nicolau, Jose, additional, Tauras, James, additional, Zivkovic, Sasa, additional, Tallaj, Jose, additional, and Lenihan, Daniel, additional

Published
2021
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32. Temporal Trends of Wild-Type Transthyretin Amyloid Cardiomyopathy in the Transthyretin Amyloidosis Outcomes Survey

Author

Nativi-Nicolau, Jose, primary, Siu, Alfonso, additional, Dispenzieri, Angela, additional, Maurer, Mathew S., additional, Rapezzi, Claudio, additional, Kristen, Arnt V., additional, Garcia-Pavia, Pablo, additional, LoRusso, Samantha, additional, Waddington-Cruz, Márcia, additional, Lairez, Olivier, additional, Witteles, Ronald, additional, Chapman, Doug, additional, Amass, Leslie, additional, Grogan, Martha, additional, Barroso, Fabio Adrian, additional, Van Cleemput, Johan, additional, Fine, Nowell, additional, Schmidt, Hartmut, additional, Gess, Burkhard, additional, Moelgaard, Henning, additional, Planté-Bordeneuve, Violaine, additional, Adams, David, additional, Inamo, Jocelyn, additional, Vita, Giuseppe, additional, Cirami, Calogero Lino, additional, Luigetti, Marco, additional, Emdin, Michele, additional, Sekijima, Yoshiki, additional, Yamashita, Taro, additional, Jeon, Eun-Seok, additional, Gonzalez Duarte Briseno, Maria Alejandra, additional, Nienhuis, Hans, additional, Azevedo, Olga, additional, Campistol Plana, Josep Maria, additional, Moreno, Juan Gonzalez, additional, Costello, Jose Gonzalez, additional, Wixner, Jonas, additional, Parman, Yesim, additional, Shah, Sanjiv, additional, Quan, Dianna, additional, Marburger, Tessa, additional, Polydefkis, Michael, additional, Gottlieb, Stephen, additional, Ralph, Jeffrey, additional, Sarswat, Nitasha, additional, Luo, Jin, additional, Murali, Srinivas, additional, Cotts, William, additional, Drachman, Brian, additional, Steidley, David, additional, Hummel, Scott, additional, Slosky, David, additional, Ventura, Hector, additional, Jacoby, Daniel, additional, Hoffman, James, additional, Tauras, James, additional, Zivkovic, Sasa, additional, Tallaj, Jose, additional, Lenihan, Daniel, additional, and Mueller, Christopher, additional

Published
2021
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37. sj-pdf-1-cic-10.1177_11795468211015230 – Supplemental material for Best Practices in Specialized Amyloidosis Centers in the United States: A Survey of Cardiologists, Nurses, Patients, and Patient Advocates

Author

Nativi-Nicolau, Jose, Sarswat, Nitasha, Fajardo, Johana, Finkel, Muriel, Abdulsattar, Younos, Castaño, Adam, Klein, Lori, and Haddad-Angulo, Alexandra

Subjects
Cardiology
Abstract

Supplemental material, sj-pdf-1-cic-10.1177_11795468211015230 for Best Practices in Specialized Amyloidosis Centers in the United States: A Survey of Cardiologists, Nurses, Patients, and Patient Advocates by Jose Nativi-Nicolau, Nitasha Sarswat, Johana Fajardo, Muriel Finkel, Younos Abdulsattar, Adam Castaño, Lori Klein and Alexandra Haddad-Angulo in Clinical Medicine Insights: Cardiology

Published
2021
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38. Expert consensus on the monitoring of transthyretin amyloid cardiomyopathy

Author

Garcia‐Pavia, Pablo, primary, Bengel, Frank, additional, Brito, Dulce, additional, Damy, Thibaud, additional, Duca, Franz, additional, Dorbala, Sharmila, additional, Nativi‐Nicolau, Jose, additional, Obici, Laura, additional, Rapezzi, Claudio, additional, Sekijima, Yoshiki, additional, and Elliott, Perry M., additional

Published
2021
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45. PREDICTORS OF MORTALITY IN ACUTE CORONARY SYNDROME-RELATED CARDIOGENIC SHOCK REQUIRING SHORT-TERM MECHANICAL CIRCULATORY SUPPORT

Author

Marashly, Qussay, primary, Taleb, Iosif, additional, Dranow, Elizabeth, additional, Nourian, Kimiya, additional, Burnham, Tyson, additional, Tandar, Anwar, additional, Abraham, Anu, additional, Welt, Frederick, additional, Tonna, Joseph, additional, Overton, Sean, additional, McKellar, Stephen, additional, Koliopoulou, Antigone, additional, Kemeyou, Line, additional, Fang, James, additional, Stehlik, Josef, additional, Nativi-Nicolau, Jose, additional, and Drakos, Stavros, additional

Published
2020
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46. SCAI CARDIOGENIC SHOCK CLASSIFICATION SYSTEM TO PREDICT SURVIVAL

Author

Jones, Tara, primary, Taleb, Iosif, additional, Dranow, Elizabeth, additional, Chaney, Jason, additional, McKellar, Stephen, additional, Koliopoulou, Antigone G., additional, Selzman, Craig, additional, Fang, James, additional, Nativi-Nicolau, Jose, additional, Tonna, Joseph, additional, Overton, Sean, additional, Stehlik, Josef, additional, Welt, Frederick, additional, Tandar, Anwar, additional, and Drakos, Stavros, additional

Published
2020
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47. Expert Consensus Recommendations for the Suspicion and Diagnosis of Cardiac ATTR Amyloidosis

Author

Maurer, Mathew S., Bokhari, Sabahat, Damy, Thibaud, Dorbala, Sharmila, Drachman, Brian M., Fontana, Marianna, Grogan, Martha, Kristen, Arnt V., Lousada, Isabelle, Nativi-Nicolau, Jose, Quarta, Candida Cristina, Rapezzi, Claudio, Ruberg, Frederick L., Witteles, Ronald, and Merlini, Giampaolo

Subjects
Amyloid Neuropathies, Familial, Consensus, Practice Guidelines as Topic, Humans, Cardiomyopathies, Article
Abstract

Cardiomyopathy is a manifestation of transthyretin amyloidosis (ATTR), which is an underrecognized systemic disease whereby the transthyretin protein misfolds to form fibrils that deposit in various tissues and organs. ATTR amyloidosis is debilitating and associated with poor life expectancy, especially in those with cardiac dysfunction, but a variety of treatment options have recently become available. Considered a rare disease, ATTR amyloidosis may be more prevalent than thought, particularly in older persons. Diagnosis is often delayed because of a lack of disease awareness and the heterogeneity of symptoms at presentation. Given the recent availability of effective treatments, early recognition and diagnosis are especially critical because treatment is likely more effective earlier in the disease course. The Amyloidosis Research Consortium recently convened a group of experts in ATTR amyloidosis who, through an iterative process, agreed on best practices for suspicion, diagnosis, and characterization of disease. This review describes these consensus recommendations for ATTR associated with cardiomyopathy as a resource to aid cardiologists and others in the recognition and diagnosis of ATTR associated with cardiomyopathy. Included in this review is an overview of red flag signs and symptoms and a recommended diagnostic approach, including testing for monoclonal protein, scintigraphy, or biopsy and, if ATTR associated with cardiomyopathy is identified, TTR genotyping.

Published
2019

48. PATIENT HEALTH STATUS TRAJECTORIES IN HEART FAILURE WITH RECOVERED EJECTION FRACTION

Author

Wohlfahrt, Peter, primary, Nativi-Nicolau, Jose, additional, Zhang, Mingyuan, additional, Selzman, Craig, additional, Greene, Tom, additional, Conte, Jorge, additional, Biber, Joshua, additional, Hess, Rachel, additional, Wever-Pinzon, Omar, additional, Drakos, Stavros, additional, Gilbert, Edward, additional, Kemeyou, Line, additional, LaSalle, Bernie, additional, Kfoury, Abdallah, additional, Steinberg, Benjamin, additional, Shah, Rashmee, additional, Fang, James, additional, Spertus, John A., additional, and Stehlik, Josef, additional

Published
2019
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50. PROVIDER PERSPECTIVES ON THE FEASIBILITY AND UTILITY OF ROUTINE PATIENT-REPORTED OUTCOMES ASSESSMENT IN HEART FAILURE: A QUALITATIVE ANALYSIS

Author

Wohlfahrt, Peter, primary, Zickmund, Susan, additional, Slager, Stacey, additional, Allen, Larry, additional, Nativi-Nicolau, Jose, additional, Kfoury, Abdallah, additional, Felker, G. Michael, additional, DeVore, Adam, additional, Hess, Rachel, additional, Spertus, John A., additional, and Stehlik, Josef, additional

Published
2019
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