Table 1.

Baseline Characteristics and Clinical Outcomes of Patients With Hematologic Malignancy and Respiratory Viral Infection, by Site of Infection

VariableaTotal (N = 490)LRI (n = 206)URI (n = 284)P Value
Demographics
 Age at RVI diagnosis, y, mean ± SD61.8 ± 13.863.9 ± 13.260.2 ± 14.0.003
 Sex
  Female216 (44.1)90 (43.7)126 (44.4).882
  Male274 (55.9)116 (56.3)158 (55.6)
 Race/ethnicity
  Non-Hispanic White277 (56.5)116 (56.3)161 (56.6).840
  Hispanic88 (18.0)39 (18.9)49 (17.3)
  Black92 (18.8)40 (19.4)52 (18.3)
  Asian29 (5.9)10 (4.9)19 (6.7)
  Other4 (0.8)1 (0.5)3 (1.1)
 Smoking statusb
  Never314 (64.2)119 (58.1)195 (68.7).048
  Former161 (32.9)80 (39.0)81 (28.5)
  Current14 (2.9)6 (2.9)8 (2.8)
 Influenza vaccination (current season)130 (26.5)51 (24.8)79 (27.8).449
HM characteristics
 HM diagnosis
  Hodgkin lymphoma31 (6.3)11 (5.3)20 (7.0).163
  Non-Hodgkin lymphoma162 (33.1)60 (29.1)102 (35.9)
  Multiple myeloma297 (60.6)135 (65.6)162 (57.1)
 Active malignancy at RVI diagnosis351 (71.6)167 (81.1)184 (64.8)<.001
 Active antineoplastic treatment at RVI diagnosis385 (78.6)174 (84.5)211 (74.3).007
 Steroid use within 30 d of RVI diagnosis (mg prednisone equivalent)
  Any296 (60.4)151 (73.3)145 (51.1)<.001
  30-d cumulative steroid dosage, median (IQR)c533 (240–1066)533 (266–997)533 (172–1066).597
  Peak dose of ≤1 mg/kg/dd86 (29.2)43 (28.5)43 (29.9).794
  Peak dose of >1 mg/kg/dd209 (70.8)108 (71.5)101 (70.1)
 Previous chest radiotherapy96 (19.6)47 (22.8)49 (17.3).126
 History of HCT
  None266 (54.3)107 (51.9)159 (56.0).395
  Autologous214 (43.7)93 (45.2)121 (42.6)
  Allogeneic10 (2.0)6 (2.9)4 (1.4)
 History of CAR-T therapy36 (7.3)11 (5.3)25 (8.8).147
RVI clinical course
 Pathogen.006
  RSV232 (47.3)112 (54.4)120 (42.3)
  Influenza256 (52.3)92 (44.6)164 (57.7)
  RSV + influenza2 (0.4)2 (1.0)0 (0.0)
 Respiratory viral coinfections (during ±2 wk)e85 (17.3)40 (19.4)45 (15.8).303
 Year of infection
  201645 (9.2)27 (13.1)18 (6.3).132
  201798 (20.0)35 (17.0)63 (22.3)
  201873 (14.9)34 (16.5)39 (13.7)
  2019115 (23.5)47 (22.8)68 (23.9)
  202053 (10.8)19 (9.2)34 (12.0)
  202136 (7.3)17 (8.3)19 (6.7)
  202270 (14.3)27 (13.1)43 (15.1)
 Time period of infection
  Pre-COVID-19 era (Jan 2016–Feb 2020)376 (76.7)158 (76.7)218 (76.8).987
  COVID-19 era (Mar 2020–Dec 2022)114 (23.3)48 (23.3)66 (23.2)
 LRI typec
  Probable170 (82.5)
  Laboratory confirmed36 (17.5)
 RVI symptoms
  Cough428 (87.3)184 (89.3)244 (85.9).263
  Fever250 (51.0)116 (56.3)134 (47.2).046
  Shortness of breath162 (33.1)95 (46.1)67 (23.6)<.001
  Rhinorrhea148 (30.2)40 (19.4)108 (38.0)<.001
  Nasal congestion151 (30.8)51 (24.8)100 (35.2).013
  Fatigue149 (30.4)69 (33.5)80 (28.2).206
  Sore throat73 (14.9)26 (12.6)47 (16.5).228
  Chills81 (16.5)37 (18.0)44 (15.5).468
  Headache54 (11.0)20 (9.7)34 (12.0).430
  Nausea/vomiting55 (11.2)25 (12.1)30 (10.6).586
  Myalgia46 (9.4)16 (7.8)30 (10.6).295
  Diarrhea38 (7.8)19 (9.2)19 (6.7).301
  Chest pain33 (6.7)18 (8.7)15 (5.3).132
  Arthralgia14 (2.9)4 (1.9)10 (3.5).300
 Hypoxia at presentation (≤92%) in room airf49 (10.6)43 (21.1)g6 (2.3)h<.001
 Nosocomial infection20 (4.1)12 (5.8)8 (2.8).097
 Bronchoscopy42 (8.6)41 (19.9)1 (0.4)<.001
 Lymphopenia (<200 cells/mL)60 (12.2)44 (21.4)16 (5.6)<.001
 Neutropenia (<500 cells/mL)28 (5.7)19 (9.2)9 (3.2).004
 Lymphopenia and neutropenia17 (3.5)14 (6.8)3 (1.1).001
 Elevated creatinine (≥1.2 mg/dL)146 (29.8)80 (38.8)66 (23.2)<.001
 Antiviral therapy
  Any therapy390 (79.6)184 (89.3)206 (72.5)<.001
  Ribavirin142 (29.0)92 (44.7)50 (17.6)<.001
  Oseltamiviri245 (50.0)91 (44.2)154 (54.2).028
  IVIG67 (13.7)54 (26.2)13 (4.6)<.001
 Antiviral timing from symptom onset
  No treatment100 (20.4)22 (10.7)78 (27.5)<.001
  Within 48 h139 (28.4)56 (27.2)83 (29.2)
  After 48 h251 (51.2)128 (62.1)123 (43.3)
RVI outcomes
 Hospital admission
  Any280 (57.1)180 (87.4)100 (35.2)<.001
  Secondary to RVI232 (47.3)154 (74.8)78 (27.5)<.001
  Length of stay, d, median (IQR)j5 (3–9)7 (4–12)3 (2–5)<.001
 ICU admission38 (7.8)36 (17.5)2 (0.7)<.001
  Oxygen requirement (maximal)
   None332 (67.8)74 (35.8)258 (90.8)<.001
   Nasal cannula98 (20.0)72 (35.0)26 (9.2)
   Face mask8 (1.6)8 (3.9)0 (0.0)
   HFNC20 (4.1)20 (9.7)0 (0.0)
   BiPAP15 (3.1)15 (7.3)0 (0.0)
   Mechanical ventilation17 (3.5)17 (8.3)0 (0.0)
 Follow-up duration, d, median (IQR)90 (90–90)90 (90–90)90 (90–90)<.001
 30-d all-cause mortality20 (4.1)20 (9.7)0 (0.0)<.001
 30-d RVI-related mortality19 (3.9)19 (9.2)0 (0.0)<.001
 90-d all-cause mortality32 (6.5)27 (13.1)5 (1.8)<.001
VariableaTotal (N = 490)LRI (n = 206)URI (n = 284)P Value
Demographics
 Age at RVI diagnosis, y, mean ± SD61.8 ± 13.863.9 ± 13.260.2 ± 14.0.003
 Sex
  Female216 (44.1)90 (43.7)126 (44.4).882
  Male274 (55.9)116 (56.3)158 (55.6)
 Race/ethnicity
  Non-Hispanic White277 (56.5)116 (56.3)161 (56.6).840
  Hispanic88 (18.0)39 (18.9)49 (17.3)
  Black92 (18.8)40 (19.4)52 (18.3)
  Asian29 (5.9)10 (4.9)19 (6.7)
  Other4 (0.8)1 (0.5)3 (1.1)
 Smoking statusb
  Never314 (64.2)119 (58.1)195 (68.7).048
  Former161 (32.9)80 (39.0)81 (28.5)
  Current14 (2.9)6 (2.9)8 (2.8)
 Influenza vaccination (current season)130 (26.5)51 (24.8)79 (27.8).449
HM characteristics
 HM diagnosis
  Hodgkin lymphoma31 (6.3)11 (5.3)20 (7.0).163
  Non-Hodgkin lymphoma162 (33.1)60 (29.1)102 (35.9)
  Multiple myeloma297 (60.6)135 (65.6)162 (57.1)
 Active malignancy at RVI diagnosis351 (71.6)167 (81.1)184 (64.8)<.001
 Active antineoplastic treatment at RVI diagnosis385 (78.6)174 (84.5)211 (74.3).007
 Steroid use within 30 d of RVI diagnosis (mg prednisone equivalent)
  Any296 (60.4)151 (73.3)145 (51.1)<.001
  30-d cumulative steroid dosage, median (IQR)c533 (240–1066)533 (266–997)533 (172–1066).597
  Peak dose of ≤1 mg/kg/dd86 (29.2)43 (28.5)43 (29.9).794
  Peak dose of >1 mg/kg/dd209 (70.8)108 (71.5)101 (70.1)
 Previous chest radiotherapy96 (19.6)47 (22.8)49 (17.3).126
 History of HCT
  None266 (54.3)107 (51.9)159 (56.0).395
  Autologous214 (43.7)93 (45.2)121 (42.6)
  Allogeneic10 (2.0)6 (2.9)4 (1.4)
 History of CAR-T therapy36 (7.3)11 (5.3)25 (8.8).147
RVI clinical course
 Pathogen.006
  RSV232 (47.3)112 (54.4)120 (42.3)
  Influenza256 (52.3)92 (44.6)164 (57.7)
  RSV + influenza2 (0.4)2 (1.0)0 (0.0)
 Respiratory viral coinfections (during ±2 wk)e85 (17.3)40 (19.4)45 (15.8).303
 Year of infection
  201645 (9.2)27 (13.1)18 (6.3).132
  201798 (20.0)35 (17.0)63 (22.3)
  201873 (14.9)34 (16.5)39 (13.7)
  2019115 (23.5)47 (22.8)68 (23.9)
  202053 (10.8)19 (9.2)34 (12.0)
  202136 (7.3)17 (8.3)19 (6.7)
  202270 (14.3)27 (13.1)43 (15.1)
 Time period of infection
  Pre-COVID-19 era (Jan 2016–Feb 2020)376 (76.7)158 (76.7)218 (76.8).987
  COVID-19 era (Mar 2020–Dec 2022)114 (23.3)48 (23.3)66 (23.2)
 LRI typec
  Probable170 (82.5)
  Laboratory confirmed36 (17.5)
 RVI symptoms
  Cough428 (87.3)184 (89.3)244 (85.9).263
  Fever250 (51.0)116 (56.3)134 (47.2).046
  Shortness of breath162 (33.1)95 (46.1)67 (23.6)<.001
  Rhinorrhea148 (30.2)40 (19.4)108 (38.0)<.001
  Nasal congestion151 (30.8)51 (24.8)100 (35.2).013
  Fatigue149 (30.4)69 (33.5)80 (28.2).206
  Sore throat73 (14.9)26 (12.6)47 (16.5).228
  Chills81 (16.5)37 (18.0)44 (15.5).468
  Headache54 (11.0)20 (9.7)34 (12.0).430
  Nausea/vomiting55 (11.2)25 (12.1)30 (10.6).586
  Myalgia46 (9.4)16 (7.8)30 (10.6).295
  Diarrhea38 (7.8)19 (9.2)19 (6.7).301
  Chest pain33 (6.7)18 (8.7)15 (5.3).132
  Arthralgia14 (2.9)4 (1.9)10 (3.5).300
 Hypoxia at presentation (≤92%) in room airf49 (10.6)43 (21.1)g6 (2.3)h<.001
 Nosocomial infection20 (4.1)12 (5.8)8 (2.8).097
 Bronchoscopy42 (8.6)41 (19.9)1 (0.4)<.001
 Lymphopenia (<200 cells/mL)60 (12.2)44 (21.4)16 (5.6)<.001
 Neutropenia (<500 cells/mL)28 (5.7)19 (9.2)9 (3.2).004
 Lymphopenia and neutropenia17 (3.5)14 (6.8)3 (1.1).001
 Elevated creatinine (≥1.2 mg/dL)146 (29.8)80 (38.8)66 (23.2)<.001
 Antiviral therapy
  Any therapy390 (79.6)184 (89.3)206 (72.5)<.001
  Ribavirin142 (29.0)92 (44.7)50 (17.6)<.001
  Oseltamiviri245 (50.0)91 (44.2)154 (54.2).028
  IVIG67 (13.7)54 (26.2)13 (4.6)<.001
 Antiviral timing from symptom onset
  No treatment100 (20.4)22 (10.7)78 (27.5)<.001
  Within 48 h139 (28.4)56 (27.2)83 (29.2)
  After 48 h251 (51.2)128 (62.1)123 (43.3)
RVI outcomes
 Hospital admission
  Any280 (57.1)180 (87.4)100 (35.2)<.001
  Secondary to RVI232 (47.3)154 (74.8)78 (27.5)<.001
  Length of stay, d, median (IQR)j5 (3–9)7 (4–12)3 (2–5)<.001
 ICU admission38 (7.8)36 (17.5)2 (0.7)<.001
  Oxygen requirement (maximal)
   None332 (67.8)74 (35.8)258 (90.8)<.001
   Nasal cannula98 (20.0)72 (35.0)26 (9.2)
   Face mask8 (1.6)8 (3.9)0 (0.0)
   HFNC20 (4.1)20 (9.7)0 (0.0)
   BiPAP15 (3.1)15 (7.3)0 (0.0)
   Mechanical ventilation17 (3.5)17 (8.3)0 (0.0)
 Follow-up duration, d, median (IQR)90 (90–90)90 (90–90)90 (90–90)<.001
 30-d all-cause mortality20 (4.1)20 (9.7)0 (0.0)<.001
 30-d RVI-related mortality19 (3.9)19 (9.2)0 (0.0)<.001
 90-d all-cause mortality32 (6.5)27 (13.1)5 (1.8)<.001

The difference in follow-up duration is more clearly illustrated when presented as the mean ± SD rather than the median and IQR. In the URI group, the mean duration was 85.4 ± 18.5 years, compared to 78.2 ± 26.5 years in the LRI group. P values less than .05 are indicated in bold format.

Abbreviations: BiPAP, bilevel positive airway pressure; CAR-T, chimeric antigen receptor T-cell; COVID-19, coronavirus disease 2019; HCT, hematopoietic stem cell transplantation; HFNC, high-flow nasal cannula; HM, hematologic malignancy; ICU, intensive care unit; IQR, interquartile range; IVIG, intravenous immunoglobulin; LRI, lower respiratory tract infection; RSV, respiratory syncytial virus; RVI, respiratory virus infection; SD, standard deviation; URI, upper respiratory tract infection.

aData are presented as No. (%) unless otherwise specified.

bn = 489.

cn = 294.

dn = 295.

eViral coinfections included rhinovirus (n = 34), seasonal human coronavirus (non–severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2]) (n = 31), SARS-CoV-2 (n = 4), parainfluenza (n = 10), human metapneumovirus (n = 7), adenovirus (n = 1), and cytomegalovirus pneumonitis (n = 3).

fn = 462.

gn = 204.

hn = 258.

iThree RSV-infected patients were treated empirically with oseltamivir before the respiratory virus panel results were received.

jn = 280.

Table 1.

Baseline Characteristics and Clinical Outcomes of Patients With Hematologic Malignancy and Respiratory Viral Infection, by Site of Infection

VariableaTotal (N = 490)LRI (n = 206)URI (n = 284)P Value
Demographics
 Age at RVI diagnosis, y, mean ± SD61.8 ± 13.863.9 ± 13.260.2 ± 14.0.003
 Sex
  Female216 (44.1)90 (43.7)126 (44.4).882
  Male274 (55.9)116 (56.3)158 (55.6)
 Race/ethnicity
  Non-Hispanic White277 (56.5)116 (56.3)161 (56.6).840
  Hispanic88 (18.0)39 (18.9)49 (17.3)
  Black92 (18.8)40 (19.4)52 (18.3)
  Asian29 (5.9)10 (4.9)19 (6.7)
  Other4 (0.8)1 (0.5)3 (1.1)
 Smoking statusb
  Never314 (64.2)119 (58.1)195 (68.7).048
  Former161 (32.9)80 (39.0)81 (28.5)
  Current14 (2.9)6 (2.9)8 (2.8)
 Influenza vaccination (current season)130 (26.5)51 (24.8)79 (27.8).449
HM characteristics
 HM diagnosis
  Hodgkin lymphoma31 (6.3)11 (5.3)20 (7.0).163
  Non-Hodgkin lymphoma162 (33.1)60 (29.1)102 (35.9)
  Multiple myeloma297 (60.6)135 (65.6)162 (57.1)
 Active malignancy at RVI diagnosis351 (71.6)167 (81.1)184 (64.8)<.001
 Active antineoplastic treatment at RVI diagnosis385 (78.6)174 (84.5)211 (74.3).007
 Steroid use within 30 d of RVI diagnosis (mg prednisone equivalent)
  Any296 (60.4)151 (73.3)145 (51.1)<.001
  30-d cumulative steroid dosage, median (IQR)c533 (240–1066)533 (266–997)533 (172–1066).597
  Peak dose of ≤1 mg/kg/dd86 (29.2)43 (28.5)43 (29.9).794
  Peak dose of >1 mg/kg/dd209 (70.8)108 (71.5)101 (70.1)
 Previous chest radiotherapy96 (19.6)47 (22.8)49 (17.3).126
 History of HCT
  None266 (54.3)107 (51.9)159 (56.0).395
  Autologous214 (43.7)93 (45.2)121 (42.6)
  Allogeneic10 (2.0)6 (2.9)4 (1.4)
 History of CAR-T therapy36 (7.3)11 (5.3)25 (8.8).147
RVI clinical course
 Pathogen.006
  RSV232 (47.3)112 (54.4)120 (42.3)
  Influenza256 (52.3)92 (44.6)164 (57.7)
  RSV + influenza2 (0.4)2 (1.0)0 (0.0)
 Respiratory viral coinfections (during ±2 wk)e85 (17.3)40 (19.4)45 (15.8).303
 Year of infection
  201645 (9.2)27 (13.1)18 (6.3).132
  201798 (20.0)35 (17.0)63 (22.3)
  201873 (14.9)34 (16.5)39 (13.7)
  2019115 (23.5)47 (22.8)68 (23.9)
  202053 (10.8)19 (9.2)34 (12.0)
  202136 (7.3)17 (8.3)19 (6.7)
  202270 (14.3)27 (13.1)43 (15.1)
 Time period of infection
  Pre-COVID-19 era (Jan 2016–Feb 2020)376 (76.7)158 (76.7)218 (76.8).987
  COVID-19 era (Mar 2020–Dec 2022)114 (23.3)48 (23.3)66 (23.2)
 LRI typec
  Probable170 (82.5)
  Laboratory confirmed36 (17.5)
 RVI symptoms
  Cough428 (87.3)184 (89.3)244 (85.9).263
  Fever250 (51.0)116 (56.3)134 (47.2).046
  Shortness of breath162 (33.1)95 (46.1)67 (23.6)<.001
  Rhinorrhea148 (30.2)40 (19.4)108 (38.0)<.001
  Nasal congestion151 (30.8)51 (24.8)100 (35.2).013
  Fatigue149 (30.4)69 (33.5)80 (28.2).206
  Sore throat73 (14.9)26 (12.6)47 (16.5).228
  Chills81 (16.5)37 (18.0)44 (15.5).468
  Headache54 (11.0)20 (9.7)34 (12.0).430
  Nausea/vomiting55 (11.2)25 (12.1)30 (10.6).586
  Myalgia46 (9.4)16 (7.8)30 (10.6).295
  Diarrhea38 (7.8)19 (9.2)19 (6.7).301
  Chest pain33 (6.7)18 (8.7)15 (5.3).132
  Arthralgia14 (2.9)4 (1.9)10 (3.5).300
 Hypoxia at presentation (≤92%) in room airf49 (10.6)43 (21.1)g6 (2.3)h<.001
 Nosocomial infection20 (4.1)12 (5.8)8 (2.8).097
 Bronchoscopy42 (8.6)41 (19.9)1 (0.4)<.001
 Lymphopenia (<200 cells/mL)60 (12.2)44 (21.4)16 (5.6)<.001
 Neutropenia (<500 cells/mL)28 (5.7)19 (9.2)9 (3.2).004
 Lymphopenia and neutropenia17 (3.5)14 (6.8)3 (1.1).001
 Elevated creatinine (≥1.2 mg/dL)146 (29.8)80 (38.8)66 (23.2)<.001
 Antiviral therapy
  Any therapy390 (79.6)184 (89.3)206 (72.5)<.001
  Ribavirin142 (29.0)92 (44.7)50 (17.6)<.001
  Oseltamiviri245 (50.0)91 (44.2)154 (54.2).028
  IVIG67 (13.7)54 (26.2)13 (4.6)<.001
 Antiviral timing from symptom onset
  No treatment100 (20.4)22 (10.7)78 (27.5)<.001
  Within 48 h139 (28.4)56 (27.2)83 (29.2)
  After 48 h251 (51.2)128 (62.1)123 (43.3)
RVI outcomes
 Hospital admission
  Any280 (57.1)180 (87.4)100 (35.2)<.001
  Secondary to RVI232 (47.3)154 (74.8)78 (27.5)<.001
  Length of stay, d, median (IQR)j5 (3–9)7 (4–12)3 (2–5)<.001
 ICU admission38 (7.8)36 (17.5)2 (0.7)<.001
  Oxygen requirement (maximal)
   None332 (67.8)74 (35.8)258 (90.8)<.001
   Nasal cannula98 (20.0)72 (35.0)26 (9.2)
   Face mask8 (1.6)8 (3.9)0 (0.0)
   HFNC20 (4.1)20 (9.7)0 (0.0)
   BiPAP15 (3.1)15 (7.3)0 (0.0)
   Mechanical ventilation17 (3.5)17 (8.3)0 (0.0)
 Follow-up duration, d, median (IQR)90 (90–90)90 (90–90)90 (90–90)<.001
 30-d all-cause mortality20 (4.1)20 (9.7)0 (0.0)<.001
 30-d RVI-related mortality19 (3.9)19 (9.2)0 (0.0)<.001
 90-d all-cause mortality32 (6.5)27 (13.1)5 (1.8)<.001
VariableaTotal (N = 490)LRI (n = 206)URI (n = 284)P Value
Demographics
 Age at RVI diagnosis, y, mean ± SD61.8 ± 13.863.9 ± 13.260.2 ± 14.0.003
 Sex
  Female216 (44.1)90 (43.7)126 (44.4).882
  Male274 (55.9)116 (56.3)158 (55.6)
 Race/ethnicity
  Non-Hispanic White277 (56.5)116 (56.3)161 (56.6).840
  Hispanic88 (18.0)39 (18.9)49 (17.3)
  Black92 (18.8)40 (19.4)52 (18.3)
  Asian29 (5.9)10 (4.9)19 (6.7)
  Other4 (0.8)1 (0.5)3 (1.1)
 Smoking statusb
  Never314 (64.2)119 (58.1)195 (68.7).048
  Former161 (32.9)80 (39.0)81 (28.5)
  Current14 (2.9)6 (2.9)8 (2.8)
 Influenza vaccination (current season)130 (26.5)51 (24.8)79 (27.8).449
HM characteristics
 HM diagnosis
  Hodgkin lymphoma31 (6.3)11 (5.3)20 (7.0).163
  Non-Hodgkin lymphoma162 (33.1)60 (29.1)102 (35.9)
  Multiple myeloma297 (60.6)135 (65.6)162 (57.1)
 Active malignancy at RVI diagnosis351 (71.6)167 (81.1)184 (64.8)<.001
 Active antineoplastic treatment at RVI diagnosis385 (78.6)174 (84.5)211 (74.3).007
 Steroid use within 30 d of RVI diagnosis (mg prednisone equivalent)
  Any296 (60.4)151 (73.3)145 (51.1)<.001
  30-d cumulative steroid dosage, median (IQR)c533 (240–1066)533 (266–997)533 (172–1066).597
  Peak dose of ≤1 mg/kg/dd86 (29.2)43 (28.5)43 (29.9).794
  Peak dose of >1 mg/kg/dd209 (70.8)108 (71.5)101 (70.1)
 Previous chest radiotherapy96 (19.6)47 (22.8)49 (17.3).126
 History of HCT
  None266 (54.3)107 (51.9)159 (56.0).395
  Autologous214 (43.7)93 (45.2)121 (42.6)
  Allogeneic10 (2.0)6 (2.9)4 (1.4)
 History of CAR-T therapy36 (7.3)11 (5.3)25 (8.8).147
RVI clinical course
 Pathogen.006
  RSV232 (47.3)112 (54.4)120 (42.3)
  Influenza256 (52.3)92 (44.6)164 (57.7)
  RSV + influenza2 (0.4)2 (1.0)0 (0.0)
 Respiratory viral coinfections (during ±2 wk)e85 (17.3)40 (19.4)45 (15.8).303
 Year of infection
  201645 (9.2)27 (13.1)18 (6.3).132
  201798 (20.0)35 (17.0)63 (22.3)
  201873 (14.9)34 (16.5)39 (13.7)
  2019115 (23.5)47 (22.8)68 (23.9)
  202053 (10.8)19 (9.2)34 (12.0)
  202136 (7.3)17 (8.3)19 (6.7)
  202270 (14.3)27 (13.1)43 (15.1)
 Time period of infection
  Pre-COVID-19 era (Jan 2016–Feb 2020)376 (76.7)158 (76.7)218 (76.8).987
  COVID-19 era (Mar 2020–Dec 2022)114 (23.3)48 (23.3)66 (23.2)
 LRI typec
  Probable170 (82.5)
  Laboratory confirmed36 (17.5)
 RVI symptoms
  Cough428 (87.3)184 (89.3)244 (85.9).263
  Fever250 (51.0)116 (56.3)134 (47.2).046
  Shortness of breath162 (33.1)95 (46.1)67 (23.6)<.001
  Rhinorrhea148 (30.2)40 (19.4)108 (38.0)<.001
  Nasal congestion151 (30.8)51 (24.8)100 (35.2).013
  Fatigue149 (30.4)69 (33.5)80 (28.2).206
  Sore throat73 (14.9)26 (12.6)47 (16.5).228
  Chills81 (16.5)37 (18.0)44 (15.5).468
  Headache54 (11.0)20 (9.7)34 (12.0).430
  Nausea/vomiting55 (11.2)25 (12.1)30 (10.6).586
  Myalgia46 (9.4)16 (7.8)30 (10.6).295
  Diarrhea38 (7.8)19 (9.2)19 (6.7).301
  Chest pain33 (6.7)18 (8.7)15 (5.3).132
  Arthralgia14 (2.9)4 (1.9)10 (3.5).300
 Hypoxia at presentation (≤92%) in room airf49 (10.6)43 (21.1)g6 (2.3)h<.001
 Nosocomial infection20 (4.1)12 (5.8)8 (2.8).097
 Bronchoscopy42 (8.6)41 (19.9)1 (0.4)<.001
 Lymphopenia (<200 cells/mL)60 (12.2)44 (21.4)16 (5.6)<.001
 Neutropenia (<500 cells/mL)28 (5.7)19 (9.2)9 (3.2).004
 Lymphopenia and neutropenia17 (3.5)14 (6.8)3 (1.1).001
 Elevated creatinine (≥1.2 mg/dL)146 (29.8)80 (38.8)66 (23.2)<.001
 Antiviral therapy
  Any therapy390 (79.6)184 (89.3)206 (72.5)<.001
  Ribavirin142 (29.0)92 (44.7)50 (17.6)<.001
  Oseltamiviri245 (50.0)91 (44.2)154 (54.2).028
  IVIG67 (13.7)54 (26.2)13 (4.6)<.001
 Antiviral timing from symptom onset
  No treatment100 (20.4)22 (10.7)78 (27.5)<.001
  Within 48 h139 (28.4)56 (27.2)83 (29.2)
  After 48 h251 (51.2)128 (62.1)123 (43.3)
RVI outcomes
 Hospital admission
  Any280 (57.1)180 (87.4)100 (35.2)<.001
  Secondary to RVI232 (47.3)154 (74.8)78 (27.5)<.001
  Length of stay, d, median (IQR)j5 (3–9)7 (4–12)3 (2–5)<.001
 ICU admission38 (7.8)36 (17.5)2 (0.7)<.001
  Oxygen requirement (maximal)
   None332 (67.8)74 (35.8)258 (90.8)<.001
   Nasal cannula98 (20.0)72 (35.0)26 (9.2)
   Face mask8 (1.6)8 (3.9)0 (0.0)
   HFNC20 (4.1)20 (9.7)0 (0.0)
   BiPAP15 (3.1)15 (7.3)0 (0.0)
   Mechanical ventilation17 (3.5)17 (8.3)0 (0.0)
 Follow-up duration, d, median (IQR)90 (90–90)90 (90–90)90 (90–90)<.001
 30-d all-cause mortality20 (4.1)20 (9.7)0 (0.0)<.001
 30-d RVI-related mortality19 (3.9)19 (9.2)0 (0.0)<.001
 90-d all-cause mortality32 (6.5)27 (13.1)5 (1.8)<.001

The difference in follow-up duration is more clearly illustrated when presented as the mean ± SD rather than the median and IQR. In the URI group, the mean duration was 85.4 ± 18.5 years, compared to 78.2 ± 26.5 years in the LRI group. P values less than .05 are indicated in bold format.

Abbreviations: BiPAP, bilevel positive airway pressure; CAR-T, chimeric antigen receptor T-cell; COVID-19, coronavirus disease 2019; HCT, hematopoietic stem cell transplantation; HFNC, high-flow nasal cannula; HM, hematologic malignancy; ICU, intensive care unit; IQR, interquartile range; IVIG, intravenous immunoglobulin; LRI, lower respiratory tract infection; RSV, respiratory syncytial virus; RVI, respiratory virus infection; SD, standard deviation; URI, upper respiratory tract infection.

aData are presented as No. (%) unless otherwise specified.

bn = 489.

cn = 294.

dn = 295.

eViral coinfections included rhinovirus (n = 34), seasonal human coronavirus (non–severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2]) (n = 31), SARS-CoV-2 (n = 4), parainfluenza (n = 10), human metapneumovirus (n = 7), adenovirus (n = 1), and cytomegalovirus pneumonitis (n = 3).

fn = 462.

gn = 204.

hn = 258.

iThree RSV-infected patients were treated empirically with oseltamivir before the respiratory virus panel results were received.

jn = 280.

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