factuality_value
stringclasses
7 values
predicat@xml:space
stringclasses
1 value
predicat@charOffset
stringlengths
3
9
predicat@headOffset
stringlengths
3
9
predicat@id
stringclasses
206 values
predicat@text
stringlengths
2
124
predicat@type
stringclasses
29 values
predicat@charOffsetMin
int64
0
3.96k
predicat@charOffsetMax
int64
6
3.97k
subject@xml:space
stringclasses
1 value
subject@charOffset
stringlengths
3
9
subject@headOffset
stringlengths
3
9
subject@id
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197 values
subject@text
stringlengths
2
49
subject@type
stringclasses
72 values
subject@charOffsetMin
int64
0
3.98k
subject@charOffsetMax
int64
3
4k
object@xml:space
stringclasses
1 value
object@charOffset
stringlengths
3
9
object@headOffset
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3
9
object@id
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198 values
object@text
stringlengths
2
53
object@type
stringclasses
73 values
object@charOffsetMin
int64
0
3.93k
object@charOffsetMax
int64
4
3.94k
id
stringclasses
58 values
raw_sent_text
stringlengths
20
749
sent_charOffset
stringlengths
4
9
sent_charOffsetMin
int64
0
3.88k
sent_charOffsetMax
int64
26
4.2k
formated_sentence
stringlengths
34
768
Fact
preserve
1226-1232
1226-1232
T67
blocks
INHIBITS
1,226
1,232
preserve
1197-1220
1213-1220
T57
receptor fusion protein
AminoAcidPeptideOrProtein
1,197
1,220
preserve
1233-1254
1248-1254
T58
tumor necrosis factor
AminoAcidPeptideOrProtein
1,233
1,254
A5
Etanercept, a bioengineered soluble receptor fusion protein that blocks tumor necrosis factor activity, is the first compound in this class to be approved for treatment of patients with refractory rheumatoid arthritis.
1155-1391
1,155
1,391
Etanercept, a bioengineered soluble @SUBJECT$ that @PREDICAT$ @OBJECT$ activity, is the first compound in this class to be approved for treatment of patients with refractory rheumatoid arthritis.
Fact
preserve
774-783
774-783
T42
Treatment
TREATS
774
783
preserve
833-870
865-870
T36
disease-modifying antirheumatic drugs
PharmacologicSubstance
833
870
preserve
787-807
798-807
T35
rheumatoid arthritis
DiseaseOrSyndrome
787
807
A6
Treatment of rheumatoid arthritis typically involves disease-modifying antirheumatic drugs, nonsteroidal anti-inflammatory drugs, and low-dose corticosteroids--often used in combination.
774-973
774
973
@PREDICAT$ of @OBJECT$ typically involves @SUBJECT$ , nonsteroidal anti-inflammatory drugs, and low-dose corticosteroids--often used in combination.
Probable
preserve
153-158
153-158
T9
cause
CAUSES
153
158
preserve
115-143
136-143
T6
chronic inflammatory disease
DiseaseOrSyndrome
115
143
preserve
181-191
181-191
T8
disability
PathologicFunction
181
191
A7
Rheumatoid arthritis is a chronic inflammatory disease that can cause severe pain and disability.
89-192
89
192
Rheumatoid arthritis is a @SUBJECT$ that can @PREDICAT$ severe pain and @OBJECT$ .
Fact
preserve
1547-1551
1547-1551
T83
with
PROCESS_OF
1,547
1,551
preserve
1552-1572
1563-1572
T79
rheumatoid arthritis
DiseaseOrSyndrome
1,552
1,572
preserve
1539-1546
1539-1546
T78
persons
PopulationGroup
1,539
1,546
A8
Therapeutic trials indicate that etanercept can reduce disease activity with relatively few drug-related adverse effects, thus helping persons with rheumatoid arthritis return to more normal, healthy lives.
1392-1616
1,392
1,616
Therapeutic trials indicate that etanercept can reduce disease activity with relatively few drug-related adverse effects, thus helping @OBJECT$ @PREDICAT$ @SUBJECT$ return to more normal, healthy lives.
Probable
preserve
153-158
153-158
T9
cause
CAUSES
153
158
preserve
115-143
136-143
T6
chronic inflammatory disease
DiseaseOrSyndrome
115
143
preserve
159-170
166-170
T7
severe pain
SignOrSymptom
159
170
A9
Rheumatoid arthritis is a chronic inflammatory disease that can cause severe pain and disability.
89-192
89
192
Rheumatoid arthritis is a @SUBJECT$ that can @PREDICAT$ @OBJECT$ and disability.
Fact
preserve
386-390
386-390
T21
with
PROCESS_OF
386
390
preserve
391-411
402-411
T18
rheumatoid arthritis
DiseaseOrSyndrome
391
411
preserve
377-385
377-385
T17
patients
PatientOrDisabledGroup
377
385
A10
However, the demonstration of early joint damage in patients with rheumatoid arthritis has emphasized the importance of early identification and treatment.
319-486
319
486
However, the demonstration of early joint damage in @OBJECT$ @PREDICAT$ @SUBJECT$ has emphasized the importance of early identification and treatment.
Fact
preserve
1326-1335
1326-1335
T68
treatment
TREATS
1,326
1,335
preserve
1155-1165
1155-1165
T54
Etanercept
AminoAcidPeptideOrProtein
1,155
1,165
preserve
1370-1390
1381-1390
T66
rheumatoid arthritis
DiseaseOrSyndrome
1,370
1,390
A11
Etanercept, a bioengineered soluble receptor fusion protein that blocks tumor necrosis factor activity, is the first compound in this class to be approved for treatment of patients with refractory rheumatoid arthritis.
1155-1391
1,155
1,391
@SUBJECT$ , a bioengineered soluble receptor fusion protein that blocks tumor necrosis factor activity, is the first compound in this class to be approved for @PREDICAT$ of patients with refractory @OBJECT$ .
Fact
preserve
774-783
774-783
T42
Treatment
TREATS
774
783
preserve
930-945
930-945
T39
corticosteroids
Hormone
930
945
preserve
787-807
798-807
T35
rheumatoid arthritis
DiseaseOrSyndrome
787
807
A12
Treatment of rheumatoid arthritis typically involves disease-modifying antirheumatic drugs, nonsteroidal anti-inflammatory drugs, and low-dose corticosteroids--often used in combination.
774-973
774
973
@PREDICAT$ of @OBJECT$ typically involves disease-modifying antirheumatic drugs, nonsteroidal anti-inflammatory drugs, and low-dose @SUBJECT$ --often used in combination.
Fact
preserve
782-791
782-791
T66
treatment
TREATS
782
791
preserve
825-829
825-829
T58
DSCG
OrganicChemical
825
829
preserve
795-804
795-804
T56
asthmatic
DiseaseOrSyndrome
795
804
A1
The treatment of asthmatic patients with DSCG downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
778-962
778
962
The @PREDICAT$ of @OBJECT$ patients with @SUBJECT$ downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
Fact
preserve
830-843
830-843
T68
downregulated
DISRUPTS
830
843
preserve
825-829
825-829
T58
DSCG
OrganicChemical
825
829
preserve
857-865
857-865
T60
adhesion
AcquiredAbnormality
857
865
A2
The treatment of asthmatic patients with DSCG downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
778-962
778
962
The treatment of asthmatic patients with @SUBJECT$ @PREDICAT$ the monocyte @OBJECT$ to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
Fact
preserve
186-188
186-188
T31
of
LOCATION_OF
186
188
preserve
189-223
218-223
T19
peripheral blood mononuclear cells
Cell
189
223
preserve
177-185
177-185
T18
adhesion
AcquiredAbnormality
177
185
A3
In this study we have compared the adhesion of peripheral blood mononuclear cells (PBMC) to human umbilical vein endothelial cells (HUVEC) in a healthy control group with two groups of allergic asthmatics, not treated or treated with disodium cromoglycate (DSCG).
142-423
142
423
In this study we have compared the @OBJECT$ @PREDICAT$ @SUBJECT$ (PBMC) to human umbilical vein endothelial cells (HUVEC) in a healthy control group with two groups of allergic asthmatics, not treated or treated with disodium cromoglycate (DSCG).
Fact
preserve
375-382
375-382
T32
treated
TREATS
375
382
preserve
394-415
403-415
T30
disodium cromoglycate
OrganicChemical
394
415
preserve
348-358
348-358
T28
asthmatics
DiseaseOrSyndrome
348
358
A4
In this study we have compared the adhesion of peripheral blood mononuclear cells (PBMC) to human umbilical vein endothelial cells (HUVEC) in a healthy control group with two groups of allergic asthmatics, not treated or treated with disodium cromoglycate (DSCG).
142-423
142
423
In this study we have compared the adhesion of peripheral blood mononuclear cells (PBMC) to human umbilical vein endothelial cells (HUVEC) in a healthy control group with two groups of allergic @OBJECT$ , not treated or @PREDICAT$ with @SUBJECT$ (DSCG).
Fact
preserve
1029-1046
1038-1046
T80
monocyte adhesion
LOCATION_OF
1,029
1,046
preserve
1029-1037
1029-1037
T74
monocyte
Cell
1,029
1,037
preserve
1038-1046
1038-1046
T75
adhesion
AcquiredAbnormality
1,038
1,046
A5
The DSCG may have a therapeutic effect on the regulation of monocyte adhesion in inflammatory and allergic diseases.
963-1092
963
1,092
The DSCG may have a therapeutic effect on the regulation of @SUBJECT$ @PREDICAT$ @OBJECT$ in inflammatory and allergic diseases.
Fact
preserve
782-791
782-791
T66
treatment
TREATS
782
791
preserve
825-829
825-829
T58
DSCG
OrganicChemical
825
829
preserve
811-819
811-819
T57
patients
PatientOrDisabledGroup
811
819
A6
The treatment of asthmatic patients with DSCG downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
778-962
778
962
The @PREDICAT$ of asthmatic @OBJECT$ with @SUBJECT$ downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
Fact
preserve
45-93
85-93
T13
peripheral blood mononuclear cell adhesion
LOCATION_OF
45
93
preserve
45-78
74-78
T4
peripheral blood mononuclear cell
Cell
45
78
preserve
85-93
85-93
T5
adhesion
AcquiredAbnormality
85
93
A7
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
0-141
0
141
Effect of disodium cromoglycate treatment on @SUBJECT$ @PREDICAT$ @OBJECT$ to cultured endothelium in allergic asthmatics.
Fact
preserve
10-41
32-41
T15
disodium cromoglycate treatment
AFFECTS
10
41
preserve
10-31
19-31
T2
disodium cromoglycate
OrganicChemical
10
31
preserve
85-93
85-93
T5
adhesion
AcquiredAbnormality
85
93
A10
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
0-141
0
141
Effect of @SUBJECT$ @PREDICAT$ on peripheral blood mononuclear cell @OBJECT$ to cultured endothelium in allergic asthmatics.
Fact
preserve
0-6
0-6
T11
Effect
AFFECTS
0
6
preserve
32-41
32-41
T3
treatment
TherapeuticOrPreventiveProcedure
32
41
preserve
85-93
85-93
T5
adhesion
AcquiredAbnormality
85
93
A11
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
0-141
0
141
@PREDICAT$ of disodium cromoglycate @SUBJECT$ on peripheral blood mononuclear cell @OBJECT$ to cultured endothelium in allergic asthmatics.
Fact
preserve
795-819
811-819
T67
asthmatic patients
PROCESS_OF
795
819
preserve
795-804
795-804
T56
asthmatic
DiseaseOrSyndrome
795
804
preserve
811-819
811-819
T57
patients
PatientOrDisabledGroup
811
819
A13
The treatment of asthmatic patients with DSCG downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
778-962
778
962
The treatment of @SUBJECT$ @PREDICAT$ @OBJECT$ with DSCG downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
Fact
preserve
848-865
857-865
T69
monocyte adhesion
LOCATION_OF
848
865
preserve
848-856
848-856
T59
monocyte
Cell
848
856
preserve
857-865
857-865
T60
adhesion
AcquiredAbnormality
857
865
A14
The treatment of asthmatic patients with DSCG downregulated the monocyte adhesion to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
778-962
778
962
The treatment of asthmatic patients with DSCG downregulated the @SUBJECT$ @PREDICAT$ @OBJECT$ to cultured endothelial cells (ECs) and this was comparable to the group of normal donors.
Fact
preserve
10-41
32-41
T10
disodium cromoglycate treatment
ISA
10
41
preserve
10-31
19-31
T2
disodium cromoglycate
OrganicChemical
10
31
preserve
32-41
32-41
T3
treatment
TherapeuticOrPreventiveProcedure
32
41
A15
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
0-141
0
141
Effect of @SUBJECT$ @PREDICAT$ @OBJECT$ on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
Fact
preserve
10-41
32-41
T12
disodium cromoglycate treatment
USES
10
41
preserve
32-41
32-41
T3
treatment
TherapeuticOrPreventiveProcedure
32
41
preserve
10-31
19-31
T2
disodium cromoglycate
OrganicChemical
10
31
A16
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
0-141
0
141
Effect of @OBJECT$ @PREDICAT$ @SUBJECT$ on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
Fact
preserve
559-561
559-561
T43
of
LOCATION_OF
559
561
preserve
562-573
562-573
T41
lymphocytes
Cell
562
573
preserve
544-552
544-552
T40
adhesion
AcquiredAbnormality
544
552
A17
No differences in the adhesion of lymphocytes were observed in any of the groups.
522-609
522
609
No differences in the @OBJECT$ @PREDICAT$ @SUBJECT$ were observed in any of the groups.
Fact
preserve
118-120
118-120
T14
in
COEXISTS_WITH
118
120
preserve
85-93
85-93
T5
adhesion
AcquiredAbnormality
85
93
preserve
130-140
130-140
T9
asthmatics
DiseaseOrSyndrome
130
140
A18
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell adhesion to cultured endothelium in allergic asthmatics.
0-141
0
141
Effect of disodium cromoglycate treatment on peripheral blood mononuclear cell @SUBJECT$ to cultured endothelium @PREDICAT$ allergic @OBJECT$ .
Fact
preserve
1015-1025
1015-1025
T79
regulation
AFFECTS
1,015
1,025
preserve
967-971
967-971
T71
DSCG
OrganicChemical
967
971
preserve
1038-1046
1038-1046
T75
adhesion
AcquiredAbnormality
1,038
1,046
A20
The DSCG may have a therapeutic effect on the regulation of monocyte adhesion in inflammatory and allergic diseases.
963-1092
963
1,092
The @SUBJECT$ may have a therapeutic effect on the @PREDICAT$ of monocyte @OBJECT$ in inflammatory and allergic diseases.
Fact
preserve
939-955
948-955
T73
levodopa therapy
ISA
939
955
preserve
939-947
939-947
T70
levodopa
AminoAcidPeptideOrProtein
939
947
preserve
948-955
948-955
T71
therapy
TherapeuticOrPreventiveProcedure
948
955
A1
Goals of therapy in patients less than 60 years of age include sparing levodopa therapy and providing neuroprotection.
862-992
862
992
Goals of therapy in patients less than 60 years of age include sparing @SUBJECT$ @PREDICAT$ @OBJECT$ and providing neuroprotection.
Fact
preserve
793-815
808-815
T63
levodopa therapy
USES
793
815
preserve
808-815
808-815
T59
therapy
TherapeuticOrPreventiveProcedure
808
815
preserve
793-801
793-801
T58
levodopa
AminoAcidPeptideOrProtein
793
801
A2
COMT inhibitors may be useful adjuncts to levodopa therapy but are plagued with serious adverse effects.
751-861
751
861
COMT inhibitors may be useful adjuncts to @OBJECT$ @PREDICAT$ @SUBJECT$ but are plagued with serious adverse effects.
Fact
preserve
564-575
564-575
T48
stimulation
STIMULATES
564
575
preserve
501-518
510-518
T39
Dopamine agonists
PharmacologicSubstance
501
518
preserve
579-597
588-597
T44
dopamine receptors
AminoAcidPeptideOrProtein
579
597
A3
Dopamine agonists hold promise because of more sustained stimulation of dopamine receptors and possibly an antioxidant effect.
501-633
501
633
@SUBJECT$ hold promise because of more sustained @PREDICAT$ of @OBJECT$ and possibly an antioxidant effect.
Fact
preserve
939-955
948-955
T75
levodopa therapy
USES
939
955
preserve
948-955
948-955
T71
therapy
TherapeuticOrPreventiveProcedure
948
955
preserve
939-947
939-947
T70
levodopa
AminoAcidPeptideOrProtein
939
947
A4
Goals of therapy in patients less than 60 years of age include sparing levodopa therapy and providing neuroprotection.
862-992
862
992
Goals of therapy in patients less than 60 years of age include sparing @OBJECT$ @PREDICAT$ @SUBJECT$ and providing neuroprotection.
Fact
preserve
735-737
735-737
T53
in
TREATS
735
737
preserve
662-678
662-678
T51
anticholinergics
PharmacologicSubstance
662
678
preserve
742-749
742-749
T52
elderly
AgeGroup
742
749
A5
Selegiline, amantadine, and anticholinergics are still used but must be employed with caution in the elderly.
634-750
634
750
Selegiline, amantadine, and @SUBJECT$ are still used but must be employed with caution @PREDICAT$ the @OBJECT$ .
Fact
preserve
354-395
391-395
T35
Levodopa is the most effective drug
ISA
354
395
preserve
354-362
354-362
T25
Levodopa
AminoAcidPeptideOrProtein
354
362
preserve
391-395
391-395
T28
drug
PharmacologicSubstance
391
395
A6
Levodopa is the most effective drug for Parkinson's disease, but its long-term use is associated with significant motor complications.
354-500
354
500
@SUBJECT$ @PREDICAT$ @OBJECT$ for Parkinson's disease, but its long-term use is associated with significant motor complications.
Fact
preserve
735-737
735-737
T53
in
TREATS
735
737
preserve
634-644
634-644
T49
Selegiline
OrganicChemical
634
644
preserve
742-749
742-749
T52
elderly
AgeGroup
742
749
A7
Selegiline, amantadine, and anticholinergics are still used but must be employed with caution in the elderly.
634-750
634
750
@SUBJECT$ , amantadine, and anticholinergics are still used but must be employed with caution @PREDICAT$ the @OBJECT$ .
Fact
preserve
354-395
391-395
T38
Levodopa is the most effective drug
TREATS
354
395
preserve
354-362
354-362
T25
Levodopa
AminoAcidPeptideOrProtein
354
362
preserve
400-419
412-419
T29
Parkinson's disease
DiseaseOrSyndrome
400
419
A9
Levodopa is the most effective drug for Parkinson's disease, but its long-term use is associated with significant motor complications.
354-500
354
500
@SUBJECT$ @PREDICAT$ for @OBJECT$ , but its long-term use is associated with significant motor complications.
Fact
preserve
446-456
446-456
T37
associated
ASSOCIATED_WITH
446
456
preserve
354-362
354-362
T25
Levodopa
AminoAcidPeptideOrProtein
354
362
preserve
486-499
486-499
T34
complications
PathologicFunction
486
499
A10
Levodopa is the most effective drug for Parkinson's disease, but its long-term use is associated with significant motor complications.
354-500
354
500
@SUBJECT$ is the most effective drug for Parkinson's disease, but its long-term use is @PREDICAT$ with significant motor @OBJECT$ .
Fact
preserve
793-815
808-815
T62
levodopa therapy
ISA
793
815
preserve
793-801
793-801
T58
levodopa
AminoAcidPeptideOrProtein
793
801
preserve
808-815
808-815
T59
therapy
TherapeuticOrPreventiveProcedure
808
815
A12
COMT inhibitors may be useful adjuncts to levodopa therapy but are plagued with serious adverse effects.
751-861
751
861
COMT inhibitors may be useful adjuncts to @SUBJECT$ @PREDICAT$ @OBJECT$ but are plagued with serious adverse effects.
Fact
preserve
153-169
162-169
T16
surgical therapy
ISA
153
169
preserve
153-161
153-161
T11
surgical
TherapeuticOrPreventiveProcedure
153
161
preserve
162-169
162-169
T12
therapy
TherapeuticOrPreventiveProcedure
162
169
A13
Despite new medical and surgical therapy, mortality rates for Parkinson's disease remain unchanged.
129-234
129
234
Despite new medical and @SUBJECT$ @PREDICAT$ @OBJECT$ , mortality rates for Parkinson's disease remain unchanged.
Fact
preserve
153-169
162-169
T18
surgical therapy
TREATS
153
169
preserve
153-161
153-161
T11
surgical
TherapeuticOrPreventiveProcedure
153
161
preserve
191-210
203-210
T14
Parkinson's disease
DiseaseOrSyndrome
191
210
A15
Despite new medical and surgical therapy, mortality rates for Parkinson's disease remain unchanged.
129-234
129
234
Despite new medical and @SUBJECT$ @PREDICAT$ , mortality rates for @OBJECT$ remain unchanged.
Fact
preserve
735-737
735-737
T53
in
TREATS
735
737
preserve
646-656
646-656
T50
amantadine
OrganicChemical
646
656
preserve
742-749
742-749
T52
elderly
AgeGroup
742
749
A16
Selegiline, amantadine, and anticholinergics are still used but must be employed with caution in the elderly.
634-750
634
750
Selegiline, @SUBJECT$ , and anticholinergics are still used but must be employed with caution @PREDICAT$ the @OBJECT$ .
Fact
preserve
396-399
396-399
T36
for
TREATS
396
399
preserve
391-395
391-395
T28
drug
PharmacologicSubstance
391
395
preserve
400-419
412-419
T29
Parkinson's disease
DiseaseOrSyndrome
400
419
A17
Levodopa is the most effective drug for Parkinson's disease, but its long-term use is associated with significant motor complications.
354-500
354
500
Levodopa is the most effective @SUBJECT$ @PREDICAT$ @OBJECT$ , but its long-term use is associated with significant motor complications.
Fact
preserve
879-881
879-881
T74
in
TREATS
879
881
preserve
871-878
871-878
T66
therapy
TherapeuticOrPreventiveProcedure
871
878
preserve
888-896
888-896
T67
patients
PatientOrDisabledGroup
888
896
A18
Goals of therapy in patients less than 60 years of age include sparing levodopa therapy and providing neuroprotection.
862-992
862
992
Goals of @SUBJECT$ @PREDICAT$ @OBJECT$ less than 60 years of age include sparing levodopa therapy and providing neuroprotection.
Fact
preserve
2165-2173
2165-2173
T136
suffered
PROCESS_OF
2,165
2,173
preserve
2174-2188
2182-2188
T128
cardiac events
DiseaseOrSyndrome
2,174
2,188
preserve
2119-2127
2119-2127
T124
patients
PatientOrDisabledGroup
2,119
2,127
A1
Four of the 36 patients with a negative symptom limited test suffered cardiac events within a year (two patients had a myocardial infarction and two had bypass surgery).
2097-2279
2,097
2,279
Four of the 36 @OBJECT$ with a negative symptom limited test @PREDICAT$ @SUBJECT$ within a year (two patients had a myocardial infarction and two had bypass surgery).
Fact
preserve
1873-1876
1873-1876
T122
had
PROCESS_OF
1,873
1,876
preserve
1879-1892
1887-1892
T107
cardiac event
DiseaseOrSyndrome
1,879
1,892
preserve
1827-1835
1827-1835
T105
patients
PatientOrDisabledGroup
1,827
1,835
A2
Twenty three of the 75 patients who performed an exercise test had a cardiac event within one year (death, myocardial infarction, bypass surgery or PTCA); of these, 19 had a positive symptom limited exercise test and nine had a positive low level exercise test (p = 0.025).
1804-2096
1,804
2,096
Twenty three of the 75 @OBJECT$ who performed an exercise test @PREDICAT$ a @SUBJECT$ within one year (death, myocardial infarction, bypass surgery or PTCA); of these, 19 had a positive symptom limited exercise test and nine had a positive low level exercise test (p = 0.025).
Fact
preserve
1453-1455
1453-1455
T83
in
PROCESS_OF
1,453
1,455
preserve
1426-1438
1431-1438
T75
test results
Finding
1,426
1,438
preserve
1459-1467
1459-1467
T77
patients
PatientOrDisabledGroup
1,459
1,467
A3
The test results were positive in 15 patients at the low level end point and in 39 patients (p < 0.001) at the symptom limited end point.
1416-1565
1,416
1,565
The @SUBJECT$ were positive @PREDICAT$ 15 @OBJECT$ at the low level end point and in 39 patients (p < 0.001) at the symptom limited end point.
Fact
preserve
1453-1455
1453-1455
T83
in
PROCESS_OF
1,453
1,455
preserve
1426-1438
1431-1438
T75
test results
Finding
1,426
1,438
preserve
1511-1519
1511-1519
T80
patients
PatientOrDisabledGroup
1,511
1,519
A4
The test results were positive in 15 patients at the low level end point and in 39 patients (p < 0.001) at the symptom limited end point.
1416-1565
1,416
1,565
The @SUBJECT$ were positive @PREDICAT$ 15 patients at the low level end point and in 39 @OBJECT$ (p < 0.001) at the symptom limited end point.
Fact
preserve
1752-1755
1752-1755
T103
had
PROCESS_OF
1,752
1,755
preserve
1773-1780
1773-1780
T101
symptom
SignOrSymptom
1,773
1,780
preserve
1695-1703
1695-1703
T95
patients
PatientOrDisabledGroup
1,695
1,703
A6
Two of these six patients had a positive low level exercise test and four had a positive symptom limited exercise test.
1672-1803
1,672
1,803
Two of these six @OBJECT$ had a positive low level exercise test and four @PREDICAT$ a positive @SUBJECT$ limited exercise test.
Fact
preserve
948-955
948-955
T50
perform
ADMINISTERED_TO
948
955
preserve
971-984
980-984
T49
exercise test
DiagnosticProcedure
971
984
preserve
926-934
926-934
T47
patients
PatientOrDisabledGroup
926
934
A7
RESULTS: 75 of the 98 patients were able to perform a predischarge exercise test.
898-985
898
985
RESULTS: 75 of the 98 @OBJECT$ were able to @PREDICAT$ a predischarge @SUBJECT$ .
Fact
preserve
2418-2422
2418-2422
T149
with
PROCESS_OF
2,418
2,422
preserve
2440-2459
2449-2459
T144
ST depression
Finding
2,440
2,459
preserve
2409-2417
2409-2417
T142
patients
PatientOrDisabledGroup
2,409
2,417
A8
CONCLUSION: Symptom limited exercise testing soon after thrombolytically treated myocardial infarction will identify more patients with exercise induced ST depression or chest pain than a low level test, and seems safe.
2280-2512
2,280
2,512
CONCLUSION: Symptom limited exercise testing soon after thrombolytically treated myocardial infarction will identify more @OBJECT$ @PREDICAT$ exercise induced @SUBJECT$ or chest pain than a low level test, and seems safe.
Fact
preserve
110-114
110-114
T10
with
PROCESS_OF
110
114
preserve
115-136
126-136
T7
myocardial infarction
DiseaseOrSyndrome
115
136
preserve
101-109
101-109
T6
patients
PatientOrDisabledGroup
101
109
A11
Prognostic value of symptom limited versus low level exercise stress test before discharge in patients with myocardial infarction treated with thrombolytics.
0-164
0
164
Prognostic value of symptom limited versus low level exercise stress test before discharge in @OBJECT$ @PREDICAT$ @SUBJECT$ treated with thrombolytics.
Fact
preserve
1840-1849
1840-1849
T121
performed
ADMINISTERED_TO
1,840
1,849
preserve
1859-1872
1868-1872
T106
exercise test
DiagnosticProcedure
1,859
1,872
preserve
1827-1835
1827-1835
T105
patients
PatientOrDisabledGroup
1,827
1,835
A12
Twenty three of the 75 patients who performed an exercise test had a cardiac event within one year (death, myocardial infarction, bypass surgery or PTCA); of these, 19 had a positive symptom limited exercise test and nine had a positive low level exercise test (p = 0.025).
1804-2096
1,804
2,096
Twenty three of the 75 @OBJECT$ who @PREDICAT$ an @SUBJECT$ had a cardiac event within one year (death, myocardial infarction, bypass surgery or PTCA); of these, 19 had a positive symptom limited exercise test and nine had a positive low level exercise test (p = 0.025).
Fact
preserve
98-100
98-100
T9
in
PROCESS_OF
98
100
preserve
20-27
20-27
T2
symptom
SignOrSymptom
20
27
preserve
101-109
101-109
T6
patients
PatientOrDisabledGroup
101
109
A13
Prognostic value of symptom limited versus low level exercise stress test before discharge in patients with myocardial infarction treated with thrombolytics.
0-164
0
164
Prognostic value of @SUBJECT$ limited versus low level exercise stress test before discharge @PREDICAT$ @OBJECT$ with myocardial infarction treated with thrombolytics.
Counterfact
preserve
2128-2132
2128-2132
T135
with
PROCESS_OF
2,128
2,132
preserve
2144-2151
2144-2151
T126
symptom
SignOrSymptom
2,144
2,151
preserve
2119-2127
2119-2127
T124
patients
PatientOrDisabledGroup
2,119
2,127
A14
Four of the 36 patients with a negative symptom limited test suffered cardiac events within a year (two patients had a myocardial infarction and two had bypass surgery).
2097-2279
2,097
2,279
Four of the 36 @OBJECT$ @PREDICAT$ a negative @SUBJECT$ limited test suffered cardiac events within a year (two patients had a myocardial infarction and two had bypass surgery).
Fact
preserve
137-144
137-144
T11
treated
TREATS
137
144
preserve
150-163
150-163
T8
thrombolytics
PharmacologicSubstance
150
163
preserve
115-136
126-136
T7
myocardial infarction
DiseaseOrSyndrome
115
136
A15
Prognostic value of symptom limited versus low level exercise stress test before discharge in patients with myocardial infarction treated with thrombolytics.
0-164
0
164
Prognostic value of symptom limited versus low level exercise stress test before discharge in patients with @OBJECT$ @PREDICAT$ with @SUBJECT$ .
Fact
preserve
1643-1646
1643-1646
T92
had
PROCESS_OF
1,643
1,646
preserve
1649-1670
1660-1670
T91
myocardial infarction
DiseaseOrSyndrome
1,649
1,670
preserve
1626-1634
1626-1634
T90
patients
PatientOrDisabledGroup
1,626
1,634
A16
During a follow up period of one year, six of the 75 patients died or had a myocardial infarction.
1566-1671
1,566
1,671
During a follow up period of one year, six of the 75 @OBJECT$ died or @PREDICAT$ a @SUBJECT$ .
Counterfact
preserve
1035-1042
1035-1042
T69
perform
ADMINISTERED_TO
1,035
1,042
preserve
1052-1065
1061-1065
T55
exercise test
DiagnosticProcedure
1,052
1,065
preserve
1012-1020
1012-1020
T52
patients
PatientOrDisabledGroup
1,012
1,020
A17
Of the remaining 23 patients who could not perform an early exercise test (because of unstable angina, heart failure, or thrombus detected at echocardiography), five died or had a myocardial infarction and six underwent bypass surgery or percutaneous transluminal coronary angioplasty (PTCA) during a follow up period of one year.
986-1340
986
1,340
Of the remaining 23 @OBJECT$ who could not @PREDICAT$ an early @SUBJECT$ (because of unstable angina, heart failure, or thrombus detected at echocardiography), five died or had a myocardial infarction and six underwent bypass surgery or percutaneous transluminal coronary angioplasty (PTCA) during a follow up period of one year.
Fact
preserve
2418-2422
2418-2422
T149
with
PROCESS_OF
2,418
2,422
preserve
2463-2473
2469-2473
T145
chest pain
SignOrSymptom
2,463
2,473
preserve
2409-2417
2409-2417
T142
patients
PatientOrDisabledGroup
2,409
2,417
A18
CONCLUSION: Symptom limited exercise testing soon after thrombolytically treated myocardial infarction will identify more patients with exercise induced ST depression or chest pain than a low level test, and seems safe.
2280-2512
2,280
2,512
CONCLUSION: Symptom limited exercise testing soon after thrombolytically treated myocardial infarction will identify more @OBJECT$ @PREDICAT$ exercise induced ST depression or @SUBJECT$ than a low level test, and seems safe.
Fact
preserve
2223-2226
2223-2226
T137
had
PROCESS_OF
2,223
2,226
preserve
2229-2250
2240-2250
T132
myocardial infarction
DiseaseOrSyndrome
2,229
2,250
preserve
2214-2222
2214-2222
T131
patients
PatientOrDisabledGroup
2,214
2,222
A19
Four of the 36 patients with a negative symptom limited test suffered cardiac events within a year (two patients had a myocardial infarction and two had bypass surgery).
2097-2279
2,097
2,279
Four of the 36 patients with a negative symptom limited test suffered cardiac events within a year (two @OBJECT$ @PREDICAT$ a @SUBJECT$ and two had bypass surgery).
Fact
preserve
937-943
937-943
T81
caused
CAUSES
937
943
preserve
954-962
954-962
T67
symptoms
SignOrSymptom
954
962
preserve
921-936
927-936
T65
early awakening
SignOrSymptom
921
936
A1
During a run-in period, patients had to show at least one nocturnal or early awakening caused by asthma symptoms that required rescue medication, and a >/= 15% overnight decrease in peak expiratory flow (PEF) on 3 of the preceding 7 d, in order to be randomized into this double-blind, double dummy, multicenter parallel group study (2-wk run-in period and 6 wk of treatment).
844-1250
844
1,250
During a run-in period, patients had to show at least one nocturnal or @OBJECT$ @PREDICAT$ by asthma @SUBJECT$ that required rescue medication, and a >/= 15% overnight decrease in peak expiratory flow (PEF) on 3 of the preceding 7 d, in order to be randomized into this double-blind, double dummy, multicenter parallel group study (2-wk run-in period and 6 wk of treatment).
Fact
preserve
439-441
439-441
T48
in
TREATS
439
441
preserve
394-404
394-404
T32
salmeterol
OrganicChemical
394
404
preserve
446-455
446-455
T35
asthmatic
DiseaseOrSyndrome
446
455
A2
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
289-686
289
686
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled @SUBJECT$ at 50 microgram taken twice daily @PREDICAT$ 126 @OBJECT$ patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
Fact
preserve
439-441
439-441
T48
in
TREATS
439
441
preserve
312-322
312-322
T27
bambuterol
OrganicChemical
312
322
preserve
446-455
446-455
T35
asthmatic
DiseaseOrSyndrome
446
455
A3
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
289-686
289
686
We compared oral @SUBJECT$ in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily @PREDICAT$ 126 @OBJECT$ patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
Fact
preserve
0-10
0-10
T10
Comparison
compared_with
0
10
preserve
19-29
19-29
T2
bambuterol
OrganicChemical
19
29
preserve
42-52
42-52
T4
salmeterol
OrganicChemical
42
52
A4
Comparison of oral bambuterol and inhaled salmeterol in patients with symptomatic asthma and using inhaled corticosteroids.
0-129
0
129
@PREDICAT$ of oral @SUBJECT$ and inhaled @OBJECT$ in patients with symptomatic asthma and using inhaled corticosteroids.
Fact
preserve
298-306
298-306
T46
compared
compared_with
298
306
preserve
312-322
312-322
T27
bambuterol
OrganicChemical
312
322
preserve
394-404
394-404
T32
salmeterol
OrganicChemical
394
404
A6
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
289-686
289
686
We @PREDICAT$ oral @SUBJECT$ in a dose of 20 mg taken once daily in the evening with inhaled @OBJECT$ at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
Fact
preserve
446-464
456-464
T47
asthmatic patients
PROCESS_OF
446
464
preserve
446-455
446-455
T35
asthmatic
DiseaseOrSyndrome
446
455
preserve
456-464
456-464
T36
patients
PatientOrDisabledGroup
456
464
A8
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
289-686
289
686
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 @SUBJECT$ @PREDICAT$ @OBJECT$ (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
Fact
preserve
439-441
439-441
T48
in
TREATS
439
441
preserve
312-322
312-322
T27
bambuterol
OrganicChemical
312
322
preserve
456-464
456-464
T36
patients
PatientOrDisabledGroup
456
464
A9
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
289-686
289
686
We compared oral @SUBJECT$ in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily @PREDICAT$ 126 asthmatic @OBJECT$ (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
Fact
preserve
65-69
65-69
T13
with
PROCESS_OF
65
69
preserve
88-94
88-94
T7
asthma
DiseaseOrSyndrome
88
94
preserve
56-64
56-64
T5
patients
PatientOrDisabledGroup
56
64
A10
Comparison of oral bambuterol and inhaled salmeterol in patients with symptomatic asthma and using inhaled corticosteroids.
0-129
0
129
Comparison of oral bambuterol and inhaled salmeterol in @OBJECT$ @PREDICAT$ symptomatic @SUBJECT$ and using inhaled corticosteroids.
Fact
preserve
53-55
53-55
T11
in
TREATS
53
55
preserve
19-29
19-29
T2
bambuterol
OrganicChemical
19
29
preserve
56-64
56-64
T5
patients
PatientOrDisabledGroup
56
64
A11
Comparison of oral bambuterol and inhaled salmeterol in patients with symptomatic asthma and using inhaled corticosteroids.
0-129
0
129
Comparison of oral @SUBJECT$ and inhaled salmeterol @PREDICAT$ @OBJECT$ with symptomatic asthma and using inhaled corticosteroids.
Fact
preserve
2001-2004
2001-2004
T137
for
TREATS
2,001
2,004
preserve
1990-2000
1990-2000
T133
salmeterol
OrganicChemical
1,990
2,000
preserve
2024-2030
2024-2030
T136
asthma
DiseaseOrSyndrome
2,024
2,030
A12
Once-daily oral bambuterol is a convenient, effective, and less expensive alternative to twice-daily inhaled salmeterol for treating nocturnal asthma.
1869-2031
1,869
2,031
Once-daily oral bambuterol is a convenient, effective, and less expensive alternative to twice-daily inhaled @SUBJECT$ @PREDICAT$ treating nocturnal @OBJECT$ .
Fact
preserve
215-224
215-224
T25
treatment
TREATS
215
224
preserve
130-140
130-140
T16
Salmeterol
OrganicChemical
130
140
preserve
228-234
228-234
T22
asthma
DiseaseOrSyndrome
228
234
A13
Salmeterol inhaled twice-daily is now being used more frequently as additional treatment in asthma insufficiently controlled by inhaled corticosteroids.
130-288
130
288
@SUBJECT$ inhaled twice-daily is now being used more frequently as additional @PREDICAT$ in @OBJECT$ insufficiently controlled by inhaled corticosteroids.
Fact
preserve
53-55
53-55
T11
in
TREATS
53
55
preserve
19-29
19-29
T2
bambuterol
OrganicChemical
19
29
preserve
88-94
88-94
T7
asthma
DiseaseOrSyndrome
88
94
A14
Comparison of oral bambuterol and inhaled salmeterol in patients with symptomatic asthma and using inhaled corticosteroids.
0-129
0
129
Comparison of oral @SUBJECT$ and inhaled salmeterol @PREDICAT$ patients with symptomatic @OBJECT$ and using inhaled corticosteroids.
Fact
preserve
439-441
439-441
T48
in
TREATS
439
441
preserve
394-404
394-404
T32
salmeterol
OrganicChemical
394
404
preserve
456-464
456-464
T36
patients
PatientOrDisabledGroup
456
464
A15
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled salmeterol at 50 microgram taken twice daily in 126 asthmatic patients (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
289-686
289
686
We compared oral bambuterol in a dose of 20 mg taken once daily in the evening with inhaled @SUBJECT$ at 50 microgram taken twice daily @PREDICAT$ 126 asthmatic @OBJECT$ (60 bambuterol, 66 salmeterol) aged 18 to 74 yr who were treated for at least 4 wk with inhaled corticosteroids at a constant dose of 400 to 2,000 microgram/d or with oral corticosteroids at </= 20 mg/d.
Fact
preserve
53-55
53-55
T11
in
TREATS
53
55
preserve
42-52
42-52
T4
salmeterol
OrganicChemical
42
52
preserve
56-64
56-64
T5
patients
PatientOrDisabledGroup
56
64
A16
Comparison of oral bambuterol and inhaled salmeterol in patients with symptomatic asthma and using inhaled corticosteroids.
0-129
0
129
Comparison of oral bambuterol and inhaled @SUBJECT$ @PREDICAT$ @OBJECT$ with symptomatic asthma and using inhaled corticosteroids.
Fact
preserve
53-55
53-55
T11
in
TREATS
53
55
preserve
42-52
42-52
T4
salmeterol
OrganicChemical
42
52
preserve
88-94
88-94
T7
asthma
DiseaseOrSyndrome
88
94
A17
Comparison of oral bambuterol and inhaled salmeterol in patients with symptomatic asthma and using inhaled corticosteroids.
0-129
0
129
Comparison of oral bambuterol and inhaled @SUBJECT$ @PREDICAT$ patients with symptomatic @OBJECT$ and using inhaled corticosteroids.
Fact
preserve
422-431
422-431
T42
treatment
TREATS
422
431
preserve
364-384
375-384
T34
salmeterol xinafoate
OrganicChemical
364
384
preserve
446-452
446-452
T39
asthma
DiseaseOrSyndrome
446
452
A1
OBJECTIVE: We sought to compare the effect of 4 weeks of treatment with inhaled salmeterol xinafoate versus oral zafirlukast in the treatment of persistent asthma.
278-453
278
453
OBJECTIVE: We sought to compare the effect of 4 weeks of treatment with inhaled @SUBJECT$ versus oral zafirlukast in the @PREDICAT$ of persistent @OBJECT$ .
Fact
preserve
385-391
385-391
T41
versus
compared_with
385
391
preserve
364-384
375-384
T34
salmeterol xinafoate
OrganicChemical
364
384
preserve
397-408
397-408
T36
zafirlukast
OrganicChemical
397
408
A3
OBJECTIVE: We sought to compare the effect of 4 weeks of treatment with inhaled salmeterol xinafoate versus oral zafirlukast in the treatment of persistent asthma.
278-453
278
453
OBJECTIVE: We sought to compare the effect of 4 weeks of treatment with inhaled @SUBJECT$ @PREDICAT$ oral @OBJECT$ in the treatment of persistent asthma.
Fact
preserve
1306-1326
1317-1326
T120
Salmeterol treatment
compared_with
1,306
1,326
preserve
1306-1316
1306-1316
T99
Salmeterol
OrganicChemical
1,306
1,316
preserve
1414-1425
1414-1425
T103
zafirlukast
OrganicChemical
1,414
1,425
A4
Salmeterol treatment resulted in significantly greater improvements from baseline compared with zafirlukast for most efficacy measurements, including morning PEF (29.6 vs 13.0 L/min; P </= .001), percentage of symptom-free days (22.4% vs 8.8%; P </= .001), and percentage of days and nights with no supplemental albuterol use (30.5% vs 11.3%; P </= .001).
1306-1692
1,306
1,692
@SUBJECT$ @PREDICAT$ resulted in significantly greater improvements from baseline compared with @OBJECT$ for most efficacy measurements, including morning PEF (29.6 vs 13.0 L/min; P </= .001), percentage of symptom-free days (22.4% vs 8.8%; P </= .001), and percentage of days and nights with no supplemental albuterol use (30.5% vs 11.3%; P </= .001).
Fact
preserve
1870-1875
1870-1875
T145
using
ADMINISTERED_TO
1,870
1,875
preserve
1884-1899
1884-1899
T130
corticosteroids
Hormone
1,884
1,899
preserve
1800-1808
1800-1808
T125
patients
PatientOrDisabledGroup
1,800
1,808
A6
CONCLUSION: In patients with persistent asthma, most of whom were concurrently using inhaled corticosteroids, treatment with inhaled salmeterol provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
1785-2071
1,785
2,071
CONCLUSION: In @OBJECT$ with persistent asthma, most of whom were concurrently @PREDICAT$ inhaled @SUBJECT$ , treatment with inhaled salmeterol provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
Fact
preserve
244-246
244-246
T27
in
PROCESS_OF
244
246
preserve
231-237
231-237
T21
asthma
DiseaseOrSyndrome
231
237
preserve
247-257
247-257
T22
adolescent
AgeGroup
247
257
A7
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and zafirlukast, a leukotriene receptor antagonist, are both indicated for the treatment of asthma in adolescent and adult patients.
79-277
79
277
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and zafirlukast, a leukotriene receptor antagonist, are both indicated for the treatment of @SUBJECT$ @PREDICAT$ @OBJECT$ and adult patients.
Fact
preserve
66-70
66-70
T10
with
PROCESS_OF
66
70
preserve
71-77
71-77
T6
asthma
DiseaseOrSyndrome
71
77
preserve
57-65
57-65
T5
patients
PatientOrDisabledGroup
57
65
A9
Comparison of inhaled salmeterol and oral zafirlukast in patients with asthma.
0-78
0
78
Comparison of inhaled salmeterol and oral zafirlukast in @OBJECT$ @PREDICAT$ @SUBJECT$ .
Fact
preserve
137-189
179-189
T29
zafirlukast, a leukotriene receptor antagonist
TREATS
137
189
preserve
137-148
137-148
T18
zafirlukast
OrganicChemical
137
148
preserve
231-237
231-237
T21
asthma
DiseaseOrSyndrome
231
237
A10
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and zafirlukast, a leukotriene receptor antagonist, are both indicated for the treatment of asthma in adolescent and adult patients.
79-277
79
277
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and @SUBJECT$ @PREDICAT$ , are both indicated for the treatment of @OBJECT$ in adolescent and adult patients.
Fact
preserve
137-189
179-189
T25
zafirlukast, a leukotriene receptor antagonist
ISA
137
189
preserve
137-148
137-148
T18
zafirlukast
OrganicChemical
137
148
preserve
158-189
179-189
T19
leukotriene receptor antagonist
OrganicChemical
158
189
A12
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and zafirlukast, a leukotriene receptor antagonist, are both indicated for the treatment of asthma in adolescent and adult patients.
79-277
79
277
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and @SUBJECT$ @PREDICAT$ @OBJECT$ , are both indicated for the treatment of asthma in adolescent and adult patients.
Fact
preserve
54-56
54-56
T8
in
TREATS
54
56
preserve
22-32
22-32
T2
salmeterol
OrganicChemical
22
32
preserve
71-77
71-77
T6
asthma
DiseaseOrSyndrome
71
77
A13
Comparison of inhaled salmeterol and oral zafirlukast in patients with asthma.
0-78
0
78
Comparison of inhaled @SUBJECT$ and oral zafirlukast @PREDICAT$ patients with @OBJECT$ .
Fact
preserve
54-56
54-56
T8
in
TREATS
54
56
preserve
42-53
42-53
T4
zafirlukast
OrganicChemical
42
53
preserve
57-65
57-65
T5
patients
PatientOrDisabledGroup
57
65
A14
Comparison of inhaled salmeterol and oral zafirlukast in patients with asthma.
0-78
0
78
Comparison of inhaled salmeterol and oral @SUBJECT$ @PREDICAT$ @OBJECT$ with asthma.
Fact
preserve
1809-1813
1809-1813
T144
with
PROCESS_OF
1,809
1,813
preserve
1825-1831
1825-1831
T127
asthma
DiseaseOrSyndrome
1,825
1,831
preserve
1800-1808
1800-1808
T125
patients
PatientOrDisabledGroup
1,800
1,808
A15
CONCLUSION: In patients with persistent asthma, most of whom were concurrently using inhaled corticosteroids, treatment with inhaled salmeterol provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
1785-2071
1,785
2,071
CONCLUSION: In @OBJECT$ @PREDICAT$ persistent @SUBJECT$ , most of whom were concurrently using inhaled corticosteroids, treatment with inhaled salmeterol provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
Fact
preserve
1306-1326
1317-1326
T119
Salmeterol treatment
USES
1,306
1,326
preserve
1317-1326
1317-1326
T100
treatment
TherapeuticOrPreventiveProcedure
1,317
1,326
preserve
1306-1316
1306-1316
T99
Salmeterol
OrganicChemical
1,306
1,316
A16
Salmeterol treatment resulted in significantly greater improvements from baseline compared with zafirlukast for most efficacy measurements, including morning PEF (29.6 vs 13.0 L/min; P </= .001), percentage of symptom-free days (22.4% vs 8.8%; P </= .001), and percentage of days and nights with no supplemental albuterol use (30.5% vs 11.3%; P </= .001).
1306-1692
1,306
1,692
@OBJECT$ @PREDICAT$ @SUBJECT$ resulted in significantly greater improvements from baseline compared with zafirlukast for most efficacy measurements, including morning PEF (29.6 vs 13.0 L/min; P </= .001), percentage of symptom-free days (22.4% vs 8.8%; P </= .001), and percentage of days and nights with no supplemental albuterol use (30.5% vs 11.3%; P </= .001).
Fact
preserve
0-10
0-10
T7
Comparison
compared_with
0
10
preserve
22-32
22-32
T2
salmeterol
OrganicChemical
22
32
preserve
42-53
42-53
T4
zafirlukast
OrganicChemical
42
53
A18
Comparison of inhaled salmeterol and oral zafirlukast in patients with asthma.
0-78
0
78
@PREDICAT$ of inhaled @SUBJECT$ and oral @OBJECT$ in patients with asthma.
Fact
preserve
422-431
422-431
T42
treatment
TREATS
422
431
preserve
397-408
397-408
T36
zafirlukast
OrganicChemical
397
408
preserve
446-452
446-452
T39
asthma
DiseaseOrSyndrome
446
452
A19
OBJECTIVE: We sought to compare the effect of 4 weeks of treatment with inhaled salmeterol xinafoate versus oral zafirlukast in the treatment of persistent asthma.
278-453
278
453
OBJECTIVE: We sought to compare the effect of 4 weeks of treatment with inhaled salmeterol xinafoate versus oral @SUBJECT$ in the @PREDICAT$ of persistent @OBJECT$ .
Fact
preserve
54-56
54-56
T8
in
TREATS
54
56
preserve
22-32
22-32
T2
salmeterol
OrganicChemical
22
32
preserve
57-65
57-65
T5
patients
PatientOrDisabledGroup
57
65
A20
Comparison of inhaled salmeterol and oral zafirlukast in patients with asthma.
0-78
0
78
Comparison of inhaled @SUBJECT$ and oral zafirlukast @PREDICAT$ @OBJECT$ with asthma.
Fact
preserve
1911-1915
1911-1915
T146
with
USES
1,911
1,915
preserve
1901-1910
1901-1910
T131
treatment
TherapeuticOrPreventiveProcedure
1,901
1,910
preserve
1930-1940
1930-1940
T133
salmeterol
OrganicChemical
1,930
1,940
A21
CONCLUSION: In patients with persistent asthma, most of whom were concurrently using inhaled corticosteroids, treatment with inhaled salmeterol provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
1785-2071
1,785
2,071
CONCLUSION: In patients with persistent asthma, most of whom were concurrently using inhaled corticosteroids, @SUBJECT$ @PREDICAT$ inhaled @OBJECT$ provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
Fact
preserve
2030-2037
2030-2037
T147
control
TREATS
2,030
2,037
preserve
1994-2005
1994-2005
T136
zafirlukast
OrganicChemical
1,994
2,005
preserve
2023-2029
2023-2029
T138
asthma
DiseaseOrSyndrome
2,023
2,029
A22
CONCLUSION: In patients with persistent asthma, most of whom were concurrently using inhaled corticosteroids, treatment with inhaled salmeterol provided significantly greater improvement than oral zafirlukast in overall asthma control over the 4-week treatment period.
1785-2071
1,785
2,071
CONCLUSION: In patients with persistent asthma, most of whom were concurrently using inhaled corticosteroids, treatment with inhaled salmeterol provided significantly greater improvement than oral @SUBJECT$ in overall @OBJECT$ @PREDICAT$ over the 4-week treatment period.
Fact
preserve
244-246
244-246
T27
in
PROCESS_OF
244
246
preserve
231-237
231-237
T21
asthma
DiseaseOrSyndrome
231
237
preserve
268-276
268-276
T24
patients
PatientOrDisabledGroup
268
276
A23
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and zafirlukast, a leukotriene receptor antagonist, are both indicated for the treatment of asthma in adolescent and adult patients.
79-277
79
277
BACKGROUND: Salmeterol, a long-acting beta2 -agonist, and zafirlukast, a leukotriene receptor antagonist, are both indicated for the treatment of @SUBJECT$ @PREDICAT$ adolescent and adult @OBJECT$ .
Fact
preserve
54-56
54-56
T8
in
TREATS
54
56
preserve
42-53
42-53
T4
zafirlukast
OrganicChemical
42
53
preserve
71-77
71-77
T6
asthma
DiseaseOrSyndrome
71
77
A24
Comparison of inhaled salmeterol and oral zafirlukast in patients with asthma.
0-78
0
78
Comparison of inhaled salmeterol and oral @SUBJECT$ @PREDICAT$ patients with @OBJECT$ .
Fact
preserve
1306-1326
1317-1326
T118
Salmeterol treatment
ISA
1,306
1,326
preserve
1306-1316
1306-1316
T99
Salmeterol
OrganicChemical
1,306
1,316
preserve
1317-1326
1317-1326
T100
treatment
TherapeuticOrPreventiveProcedure
1,317
1,326
A25
Salmeterol treatment resulted in significantly greater improvements from baseline compared with zafirlukast for most efficacy measurements, including morning PEF (29.6 vs 13.0 L/min; P </= .001), percentage of symptom-free days (22.4% vs 8.8%; P </= .001), and percentage of days and nights with no supplemental albuterol use (30.5% vs 11.3%; P </= .001).
1306-1692
1,306
1,692
@SUBJECT$ @PREDICAT$ @OBJECT$ resulted in significantly greater improvements from baseline compared with zafirlukast for most efficacy measurements, including morning PEF (29.6 vs 13.0 L/min; P </= .001), percentage of symptom-free days (22.4% vs 8.8%; P </= .001), and percentage of days and nights with no supplemental albuterol use (30.5% vs 11.3%; P </= .001).
Fact
preserve
626-648
641-648
T67
corticosteroid regimen
USES
626
648
preserve
641-648
641-648
T55
regimen
ResearchActivity
641
648
preserve
626-640
626-640
T54
corticosteroid
Hormone
626
640
A26
Patients, over 80% of whom were on a concurrent inhaled corticosteroid regimen, were treated for 4 weeks with either inhaled salmeterol xinafoate 42 microgram twice daily administered by means of a metered-dose inhaler or oral zafirlukast 20 mg twice daily.
564-845
564
845
Patients, over 80% of whom were on a concurrent inhaled @OBJECT$ @PREDICAT$ @SUBJECT$ , were treated for 4 weeks with either inhaled salmeterol xinafoate 42 microgram twice daily administered by means of a metered-dose inhaler or oral zafirlukast 20 mg twice daily.
Fact
preserve
1047-1049
1047-1049
T52
in
PROCESS_OF
1,047
1,049
preserve
1029-1036
1029-1036
T49
obesity
DiseaseOrSyndrome
1,029
1,036
preserve
1050-1053
1050-1053
T50
men
PopulationGroup
1,050
1,053
A3
RESULTS: Prevalence of obesity was 12.1% in men and 18.4% in women.
1006-1073
1,006
1,073
RESULTS: Prevalence of @SUBJECT$ was 12.1% @PREDICAT$ @OBJECT$ and 18.4% in women.
Fact
preserve
183-193
183-193
T10
prevalence
OCCURS_IN
183
193
preserve
197-204
197-204
T7
obesity
DiseaseOrSyndrome
197
204
preserve
220-244
234-244
T9
general population
PopulationGroup
220
244
A4
OBJECTIVE: To examine associations between sociodemographic, dietary factors and physical activity and the prevalence of obesity in the Belgian general population.
69-245
69
245
OBJECTIVE: To examine associations between sociodemographic, dietary factors and physical activity and the @PREDICAT$ of @SUBJECT$ in the Belgian @OBJECT$ .
Fact
preserve
1137-1139
1137-1139
T57
in
PROCESS_OF
1,137
1,139
preserve
1109-1116
1109-1116
T53
obesity
DiseaseOrSyndrome
1,109
1,116
preserve
1153-1165
1157-1165
T55
age category
AgeGroup
1,153
1,165
A5
In both sexes, prevalence of obesity increased gradually in each 10-year age category (P<0.0001) and steeply decreased with level of education.
1074-1229
1,074
1,229
In both sexes, prevalence of @SUBJECT$ increased gradually @PREDICAT$ each 10-year @OBJECT$ (P<0.0001) and steeply decreased with level of education.
Possible
preserve
1910-1913
1910-1913
T97
for
TREATS
1,910
1,913
preserve
1880-1895
1880-1895
T92
antidepressants
PharmacologicSubstance
1,880
1,895
preserve
1935-1951
1941-1951
T94
major depression
MentalOrBehavioralDysfunction
1,935
1,951
A1
Adjunctive antidepressants may be useful for patients with major depression who are not acutely ill.
1869-1976
1,869
1,976
Adjunctive @SUBJECT$ may be useful @PREDICAT$ patients with @OBJECT$ who are not acutely ill.
Possible
preserve
1910-1913
1910-1913
T97
for
TREATS
1,910
1,913
preserve
1880-1895
1880-1895
T92
antidepressants
PharmacologicSubstance
1,880
1,895
preserve
1914-1922
1914-1922
T93
patients
PatientOrDisabledGroup
1,914
1,922
A2
Adjunctive antidepressants may be useful for patients with major depression who are not acutely ill.
1869-1976
1,869
1,976
Adjunctive @SUBJECT$ may be useful @PREDICAT$ @OBJECT$ with major depression who are not acutely ill.
Fact
preserve
1639-1641
1639-1641
T81
in
PROCESS_OF
1,639
1,641
preserve
1624-1638
1630-1638
T77
manic symptoms
MentalOrBehavioralDysfunction
1,624
1,638
preserve
1642-1650
1642-1650
T78
patients
PatientOrDisabledGroup
1,642
1,650
A3
There was little evidence to support adjunctive lithium for depressive symptoms and no evidence concerning its use for manic symptoms in patients with schizophrenia.
1493-1670
1,493
1,670
There was little evidence to support adjunctive lithium for depressive symptoms and no evidence concerning its use for @SUBJECT$ @PREDICAT$ @OBJECT$ with schizophrenia.
Fact
preserve
1651-1655
1651-1655
T82
with
PROCESS_OF
1,651
1,655
preserve
1656-1669
1656-1669
T79
schizophrenia
MentalOrBehavioralDysfunction
1,656
1,669
preserve
1642-1650
1642-1650
T78
patients
PatientOrDisabledGroup
1,642
1,650
A4
There was little evidence to support adjunctive lithium for depressive symptoms and no evidence concerning its use for manic symptoms in patients with schizophrenia.
1493-1670
1,493
1,670
There was little evidence to support adjunctive lithium for depressive symptoms and no evidence concerning its use for manic symptoms in @OBJECT$ @PREDICAT$ @SUBJECT$ .
Probable
preserve
1745-1752
1745-1752
T89
treated
TREATS
1,745
1,752
preserve
1806-1829
1815-1829
T87
atypical antipsychotics
PharmacologicSubstance
1,806
1,829
preserve
1727-1735
1727-1735
T84
patients
PatientOrDisabledGroup
1,727
1,735
A5
CONCLUSIONS: Empirical data suggest that both groups of patients are best treated by optimizing antipsychotic treatment and that atypical antipsychotics may prove to be most effective.
1671-1868
1,671
1,868
CONCLUSIONS: Empirical data suggest that both groups of @OBJECT$ are best @PREDICAT$ by optimizing antipsychotic treatment and that @SUBJECT$ may prove to be most effective.
Fact
preserve
1262-1286
1277-1286
T70
antidepressant treatment
USES
1,262
1,286
preserve
1277-1286
1277-1286
T62
treatment
TherapeuticOrPreventiveProcedure
1,277
1,286
preserve
1262-1276
1262-1276
T61
antidepressant
PharmacologicSubstance
1,262
1,276
A6
There was evidence supporting adjunctive antidepressant treatment for schizophrenic and schizoaffective patients who develop a major depressive syndrome after remission of acute psychosis, but there were mixed results for treatment of subsyndromal depression.
1215-1492
1,215
1,492
There was evidence supporting adjunctive @OBJECT$ @PREDICAT$ @SUBJECT$ for schizophrenic and schizoaffective patients who develop a major depressive syndrome after remission of acute psychosis, but there were mixed results for treatment of subsyndromal depression.