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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
stringclasses
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
stringlengths
3
9
object@id
stringclasses
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
1290-1293
1290-1293
T80
for
TREATS
1,290
1,293
preserve
1241-1254
1241-1254
T73
streptokinase
AminoAcidPeptideOrProtein
1,241
1,254
preserve
1294-1302
1294-1302
T76
patients
PatientOrDisabledGroup
1,294
1,302
A2
RESULTS: In the absence of streptokinase resistance, streptokinase is a cost effective strategy for patients with suspected myocardial infarction, even when the expected mortality is low.
1182-1387
1,182
1,387
RESULTS: In the absence of streptokinase resistance, @SUBJECT$ is a cost effective strategy @PREDICAT$ @OBJECT$ with suspected myocardial infarction, even when the expected mortality is low.
Fact
preserve
1303-1307
1303-1307
T81
with
PROCESS_OF
1,303
1,307
preserve
1318-1339
1329-1339
T77
myocardial infarction
DiseaseOrSyndrome
1,318
1,339
preserve
1294-1302
1294-1302
T76
patients
PatientOrDisabledGroup
1,294
1,302
A4
RESULTS: In the absence of streptokinase resistance, streptokinase is a cost effective strategy for patients with suspected myocardial infarction, even when the expected mortality is low.
1182-1387
1,182
1,387
RESULTS: In the absence of streptokinase resistance, streptokinase is a cost effective strategy for @OBJECT$ @PREDICAT$ suspected @SUBJECT$ , even when the expected mortality is low.
Fact
preserve
93-100
93-100
T6
treated
TREATS
93
100
preserve
106-119
106-119
T5
streptokinase
AminoAcidPeptideOrProtein
106
119
preserve
67-75
67-75
T4
patients
PatientOrDisabledGroup
67
75
A5
Potential cost effectiveness of tissue plasminogen activator among patients previously treated with streptokinase.
0-120
0
120
Potential cost effectiveness of tissue plasminogen activator among @OBJECT$ previously @PREDICAT$ with @SUBJECT$ .
Fact
preserve
1290-1293
1290-1293
T80
for
TREATS
1,290
1,293
preserve
1241-1254
1241-1254
T73
streptokinase
AminoAcidPeptideOrProtein
1,241
1,254
preserve
1318-1339
1329-1339
T77
myocardial infarction
DiseaseOrSyndrome
1,318
1,339
A6
RESULTS: In the absence of streptokinase resistance, streptokinase is a cost effective strategy for patients with suspected myocardial infarction, even when the expected mortality is low.
1182-1387
1,182
1,387
RESULTS: In the absence of streptokinase resistance, @SUBJECT$ is a cost effective strategy @PREDICAT$ patients with suspected @OBJECT$ , even when the expected mortality is low.
Fact
preserve
2217-2219
2217-2219
T141
in
TREATS
2,217
2,219
preserve
2212-2216
2212-2216
T123
t-PA
AminoAcidPeptideOrProtein
2,212
2,216
preserve
2227-2235
2227-2235
T124
patients
PatientOrDisabledGroup
2,227
2,235
A7
CONCLUSIONS: This analysis shows that using t-PA in patients previously treated with streptokinase is a cost effective strategy.
2168-2303
2,168
2,303
CONCLUSIONS: This analysis shows that using @SUBJECT$ @PREDICAT$ @OBJECT$ previously treated with streptokinase is a cost effective strategy.
Fact
preserve
921-933
921-933
T55
administered
ADMINISTERED_TO
921
933
preserve
870-883
870-883
T51
streptokinase
AminoAcidPeptideOrProtein
870
883
preserve
967-975
967-975
T54
patients
PatientOrDisabledGroup
967
975
A8
It was assumed that streptokinase would be clinically ineffective when administered to streptokinase-resistant patients.
844-976
844
976
It was assumed that @SUBJECT$ would be clinically ineffective when @PREDICAT$ to streptokinase-resistant @OBJECT$ .
Fact
preserve
1153-1161
1153-1161
T68
compared
compared_with
1,153
1,161
preserve
1148-1152
1148-1152
T66
t-PA
AminoAcidPeptideOrProtein
1,148
1,152
preserve
1167-1180
1167-1180
T67
streptokinase
AminoAcidPeptideOrProtein
1,167
1,180
A10
Sensitivity analyses were performed varying the baseline mortality, the proportion of patients resistant to streptokinase and the absolute survival benefit of t-PA compared with streptokinase.
977-1181
977
1,181
Sensitivity analyses were performed varying the baseline mortality, the proportion of patients resistant to streptokinase and the absolute survival benefit of @SUBJECT$ @PREDICAT$ with @OBJECT$ .
Fact
preserve
316-337
330-337
T19
streptokinase therapy
USES
316
337
preserve
316-329
316-329
T16
streptokinase
AminoAcidPeptideOrProtein
316
329
preserve
316-329
316-329
T16
streptokinase
AminoAcidPeptideOrProtein
316
329
A13
BACKGROUND: A major limitation of streptokinase is the development and persistence of problematic neutralizing antibodies that have the potential to limit the effectiveness of repeat streptokinase therapy.
121-338
121
338
BACKGROUND: A major limitation of streptokinase is the development and persistence of problematic neutralizing antibodies that have the potential to limit the effectiveness of repeat @OBJECT$ @SUBJECT$ @PREDICAT$ .
Fact
preserve
525-529
525-529
T34
with
USES
525
529
preserve
515-524
515-524
T30
treatment
TherapeuticOrPreventiveProcedure
515
524
preserve
537-550
537-550
T31
streptokinase
AminoAcidPeptideOrProtein
537
550
A16
Accordingly, tissue-type plasminogen activator (t-PA) is frequently administered to patients with recurrent infarction presenting more than four days from previous treatment with streptokinase.
339-551
339
551
Accordingly, tissue-type plasminogen activator (t-PA) is frequently administered to patients with recurrent infarction presenting more than four days from previous @SUBJECT$ @PREDICAT$ @OBJECT$ .
Fact
preserve
438-442
438-442
T33
with
PROCESS_OF
438
442
preserve
459-469
459-469
T25
infarction
PathologicFunction
459
469
preserve
429-437
429-437
T23
patients
PatientOrDisabledGroup
429
437
A17
Accordingly, tissue-type plasminogen activator (t-PA) is frequently administered to patients with recurrent infarction presenting more than four days from previous treatment with streptokinase.
339-551
339
551
Accordingly, tissue-type plasminogen activator (t-PA) is frequently administered to @OBJECT$ @PREDICAT$ recurrent @SUBJECT$ presenting more than four days from previous treatment with streptokinase.
Fact
preserve
316-337
330-337
T18
streptokinase therapy
ISA
316
337
preserve
316-329
316-329
T16
streptokinase
AminoAcidPeptideOrProtein
316
329
preserve
330-337
330-337
T17
therapy
TherapeuticOrPreventiveProcedure
330
337
A19
BACKGROUND: A major limitation of streptokinase is the development and persistence of problematic neutralizing antibodies that have the potential to limit the effectiveness of repeat streptokinase therapy.
121-338
121
338
BACKGROUND: A major limitation of streptokinase is the development and persistence of problematic neutralizing antibodies that have the potential to limit the effectiveness of repeat @SUBJECT$ @PREDICAT$ @OBJECT$ .
Probable
preserve
413-425
413-425
T32
administered
ADMINISTERED_TO
413
425
preserve
352-391
382-391
T21
tissue-type plasminogen activator
AminoAcidPeptideOrProtein
352
391
preserve
429-437
429-437
T23
patients
PatientOrDisabledGroup
429
437
A21
Accordingly, tissue-type plasminogen activator (t-PA) is frequently administered to patients with recurrent infarction presenting more than four days from previous treatment with streptokinase.
339-551
339
551
Accordingly, @SUBJECT$ (t-PA) is frequently @PREDICAT$ to @OBJECT$ with recurrent infarction presenting more than four days from previous treatment with streptokinase.
Fact
preserve
1069-1072
1069-1072
T63
for
TREATS
1,069
1,072
preserve
1049-1068
1061-1068
T57
acupuncture therapy
TherapeuticOrPreventiveProcedure
1,049
1,068
preserve
1086-1094
1086-1094
T59
patients
PatientOrDisabledGroup
1,086
1,094
A1
This result did not postulate the previous study that acupuncture therapy for stroke patients should depend on needle manual and "de qi" response.
988-1147
988
1,147
This result did not postulate the previous study that @SUBJECT$ @PREDICAT$ stroke @OBJECT$ should depend on needle manual and "de qi" response.
Fact
preserve
1069-1072
1069-1072
T63
for
TREATS
1,069
1,072
preserve
1049-1068
1061-1068
T57
acupuncture therapy
TherapeuticOrPreventiveProcedure
1,049
1,068
preserve
1073-1079
1073-1079
T58
stroke
DiseaseOrSyndrome
1,073
1,079
A2
This result did not postulate the previous study that acupuncture therapy for stroke patients should depend on needle manual and "de qi" response.
988-1147
988
1,147
This result did not postulate the previous study that @SUBJECT$ @PREDICAT$ @OBJECT$ patients should depend on needle manual and "de qi" response.
Fact
preserve
1343-1358
1350-1358
T77
stroke patients
PROCESS_OF
1,343
1,358
preserve
1343-1349
1343-1349
T74
stroke
DiseaseOrSyndrome
1,343
1,349
preserve
1350-1358
1350-1358
T75
patients
PatientOrDisabledGroup
1,350
1,358
A3
We suggest that electrical acupuncture through adhesive surface electrodes in conjunction with current optimal rehabilitation programs is a convenient and effective therapy for stroke patients.
1148-1359
1,148
1,359
We suggest that electrical acupuncture through adhesive surface electrodes in conjunction with current optimal rehabilitation programs is a convenient and effective therapy for @SUBJECT$ @PREDICAT$ @OBJECT$ .
Fact
preserve
252-259
252-259
T20
receive
ADMINISTERED_TO
252
259
preserve
318-329
318-329
T17
acupuncture
TherapeuticOrPreventiveProcedure
318
329
preserve
206-214
206-214
T13
patients
PatientOrDisabledGroup
206
214
A4
To assess the efficacy of electrical acupuncture in the rehabilitation of patients with hemiplegia in stroke, we randomized 128 patients within 2 wk of stroke onset to receive either comprehensive rehabilitation plus electrical acupuncture (n = 59) or comprehensive rehabilitation only (n = 59).
72-385
72
385
To assess the efficacy of electrical acupuncture in the rehabilitation of patients with hemiplegia in stroke, we randomized 128 @OBJECT$ within 2 wk of stroke onset to @PREDICAT$ either comprehensive rehabilitation plus electrical @SUBJECT$ (n = 59) or comprehensive rehabilitation only (n = 59).
Fact
preserve
1073-1094
1086-1094
T62
stroke patients
PROCESS_OF
1,073
1,094
preserve
1073-1079
1073-1079
T58
stroke
DiseaseOrSyndrome
1,073
1,079
preserve
1086-1094
1086-1094
T59
patients
PatientOrDisabledGroup
1,086
1,094
A5
This result did not postulate the previous study that acupuncture therapy for stroke patients should depend on needle manual and "de qi" response.
988-1147
988
1,147
This result did not postulate the previous study that acupuncture therapy for @SUBJECT$ @PREDICAT$ @OBJECT$ should depend on needle manual and "de qi" response.
Fact
preserve
717-724
717-724
T53
treated
TREATS
717
724
preserve
747-758
747-758
T40
acupuncture
TherapeuticOrPreventiveProcedure
747
758
preserve
708-716
708-716
T38
Patients
PatientOrDisabledGroup
708
716
A6
Patients treated with electrical acupuncture had a shorter duration of hospital stay for rehabilitation and better neurological and functional outcomes than the control group had, with a significant difference in scores for self-care and locomotion (P = 0.02).
708-987
708
987
@OBJECT$ @PREDICAT$ with electrical @SUBJECT$ had a shorter duration of hospital stay for rehabilitation and better neurological and functional outcomes than the control group had, with a significant difference in scores for self-care and locomotion (P = 0.02).
Fact
preserve
161-165
161-165
T18
with
PROCESS_OF
161
165
preserve
166-176
166-176
T11
hemiplegia
SignOrSymptom
166
176
preserve
152-160
152-160
T10
patients
PatientOrDisabledGroup
152
160
A7
To assess the efficacy of electrical acupuncture in the rehabilitation of patients with hemiplegia in stroke, we randomized 128 patients within 2 wk of stroke onset to receive either comprehensive rehabilitation plus electrical acupuncture (n = 59) or comprehensive rehabilitation only (n = 59).
72-385
72
385
To assess the efficacy of electrical acupuncture in the rehabilitation of @OBJECT$ @PREDICAT$ @SUBJECT$ in stroke, we randomized 128 patients within 2 wk of stroke onset to receive either comprehensive rehabilitation plus electrical acupuncture (n = 59) or comprehensive rehabilitation only (n = 59).
Probable
preserve
1325-1332
1325-1332
T76
therapy
TREATS
1,325
1,332
preserve
1181-1192
1181-1192
T66
acupuncture
TherapeuticOrPreventiveProcedure
1,181
1,192
preserve
1343-1349
1343-1349
T74
stroke
DiseaseOrSyndrome
1,343
1,349
A8
We suggest that electrical acupuncture through adhesive surface electrodes in conjunction with current optimal rehabilitation programs is a convenient and effective therapy for stroke patients.
1148-1359
1,148
1,359
We suggest that electrical @SUBJECT$ through adhesive surface electrodes in conjunction with current optimal rehabilitation programs is a convenient and effective @PREDICAT$ for @OBJECT$ patients.
Fact
preserve
55-70
62-70
T7
stroke patients
PROCESS_OF
55
70
preserve
55-61
55-61
T5
stroke
DiseaseOrSyndrome
55
61
preserve
62-70
62-70
T6
patients
PatientOrDisabledGroup
62
70
A9
Clinical trial of electrical acupuncture on hemiplegic stroke patients.
0-71
0
71
Clinical trial of electrical acupuncture on hemiplegic @SUBJECT$ @PREDICAT$ @OBJECT$ .
Fact
preserve
177-179
177-179
T19
in
ASSOCIATED_WITH
177
179
preserve
166-176
166-176
T11
hemiplegia
SignOrSymptom
166
176
preserve
180-186
180-186
T12
stroke
DiseaseOrSyndrome
180
186
A10
To assess the efficacy of electrical acupuncture in the rehabilitation of patients with hemiplegia in stroke, we randomized 128 patients within 2 wk of stroke onset to receive either comprehensive rehabilitation plus electrical acupuncture (n = 59) or comprehensive rehabilitation only (n = 59).
72-385
72
385
To assess the efficacy of electrical acupuncture in the rehabilitation of patients with @SUBJECT$ @PREDICAT$ @OBJECT$ , we randomized 128 patients within 2 wk of stroke onset to receive either comprehensive rehabilitation plus electrical acupuncture (n = 59) or comprehensive rehabilitation only (n = 59).
Probable
preserve
1325-1332
1325-1332
T76
therapy
TREATS
1,325
1,332
preserve
1181-1192
1181-1192
T66
acupuncture
TherapeuticOrPreventiveProcedure
1,181
1,192
preserve
1350-1358
1350-1358
T75
patients
PatientOrDisabledGroup
1,350
1,358
A11
We suggest that electrical acupuncture through adhesive surface electrodes in conjunction with current optimal rehabilitation programs is a convenient and effective therapy for stroke patients.
1148-1359
1,148
1,359
We suggest that electrical @SUBJECT$ through adhesive surface electrodes in conjunction with current optimal rehabilitation programs is a convenient and effective @PREDICAT$ for stroke @OBJECT$ .
Fact
preserve
432-434
432-434
T31
by
METHOD_OF
432
434
preserve
435-457
446-457
T23
electrical stimulation
LaboratoryProcedure
435
457
preserve
403-414
403-414
T22
acupuncture
TherapeuticOrPreventiveProcedure
403
414
A12
Electrical acupuncture was administered by electrical stimulation of acupuncture points through adhesive surface electrodes five times per week.
386-542
386
542
Electrical @OBJECT$ was administered @PREDICAT$ @SUBJECT$ of acupuncture points through adhesive surface electrodes five times per week.
Fact
preserve
612-637
627-637
T40
antidepressant treatments
USES
612
637
preserve
627-637
627-637
T33
treatments
TherapeuticOrPreventiveProcedure
627
637
preserve
612-626
612-626
T32
antidepressant
PharmacologicSubstance
612
626
A1
The different classes of antidepressant treatments were subsequently shown to enhance serotonin neurotransmission albeit via different pre- and postsynaptic mechanisms.
581-761
581
761
The different classes of @OBJECT$ @PREDICAT$ @SUBJECT$ were subsequently shown to enhance serotonin neurotransmission albeit via different pre- and postsynaptic mechanisms.
Uncommitted
preserve
49-51
49-51
T7
in
ASSOCIATED_WITH
49
51
preserve
0-9
0-9
T1
Serotonin
NeuroreactiveSubstanceOrBiogenicAmine
0
9
preserve
101-116
107-116
T6
panic disorders
MentalOrBehavioralDysfunction
101
116
A2
Serotonin and drug-induced therapeutic responses in major depression, obsessive-compulsive and panic disorders.
0-117
0
117
@SUBJECT$ and drug-induced therapeutic responses @PREDICAT$ major depression, obsessive-compulsive and @OBJECT$ .
Uncommitted
preserve
49-51
49-51
T7
in
ASSOCIATED_WITH
49
51
preserve
0-9
0-9
T1
Serotonin
NeuroreactiveSubstanceOrBiogenicAmine
0
9
preserve
52-68
58-68
T5
major depression
MentalOrBehavioralDysfunction
52
68
A3
Serotonin and drug-induced therapeutic responses in major depression, obsessive-compulsive and panic disorders.
0-117
0
117
@SUBJECT$ and drug-induced therapeutic responses @PREDICAT$ @OBJECT$ , obsessive-compulsive and panic disorders.
Fact
preserve
172-174
172-174
T13
in
TREATS
172
174
preserve
151-171
166-171
T11
antidepressant drugs
PharmacologicSubstance
151
171
preserve
175-191
181-191
T12
major depression
MentalOrBehavioralDysfunction
175
191
A4
The therapeutic effectiveness of antidepressant drugs in major depression was discovered by pure serendipity.
118-233
118
233
The therapeutic effectiveness of @SUBJECT$ @PREDICAT$ @OBJECT$ was discovered by pure serendipity.
Fact
preserve
1247-1250
1247-1250
T65
for
TREATS
1,247
1,250
preserve
1226-1235
1226-1235
T62
treatment
TherapeuticOrPreventiveProcedure
1,226
1,235
preserve
1257-1266
1257-1266
T64
disorders
DiseaseOrSyndrome
1,257
1,266
A5
It is expected that the better understanding recently obtained of the mechanism of action of certain antidepressant drugs in obsessive-compulsive and panic disorders will also lead to more effective treatment strategies for those disorders.
1008-1267
1,008
1,267
It is expected that the better understanding recently obtained of the mechanism of action of certain antidepressant drugs in obsessive-compulsive and panic disorders will also lead to more effective @SUBJECT$ strategies @PREDICAT$ those @OBJECT$ .
Fact
preserve
736-743
736-743
T37
treated
TREATS
736
743
preserve
749-764
749-764
T35
glucocorticoids
Hormone
749
764
preserve
708-714
708-714
T34
asthma
DiseaseOrSyndrome
708
714
A1
Adults with stable asthma, either untreated or treated with glucocorticoids (GCs), were enrolled.
683-792
683
792
Adults with stable @OBJECT$ , either untreated or @PREDICAT$ with @SUBJECT$ (GCs), were enrolled.
Fact
preserve
1525-1527
1525-1527
T78
in
PROCESS_OF
1,525
1,527
preserve
1482-1490
1482-1490
T74
fibrosis
PathologicFunction
1,482
1,490
preserve
1528-1536
1528-1536
T75
patients
PatientOrDisabledGroup
1,528
1,536
A2
This observation has important implications, since an excess of TIMP-1 could lead to airway fibrosis, a hallmark of airway remodelling in patients with chronic asthma.
1384-1564
1,384
1,564
This observation has important implications, since an excess of TIMP-1 could lead to airway @SUBJECT$ , a hallmark of airway remodelling @PREDICAT$ @OBJECT$ with chronic asthma.
Uncommitted
preserve
521-523
521-523
T24
in
PROCESS_OF
521
523
preserve
448-457
448-457
T18
imbalance
SignOrSymptom
448
457
preserve
535-543
535-543
T21
patients
PatientOrDisabledGroup
535
543
A3
The accumulation in the submucosa of fibrous proteins that are substrates of matrix metalloproteinases (MMP), and the demonstration of increased levels of MMP-9 in bronchoalveolar lavage fluid, prompted us to determine whether there was an imbalance between MMPs and tissue inhibitors of metalloproteinase (TIMP) in such patients.
190-544
190
544
The accumulation in the submucosa of fibrous proteins that are substrates of matrix metalloproteinases (MMP), and the demonstration of increased levels of MMP-9 in bronchoalveolar lavage fluid, prompted us to determine whether there was an @SUBJECT$ between MMPs and tissue inhibitors of metalloproteinase (TIMP) @PREDICAT$ such @OBJECT$ .
Fact
preserve
736-743
736-743
T37
treated
TREATS
736
743
preserve
749-764
749-764
T35
glucocorticoids
Hormone
749
764
preserve
683-689
683-689
T33
Adults
AgeGroup
683
689
A4
Adults with stable asthma, either untreated or treated with glucocorticoids (GCs), were enrolled.
683-792
683
792
@OBJECT$ with stable asthma, either untreated or @PREDICAT$ with @SUBJECT$ (GCs), were enrolled.
Fact
preserve
690-694
690-694
T36
with
PROCESS_OF
690
694
preserve
708-714
708-714
T34
asthma
DiseaseOrSyndrome
708
714
preserve
683-689
683-689
T33
Adults
AgeGroup
683
689
A5
Adults with stable asthma, either untreated or treated with glucocorticoids (GCs), were enrolled.
683-792
683
792
@OBJECT$ @PREDICAT$ stable @SUBJECT$ , either untreated or treated with glucocorticoids (GCs), were enrolled.
Fact
preserve
253-263
253-263
T22
substrates
INTERACTS_WITH
253
263
preserve
227-243
235-243
T12
fibrous proteins
AminoAcidPeptideOrProtein
227
243
preserve
273-298
280-298
T13
matrix metalloproteinases
AminoAcidPeptideOrProtein
273
298
A6
The accumulation in the submucosa of fibrous proteins that are substrates of matrix metalloproteinases (MMP), and the demonstration of increased levels of MMP-9 in bronchoalveolar lavage fluid, prompted us to determine whether there was an imbalance between MMPs and tissue inhibitors of metalloproteinase (TIMP) in such patients.
190-544
190
544
The accumulation in the submucosa of @SUBJECT$ that are @PREDICAT$ of @OBJECT$ (MMP), and the demonstration of increased levels of MMP-9 in bronchoalveolar lavage fluid, prompted us to determine whether there was an imbalance between MMPs and tissue inhibitors of metalloproteinase (TIMP) in such patients.
Fact
preserve
169-173
169-173
T11
with
PROCESS_OF
169
173
preserve
182-188
182-188
T10
asthma
DiseaseOrSyndrome
182
188
preserve
160-168
160-168
T8
patients
PatientOrDisabledGroup
160
168
A7
Airway remodeling is a well-recognized feature in patients with chronic asthma.
110-189
110
189
Airway remodeling is a well-recognized feature in @OBJECT$ @PREDICAT$ chronic @SUBJECT$ .
Fact
preserve
363-365
363-365
T23
in
LOCATION_OF
363
365
preserve
366-394
389-394
T17
bronchoalveolar lavage fluid
BodySubstance
366
394
preserve
357-362
357-362
T16
MMP-9
AminoAcidPeptideOrProtein
357
362
A8
The accumulation in the submucosa of fibrous proteins that are substrates of matrix metalloproteinases (MMP), and the demonstration of increased levels of MMP-9 in bronchoalveolar lavage fluid, prompted us to determine whether there was an imbalance between MMPs and tissue inhibitors of metalloproteinase (TIMP) in such patients.
190-544
190
544
The accumulation in the submucosa of fibrous proteins that are substrates of matrix metalloproteinases (MMP), and the demonstration of increased levels of @OBJECT$ @PREDICAT$ @SUBJECT$ , prompted us to determine whether there was an imbalance between MMPs and tissue inhibitors of metalloproteinase (TIMP) in such patients.
Fact
preserve
1537-1541
1537-1541
T79
with
PROCESS_OF
1,537
1,541
preserve
1557-1563
1557-1563
T77
asthma
DiseaseOrSyndrome
1,557
1,563
preserve
1528-1536
1528-1536
T75
patients
PatientOrDisabledGroup
1,528
1,536
A9
This observation has important implications, since an excess of TIMP-1 could lead to airway fibrosis, a hallmark of airway remodelling in patients with chronic asthma.
1384-1564
1,384
1,564
This observation has important implications, since an excess of TIMP-1 could lead to airway fibrosis, a hallmark of airway remodelling in @OBJECT$ @PREDICAT$ chronic @SUBJECT$ .
Fact
preserve
1996-2005
1996-2005
T116
treatment
TREATS
1,996
2,005
preserve
2013-2040
2031-2040
T112
monoamine oxidase inhibitor
PharmacologicSubstance
2,013
2,040
preserve
2069-2094
2086-2094
T114
major depressive disorder
MentalOrBehavioralDysfunction
2,069
2,094
A1
CONCLUSIONS: Cognitive therapy may offer an effective alternative to standard acute-phase treatment with a monoamine oxidase inhibitor for outpatients with major depressive disorder and atypical features.
1900-2117
1,900
2,117
CONCLUSIONS: Cognitive therapy may offer an effective alternative to standard acute-phase @PREDICAT$ with a @SUBJECT$ for outpatients with @OBJECT$ and atypical features.
Fact
preserve
1514-1518
1514-1518
T94
than
compared_with
1,514
1,518
preserve
1434-1444
1434-1444
T80
Phenelzine
OrganicChemical
1,434
1,444
preserve
1519-1526
1519-1526
T84
placebo
MedicalDevice
1,519
1,526
A3
Phenelzine and cognitive therapy also reduced symptoms significantly more than placebo according to contrasts after a repeated-measures analysis of covariance and random regression with the use of the blind evaluator's final Hamilton Rating Scale for Depression score.
1434-1727
1,434
1,727
@SUBJECT$ and cognitive therapy also reduced symptoms significantly more @PREDICAT$ @OBJECT$ according to contrasts after a repeated-measures analysis of covariance and random regression with the use of the blind evaluator's final Hamilton Rating Scale for Depression score.
Fact
preserve
1996-2005
1996-2005
T116
treatment
TREATS
1,996
2,005
preserve
2013-2040
2031-2040
T112
monoamine oxidase inhibitor
PharmacologicSubstance
2,013
2,040
preserve
2052-2063
2052-2063
T113
outpatients
PatientOrDisabledGroup
2,052
2,063
A4
CONCLUSIONS: Cognitive therapy may offer an effective alternative to standard acute-phase treatment with a monoamine oxidase inhibitor for outpatients with major depressive disorder and atypical features.
1900-2117
1,900
2,117
CONCLUSIONS: Cognitive therapy may offer an effective alternative to standard acute-phase @PREDICAT$ with a @SUBJECT$ for @OBJECT$ with major depressive disorder and atypical features.
Fact
preserve
501-509
501-509
T30
compared
compared_with
501
509
preserve
483-500
493-500
T28
cognitive therapy
TherapeuticOrPreventiveProcedure
483
500
preserve
517-550
541-550
T29
monoamine oxidase inhibitor
PharmacologicSubstance
517
550
A5
There are no prospective, randomized, controlled trials, to our knowledge, of psychotherapy for atypical depression or of cognitive therapy compared with a monoamine oxidase inhibitor.
349-551
349
551
There are no prospective, randomized, controlled trials, to our knowledge, of psychotherapy for atypical depression or of @SUBJECT$ @PREDICAT$ with a @OBJECT$ .
Fact
preserve
722-726
722-726
T55
with
PROCESS_OF
722
726
preserve
737-762
754-762
T45
major depressive disorder
MentalOrBehavioralDysfunction
737
762
preserve
710-721
710-721
T43
Outpatients
PatientOrDisabledGroup
710
721
A6
METHODS: Outpatients with DSM-III-R major depressive disorder and atypical features (N = 108) were treated in a 10-week, double-blind, randomized, controlled trial comparing acute-phase cognitive therapy or clinical management plus either phenelzine sulfate or placebo.
701-988
701
988
METHODS: @OBJECT$ @PREDICAT$ DSM-III-R @SUBJECT$ and atypical features (N = 108) were treated in a 10-week, double-blind, randomized, controlled trial comparing acute-phase cognitive therapy or clinical management plus either phenelzine sulfate or placebo.
Fact
preserve
685-688
685-688
T41
for
TREATS
685
688
preserve
671-684
671-684
T39
psychotherapy
TherapeuticOrPreventiveProcedure
671
684
preserve
689-699
689-699
T40
depression
MentalOrBehavioralDysfunction
689
699
A7
Since there is only 1 placebo-controlled trial of cognitive therapy, this trial fills a gap in the literature on psychotherapy for depression.
552-700
552
700
Since there is only 1 placebo-controlled trial of cognitive therapy, this trial fills a gap in the literature on @SUBJECT$ @PREDICAT$ @OBJECT$ .
Fact
preserve
0-9
0-9
T8
Treatment
TREATS
0
9
preserve
59-69
59-69
T4
phenelzine
OrganicChemical
59
69
preserve
13-32
22-32
T2
atypical depression
MentalOrBehavioralDysfunction
13
32
A8
Treatment of atypical depression with cognitive therapy or phenelzine: a double-blind, placebo-controlled trial.
0-118
0
118
@PREDICAT$ of @OBJECT$ with cognitive therapy or @SUBJECT$ : a double-blind, placebo-controlled trial.
Fact
preserve
2064-2068
2064-2068
T117
with
PROCESS_OF
2,064
2,068
preserve
2069-2094
2086-2094
T114
major depressive disorder
MentalOrBehavioralDysfunction
2,069
2,094
preserve
2052-2063
2052-2063
T113
outpatients
PatientOrDisabledGroup
2,052
2,063
A9
CONCLUSIONS: Cognitive therapy may offer an effective alternative to standard acute-phase treatment with a monoamine oxidase inhibitor for outpatients with major depressive disorder and atypical features.
1900-2117
1,900
2,117
CONCLUSIONS: Cognitive therapy may offer an effective alternative to standard acute-phase treatment with a monoamine oxidase inhibitor for @OBJECT$ @PREDICAT$ @SUBJECT$ and atypical features.
Fact
preserve
0-9
0-9
T8
Treatment
TREATS
0
9
preserve
38-55
48-55
T3
cognitive therapy
TherapeuticOrPreventiveProcedure
38
55
preserve
13-32
22-32
T2
atypical depression
MentalOrBehavioralDysfunction
13
32
A10
Treatment of atypical depression with cognitive therapy or phenelzine: a double-blind, placebo-controlled trial.
0-118
0
118
@PREDICAT$ of @OBJECT$ with @SUBJECT$ or phenelzine: a double-blind, placebo-controlled trial.
Fact
preserve
140-144
140-144
T16
with
PROCESS_OF
140
144
preserve
145-164
154-164
T11
atypical depression
MentalOrBehavioralDysfunction
145
164
preserve
131-139
131-139
T10
Patients
PatientOrDisabledGroup
131
139
A11
BACKGROUND: Patients with atypical depression are more likely to respond to monoamine oxidase inhibitors than to tricyclic antidepressants.
119-264
119
264
BACKGROUND: @OBJECT$ @PREDICAT$ @SUBJECT$ are more likely to respond to monoamine oxidase inhibitors than to tricyclic antidepressants.
Fact
preserve
1514-1518
1514-1518
T95
than
higher_than
1,514
1,518
preserve
1434-1444
1434-1444
T80
Phenelzine
OrganicChemical
1,434
1,444
preserve
1519-1526
1519-1526
T84
placebo
MedicalDevice
1,519
1,526
A12
Phenelzine and cognitive therapy also reduced symptoms significantly more than placebo according to contrasts after a repeated-measures analysis of covariance and random regression with the use of the blind evaluator's final Hamilton Rating Scale for Depression score.
1434-1727
1,434
1,727
@SUBJECT$ and cognitive therapy also reduced symptoms significantly more @PREDICAT$ @OBJECT$ according to contrasts after a repeated-measures analysis of covariance and random regression with the use of the blind evaluator's final Hamilton Rating Scale for Depression score.
Fact
preserve
453-456
453-456
T31
for
TREATS
453
456
preserve
433-446
433-446
T26
psychotherapy
TherapeuticOrPreventiveProcedure
433
446
preserve
457-476
466-476
T27
atypical depression
MentalOrBehavioralDysfunction
457
476
A13
There are no prospective, randomized, controlled trials, to our knowledge, of psychotherapy for atypical depression or of cognitive therapy compared with a monoamine oxidase inhibitor.
349-551
349
551
There are no prospective, randomized, controlled trials, to our knowledge, of @SUBJECT$ @PREDICAT$ @OBJECT$ or of cognitive therapy compared with a monoamine oxidase inhibitor.
Probable
preserve
867-874
867-874
T67
therapy
TREATS
867
874
preserve
846-856
846-856
T64
salmeterol
OrganicChemical
846
856
preserve
860-866
860-866
T65
asthma
DiseaseOrSyndrome
860
866
A1
The above results indicate the great efficacy of salmeterol in asthma therapy.
791-875
791
875
The above results indicate the great efficacy of @SUBJECT$ in @OBJECT$ @PREDICAT$ .
Fact
preserve
165-172
165-172
T19
therapy
TREATS
165
172
preserve
138-148
138-148
T16
salmeterol
OrganicChemical
138
148
preserve
152-158
152-158
T17
asthma
DiseaseOrSyndrome
152
158
A2
The purpose of the study was to evaluate the efficacy of salmeterol in asthma therapy.
81-173
81
173
The purpose of the study was to evaluate the efficacy of @SUBJECT$ in @OBJECT$ @PREDICAT$ .
Fact
preserve
215-239
231-239
T26
allergic asthma patients
PROCESS_OF
215
239
preserve
215-230
224-230
T22
allergic asthma
DiseaseOrSyndrome
215
230
preserve
231-239
231-239
T23
patients
PatientOrDisabledGroup
231
239
A3
The study was performed on a group of 16 allergic asthma patients sensitive to house dust mite allergens.
174-285
174
285
The study was performed on a group of 16 @SUBJECT$ @PREDICAT$ @OBJECT$ sensitive to house dust mite allergens.
Fact
preserve
51-53
51-53
T10
in
TREATS
51
53
preserve
43-50
43-50
T4
therapy
TherapeuticOrPreventiveProcedure
43
50
preserve
70-78
70-78
T6
patients
PatientOrDisabledGroup
70
78
A5
[Clinical evaluation of 12 week salmeterol therapy in allergic asthma patients].
0-80
0
80
[Clinical evaluation of 12 week salmeterol @SUBJECT$ @PREDICAT$ allergic asthma @OBJECT$ ].
Fact
preserve
51-53
51-53
T10
in
TREATS
51
53
preserve
43-50
43-50
T4
therapy
TherapeuticOrPreventiveProcedure
43
50
preserve
54-69
63-69
T5
allergic asthma
DiseaseOrSyndrome
54
69
A6
[Clinical evaluation of 12 week salmeterol therapy in allergic asthma patients].
0-80
0
80
[Clinical evaluation of 12 week salmeterol @SUBJECT$ @PREDICAT$ @OBJECT$ patients].
Fact
preserve
32-50
43-50
T12
salmeterol therapy
TREATS
32
50
preserve
32-42
32-42
T3
salmeterol
OrganicChemical
32
42
preserve
70-78
70-78
T6
patients
PatientOrDisabledGroup
70
78
A7
[Clinical evaluation of 12 week salmeterol therapy in allergic asthma patients].
0-80
0
80
[Clinical evaluation of 12 week @SUBJECT$ @PREDICAT$ in allergic asthma @OBJECT$ ].
Fact
preserve
32-50
43-50
T8
salmeterol therapy
USES
32
50
preserve
43-50
43-50
T4
therapy
TherapeuticOrPreventiveProcedure
43
50
preserve
32-42
32-42
T3
salmeterol
OrganicChemical
32
42
A8
[Clinical evaluation of 12 week salmeterol therapy in allergic asthma patients].
0-80
0
80
[Clinical evaluation of 12 week @OBJECT$ @PREDICAT$ @SUBJECT$ in allergic asthma patients].
Fact
preserve
565-588
578-588
T48
clinic spirometry
USES
565
588
preserve
578-588
578-588
T47
spirometry
DiagnosticProcedure
578
588
preserve
565-571
565-571
T46
clinic
HealthCareRelatedOrganization
565
571
A9
On the visit to the clinic spirometry was performed.
545-603
545
603
On the visit to the @OBJECT$ @PREDICAT$ @SUBJECT$ was performed.
Fact
preserve
32-50
43-50
T7
salmeterol therapy
ISA
32
50
preserve
32-42
32-42
T3
salmeterol
OrganicChemical
32
42
preserve
43-50
43-50
T4
therapy
TherapeuticOrPreventiveProcedure
43
50
A10
[Clinical evaluation of 12 week salmeterol therapy in allergic asthma patients].
0-80
0
80
[Clinical evaluation of 12 week @SUBJECT$ @PREDICAT$ @OBJECT$ in allergic asthma patients].
Fact
preserve
54-78
70-78
T9
allergic asthma patients
PROCESS_OF
54
78
preserve
54-69
63-69
T5
allergic asthma
DiseaseOrSyndrome
54
69
preserve
70-78
70-78
T6
patients
PatientOrDisabledGroup
70
78
A11
[Clinical evaluation of 12 week salmeterol therapy in allergic asthma patients].
0-80
0
80
[Clinical evaluation of 12 week salmeterol therapy in @SUBJECT$ @PREDICAT$ @OBJECT$ ].
Fact
preserve
332-339
332-339
T35
treated
TREATS
332
339
preserve
345-355
345-355
T30
salmeterol
OrganicChemical
345
355
preserve
312-320
312-320
T29
patients
PatientOrDisabledGroup
312
320
A12
After a run-in period the patients were treated with salmeterol, 2 x 50 micrograms, for a period of 12 weeks.
286-401
286
401
After a run-in period the @OBJECT$ were @PREDICAT$ with @SUBJECT$ , 2 x 50 micrograms, for a period of 12 weeks.
Fact
preserve
834-841
834-841
T45
treated
TREATS
834
841
preserve
847-860
847-860
T43
streptokinase
AminoAcidPeptideOrProtein
847
860
preserve
825-833
825-833
T42
patients
PatientOrDisabledGroup
825
833
A1
The cumulative 1-, 5- and 10-year survival rates were 91%, 81% and 69% in patients treated with streptokinase and 84%, 71% and 59% in the control group, respectively (P=0.02).
745-932
745
932
The cumulative 1-, 5- and 10-year survival rates were 91%, 81% and 69% in @OBJECT$ @PREDICAT$ with @SUBJECT$ and 84%, 71% and 59% in the control group, respectively (P=0.02).
Probable
preserve
1156-1161
1156-1161
T59
after
PRECEDES
1,156
1,161
preserve
1162-1182
1175-1182
T58
thrombolytic therapy
TherapeuticOrPreventiveProcedure
1,162
1,182
preserve
1079-1093
1086-1093
T54
bypass surgery
TherapeuticOrPreventiveProcedure
1,079
1,093
A3
Coronary bypass surgery and coronary angioplasty were more frequently performed after thrombolytic therapy.
1070-1183
1,070
1,183
Coronary @OBJECT$ and coronary angioplasty were more frequently performed @PREDICAT$ @SUBJECT$ .
Fact
preserve
70-72
70-72
T7
in
TREATS
70
72
preserve
49-69
62-69
T5
thrombolytic therapy
TherapeuticOrPreventiveProcedure
49
69
preserve
79-100
90-100
T6
myocardial infarction
DiseaseOrSyndrome
79
100
A5
Sustained benefit at 10-14 years follow-up after thrombolytic therapy in myocardial infarction.
0-101
0
101
Sustained benefit at 10-14 years follow-up after @SUBJECT$ @PREDICAT$ @OBJECT$ .
Fact
preserve
633-655
646-655
T38
thrombolytic treatment
USES
633
655
preserve
646-655
646-655
T34
treatment
TherapeuticOrPreventiveProcedure
646
655
preserve
633-645
633-645
T33
thrombolytic
PharmacologicSubstance
633
645
A6
At follow-up, 158 patients (59%) of the 269 patients allocated to thrombolytic treatment and only 129 patients (49%) of the 264 conventionally treated patients were alive.
561-744
561
744
At follow-up, 158 patients (59%) of the 269 patients allocated to @OBJECT$ @PREDICAT$ @SUBJECT$ and only 129 patients (49%) of the 264 conventionally treated patients were alive.
Probable
preserve
1156-1161
1156-1161
T59
after
PRECEDES
1,156
1,161
preserve
1162-1182
1175-1182
T58
thrombolytic therapy
TherapeuticOrPreventiveProcedure
1,162
1,182
preserve
1098-1118
1107-1118
T55
coronary angioplasty
TherapeuticOrPreventiveProcedure
1,098
1,118
A7
Coronary bypass surgery and coronary angioplasty were more frequently performed after thrombolytic therapy.
1070-1183
1,070
1,183
Coronary bypass surgery and @OBJECT$ were more frequently performed @PREDICAT$ @SUBJECT$ .
Fact
preserve
1497-1499
1497-1499
T92
in
TREATS
1,497
1,499
preserve
1442-1455
1442-1455
T82
Beta-blockers
PharmacologicSubstance
1,442
1,455
preserve
1500-1508
1500-1508
T84
patients
PatientOrDisabledGroup
1,500
1,508
A1
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
1442-1642
1,442
1,642
@SUBJECT$ seem to be safe and well tolerated @PREDICAT$ @OBJECT$ with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
Fact
preserve
1688-1692
1688-1692
T103
with
PROCESS_OF
1,688
1,692
preserve
1693-1699
1693-1699
T101
asthma
DiseaseOrSyndrome
1,693
1,699
preserve
1679-1687
1679-1687
T100
patients
PatientOrDisabledGroup
1,679
1,687
A2
Beta-blockers should not be used in patients with asthma.
1643-1700
1,643
1,700
Beta-blockers should not be used in @OBJECT$ @PREDICAT$ @SUBJECT$ .
Fact
preserve
1351-1353
1351-1353
T80
in
PROCESS_OF
1,351
1,353
preserve
1321-1326
1321-1326
T71
death
OrganismFunction
1,321
1,326
preserve
1382-1390
1382-1390
T76
patients
PatientOrDisabledGroup
1,382
1,390
A3
Calcium channel antagonists may have some effect in retarding progression of diabetic nephropathy although a recent trial found a higher incidence of death as a secondary endpoint in hypertensive diabetic patients who were treated with calcium channel antagonists.
1158-1441
1,158
1,441
Calcium channel antagonists may have some effect in retarding progression of diabetic nephropathy although a recent trial found a higher incidence of @SUBJECT$ as a secondary endpoint @PREDICAT$ hypertensive diabetic @OBJECT$ who were treated with calcium channel antagonists.
Counterfact
preserve
1676-1678
1676-1678
T102
in
TREATS
1,676
1,678
preserve
1643-1656
1643-1656
T98
Beta-blockers
PharmacologicSubstance
1,643
1,656
preserve
1679-1687
1679-1687
T100
patients
PatientOrDisabledGroup
1,679
1,687
A4
Beta-blockers should not be used in patients with asthma.
1643-1700
1,643
1,700
@SUBJECT$ should not be used @PREDICAT$ @OBJECT$ with asthma.
Fact
preserve
1032-1036
1032-1036
T53
have
PROCESS_OF
1,032
1,036
preserve
1043-1059
1043-1059
T49
microalbuminuria
DiseaseOrSyndrome
1,043
1,059
preserve
999-1007
999-1007
T47
patients
PatientOrDisabledGroup
999
1,007
A5
In patients with diabetes, ACE inhibitors are effective first-line agents in type 1 and type 2 diabetic patients who are hypertensive or have microalbuminuria.
889-1060
889
1,060
In patients with diabetes, ACE inhibitors are effective first-line agents in type 1 and type 2 diabetic @OBJECT$ who are hypertensive or @PREDICAT$ @SUBJECT$ .
Fact
preserve
1962-1967
1962-1967
T132
raise
AUGMENTS
1,962
1,967
preserve
1928-1937
1928-1937
T122
piroxicam
OrganicChemical
1,928
1,937
preserve
1968-1987
1979-1987
T124
mean blood pressure
Finding
1,968
1,987
A6
NSAIDs, particularly piroxicam and indomethacin, raise mean blood pressure by approximately 5 mm Hg, enough to consider a change of either NSAID or antihypertensive to one that is not as affected by NSAIDs.
1907-2131
1,907
2,131
NSAIDs, particularly @SUBJECT$ and indomethacin, @PREDICAT$ @OBJECT$ by approximately 5 mm Hg, enough to consider a change of either NSAID or antihypertensive to one that is not as affected by NSAIDs.
Fact
preserve
1795-1797
1795-1797
T116
in
PROCESS_OF
1,795
1,797
preserve
1782-1794
1782-1794
T110
hypertension
DiseaseOrSyndrome
1,782
1,794
preserve
1798-1806
1798-1806
T111
patients
PatientOrDisabledGroup
1,798
1,806
A7
Dihydropyridine calcium channel antagonists are the preferred treatment of hypertension in patients with Raynaud's but should be avoided in patients with severe gastroesophageal reflux disease.
1701-1906
1,701
1,906
Dihydropyridine calcium channel antagonists are the preferred treatment of @SUBJECT$ @PREDICAT$ @OBJECT$ with Raynaud's but should be avoided in patients with severe gastroesophageal reflux disease.
Probable
preserve
1094-1096
1094-1096
T59
in
TREATS
1,094
1,096
preserve
1061-1075
1065-1075
T55
ACE inhibitors
PharmacologicSubstance
1,061
1,075
preserve
1097-1105
1097-1105
T56
patients
PatientOrDisabledGroup
1,097
1,105
A8
ACE inhibitors may be beneficial in patients with nondiabetic renal insufficiency as well.
1061-1157
1,061
1,157
@SUBJECT$ may be beneficial @PREDICAT$ @OBJECT$ with nondiabetic renal insufficiency as well.
Fact
preserve
1582-1586
1582-1586
T94
with
PROCESS_OF
1,582
1,586
preserve
1587-1596
1592-1596
T88
rest pain
SignOrSymptom
1,587
1,596
preserve
1573-1581
1573-1581
T87
patients
PatientOrDisabledGroup
1,573
1,581
A9
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
1442-1642
1,442
1,642
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although @OBJECT$ @PREDICAT$ @SUBJECT$ or limb ischemia have not been studied.
Fact
preserve
901-905
901-905
T50
with
PROCESS_OF
901
905
preserve
906-914
906-914
T38
diabetes
DiseaseOrSyndrome
906
914
preserve
892-900
892-900
T37
patients
PatientOrDisabledGroup
892
900
A10
In patients with diabetes, ACE inhibitors are effective first-line agents in type 1 and type 2 diabetic patients who are hypertensive or have microalbuminuria.
889-1060
889
1,060
In @OBJECT$ @PREDICAT$ @SUBJECT$ , ACE inhibitors are effective first-line agents in type 1 and type 2 diabetic patients who are hypertensive or have microalbuminuria.
Probable
preserve
1094-1096
1094-1096
T59
in
TREATS
1,094
1,096
preserve
1061-1075
1065-1075
T55
ACE inhibitors
PharmacologicSubstance
1,061
1,075
preserve
1129-1148
1135-1148
T57
renal insufficiency
DiseaseOrSyndrome
1,129
1,148
A11
ACE inhibitors may be beneficial in patients with nondiabetic renal insufficiency as well.
1061-1157
1,061
1,157
@SUBJECT$ may be beneficial @PREDICAT$ patients with nondiabetic @OBJECT$ as well.
Fact
preserve
1582-1586
1582-1586
T94
with
PROCESS_OF
1,582
1,586
preserve
1605-1613
1605-1613
T90
ischemia
DiseaseOrSyndrome
1,605
1,613
preserve
1573-1581
1573-1581
T87
patients
PatientOrDisabledGroup
1,573
1,581
A12
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
1442-1642
1,442
1,642
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although @OBJECT$ @PREDICAT$ rest pain or limb @SUBJECT$ have not been studied.
Fact
preserve
1962-1967
1962-1967
T132
raise
AUGMENTS
1,962
1,967
preserve
1907-1913
1907-1913
T121
NSAIDs
PharmacologicSubstance
1,907
1,913
preserve
1968-1987
1979-1987
T124
mean blood pressure
Finding
1,968
1,987
A14
NSAIDs, particularly piroxicam and indomethacin, raise mean blood pressure by approximately 5 mm Hg, enough to consider a change of either NSAID or antihypertensive to one that is not as affected by NSAIDs.
1907-2131
1,907
2,131
@SUBJECT$ , particularly piroxicam and indomethacin, @PREDICAT$ @OBJECT$ by approximately 5 mm Hg, enough to consider a change of either NSAID or antihypertensive to one that is not as affected by NSAIDs.
Fact
preserve
990-1007
999-1007
T52
diabetic patients
PROCESS_OF
990
1,007
preserve
990-998
990-998
T46
diabetic
Finding
990
998
preserve
999-1007
999-1007
T47
patients
PatientOrDisabledGroup
999
1,007
A15
In patients with diabetes, ACE inhibitors are effective first-line agents in type 1 and type 2 diabetic patients who are hypertensive or have microalbuminuria.
889-1060
889
1,060
In patients with diabetes, ACE inhibitors are effective first-line agents in type 1 and type 2 @SUBJECT$ @PREDICAT$ @OBJECT$ who are hypertensive or have microalbuminuria.
Probable
preserve
2151-2157
2151-2157
T141
induce
CAUSES
2,151
2,157
preserve
2132-2146
2145-2146
T136
Cyclosporine A
AminoAcidPeptideOrProtein
2,132
2,146
preserve
2158-2170
2158-2170
T137
hypertension
DiseaseOrSyndrome
2,158
2,170
A16
Cyclosporine A can induce hypertension by its vasoconstrictive effects, particularly on the kidney.
2132-2237
2,132
2,237
@SUBJECT$ can @PREDICAT$ @OBJECT$ by its vasoconstrictive effects, particularly on the kidney.
Fact
preserve
781-790
781-790
T33
treatment
TREATS
781
790
preserve
724-733
724-733
T27
diuretics
PharmacologicSubstance
724
733
preserve
800-826
814-826
T32
uncomplicated hypertension
DiseaseOrSyndrome
800
826
A18
In the absence of contraindications, beta-blockers and diuretics are still recommended as first-line agents for treatment of uncomplicated hypertension.
663-827
663
827
In the absence of contraindications, beta-blockers and @SUBJECT$ are still recommended as first-line agents for @PREDICAT$ of @OBJECT$ .
Fact
preserve
1962-1967
1962-1967
T132
raise
AUGMENTS
1,962
1,967
preserve
1948-1960
1948-1960
T123
indomethacin
OrganicChemical
1,948
1,960
preserve
1968-1987
1979-1987
T124
mean blood pressure
Finding
1,968
1,987
A19
NSAIDs, particularly piroxicam and indomethacin, raise mean blood pressure by approximately 5 mm Hg, enough to consider a change of either NSAID or antihypertensive to one that is not as affected by NSAIDs.
1907-2131
1,907
2,131
NSAIDs, particularly piroxicam and @SUBJECT$ , @PREDICAT$ @OBJECT$ by approximately 5 mm Hg, enough to consider a change of either NSAID or antihypertensive to one that is not as affected by NSAIDs.
Counterfact
preserve
1676-1678
1676-1678
T102
in
TREATS
1,676
1,678
preserve
1643-1656
1643-1656
T98
Beta-blockers
PharmacologicSubstance
1,643
1,656
preserve
1693-1699
1693-1699
T101
asthma
DiseaseOrSyndrome
1,693
1,699
A20
Beta-blockers should not be used in patients with asthma.
1643-1700
1,643
1,700
@SUBJECT$ should not be used @PREDICAT$ patients with @OBJECT$ .
Fact
preserve
1497-1499
1497-1499
T92
in
TREATS
1,497
1,499
preserve
1442-1455
1442-1455
T82
Beta-blockers
PharmacologicSubstance
1,442
1,455
preserve
1531-1562
1550-1562
T86
intermittent claudication
DiseaseOrSyndrome
1,531
1,562
A21
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
1442-1642
1,442
1,642
@SUBJECT$ seem to be safe and well tolerated @PREDICAT$ patients with mild to moderate @OBJECT$ , although patients with rest pain or limb ischemia have not been studied.
Fact
preserve
1367-1390
1382-1390
T79
diabetic patients
PROCESS_OF
1,367
1,390
preserve
1367-1375
1367-1375
T75
diabetic
Finding
1,367
1,375
preserve
1382-1390
1382-1390
T76
patients
PatientOrDisabledGroup
1,382
1,390
A22
Calcium channel antagonists may have some effect in retarding progression of diabetic nephropathy although a recent trial found a higher incidence of death as a secondary endpoint in hypertensive diabetic patients who were treated with calcium channel antagonists.
1158-1441
1,158
1,441
Calcium channel antagonists may have some effect in retarding progression of diabetic nephropathy although a recent trial found a higher incidence of death as a secondary endpoint in hypertensive @SUBJECT$ @PREDICAT$ @OBJECT$ who were treated with calcium channel antagonists.
Fact
preserve
1856-1860
1856-1860
T119
with
PROCESS_OF
1,856
1,860
preserve
1874-1905
1898-1905
T115
gastroesophageal reflux disease
DiseaseOrSyndrome
1,874
1,905
preserve
1847-1855
1847-1855
T113
patients
PatientOrDisabledGroup
1,847
1,855
A25
Dihydropyridine calcium channel antagonists are the preferred treatment of hypertension in patients with Raynaud's but should be avoided in patients with severe gastroesophageal reflux disease.
1701-1906
1,701
1,906
Dihydropyridine calcium channel antagonists are the preferred treatment of hypertension in patients with Raynaud's but should be avoided in @OBJECT$ @PREDICAT$ severe @SUBJECT$ .
Fact
preserve
781-790
781-790
T33
treatment
TREATS
781
790
preserve
700-713
700-713
T26
beta-blockers
PharmacologicSubstance
700
713
preserve
800-826
814-826
T32
uncomplicated hypertension
DiseaseOrSyndrome
800
826
A26
In the absence of contraindications, beta-blockers and diuretics are still recommended as first-line agents for treatment of uncomplicated hypertension.
663-827
663
827
In the absence of contraindications, @SUBJECT$ and diuretics are still recommended as first-line agents for @PREDICAT$ of @OBJECT$ .
Fact
preserve
1807-1811
1807-1811
T117
with
PROCESS_OF
1,807
1,811
preserve
1812-1821
1812-1819
T112
Raynaud's
DiseaseOrSyndrome
1,812
1,821
preserve
1798-1806
1798-1806
T111
patients
PatientOrDisabledGroup
1,798
1,806
A27
Dihydropyridine calcium channel antagonists are the preferred treatment of hypertension in patients with Raynaud's but should be avoided in patients with severe gastroesophageal reflux disease.
1701-1906
1,701
1,906
Dihydropyridine calcium channel antagonists are the preferred treatment of hypertension in @OBJECT$ @PREDICAT$ @SUBJECT$ but should be avoided in patients with severe gastroesophageal reflux disease.
Fact
preserve
1106-1110
1106-1110
T60
with
PROCESS_OF
1,106
1,110
preserve
1129-1148
1135-1148
T57
renal insufficiency
DiseaseOrSyndrome
1,129
1,148
preserve
1097-1105
1097-1105
T56
patients
PatientOrDisabledGroup
1,097
1,105
A29
ACE inhibitors may be beneficial in patients with nondiabetic renal insufficiency as well.
1061-1157
1,061
1,157
ACE inhibitors may be beneficial in @OBJECT$ @PREDICAT$ nondiabetic @SUBJECT$ as well.
Fact
preserve
1600-1613
1605-1613
T96
limb ischemia
LOCATION_OF
1,600
1,613
preserve
1600-1604
1600-1604
T89
limb
BodyPartOrganOrOrganComponent
1,600
1,604
preserve
1605-1613
1605-1613
T90
ischemia
DiseaseOrSyndrome
1,605
1,613
A32
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
1442-1642
1,442
1,642
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or @SUBJECT$ @PREDICAT$ @OBJECT$ have not been studied.
Fact
preserve
1509-1513
1509-1513
T93
with
PROCESS_OF
1,509
1,513
preserve
1531-1562
1550-1562
T86
intermittent claudication
DiseaseOrSyndrome
1,531
1,562
preserve
1500-1508
1500-1508
T84
patients
PatientOrDisabledGroup
1,500
1,508
A33
Beta-blockers seem to be safe and well tolerated in patients with mild to moderate intermittent claudication, although patients with rest pain or limb ischemia have not been studied.
1442-1642
1,442
1,642
Beta-blockers seem to be safe and well tolerated in @OBJECT$ @PREDICAT$ mild to moderate @SUBJECT$ , although patients with rest pain or limb ischemia have not been studied.
Uncommitted
preserve
23-25
23-25
T6
in
TREATS
23
25
preserve
14-22
14-22
T2
exercise
DailyOrRecreationalActivity
14
22
preserve
26-36
26-36
T3
overweight
SignOrSymptom
26
36
A1
Nutrition and exercise in overweight and obese postpartum women.
0-64
0
64
Nutrition and @SUBJECT$ @PREDICAT$ @OBJECT$ and obese postpartum women.
Fact
preserve
660-664
660-664
T48
with
PROCESS_OF
660
664
preserve
665-676
665-676
T41
underweight
Finding
665
676
preserve
695-700
695-700
T43
women
PopulationGroup
695
700
A2
No differences were present when overweight and obese women were compared with underweight and normal weight women relative to nutrition and physical activity.
580-751
580
751
No differences were present when overweight and obese women were compared @PREDICAT$ @SUBJECT$ and normal weight @OBJECT$ relative to nutrition and physical activity.
Fact
preserve
807-824
819-824
T59
obese women
PROCESS_OF
807
824
preserve
807-812
807-812
T54
obese
DiseaseOrSyndrome
807
812
preserve
819-824
819-824
T55
women
PopulationGroup
819
824
A3
Nutritional imbalances were present for overweight and obese women relative to protein and fat intake.
752-860
752
860
Nutritional imbalances were present for overweight and @SUBJECT$ @PREDICAT$ @OBJECT$ relative to protein and fat intake.
Uncommitted
preserve
23-25
23-25
T6
in
TREATS
23
25
preserve
14-22
14-22
T2
exercise
DailyOrRecreationalActivity
14
22
preserve
41-46
41-46
T4
obese
DiseaseOrSyndrome
41
46
A4
Nutrition and exercise in overweight and obese postpartum women.
0-64
0
64
Nutrition and @SUBJECT$ @PREDICAT$ overweight and @OBJECT$ postpartum women.
Fact
preserve
41-63
58-63
T8
obese postpartum women
PROCESS_OF
41
63
preserve
41-46
41-46
T4
obese
DiseaseOrSyndrome
41
46
preserve
47-63
58-63
T5
postpartum women
PatientOrDisabledGroup
47
63
A5
Nutrition and exercise in overweight and obese postpartum women.
0-64
0
64
Nutrition and exercise in overweight and @SUBJECT$ @PREDICAT$ @OBJECT$ .
Fact
preserve
628-639
634-639
T47
obese women
PROCESS_OF
628
639
preserve
628-633
628-633
T39
obese
DiseaseOrSyndrome
628
633
preserve
634-639
634-639
T40
women
PopulationGroup
634
639
A7
No differences were present when overweight and obese women were compared with underweight and normal weight women relative to nutrition and physical activity.
580-751
580
751
No differences were present when overweight and @SUBJECT$ @PREDICAT$ @OBJECT$ were compared with underweight and normal weight women relative to nutrition and physical activity.
Fact
preserve
876-898
893-898
T73
obese postpartum women
PROCESS_OF
876
898
preserve
876-881
876-881
T61
obese
DiseaseOrSyndrome
876
881
preserve
882-898
893-898
T62
postpartum women
PatientOrDisabledGroup
882
898
A8
Overweight and obese postpartum women can be encouraged to lose weight using a nutritionally balanced approach by decreasing fat and protein intake, maintaining an adequate carbohydrate intake, and increasing their folacin intake.
861-1109
861
1,109
Overweight and @SUBJECT$ @PREDICAT$ @OBJECT$ can be encouraged to lose weight using a nutritionally balanced approach by decreasing fat and protein intake, maintaining an adequate carbohydrate intake, and increasing their folacin intake.
Uncommitted
preserve
23-25
23-25
T6
in
TREATS
23
25
preserve
14-22
14-22
T2
exercise
DailyOrRecreationalActivity
14
22
preserve
47-63
58-63
T5
postpartum women
PatientOrDisabledGroup
47
63
A9
Nutrition and exercise in overweight and obese postpartum women.
0-64
0
64
Nutrition and @SUBJECT$ @PREDICAT$ overweight and obese @OBJECT$ .