US3860708A - Method of delivering the intestines of human beings from bariumsulphate after barium meal examination - Google Patents
Method of delivering the intestines of human beings from bariumsulphate after barium meal examination Download PDFInfo
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- US3860708A US3860708A US416037A US41603773A US3860708A US 3860708 A US3860708 A US 3860708A US 416037 A US416037 A US 416037A US 41603773 A US41603773 A US 41603773A US 3860708 A US3860708 A US 3860708A
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- barium
- examination
- lactulose
- intestines
- bariumsulphate
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- 229910052788 barium Inorganic materials 0.000 title claims abstract description 34
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 title claims abstract description 34
- 235000012054 meals Nutrition 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims description 12
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 title abstract description 30
- 210000000936 intestine Anatomy 0.000 title abstract description 9
- 241000282414 Homo sapiens Species 0.000 title description 6
- JCQLYHFGKNRPGE-FCVZTGTOSA-N lactulose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 JCQLYHFGKNRPGE-FCVZTGTOSA-N 0.000 claims abstract description 30
- 229960000511 lactulose Drugs 0.000 claims abstract description 23
- PFCRQPBOOFTZGQ-UHFFFAOYSA-N lactulose keto form Natural products OCC(=O)C(O)C(C(O)CO)OC1OC(CO)C(O)C(O)C1O PFCRQPBOOFTZGQ-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000006188 syrup Substances 0.000 claims description 3
- 235000020357 syrup Nutrition 0.000 claims description 3
- 239000007920 enema Substances 0.000 description 10
- 206010012735 Diarrhoea Diseases 0.000 description 9
- 241000792859 Enema Species 0.000 description 8
- 210000001015 abdomen Anatomy 0.000 description 8
- 210000001072 colon Anatomy 0.000 description 7
- 229940079360 enema for constipation Drugs 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- KHOITXIGCFIULA-UHFFFAOYSA-N Alophen Chemical compound C1=CC(OC(=O)C)=CC=C1C(C=1N=CC=CC=1)C1=CC=C(OC(C)=O)C=C1 KHOITXIGCFIULA-UHFFFAOYSA-N 0.000 description 5
- 229960000503 bisacodyl Drugs 0.000 description 5
- IPQVTOJGNYVQEO-KGFNBKMBSA-N sennoside A Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=CC2=C1C(=O)C1=C(O)C=C(C(O)=O)C=C1[C@@H]2[C@H]1C2=CC(C(O)=O)=CC(O)=C2C(=O)C2=C(O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)C=CC=C21 IPQVTOJGNYVQEO-KGFNBKMBSA-N 0.000 description 5
- 229940063651 senokot Drugs 0.000 description 5
- 230000005856 abnormality Effects 0.000 description 4
- 238000011835 investigation Methods 0.000 description 4
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 3
- 208000004998 Abdominal Pain Diseases 0.000 description 3
- 206010000060 Abdominal distension Diseases 0.000 description 3
- 206010010774 Constipation Diseases 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 206010000059 abdominal discomfort Diseases 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229940095399 enema Drugs 0.000 description 3
- 229930182830 galactose Natural products 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 230000033001 locomotion Effects 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- 206010024971 Lower respiratory tract infections Diseases 0.000 description 2
- 241001249696 Senna alexandrina Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 210000001731 descending colon Anatomy 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 210000000664 rectum Anatomy 0.000 description 2
- 239000000829 suppository Substances 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- 206010000084 Abdominal pain lower Diseases 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 206010010305 Confusional state Diseases 0.000 description 1
- 206010051055 Deep vein thrombosis Diseases 0.000 description 1
- 208000020401 Depressive disease Diseases 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 206010028813 Nausea Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 206010034647 Peristalsis visible Diseases 0.000 description 1
- 206010051482 Prostatomegaly Diseases 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000004098 Tetracycline Substances 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 206010047249 Venous thrombosis Diseases 0.000 description 1
- 206010060926 abdominal symptom Diseases 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000001785 acacia senegal l. willd gum Substances 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 229960000723 ampicillin Drugs 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 208000022531 anorexia Diseases 0.000 description 1
- 210000000709 aorta Anatomy 0.000 description 1
- 210000001815 ascending colon Anatomy 0.000 description 1
- 239000000305 astragalus gummifer gum Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 208000011769 benign colon neoplasm Diseases 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 208000035269 cancer or benign tumor Diseases 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 201000011024 colonic benign neoplasm Diseases 0.000 description 1
- 238000009109 curative therapy Methods 0.000 description 1
- 206010061428 decreased appetite Diseases 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 206010013395 disorientation Diseases 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 201000005917 gastric ulcer Diseases 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 208000003243 intestinal obstruction Diseases 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 229940125722 laxative agent Drugs 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 230000008693 nausea Effects 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- -1 pcctine Substances 0.000 description 1
- OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 description 1
- 229960005205 prednisolone Drugs 0.000 description 1
- 230000001141 propulsive effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229960002180 tetracycline Drugs 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 210000003384 transverse colon Anatomy 0.000 description 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 208000022534 visible peristalsis Diseases 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
Definitions
- barium sulphate often remains in the intestines of patients after a barium meal examination. This especially readily occurs in elderly patients.
- Bisacodyl containing 4,4-(2-pyridylmethylen)diphenol diacetate as active ingredient and enemas, are not effective.
- barium sulphate can quite surprisingly be expelled from the intestines by administering orally a small but effective dose of lactulose.
- the duration of the treatment may vary from 1 to several weeks in the case some time lapsed between the barium meal examination and the curative treatment with lactulose. In the case the administration of lactulose is begun with at the time of the barium meal examination or shortly thereafter a treatment of l or 2 days to a week will suffice.
- Lactulose may be administered in solid form either alone or in admixture with one or more carriers such as glucose, galactose or lactose.
- a very satisfactory method however is to administer the lactulose in the form of a syrup, for example one containing about 50% by weight of lactulose, about 5% by weight of lactose, about 8% by weight of galactose and the remainder water.
- This composition which has a specific gravity of 1.33 (mg/ml), is called hereinafter Duphalac.
- a dry composition may contain about 40% by weight of lactulose, about 4% by weight of lactose, about 6% by weight of galactose and the remainder dextrine maltose.
- the lactulose may alternatively be worked into confectionery, candies, jelly drops, gum drops etc. each containing about 3 gram of lactulose.
- Colouring agents admitted for drugs conserving agents such as sorbicacid and its salts, jellifying agents such as pcctine, thickening agents such as tragacanth gum, arabic gum and carboxymethylcellulose flavouring agents such as citric acid and tartaric acid may be employed.
- the patient was treated with soap enemas and Bisacodyl suppositories with no effect, and later oral Senokot was given in addition. This produced only a minimal effect and she was then treated with 5 ml of Duphalac orally twice daily. This induced the passage of chalky stools, and four weeks later the large bowel no longer contained barium on the plain x-ray film.
- a plain x-ray film of the abdomen and a barium enema examination showed nothing abnormal.
- a barium meal and follow through examination was carried out and was also clear, but after this the diarrhoea stopped for the first time for 7 weeks.
- An occasional formed motion was passed but lessned in frequency and amount until two weeks after the barium meal examination the patient was no longer able to open her bowels and complained of generalized abdominal discomfort.
- a plain x-ray film of the abdomen showed barium filling the entire large bowel.
- a method of delivering the intestines of human beings from bariumsulphate after barium meal examination which method comprises administering to said human beings orally a daily effective dose of lactulose.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Lactulose has been found to be effective to expell barium sulphate from the intestines after barium meal examination.
Description
United States Patent [191 Prout [4 1 Jan. 14,1975
[75] Inventor: Brian John Prout, Truro, England [73] Assignee: U.S. Philips Corporation, New
York, NY.
[22] Filed: Nov. 15, 1973 [21] Appl. No.: 416,037
[52] US. Cl. 424/180 [51] Int. Cl A0ln 9/00 [58] Field of Search 424/l 80 Primary Examiner-Elbert L. Roberts Attorney, Agent, or Firm-Frank R. Trifari; Norman N. Spain [57] ABSTRACT Lactulose has been found to be effective to expell barium sulphate from the intestines after barium meal examination.
4 Claims, No Drawings METHOD OF DELIVERING THE INTESTINES OF HUMAN BEINGS FROM BARIUMSULPHATE AFTER BARIUM MEAL EXAMINATION The invention relates to a new and novel method of delivering the intestines of human beings from barium sulphate after barium meal examination.
It has been found that barium sulphate often remains in the intestines of patients after a barium meal examination. This especially readily occurs in elderly patients.
When the retention of barium is not early recognized serious symptones may develop, such as abdominal pains, depression, mental confusion, constipation, abdominal distension and cramping.
It appeared that common laxative agents such as Senokot containing the active constituents of cassia angustifolia,
Bisacodyl, containing 4,4-(2-pyridylmethylen)diphenol diacetate as active ingredient and enemas, are not effective.
It has now been found, that barium sulphate can quite surprisingly be expelled from the intestines by administering orally a small but effective dose of lactulose.
Generally a dose of 3.3 gram of lactulose once or twice a day suffices. These doses even appeared to be effective in the treatment of patients who had the barium meal several weeks before the installation of the lactulose treatment. This is the more remarkable as in the meantime the bariumsulphate is completely dehydrated and the colon has lost of its normal propulsive movements.
It is note worthy that also in cases wherein severe conditions including constipation could develop the said low doses, which are substantially lower than those generally required to provoke diarrhoea, were sufficient to provoke the excretion of chalky stools and to completely deliver the intestines from bariumsulphate.
In view of the serious symptomes that may develop on barium sulphate retention, it is however recommended to start the administration of lactulose immediately after the barium meal X-ray examination. Alternatively lactulose may already be given together with or even just before the barium meal.
The duration of the treatment may vary from 1 to several weeks in the case some time lapsed between the barium meal examination and the curative treatment with lactulose. In the case the administration of lactulose is begun with at the time of the barium meal examination or shortly thereafter a treatment of l or 2 days to a week will suffice.
Lactulose may be administered in solid form either alone or in admixture with one or more carriers such as glucose, galactose or lactose. A very satisfactory method however is to administer the lactulose in the form of a syrup, for example one containing about 50% by weight of lactulose, about 5% by weight of lactose, about 8% by weight of galactose and the remainder water. This composition, which has a specific gravity of 1.33 (mg/ml), is called hereinafter Duphalac.
A dry composition may contain about 40% by weight of lactulose, about 4% by weight of lactose, about 6% by weight of galactose and the remainder dextrine maltose.
The lactulose may alternatively be worked into confectionery, candies, jelly drops, gum drops etc. each containing about 3 gram of lactulose. Colouring agents admitted for drugs, conserving agents such as sorbicacid and its salts, jellifying agents such as pcctine, thickening agents such as tragacanth gum, arabic gum and carboxymethylcellulose flavouring agents such as citric acid and tartaric acid may be employed.
The invention will now be described in greater detail with reference to the following case reports.
CASE 1 A 71-year-old woman was admitted as an emergency to the psychogeriatric assessment unit on Dec. 24, 1970 with a history of vague abdominal pains, depression, and mental confusion of recent onset. Her previous history indicated long-standing abdominal discomfort. In 1966 this had been investigated in the surgical department when barium meal had revealed no abnormality. Her abdominal symptoms had recurred intermittently, and in the autumn of 1970 further investigations had been carried out as a surgical outpatient, including on Nov. 25 a barium-meal examination which showed no abnormality.
On admission to the assessment unit she was noted to be depressed, disorientated, and intermittently confused. The colon was palpable and she was constipated.
Routine measures to clear the bowel were instituted. Senokot tablets (containing the active constituents of Cassia angustifolia) two daily proved unsuccessful, and Bisacodyl (4,4'-(Z-pyridylmethylene)diphenol diacetate) tablets two nightly together with repeated enemas also had no effect. These measures were continued for two weeks after admission, when physical examination showed a ballooned and empty rectum; the descending colon was no longer palpable but the ascending colon was palpable and thickened.
A barium-enema examination was requested but the preliminary plain x-ray picture of the abdomen on Jan. 7, 1971 showed a bowelfilled with what might be described as a barium cast and no further radiological examination was carried out at that time. After this examination 5 ml of Duphalac was administered orally twice daily. The patient was subsequently noted to excrete chalky stools, and a further x-ray film of the abdomen on Feb. 15 suggested some dilution of the colonic mass of barium. At that time she improved physically and was discharged home on 10 ml of Duphalac orally twice daily.
At follow-up on May 10 she had remained well, and a plain x-ray film of the abdomen showed that all residual barium had disappeared. Further review in Aug. indicated that her progress had been maintained, and subsequent investigation confirmed that there was no evidence of an organic obstruction in the gastrointestinal tract.
CASE 2 A -year-old widow was admitted to the general medical ward on Dec. 12, 1969 with an 8-week history of cramping lower abdominal pains, abdominal distension, and constipation. For about 6 months she had been experiencing intermittent upper abdominal discomfort, nausea, and slight looseness of the motions since the death of her husband. Her practitioner had arranged for a barium meal examination, which was carried out 6 weeks before her admission.
On examination the main physical findings were a distended abdomen with slightly increased bowel sounds and occasional visible peristalsis. Because of the possibility of an intestinal obstruction plain x-ray examination of the abdomen was carried out. This showed the large bowel filled with barium, but no fluid levels could be seen.
The patient was treated with soap enemas and Bisacodyl suppositories with no effect, and later oral Senokot was given in addition. This produced only a minimal effect and she was then treated with 5 ml of Duphalac orally twice daily. This induced the passage of chalky stools, and four weeks later the large bowel no longer contained barium on the plain x-ray film.
CASE 3 A 76-year-old man had recently been treated for a chest infection and had an episode of diarrhoea presumed to be due to tetracycline therapy. The diarrhoea had cleared. Barium meal examination showed a possible small gastric ulcer on the lesser curve. As he was reluctant to take any medication because of his previous experience with side effects he was advised to take regular and frequent meals with milk drinks between. The abdominal pain gradually worsened and he became increasingly constipated.
Five weeks after the barium-meal examination he was admitted to hospital. The only physical signs of note were an empty rectum, a firm enlarged prostate on rectal examination, and a tender palpable transverse and descending colon. A plain x-ray film of the abdomen showed the colon filled with barium.
Treatment with enemas was instituted but with no effect, and later Senokot and Bisacodyl suppositories were tried with only slight effect. The patient was then treated with 5 ml of Duphalac orally initially twice and then thrice daily. Loose chalky stools were then passed and 3 weeks later the bowel was seen to be clear of barium on the plain x-ray film.
CASE 4 A 70-year-old woman was admitted to hospital on Sept. 16, 1971 with a painful swollen left leg of 4 days duration. She was found to have mild maturity onset diabetes of one months duration. There was a history of anorexia and of weight loss of 19 kg in 3 months. She had been taking a small dose of prednisolone for 3 years because of exzema.
On examination she appeared a well-preserved, elderly woman. There were signs of a deep-vein thrombosis in the left leg but no appreciable abnormalities were found in the abdomen or other main systems. A midstream specimen of urine showed a coliform urinary infection.
She responded slowly to conservative measures. It was thought that an underlying neoplasm was possibly present, and a barium meal examination was carried out on Sept. 20. Apart from a calcified aorta no abnormality was noted. On Oct. 11 it was decided to carry out a barium-enema examination. The plain x-ray film showed that the colon was loaded with barium. She was then given Senokot and enemas in an attempt to empty the colon but this resulted in water diarrhoea. A repeat plain x-ray film on Oct. 14 showed the colon still filled with barium. She was treated with 5 ml of Duphalac orally twice daily after which she began to pass chalky stools, and on Oct. 21 the colon was seen to be clear of barium.
CASE 5 An 81-year-old woman was admitted to hospital for investigation of diarrhoea. she had been receiving ampicillin for 2 weeks because of a chest infection, and the diarrhoea, which started during therapy, had been persitent for 4 weeks. There had been no response to routine treatment of the diarrhoea, and as she was well preserved and had been previously fit she was referred to the gastroenterology department for further investigation.
A plain x-ray film of the abdomen and a barium enema examination showed nothing abnormal. A barium meal and follow through examination was carried out and was also clear, but after this the diarrhoea stopped for the first time for 7 weeks. An occasional formed motion was passed but lessned in frequency and amount until two weeks after the barium meal examination the patient was no longer able to open her bowels and complained of generalized abdominal discomfort. A plain x-ray film of the abdomen showed barium filling the entire large bowel.
There was no response to two enemas and treatment with Duphalac orally was instituted simultaneously in a dose of 10 ml twice daily. This cleared the bowel within l week. There was no recurrence of the original diarrhoea and no explanation was found for this sympton. It was presumed that pH changes induced by the barium and lactulose had further altered the bacterial flora of the gut which had initially been disturbed .by the antibiotic therapy. Subsequently she remained well.
What is claimed is:
l. A method of delivering the intestines of human beings from bariumsulphate after barium meal examination which method comprises administering to said human beings orally a daily effective dose of lactulose.
2. A method as claimed in claim 1 wherein lactulose is administered in a daily amount of 3.3 20 gram.
3. A method as claimed in claim 2 wherein lactulose is administered as a 50% by weight aqueous syrup.
4. A method as claimed in claim 1 wherein the administering of lactulose is begun with immediately after the barium meal examination.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3 50 70 Dated January 151975 Inventor(s) BRIAN JOHN PROUT It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 1, line 13, "symptones" should read symptoms.
line 18, after "gustifolia," insert as the same paragraph Bisacodyl, containing 4,4-(2-pyridylmethylen) diphenol diacetate as active ingredient and enemas, are not effective line 31, "bariumsulphate" should read barium sulphate line 32, cancel "of".
Column 2, line 2, "admitted" should read permitted Column 4, line 45, bariumsulphate" should read barium sulphate Signed and Scaled this twenty-second Day of July 1975 [SEAL] Arrest.-
RUTH C. MASON C. MARSHALL DANN Arresting Offiver Commissioner of Parents and Trademarks
Claims (3)
- 2. A method as claimed in claim 1 wherein lactulose is administered in a daily amount of 3.3 - 20 gram.
- 3. A method as claimed in claim 2 wherein lactulose is administered as a 50% by weight aqueous syrup.
- 4. A method as claimed in claim 1 wherein the administering of lactulose is begun with immediately after the barium meal examination.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US416037A US3860708A (en) | 1973-11-15 | 1973-11-15 | Method of delivering the intestines of human beings from bariumsulphate after barium meal examination |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US416037A US3860708A (en) | 1973-11-15 | 1973-11-15 | Method of delivering the intestines of human beings from bariumsulphate after barium meal examination |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3860708A true US3860708A (en) | 1975-01-14 |
Family
ID=23648264
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US416037A Expired - Lifetime US3860708A (en) | 1973-11-15 | 1973-11-15 | Method of delivering the intestines of human beings from bariumsulphate after barium meal examination |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3860708A (en) |
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- 1973-11-15 US US416037A patent/US3860708A/en not_active Expired - Lifetime
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