Is there a real treatment for stroke? Clinical and statistical... treatments in 300 patients.
Transcription
Is there a real treatment for stroke? Clinical and statistical... treatments in 300 patients.
Is there a real treatment for stroke? Clinical and statistical comparison of different treatments in 300 patients. S Santambrogio, R Martinotti, F Sardella, F Porro and A Randazzo Stroke. 1978;9:130-132 doi: 10.1161/01.STR.9.2.130 Stroke is published by the American Heart Association, 7272 Greenville Avenue, Dallas, TX 75231 Copyright © 1978 American Heart Association, Inc. All rights reserved. Print ISSN: 0039-2499. Online ISSN: 1524-4628 The online version of this article, along with updated information and services, is located on the World Wide Web at: http://stroke.ahajournals.org/content/9/2/130 Permissions: Requests for permissions to reproduce figures, tables, or portions of articles originally published in Stroke can be obtained via RightsLink, a service of the Copyright Clearance Center, not the Editorial Office. Once the online version of the published article for which permission is being requested is located, click Request Permissions in the middle column of the Web page under Services. Further information about this process is available in the Permissions and Rights Question and Answer document. Reprints: Information about reprints can be found online at: http://www.lww.com/reprints Subscriptions: Information about subscribing to Stroke is online at: http://stroke.ahajournals.org//subscriptions/ Downloaded from http://stroke.ahajournals.org/ by guest on September 9, 2014 STROKE 130 VOL 9, No 2, MARCH-APRIL 1978 and perfusion in brain and heart. J Nucl Med 17: 603-612, (July) 1976 19. Symon L, Dorsch NWC, Crockard HA: The production and clinical features of a chronic stroke model in experimental primates. Stroke 6: 476^t81, (Sept-Oct) 1975 20. Pasztor E, Symon L, Dorsch NWC, Branston NM: The hydrogen clearance method in assessment of blood flow in cortex, white matter, and deep nuclei of baboons. Stroke 4: 556-567, (July-Aug) 1973 21. Zatz LM, Alvarey RE: An inaccuracy in computed tomography: The dependence of CT values. Radiology 124: 91-97, (July) 1977 22. McCullough EC: Factors affecting the use of quantitative information from a CT scanner. Radiology 124: 99-107, (July) 1977 15. Collins VJ: Pharmacology of inorganic gas anesthetics, pp. 1541-1542. In Principles of Anesthesia, 2nd edition. Philadelphia, Lea and Febiger, 1976 16. Obrist WD, Thompson HK, Wang HS, Wilkinson WE: Regional cerebral blood flow estimated by '"Xenon inhalation. Stroke 6: 245-256, (May-June) 1975 17. Kuhl DE, Reivich M, Alavi A, Nyary I, Staum MM: Local cerebral blood volume determined by three-dimensional reconstruction of radionuclide scan data. Circ Res 36: 610-619, (May) 1975 18. Phelps ME, Hoffman EJ, Coleman RE, Welch MJ, Raichle ME, Weiss ES, Sobel BE, Ter-Pergossian MM: Tomographic images of blood pool Is There a Real Treatment for Stroke? Clinical and Statistical Comparison of Different Treatments in 300 Patients SERGIO SANTAMBROGIO, M.D., RENATO MARTINOTTI, M.D., FERNANDO PORRO, M.D., FRANCESCO SARDELLA, AND ANTONIO RANDAZZO, M.D., M.D. SUMMARY In the absence of universally accepted criteria for the medical treatment of stroke, we made a rigorously randomized comparative study of different treatments in 300 patients. One group of patients received only a general supportive treatment designed to ensure adequate supplies of water, electrolytes and calories, plus whatever was needed to prevent infection and correct extant associated pathology. Three other groups of patients were treated in the same way but were also given, respectively, one of the following medications: Hydergine (Sandoz) (a mixture of three ergot alkaloids), dexamethasone, and mannitol. No statistically significant difference emerged among any of the treatment groups and the reference group in terms of objective therapeutic results. The authors concluded that, at least with the dosage used in this study, none of the treatments proved more useful than conventional supportive therapy in the first 10 days after a stroke. TREATING PATIENTS with stroke is often unrewarding. As in other fields of medicine, the lack of a basic reference treatment for stroke has generated a multitude of drug therapies, each being thought of as a cure, only to be soon abandoned. It is likely that some deaths in the first several days after a stroke are due to cerebral edema around the infarcted area rather than to the infarct itself.13 Edema reaches its peak about 3 to 4 days after the stroke, and can be responsible for transtentorial herniation of the brain, rostrocaudal deterioration, and impaired cerebral blood flow. Drugs thought to reduce edema reduce intracranial pressure which can indirectly improve brain circulation. Those used in recent years include mannitol,3"7 corticosteroids,2- *•5-"~21 and Hydergine,3'22~32 each with conflicting reports of clinical effectiveness. We have studied these 3 therapies using 1) a large number of patients; 2) random selection for treatment; 3) each drug alone; 4) results from reliable clinical parameters; 5) data evaluated by a correctly designed statistical program. mean age for the whole group was 71 years. There were 110 men (mean age 69) and 190 women (mean age 73). Of these 241 were diagnosed as having an ischemic stroke, 189 in the carotid artery territory, 40 in the vertebrobasilar territory. In 12 the classification was uncertain. At hospitalization, each patient was assigned randomly to one of the following 4 treatment groups: Group A. These patients received adequate water and electrolyte replenishment by intravenous infusion for the first 48-72 hours, and then a suitable caloric intake, in the form of a special standard diet if necessary, administered by stomach tube. These patients also received suitable antibiotics and additional treatments, such as digitalis, diuretics, tracheal aspiration and instillation of mucolytic agents, and bedsore prevention. Group B. These patients received the same treatment as those in group A, plus a proprietary mixture of dihydroergocornine, dihydroergocristine and dihydroergocriptine, 0.3 mg each (Hydergine) in a daily dosage of 6 ampoules representing 1.8 mg of each alkaloid in the mixture. Group C. Patients in group C received the same treatment as group A plus dexamethasone 24 mg daily, given in divided doses. Group D. Patients received the same treatment as group A plus a solution of 20% hypertonic mannitol given i.v. 0.8-0.9 g/kg daily. In all groups treatment was instituted between 3 and 24 hours after onset of symptoms. The period of observation was 10 days for all 4 groups. Materials and Methods We studied 300 patients with a diagnosis of stroke, hospitalized in the Emergency Medicine Division of the Polyclinic Hospital in Milan, during 1974 and 1975. The From the Emergency Medical Division, Ospedale Maggiore Policlinico, Via Francesco Sforza 35, Milan, Italy 20122. Reprint requests to Dr. Santambrogio, O.M. Policlinico, Milan, Italy. Downloaded from http://stroke.ahajournals.org/ by guest on September 9, 2014 COMPARISON OF STROKE TREATMEUTS/Santambrogio et al. Patient Classification In accordance with Locksley33 and Derouesne,1 we classified each patient as a case of hemorrhagic or ischemic stroke by the behavior of the following parameters. Cerebrovascular accidents were thought to be due to hemorrhage when the period of onset was less than 2 hours, impairment of consciousness progressing steadily to coma and a very recent history of headache and vomiting. Patients with cerebral hemorrhage generally had hypertension and bloody spinal fluid. Ischemic strokes had a longer period of onset, no history of headache or vomiting and clear spinal fluid. Overt hypertension indicated an ischemic or hemorrhagic stroke with indifferent probability, but a normal or low blood pressure was more suggestive of an ischemic than a hemorrhagic stroke.1' 33~38 We further divided patients with ischemic stroke into two groups; transient stroke (prompt resolution of the stroke episode with complete recovery in less than 24 hours) and completed stroke (persistent stable neurologic impairment during the first few days after onset).37 Our clinical material also included 4 patients with a diagnosis of cerebral embolism made on the strength of young age, extant mitral valve disease, a history of previous embolization elsewhere in the body, and sudden onset.1-36-38 Patients were classified in terms of clinical evolution using a scoring system similar to that of Bauer and Tellez:8-21 (A) stroke in evolution in which both neurologic damage and impairment of consciousness changed during the observation period; and (B) established or stationary strokes, in which such changes did not occur. Assessment of improvement or worsening was made by the following parameters: (1) state of consciousness at time of admission was classified at 4 levels, namely, wakefulness, somnolence, stupor, and coma;39 (all shifts from one level to another were recorded during the 10-day observation period); (2) neurologic signs of motor or sensory impairment with any change during the observation period, such as increasing or decreasing weakness or sensory impairment, were recorded. Each patient was evaluated at 1, 2, 4, 7 and 10 days after hospitalization. Each evaluation required scoring the level of consciousness, language function, motor function and sensory function. Total numerical scores were obtained based on the presence or absence of 30 specific points. An increasing score was associated with worsening; a declining score with improvement. The observation period was restricted to the first 10 days after the stroke. It was found that changes of focal motor and speech abnormalities were less reliable as a criterion for determining whether a stroke was improving or worsening during the first 10 days than was the state of consciousness.1 Results On reviewing our results we excluded patients with transient cerebral ischemia because the prompt abatement of symptoms and signs (within 24 hours by definition) made it impossible to judge effectiveness of treatment. Patients with cerebral embolism were excluded because of the small number of cases. Patients with cerebral hemorrhage were excluded because an early mortality of 84%, regardless of the treatment, made analysis impossible. 131 TABLE 1 Two-by-Three Contingency Tabulation by Treatment Groups in Patients with Ischemic Cerebral Stroke (ICS) Treatment groups Group A Improved Unchanged Worsened Ischemic cerebral stroke (ICS) Evolutive Established Total 14 0 18 0 9 0 14 9 18 32 9 41 Improved Unchanged Worsened 15 0 18 0 8 0 15 8 18 Total 33 8 41 Improved Unchanged Worsened 15 0 19 0 14 0 15 14 19 Total 34 14 48 12 0 16 0 8 0 12 8 16 28 8 36 Total Group B Group C Group D Improved Unchanged Worsened Total Group A, control; Group B, Hydergine; Group C, dexamethasone; Group D, mannitol. The therapeutic results obtained in patients with ischemic stroke were used for statistical evaluation. The results are shown in tables 1 and 2. No significant differences were observed for any of the treatments given. Nor were there significant differences in outcome when strokes were divided into evolving and established stroke. Patients who were not in coma at the beginning of treatment did better than those with severely impaired consciousness. Older patients, in general, did worse than younger patients. The three modes of treatment failed to show difference in outcome between treatment groups or between these and the reference group. A comparison with the reference group showed clearly that evaluation of an ischemic stroke was wholly independent of these treatments. This finding could be interpreted to mean that treatment really has no effect in determining the course of a stroke, whether the wrong treatment was used or whether the wrong parameters of change were evaluated. To test the last hypothesis, we evaluated two possible sources of error: coma at the outset of stroke and age. The role of coma as a major source of error was suggested by the very high mortality rate (86%) associated with coma TABLE 2 Statistical Comparison Between Control Group (A) and Three Treatment Groups (B, C, D) in Patients with Ischemic Cerebral Stroke (ICS) Interactions ICS (A) X ICS (B) ICS (A) X ICS (C) ICS (A) X ICS (D) x1 P 1 0 1 0.04 0.028 N.S. N.S. N.S. Degrees of freedom 1 X = cbi-equare corrected for continuity; P = statistical significance; (other symbols same as in table 1). Downloaded from http://stroke.ahajournals.org/ by guest on September 9, 2014 132 STROKE in all 3 treatment groups as well as in the control group. Coma at onset of symptoms suggests so severe an anatomical injury as to make any drug treatment futile. When we recalculated the corrected chi-square values after eliminating patients with coma from the group, we found some evidence of effectiveness of dexamethasone and Hydergine treatment groups, but this did not reach statistical significance. Age had no effect in determining outcome in the control group or in the groups treated with mannitol, Hydergine and dexamethasone. The mean age of patients who improved was less than 64.9 ± 2.08 and for those who became worse it was more than 64.9. Confining our statistical comparison to patients under this age limit and comparing them to their age mates in the control group, differences in outcome are below the minimum level of significance. In conclusion, we were unable to demonstrate that any of the given treatments, in the dosages used in these trials, had a real influence on the clinical course of ischemic cerebral stroke, during the first 10 days after onset. 15. 16. 17. 18. 19. 20. 21. 22. 23. 24. 25. 26. References 27. 1. Derouesne C: Le diagnostic des rammolisments recents. Rev Prat 9: 621-625, 1976 2. Dyken M, White PT: Evaluation of cortisone in the treatment of cerebral infarction. JAMA 162: 1531-1534, 1956 3. Pratesi F, Corsi C, Nuti A, Tesi M: Terapia dell'infarto encefalico arterio-sclerotico. Orientamenti attuali e prospettive. Giorn Arteriosclerosi 2 - 3 : 147-156, 1972 4. Candelise L, Colombo A, Spinnler H: Therapy against brain swelling in stroke patients. Stroke 6: 353-356, 1975 5. Hooshmand H, Quinn JC, Houff SA: Cerebrovascular fluid pressure changes with chemotherapy for intracerebral hemorrhage. Neurology (Minneap) 22: 56-61, 1972 6. Shenkin HA, Goluboff B, Haft H: Use of mannitol for reduction of intracranial pressure in intracranial surgery. J Neurosurg 19: 897-900, 1962 7. Wise BL, Chater N: Value of hypertonic mannitol solution in decreasing brain mass and lowering cerebrospinal fluid pressure. J Neurosurg 19: 1038-1043, 1962 8. Bauer RB, Tellez H: Dexamethasone as treatment in cerebrovascular disease. II. A controlled study in acute cerebral infarction. Stroke 4: 547-555, 1973 9. Foley JM, Chambers RA, Adams RD: Effect of cortisone on the early repair of brain wounds in Guinea pigs, (abstract). J Neuropathol Exp Neurol 12: 101-104, 1953 10. Harrison MJG, Russel RWR: Effect of dexamethasone on experimental cerebral infarction in the gerbil. J Neurol Neurosurg Psychiatry 35: 520-521, 1972 11. Hetzel BS, Lander H, Robson HN: Immediate treatment of apoplexy. Br Med J 1: 1122, 1957 12. Kahn K, Pranzarone FG, Newman T: Dexamethasone treatment of experimental cerebral infarction (abstract). Neurology 22: 406-407, 1972 13. Lee MC, Mastri AR, Waztz AG, Loewenson RB: Ineffectiveness of dexamethasone for treatment of experimental cerebral infarction. Stroke 5: 216-218, 1974 14. Patten BM, Mendell J, Bruun B, Curtin W, Carter S: Double-blind study 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. 38. 39. 40. VOL 9, No 2, MARCH-APRIL 1978 of the effects of dexamethasone on acute stroke. Neurology 22: 377-383, 1972 Plum F, Alvord EC Jr, Posner JB: Effect of steroids on experimental cerebral infarction. Arch Neurol 9: 571-573, 1963 Prados M, Strowger B, Feindez WH: Studies on cerebral edema: I. Reaction of the brain to air exposure; pathologic changes. Arch Neurol Psychiat 54: 163-174, 1945 Roberts HJ: Supportive adrenocortical steroid therapy in acute and subacute cerebro-vascular accidents with particular reference to brain stem involvement. J Am Geriatr Soc 6: 686-702, 1958 Rubenstein MK: Influence of adrenocortical steroids on severe cerebrovascular accidents. J Nerv Ment Dis 141: 291-299, 1965 Russek HI, Russek AS, Zohman BL: Cortisone in immediate therapy of apopletic stroke. JAMA 159: 102-105, 1955 Sheely RF: Effect of cortisone and hydrocortisone in hemiplegia after cerebral infarction. JAMA 158: 803-806, 1955 Tellez H, Bauer RB: Dexamethasone as treatment in cerebrovascular disease. I. Controlled study in intracerebral hemorrhage. Stroke 4:541-546, 1973 Agnoli A: Drug action on regional cerebral blood flow in cases of acute cerebrovascular involvement. Acta Neurol Scand (Suppl) 14: 143, 1965 Aradas A: II trattamento dei disturb! circolatori cerebrali con alcaloidi diidrogenati della segale cornuta, per via endovenosa a dosi subentranti. Giorn di Gerontol 8: 677-682, 1963 Berselli L, Ferracini R: Sul trattamento degli incidenti cerebrovascolari acuti. La Clinica XXV: 68-75, 1965 Betti R: Rilievi clinici sul trattamento degli episodi di insufficienze cerebrovascolari acuti. La Riforma Medica 13: 3-14, 1975 Emmenegger H, Meier-Ruge W: L'effetto dell'Hydergina a livello cerebrale. Studio istochimico, circolatorio e neurofisiologico. Pharmacology 1: 65-78, 1968 Geraud J: Traitment des troubles chroniques de la circulation cerebrale. In International Symposium on Cerebral Circulation. Paris, Sandoz, pp 305-317, 1965 Heyck H: Der einfluss der ausgangslage auf sympathikolytische effekte am hirnkreislauf bei zerebralvaskularen erkrankungen. Arzneim Forsch 15: 243-251, 1961 Iwangoff P, Enz A: Influence of various dihydroergotamine analogues on cyclicadenosine - 3' 5' - monophosphate phosphodiesterase in the grey matter of cat brain in vitro. Agents Actions 2: 223-230, 1972 Pratesi F, Dabizzi RP, Caramelli L: Traitment intracarotidien et intraveineux vaso-moteur des maladies vasculaires cerebrales. In International Symposium on Cerebral Circulation. Paris, Sandoz, pp. 296-300, 1965 Taeschler M: Pharmacologie classique de I'Hydergine. Ann Anesthesiol Fr VI: 97-104, 1965 Turon R: Le traitment medical des troubles vasculaires aigus du cerveau. In International Symposium on Cerebral Circulation. Paris, Sandoz, pp. 327-329, 1965 Locksley HB: L'ictus emorragico. In Clinical Medicine North America, Padova, (Italy) Piccin 1: 1302-1323, 1969 Agnoli A, Ruggieri S: II liquido cerebrospinale nelle vasculopatie cerebrali. Gior Arteriosclerosi 2-3: 187-197, 1972 Fager CH A: Le sindromi endocraniche acuti. In Clinical Medicine North America, Padova (Italy) Piccin 2: 885-892, 1970 Fieschi C: Problemi diagnostici dell'apoplessia cerebrale. Gior Arteriosclerosi 2-3: 83-86, 1972 Hass W: Malattie cerebro-vascolari occlusive. In Clinical Medicine North America, Padova, (Italy) Piccin, 5: 1244-1262, 1973 Lhermitte F, Mamo N: "Systeme nerveux et muscles." In Pathologic Medicale, Paris, Flammarion, 1973 Hinterbuchner LP: La valutazione del paziente in stato di incoscienza. In Clinical Medicine North America, Padova (Italy), Piccin, 6: 1519-1529, 1975 Lison L: Statistica Applicata alia Biologia Sperimentale, Milano, Ambrosiana, 1961 Downloaded from http://stroke.ahajournals.org/ by guest on September 9, 2014