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  The Indian Practitioner, (1980): December, 685
The role of Cystone in urinary tract infection Prasad, R.R., M.D.,
Resident Medical Officer, Dept. of Medicine,
Darbhanga Medical College and Hospital, Bihar, India.
 
 
 Introduction

Urinary Tract Infections are quite common in day to day practice. The most common organism generally isolated after urine culture id E. coli. Many a times E. coli is resistant to the usual line of treatment with urinary antiseptics and anti-bacterial agents.

Cystone is claimed to be effective in expelling a urinary calculus. In several recent clinical studies, its value is also claimed in urinary tract infection to E. coli in non-specific cystitis and persistent burning micturition syndrome.

The object of the present clinical study is to determine the efficacy of Cystone tablet in urinary tract infection due to E. coli.

Each tablet of Cystone contains:

Exts. Didymocarpus pedicellata 65mg

Saxifraga ligulata 49mg

Rubia cordifolia 15 mg

Cyperus scariosus 16 mg

Achyranthes aspera 16mg

Onosma bracteatum 16 mg

Vernonia cinerea 16 mg

Shilajeet (Purified) 13mg

Hajrul yahood bhasma 16mg

Hajrul yahood bhasma is prepared with Oconum basilicum, Tribulus terrestris, Mimosa pudica, Dolichos biflorus, Pavonia odorata, Equisetum arvense, Tectona grandis seed.

 Review on Literature

Cystone, a drug of vegetable-mineral origin has been effective in the conservative management of urinary calculi. The principal pharmacological action of Cystone is as follows:

Cystone disintegrates urinary calculi by acting on the mucin, which binds the particles together, and clears the urinary tract by flushing out the particles with the flow of urine. It also corrects the crystalloid-colloid with the flow of urine. It also corrects crystalloid-colloid balance (Vakil7, Sharma5, Agrawal1). Cystone acts as a urinary antiseptic. It does not alter the electrolyte balance (Subramaniam6).

In urinary tract infections, in cystitis and in non-specific persistent burning micturition syndrome, Cystone is effective in eliminating the symptoms and to make the urine sterile and has no toxic effect on the kidney (Gupta and Singh3, Sengupta and Subrato Gutpa4 and Brijkishore2).


 Patients & Methods

The present study was conducted at Darbhanga Medical College and Hospital during the period 1977 to 1979. Twenty five established cases of urinary tract infection having E. coli in urine culture were selected for the present study. All patients were subject to a thorough case history and clinical examination. In each case the routine blood, urine examination, microscopic urine examination and culture and sensitivity studies of mid-stream samples were done before administration of Cystone therapy.

These patients were given Cystone in the dose of 3 tablets three times a day.

In all these cases, investigations were repeated during Cystone therapy and clinically the patients were observed daily and their progress noted.

 Results & Observations

Table 1: Showing the number of cases of U.T.I. with symptoms and investigatory findings before Cystone therapy

No. of cases

Symptoms

Pus cells count in urine per high power filed

Albuminuria

Urine culture

25

Fever with rigor, dysuria strangury increased frequency of micturition, tenderness over the supra-public region and toxic look

15-90

0 - +

E. coli isolated

There was definite improvement in 13 cases. In these cases there was marked improvement in symptomatology, the pus cell count came to 10-20/h.p.f.; albuminuria became nil and the urine culture became sterile. These cases were put in to "Marked improvement" group.

In 7 cases there was moderate improvement in symptoms; the pus cells came down to 10-40/h.p.f., albuminuria persisted and culture remained positive. These cases were put into "Moderate improvement" group (Table 2).

In 5 cases there was no improvement at all and these cases were put in "No improvement" group (Table 2).

Table 2: Showing the results of U.T.I. after the end of one week of Cystone therapy

 

No. of cases

Symptoms

Pus cells count/h.p.f.

Albuminuria

Urine culture

Improvement

13

Marked improvement in symptomatology

10-20

Nil

Negative

Moderate improvement

7

Moderate symptoms persisting

10-40

0- +

Positive E. coli

No improvement

5

No improvement at all

15-60

+

Positive E. coli


In all these cases, the treatment continued for another week, and at the end of second week, the urine culture became negative in 18 cases. The number of pus cell count came down to 2-8/h.p.f. and they were free from symptoms.

The 18 cases which responded to Cystone therapy after the 2nd week were discharged with the advice to continue the treatment with Cystone for another two weeks at the dose of 2 tablets t.i.d.

These cases turned up in O.P.D. after two weeks and there was no relapse; the urine culture was sterile and the pus cell count was almost normal in all cases.

In 4 cases, there was moderate improvement in symptoms. The pus cells came to 5-20/h.p.f. but the culture remained positive (Table 3).

Table 3: Showing the results in U.T.I. after second week of Cystone therapy

 

No. of cases

Symptoms

Pus cells count/h.p.f.

Albuminuria

Urine culture

Marked improvement

18

Symptom free

2-8

Nil

Negative

Moderate improvement

4

Moderate symptoms persisting

5-20

0 - +

Positive

No improvement

3

Slight improvement in symptoms

15-40

+

Positive

In 3 cases there was definite fall in pus cell count and also a slight improvement in symptoms, but albuminuria was present in urine and also the culture remained positive (Table 3).

In cases with moderate improvement (Table 3) the treatment was continued into the third week. At the end of the 3rd week, the urine culture was still positive, but the pus cell count came to 5-10/h.p.f. and there was marked improvement in symptomatology. These 4 patients were treated with a suitable antibiotic along with Cystone and at the end of 4th week the urine culture in all these cases became negative. The pus cell count came down in all these 3 cases to 5-20/h.p.f. and the albumin also decreased. In these 3 patients, the same treatment was given for a further one week and at the end of 4th week the culture became negative in the remaining 2 cases also. The pus cell count came down to 2-5/h.p.f.

The role of Cystone in urinary tract infection due to E. coli seems to be effective in this clinical trial, though the number of cases treated is small.

 Summary
  1. Twenty five cases of U.T.I. due to E. coli were treated with Cystone in the dose of 3 tablets three times daily.

  2. Thirteen cases became culture-negative in one week’s therapy

  3. Five more cases became culture-negative in second week’s therapy.

  4. The remaining 7 cases did not become culture-negative even after the end of 3rd week therapy. However, on the addition of suitable antibiotics, all the 7 culture-positive cases became negative in 4th week.

  5. On Cystone therapy, marked improvement in symptoms was noticed in 1-2 weeks in 18 cases. In 7 cases moderate to mild improvement in symptoms was noticed.

  6. Pus cell count decreased gradually in all cases.

  7. Albuminuria also decreased gradually.

 Acknowledgement

I am extremely indebted, to Prof. Mohan Mishra, M.B.,B.S., M.D. M.R.C.P. (U.K.), Professor in the Department of Medicine, Darbhanga Medical College for his inspiration, valuable suggestions and guidance without which this work would not have been possible.

I must express my gratefulness to Dr. G.P. Keshari, M.B.,B.S., D.L.O. (Lond.), Superintendent Darbhanga Medical College and Hospital for kindly allowing me to undertake the trial and to make use of the hospital facilities and publish this report.

My thanks to The Himalaya Drug Company for kindly supplying me Cystone tablets for trial.

 References
  1. Agrawal, S.U. (1960): Capsule, 1: 23.

  2. Brij. Kishore and Agrawal, G.C. (1979): Capsule, 3: 55.

  3. Gupta, P.D. and Singh, L.M. (1976): Probe, 2: 108.

  4. Sengupta, B.R. and Subrato Gupta (1978): Probe, 3: 239.

  5. Sharma, A.K. (1970): Probe, 4: 179.

  6. Subramaniam, R. (1961): The Antiseptic, 2: 103.

  7. Vakil, J.N. (1955): Ind. Practit., 8: 817.