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ISSN Print: 2278 – 2648 IJRPP |Vol 3 | Issue 1 | Jan - Mar -2014
ISSN Online: 2278- 2656 Journal Home page: www.ijrpp.com
Research article Open Access
A prospective study of the pattern of drug use in primary
dysmenorrhea in a tertiary care hospital
Ramya Sugumar*1
, Vasundara Krishniah2
, Suvarna2
, H.P.Pundarikaksha2
, Prathap.B1
,
Gladius Jennifer H1
.
1
Karpaga Vinayaga Institute of Medical Sciences, Madurantakam, Kanchipuram District, Tamil
Nadu, India – 603308.
2
Kempegowda Institute of Medical Sciences, Bangalore, Karnataka, India – 560070
*Corresponding author: Ramya Sugumar.
Email address : drramya.sugumar@gmail.com
Aim
To study the pattern of drug use in primary dysmenorrhea in a tertiary care hospital.
Materials and Methods
This prospective study of nine months duration was carried in Obstetrics and Gynecology OPD, in a tertiary care
teaching hospital among 100 patients with PD. The analysis was done for the pattern of drug use, prescribing
frequency of individual drug, to evaluate association between severity of dysmenorrhea and prescription pattern and
adequacy of prescription details.
Results
The mean age of the patients was 22.32 Β± 4.5 years. Majority (61%) of patients experienced severe dysmenorrhea.
Mefenamic acid with dicyclomine combination was most frequently (72%) prescribed, followed by mefenamic acid
alone (16%) and diclofenac (12%) and none were prescribed hormonal preparations. Although majority (43%) of the
patients with severe dysmenorrhea were prescribed mefenamic acid with dicyclomine combination, the severity of
dysmenorrhea did not influence the prescription pattern and choice of drug (p>.05). Instructions regarding dose,
frequency and duration of drug administration were present in the prescriptions.
Conclusion
In our present study, NSAIDs and their combination with antispasmodics were prescribed most frequently. Majority
of the drugs were prescribed by their brand names. Instructions regarding the prophylactic benefit of NSAIDs were
not present in the prescriptions.
Keywords: Drug use study, NSAIDS, Primary dysmenorrhea, Tertiary care hospital.
INTRODUCTION
Primary dysmenorrhea (PD) is a common
gynecological disorder characterized by painful
menstruation in the absence of any underlying pelvic
pathology.1,2
Its prevalence (71.9%) among
adolescent girls is particularly high.3
The medical,
social and economic consequence of PD are
International Journal of Research in
Pharmacology & Pharmacotherapeutics
Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84]
www.ijrpp.com
~ 81~
substantial causing interference with daily activities,
disruption of educational and social life leading to
school absenteeism and loss of labour.3
Prostaglandins (PGs) have a well recognized
pathophysiological role in PD by inducing intense
uterine contractions, decreasing uterine blood flow,
increasing peripheral nerve hypersensitivity and
resulting in pain. Patients with PD usually present
with colicky suprapubic pain, nausea, vomiting,
diarrhea and rarely syncopal attacks.1
The pharmacological measures for PD include
various non-steroidal anti-inflammatory drugs
(NSAIDs), antispasmodics and hormonal therapy.
NSAIDs which are PG synthesis inhibitors form the
main stay of treatment. Among them the most
commonly used are ibuprofen, mefenamic acid,
naproxen, ketoprofen, celecoxib, diclofenac.4
Hormonal therapy in the form of oral contraceptive
pills (OCPs) are reserved for patients with suboptimal
or lack of response to NSAIDs. Medroxy
progesterone acetate, levonorgestral releasing intra
uterine device and leuprolide are the other hormonal
agents that may be used.5
PD being a common gynecological disorder requires
adequate treatment failing which it may be
responsible for the silent suffering among young
women.6
However, there is no unanimity or
universally accepted and standardized guidelines
regarding the choice of drug therapy, criteria for
selection, the dose, frequency and duration of
administration. Hence the present study is taken up to
study the pattern of drug use in PD.
MATERIALS & METHODS
Study design
A prospective observational study.
Study duration
Nine months from March 2012 – November 2012
Study subjects
100 consecutive patients attending Obstetrics &
Gynecology OPD, KIMS Hospital and Research
Centre, Bangalore and diagnosed as PD by the
gynecologist.
Study procedure
The study was conducted after prior approval from
Institutional Ethics Committee. The data from 100
patients fulfilling the inclusion and exclusion criteria
were recorded and analyzed. For each patient,
demographic data, menstrual history (including onset,
duration and severity of dysmenorrhea and its
associated symptoms), prescription details including
name of drug, dose, route and frequency of
administration, and also prescription by generic or
brand names were documented on a case record form.
Inclusion criteria
Data of patients with PD between 12-35 years of age
and with regular menstrual cycle (28Β±7 days).
Exclusion criteria
Data of patients with underlying pelvic pathology
(abnormal USG) indicating secondary dysmenorrhea.
Statistical analysis was done using SPSS version
19.0. The characteristics of demographic details,
dysmenorrhea and drug prescription patterns were
described using descriptive statistics. The association
of prescription pattern and severity of pain was
analyzed using Chi square test (p<.05 considered
statistically significant).
RESULTS
Total of 100 prescriptions of patients with PD were
analyzed. Their mean age and mean age at menarche
was 22.32 Β± 4.5 and 12.8 Β±1.7 years respectively. The
age distribution of the patients is given in Table 1.
Majority (93%) of them were from urban
background. Dysmenorrhea was experienced on 1st
day of menstrual flow by majority (76%) of patients,
1 day before menstrual flow in 13% patients, 2 days
before menstrual flow in 6% patients and >2 days
before menstrual flow in 5% patients. Mean duration
of dysmenorrhea was 2.2 days with 74% of patients
experiencing pain in the first 2-3 days of menstrual
cycle. Figure 1 shows the severity of dysmenorrhea
among the patients which was categorized using
verbal multi dimentional scoring system.7
The drug
prescribing pattern was as follows: A majority (72%)
of patients were prescribed a combination of
mefenamic acid (250mg) + dicyclomine (10mg) (MA
+ Di) t.i.d, followed by mefenamic acid (250mg)
(MA) t.i.d in 16% and diclofenac (50mg) (D) in 12%
patients respectively. Among the patients with severe
dysmenorrhea 42% were prescribed MA+Di, 10%
Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84]
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~ 82~
MA, and 9% were prescribed D. Among those with
moderate dysmenorrhea 29% were prescribed MA +
Di, 6% MA and 3% patients were prescribed D. One
percent patients with mild dysmenorrhea were
prescribed MA + Di (Table 2). There was no
statistically significant relationship between drug
prescription and severity of dysmenorrhea (p>.05)
(Table 2).
DISCUSSION
Though PD is common in adolescents, in our study
only 27% belonged to adolescent age group (12-19
years) (Table 1). This may probably be due to lack of
awareness regarding existing medical treatment for
dysmenorrhea, practice of non-pharmacological
methods and prevalence of self medication practice in
them.8,9,10,11,12
The mean age at menarche was 12.8
years which was akin to the previous studies.13,14,15
Majority (93%) of the patients were from urban
background and only 7% were from rural, indicative
of better awareness and accessibility to institutional
health care facilities among the urban population.
With respect to onset of dysmenorrhea, in our study
majority (76%) of the patients experienced it on 1st
day of menstrual flow which is similar to the results
of previous studies.16
The mean duration of
dysmenorrhea was 2.2 days and majority(74%) of
patients experienced pain on 1st
2-3 days of menstrual
cycle which is in accordance with previous study and
probably because PG levels are highest during first
two days of menses.6
The prescribing pattern for PD included mefenamic
acid with dicyclomine combination (most commonly
prescribed), mefenamic acid alone and diclofenac
which are among the most commonly preferred drugs
for PD.4
None of the patients were prescribed OCPs
as they are indicated only when there is suboptimal or
lack of response to NSAIDs and when contraception
is required in addition to pain relief.5
The severity of
dysmenorrhea did not influence the prescribing
pattern indicating that severity of pain was not taken
as a criteria for choice of drug in PD (p>.05, Table
2). Most of the drugs were prescribed by their brand
names which may undermine the essential drug
concept. Instructions to the patients regarding dose,
frequency and duration of drug administration were
present in all prescriptions but prophylactic analgesic
benefit of NSAIDs (that they can be taken 1-2 days
before the onset of menstruation) was not present. If
advice is given to the patients with severe
dysmenorrhea to take NSAIDs prophylactically the
burden of pain and its consequences can be reduced
substantially.
To conclude, the drug prescription pattern for PD
included NSAIDs and antispasmodics which were
prescribed irrespective of the severity of pain. The
results of this study along with other extensive drug
utilization studies on primary dysmenorrhea will be
helpful in the future for the appropriate and efficient
treatment and thereby decrease the social and
economic consequences associated with it.
Table 1. Age distribution of patients
Age group
(yrs)
% of patients
12-19 27
20-22 32
23-26 23
27-31 14
32-35 4
Total 100
MeanΒ±SD 22.3Β±4.5
Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84]
www.ijrpp.com
~ 83~
Figure 1: Dysmenorrhea severity based on verbal multidimensional scoring system
Table: 2 Pattern of drug prescription and severity of dysmenorrhea
*Chi square test
REFERENCES
[1] Ropkin AJ, Howe NC. Pelvic pain and dysmenorrhea. In: Berek JS, editor. Novak’s Gynecology. 14th
ed.
Philadelphia: Lippincot Williams & Wilkins; 2007. p. 505-40.
[2] Umland EM, Weinstein LC, Buchanan C. Menstruation related disorders. In Dipiro JT, Talbert RL, Yee
GC, Matzke GR, Wells BG, Posey LW, editors. Pharmacotherapy a pathophysiologic approach. 7th
ed.
New York: McGraw Hill; 2008. p. 1329-44.
[3] Agarwal AK, Agarwal A. A study of dysmenorrhea during menstruation in adolescent girls. India J
Community Med 2010;35:159-64.
[4] Mackay HT. Dysmenorrhea. In: McPhee ST, Papadakis MA, Gonzales R, Zeiger R, editors. Current
Medical Diagnosis and Treatment. 49th ed. New York:McGraw Hill Lange; 2010. p. 655-86.
[5] Sanfilippo J, Erb T. Evaluation and management of dysmenorrhea in adolescents. Clin Obstet Gynecol
2008;51:257-67.
[6] Esimai OA, Omoniyi Esan GO. Awareness of menstrual abnormality amongst college students in urban
area of Ile-Ife, Osun state, Nigeria. Indian Journal of Community Medicine 2010;35(1):63-6.
[7] Andersch B, Milsom I. An epidemiological study among young women with dysmenorrhea. Am J Obstet
Gynecol 1982;144:655-60.
[8] Kolhe S, Deb S. Dysmenorrhea. Obstetrics, Gynecology and Reproductive Medicine 2011 Nov;
21(11):311-6.
Dysmenorrhea severity MA MA + Di D
Mild 0 1 0
Modearte 6 29 3
Severe 10 42 9
Total 16 72 12
p* >.05
0
10
20
30
40
50
60
70
Mild Moderate Severe
Percentage(%)
Dysmenorrhea severity
Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84]
www.ijrpp.com
~ 84~
[9] Unsal A, Ayranci U, Tozun M. Arslan G, Calik E. Prevalence of dysmenorrhea and its effect on quality
of life among a group of female university students. Upsala Journal of Medical Sciences 2010;115:138-
45.
[10]Lefebvre G, Pinsonneault O. SOGC Clinical Practice Guideline: Primary dysmenorrhea Consensus
Guideline. JOGC 2005 Dec:1117-30.
[11]Ropkin AJ, Howe NC. Pelvic pain and dysmenorrhea. In: Berek JS editor. Novak’s Gynecology. 14th ed.
Philadelphia: Lippincot Williams & Wilkins; 2007. p. 505-40.
[12] Hillen TIJ, Grbavac SL, Johnston PJ, Straton JAY, Keogh JMF. Primary dysmenorrhea in young
Wesatern Australian women: prevalence, impact and knowledge of treatment. Journal of Adolescent
Health 1999;25:40-5.
[13]Singh A, Kiran D, Singh H, Nel B, Singh P, Tiwari P. Prevalence and severity of dysmenorrhea: A
problem related to menstruation, among first and second year female medical students. Indian J Physiol
Pharmacol 2008;52(4):389-97.
[14]Cakir M, Mungan I, Karakas T, Girisken I, Okten A. Menstrual pattern and common menstrual disorders
among university students in Turkey. Pediatr Int 2007 Dec;49(6):938-42.
[15]Demir SC, Kadayýfçý TO, Vardar MA, Atay Y. Dysfunctionsl uterine bleeding and other menstrual
problems of secondary school students in Turkey. Pediatr Int 2007 Dec;49(6):938-42.
[16]Eryilmaz G, Ozdemir F. Evaluation of menstrual pain management approaches by Northeastern
Anatolian adolescents. Pain management Nursing 2009;10(1):40-7.

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A prospective study of the pattern of drug use in primary dysmenorrhea in a tertiary care hospital

  • 1. www.ijrpp.com ~ 80~ ISSN Print: 2278 – 2648 IJRPP |Vol 3 | Issue 1 | Jan - Mar -2014 ISSN Online: 2278- 2656 Journal Home page: www.ijrpp.com Research article Open Access A prospective study of the pattern of drug use in primary dysmenorrhea in a tertiary care hospital Ramya Sugumar*1 , Vasundara Krishniah2 , Suvarna2 , H.P.Pundarikaksha2 , Prathap.B1 , Gladius Jennifer H1 . 1 Karpaga Vinayaga Institute of Medical Sciences, Madurantakam, Kanchipuram District, Tamil Nadu, India – 603308. 2 Kempegowda Institute of Medical Sciences, Bangalore, Karnataka, India – 560070 *Corresponding author: Ramya Sugumar. Email address : drramya.sugumar@gmail.com Aim To study the pattern of drug use in primary dysmenorrhea in a tertiary care hospital. Materials and Methods This prospective study of nine months duration was carried in Obstetrics and Gynecology OPD, in a tertiary care teaching hospital among 100 patients with PD. The analysis was done for the pattern of drug use, prescribing frequency of individual drug, to evaluate association between severity of dysmenorrhea and prescription pattern and adequacy of prescription details. Results The mean age of the patients was 22.32 Β± 4.5 years. Majority (61%) of patients experienced severe dysmenorrhea. Mefenamic acid with dicyclomine combination was most frequently (72%) prescribed, followed by mefenamic acid alone (16%) and diclofenac (12%) and none were prescribed hormonal preparations. Although majority (43%) of the patients with severe dysmenorrhea were prescribed mefenamic acid with dicyclomine combination, the severity of dysmenorrhea did not influence the prescription pattern and choice of drug (p>.05). Instructions regarding dose, frequency and duration of drug administration were present in the prescriptions. Conclusion In our present study, NSAIDs and their combination with antispasmodics were prescribed most frequently. Majority of the drugs were prescribed by their brand names. Instructions regarding the prophylactic benefit of NSAIDs were not present in the prescriptions. Keywords: Drug use study, NSAIDS, Primary dysmenorrhea, Tertiary care hospital. INTRODUCTION Primary dysmenorrhea (PD) is a common gynecological disorder characterized by painful menstruation in the absence of any underlying pelvic pathology.1,2 Its prevalence (71.9%) among adolescent girls is particularly high.3 The medical, social and economic consequence of PD are International Journal of Research in Pharmacology & Pharmacotherapeutics
  • 2. Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84] www.ijrpp.com ~ 81~ substantial causing interference with daily activities, disruption of educational and social life leading to school absenteeism and loss of labour.3 Prostaglandins (PGs) have a well recognized pathophysiological role in PD by inducing intense uterine contractions, decreasing uterine blood flow, increasing peripheral nerve hypersensitivity and resulting in pain. Patients with PD usually present with colicky suprapubic pain, nausea, vomiting, diarrhea and rarely syncopal attacks.1 The pharmacological measures for PD include various non-steroidal anti-inflammatory drugs (NSAIDs), antispasmodics and hormonal therapy. NSAIDs which are PG synthesis inhibitors form the main stay of treatment. Among them the most commonly used are ibuprofen, mefenamic acid, naproxen, ketoprofen, celecoxib, diclofenac.4 Hormonal therapy in the form of oral contraceptive pills (OCPs) are reserved for patients with suboptimal or lack of response to NSAIDs. Medroxy progesterone acetate, levonorgestral releasing intra uterine device and leuprolide are the other hormonal agents that may be used.5 PD being a common gynecological disorder requires adequate treatment failing which it may be responsible for the silent suffering among young women.6 However, there is no unanimity or universally accepted and standardized guidelines regarding the choice of drug therapy, criteria for selection, the dose, frequency and duration of administration. Hence the present study is taken up to study the pattern of drug use in PD. MATERIALS & METHODS Study design A prospective observational study. Study duration Nine months from March 2012 – November 2012 Study subjects 100 consecutive patients attending Obstetrics & Gynecology OPD, KIMS Hospital and Research Centre, Bangalore and diagnosed as PD by the gynecologist. Study procedure The study was conducted after prior approval from Institutional Ethics Committee. The data from 100 patients fulfilling the inclusion and exclusion criteria were recorded and analyzed. For each patient, demographic data, menstrual history (including onset, duration and severity of dysmenorrhea and its associated symptoms), prescription details including name of drug, dose, route and frequency of administration, and also prescription by generic or brand names were documented on a case record form. Inclusion criteria Data of patients with PD between 12-35 years of age and with regular menstrual cycle (28Β±7 days). Exclusion criteria Data of patients with underlying pelvic pathology (abnormal USG) indicating secondary dysmenorrhea. Statistical analysis was done using SPSS version 19.0. The characteristics of demographic details, dysmenorrhea and drug prescription patterns were described using descriptive statistics. The association of prescription pattern and severity of pain was analyzed using Chi square test (p<.05 considered statistically significant). RESULTS Total of 100 prescriptions of patients with PD were analyzed. Their mean age and mean age at menarche was 22.32 Β± 4.5 and 12.8 Β±1.7 years respectively. The age distribution of the patients is given in Table 1. Majority (93%) of them were from urban background. Dysmenorrhea was experienced on 1st day of menstrual flow by majority (76%) of patients, 1 day before menstrual flow in 13% patients, 2 days before menstrual flow in 6% patients and >2 days before menstrual flow in 5% patients. Mean duration of dysmenorrhea was 2.2 days with 74% of patients experiencing pain in the first 2-3 days of menstrual cycle. Figure 1 shows the severity of dysmenorrhea among the patients which was categorized using verbal multi dimentional scoring system.7 The drug prescribing pattern was as follows: A majority (72%) of patients were prescribed a combination of mefenamic acid (250mg) + dicyclomine (10mg) (MA + Di) t.i.d, followed by mefenamic acid (250mg) (MA) t.i.d in 16% and diclofenac (50mg) (D) in 12% patients respectively. Among the patients with severe dysmenorrhea 42% were prescribed MA+Di, 10%
  • 3. Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84] www.ijrpp.com ~ 82~ MA, and 9% were prescribed D. Among those with moderate dysmenorrhea 29% were prescribed MA + Di, 6% MA and 3% patients were prescribed D. One percent patients with mild dysmenorrhea were prescribed MA + Di (Table 2). There was no statistically significant relationship between drug prescription and severity of dysmenorrhea (p>.05) (Table 2). DISCUSSION Though PD is common in adolescents, in our study only 27% belonged to adolescent age group (12-19 years) (Table 1). This may probably be due to lack of awareness regarding existing medical treatment for dysmenorrhea, practice of non-pharmacological methods and prevalence of self medication practice in them.8,9,10,11,12 The mean age at menarche was 12.8 years which was akin to the previous studies.13,14,15 Majority (93%) of the patients were from urban background and only 7% were from rural, indicative of better awareness and accessibility to institutional health care facilities among the urban population. With respect to onset of dysmenorrhea, in our study majority (76%) of the patients experienced it on 1st day of menstrual flow which is similar to the results of previous studies.16 The mean duration of dysmenorrhea was 2.2 days and majority(74%) of patients experienced pain on 1st 2-3 days of menstrual cycle which is in accordance with previous study and probably because PG levels are highest during first two days of menses.6 The prescribing pattern for PD included mefenamic acid with dicyclomine combination (most commonly prescribed), mefenamic acid alone and diclofenac which are among the most commonly preferred drugs for PD.4 None of the patients were prescribed OCPs as they are indicated only when there is suboptimal or lack of response to NSAIDs and when contraception is required in addition to pain relief.5 The severity of dysmenorrhea did not influence the prescribing pattern indicating that severity of pain was not taken as a criteria for choice of drug in PD (p>.05, Table 2). Most of the drugs were prescribed by their brand names which may undermine the essential drug concept. Instructions to the patients regarding dose, frequency and duration of drug administration were present in all prescriptions but prophylactic analgesic benefit of NSAIDs (that they can be taken 1-2 days before the onset of menstruation) was not present. If advice is given to the patients with severe dysmenorrhea to take NSAIDs prophylactically the burden of pain and its consequences can be reduced substantially. To conclude, the drug prescription pattern for PD included NSAIDs and antispasmodics which were prescribed irrespective of the severity of pain. The results of this study along with other extensive drug utilization studies on primary dysmenorrhea will be helpful in the future for the appropriate and efficient treatment and thereby decrease the social and economic consequences associated with it. Table 1. Age distribution of patients Age group (yrs) % of patients 12-19 27 20-22 32 23-26 23 27-31 14 32-35 4 Total 100 MeanΒ±SD 22.3Β±4.5
  • 4. Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84] www.ijrpp.com ~ 83~ Figure 1: Dysmenorrhea severity based on verbal multidimensional scoring system Table: 2 Pattern of drug prescription and severity of dysmenorrhea *Chi square test REFERENCES [1] Ropkin AJ, Howe NC. Pelvic pain and dysmenorrhea. In: Berek JS, editor. Novak’s Gynecology. 14th ed. Philadelphia: Lippincot Williams & Wilkins; 2007. p. 505-40. [2] Umland EM, Weinstein LC, Buchanan C. Menstruation related disorders. In Dipiro JT, Talbert RL, Yee GC, Matzke GR, Wells BG, Posey LW, editors. Pharmacotherapy a pathophysiologic approach. 7th ed. New York: McGraw Hill; 2008. p. 1329-44. [3] Agarwal AK, Agarwal A. A study of dysmenorrhea during menstruation in adolescent girls. India J Community Med 2010;35:159-64. [4] Mackay HT. Dysmenorrhea. In: McPhee ST, Papadakis MA, Gonzales R, Zeiger R, editors. Current Medical Diagnosis and Treatment. 49th ed. New York:McGraw Hill Lange; 2010. p. 655-86. [5] Sanfilippo J, Erb T. Evaluation and management of dysmenorrhea in adolescents. Clin Obstet Gynecol 2008;51:257-67. [6] Esimai OA, Omoniyi Esan GO. Awareness of menstrual abnormality amongst college students in urban area of Ile-Ife, Osun state, Nigeria. Indian Journal of Community Medicine 2010;35(1):63-6. [7] Andersch B, Milsom I. An epidemiological study among young women with dysmenorrhea. Am J Obstet Gynecol 1982;144:655-60. [8] Kolhe S, Deb S. Dysmenorrhea. Obstetrics, Gynecology and Reproductive Medicine 2011 Nov; 21(11):311-6. Dysmenorrhea severity MA MA + Di D Mild 0 1 0 Modearte 6 29 3 Severe 10 42 9 Total 16 72 12 p* >.05 0 10 20 30 40 50 60 70 Mild Moderate Severe Percentage(%) Dysmenorrhea severity
  • 5. Ramya sugumar et al / Int. J. of Res. in Pharmacology & Pharmacotherapeutics Vol-3(1) 2014 [80-84] www.ijrpp.com ~ 84~ [9] Unsal A, Ayranci U, Tozun M. Arslan G, Calik E. Prevalence of dysmenorrhea and its effect on quality of life among a group of female university students. Upsala Journal of Medical Sciences 2010;115:138- 45. [10]Lefebvre G, Pinsonneault O. SOGC Clinical Practice Guideline: Primary dysmenorrhea Consensus Guideline. JOGC 2005 Dec:1117-30. [11]Ropkin AJ, Howe NC. Pelvic pain and dysmenorrhea. In: Berek JS editor. Novak’s Gynecology. 14th ed. Philadelphia: Lippincot Williams & Wilkins; 2007. p. 505-40. [12] Hillen TIJ, Grbavac SL, Johnston PJ, Straton JAY, Keogh JMF. Primary dysmenorrhea in young Wesatern Australian women: prevalence, impact and knowledge of treatment. Journal of Adolescent Health 1999;25:40-5. [13]Singh A, Kiran D, Singh H, Nel B, Singh P, Tiwari P. Prevalence and severity of dysmenorrhea: A problem related to menstruation, among first and second year female medical students. Indian J Physiol Pharmacol 2008;52(4):389-97. [14]Cakir M, Mungan I, Karakas T, Girisken I, Okten A. Menstrual pattern and common menstrual disorders among university students in Turkey. Pediatr Int 2007 Dec;49(6):938-42. [15]Demir SC, KadayΓ½fçý TO, Vardar MA, Atay Y. Dysfunctionsl uterine bleeding and other menstrual problems of secondary school students in Turkey. Pediatr Int 2007 Dec;49(6):938-42. [16]Eryilmaz G, Ozdemir F. Evaluation of menstrual pain management approaches by Northeastern Anatolian adolescents. Pain management Nursing 2009;10(1):40-7.