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International Journal of Women's Health logoLink to International Journal of Women's Health
. 2016 Sep 19;8:489–496. doi: 10.2147/IJWH.S112768

Primary dysmenorrhea magnitude, associated risk factors, and its effect on academic performance: evidence from female university students in Ethiopia

Solomon Hailemeskel 1, Asrate Demissie 2, Nigussie Assefa 3,
PMCID: PMC5034908  PMID: 27695366

Abstract

Background

Primary dysmenorrhea (PD) is the most common gynecologic compliant among adolescent females. There is a wide variation in the estimate of PD, which ranges from 50% to 90%, and the disorder is the most common cause of work and school absenteeism in adolescent females.

Objective

To assess the prevalence and associated risk factors of PD among female university students and understand its effects on students’ academic performance.

Methods

A cross-sectional study was employed in 440 research participants. A multistage stratified sampling technique was employed to select the study units. Structured and pretested self-administered questionnaires were used and weight and height measurements were conducted. The severity of dysmenorrheal pain was assessed by using a verbal multidimensional scoring system and visual analog scale. The data were double entered in Epi Info version 3.1 and analyzed using SPSS version 17. Descriptive statistics, chi-square test, and logistic regression analysis were performed.

Results

A total of 440 students participated in this study. The prevalence of PD was 368 (85.4%). Of these, 123 (28.5%) had mild, 164 (38.1%) moderate, and 81 (18.8%) severe primary dysmenorrheal pain. Among students with PD, 88.3% reported that PD had a negative effect on their academic performance. Of these, 80% reported school absence, 66.8% reported loss of class concentration, 56.3% reported class absence, 47.4% reported loss of class participation, 37.8% reported limited sport participation, 31.7% reported limitation in going out with friends, and 21% reported inability to do homework. Based on the multivariate logistic regression, PD was statistically significant with those who had lower monthly stipends, a history of attempt to lose weight, a history of depression or anxiety, disruption of social network of family, friends or people they love, who consumed more than four glasses of tea per day, who drunk one or more Coca-Cola or Pepsi per day, in nullipara, and students with a family history of dysmenorrhea.

Conclusion

PD is more prevalent among female students attending university. It has a significant negative impact on students’ academic performance. Thus, it needs medical attention. There are various identified associated risk factors and considering them in the management of the disorder is fundamental. It is also wise to recommend future studies to better identify risk factors for PD and lighten its effect on students’ academic performance at a larger scale in the country.

Keywords: academic performance, risk factors, dysmenorrhea, Ethiopia, adolescents, young, higher institution

Introduction

Primary dysmenorrhea (PD) is pain during menstrual bleeding without organ pathological abnormalities.1 It usually begins during adolescence.2,3 Affected females experience sharp, intermittent spasm of pain usually concentrated on the supra pubic area and which may radiate to the back of the legs. Pain usually develops within hours of the start of the menstruation and peaks as the flow becomes heaviest during the first day or two of the cycle.4

PD is a key women’s health burden5 and is also one of the public problems in the world.6 An estimated 140 million hours are lost annually from school or work because of dysmenorrhea;7 for example, in the US, ~600 million working hours are lost annually as a result of PD.8 PD is the leading cause of work or school absenteeism in women5 and a leading cause of recurrent short-term school absenteeism among adolescent girls.9

Several research findings showed that the proportions of PD and/or dysmenorrhea in young females are higher. In studies from three medical colleges of India,10 Turkish University,6 Mexican University,11 and Thailand,12 students reported that the prevalence rate of dysmenorrhea as 73.83%, 55.5%, 64%, and 84.9%, respectively. A study done among Hispanic female adolescents found that 3 months prior to the study 85% of the adolescents reported experiencing dysmenorrhea.13 A study done among 356 Naples professional institute adolescents14 and Nigeria college students in the urban area of Ile-Ife, Osun,15 found the prevalence of PD as 82.30% and 62.5%, respectively. Another study done in Dabat and Kola Diba showed 72% prevalence of dysmenorrhea in secondary school students.16

PD is believed to be associated with many factors, including behavioral and psychological aspects. Age <20 years, nulliparity, heavy menstrual flow, smoking, high socioeconomic status, attempts to lose weight, physical activity, disruption of social networks, depression, and anxiety are risk factors of dysmenorrhea.7 A long and heavy menstrual flow is related to an increase in the severity of dysmenorrhea. Concerning dietary habits of students, it was noted that a higher consumption of fish, eggs, fruit, and a lower consumption of wine was correlated with a lower frequency of dysmenorrhea.14 According to a study done in Dumlupinar University, coffee consumption, menstrual bleeding with duration ≥7 days, and positive family history of dysmenorrhea were reported as important risk factors for dysmenorrhea.17 Another study indicated that smoking status18,19 and depressive symptoms/anxiety18,20 were related to menstrual symptoms and the impact of depressive symptoms/anxiety on menstrual symptoms was strongly associated among nonsmokers as well.18 Other studies also showed that risk factors related to dysmenorrhea are heavy menstrual blood flow (prolonged or aberrant menstrual blood flow),2124 a younger age (age <20 years), low body mass index (BMI), nulliparity, smoking, early menarche, premenstrual syndrome, clinically suspected pelvic inflammatory disease, somatization, psychological disturbance, disruption of social relations with family or friends, and poor mental health, such as depression and anxiety.21,23,24

Dysmenorrhea adversely affects the personal life of adolescents and limits their social and academic performance. A study by Mexican university students found that dysmenorrhea affects 65% of students’ daily activities.25 Based on this study, the characteristics of menstrual factors that limit students’ daily activities were cramping pain in the lower abdomen (93%), swollen abdomen (67%), irritability (50%), depression (48%), painful or tender breasts (45%), backache (43%), gastrointestinal disturbances (26%), headache (24%), and swelling legs (19%).25 In addition to this, menstrual pain and distress can cause disability (loss of function and activity) and handicap (altered social roles).1,2

Affecting female students’ academic performance,12,13,26 absenteeism from school6,8,10,12,13,15,17,22,2729 and loss of work days8,22,2729 are common in a woman with dysmenorrhea or PD, which result in significant economic consequences.

This research gives insights on PD-associated risk factors, the severity of this disorder among groups of female students, and its effect on their academic performance. Besides, it also opens the window for further large scale studies.

Materials and methods

Study design and population

A cross-sectional study design was used to conduct the research in Debre Berhan University in 2012. The university is one of the public universities in Ethiopia and has been enrolling students from all regions of the country. The population of the study was all regular female students who were randomly selected from colleges and schools from first year to fourth year batches. A total of 440 female students were involved in the study.

Sampling procedure, data collection tools, and procedure

Participants were selected from all female students of the university using multistage sampling technique. Probability proportionate sampling method was also applied to allocate the sample size according to the strata. The strata are categorized based on the batch/academic year of students. In order to select colleges and schools, simple random sampling techniques were applied.

Pretest was administered to 22 students, which accounts for 5%. Regarding their background, all of them were selected from similar socioeconomic status. These students were not involved in the main study.

Structured self-administered questionnaires were used. The questionnaire items were adapted from previous studies.13,30,31 Some terms were given operational definitions. For instance, class absence was defined as when students miss individual classes because of PD during the last month prior to the data collection and school absence was to mean when students miss a school day due to primary dysmenorrheal pain during the last month prior to the data collection. The tool includes sociodemographic characteristics, student’s psychosocial factor and family planning history, dysmenorrheal status, menstrual characteristics, activities affected by PD, behavioral factors, and PD effect on student’s academic performance. The questionnaires also included visual analogue scale questions and multidimensional scoring system to assess the severity of PD.30 The questionnaires were translated to local languages.

Training for data collectors and supervisors was given in understanding the objective of the survey, methods of data collection, and ways of approaching the respondents. The supervisor checked the activities of each data collector and all the filled questionnaires for its completion, clarity, and proper identification of the respondents. Then, the questionnaires were checked again for the completion by the principal investigator.

Data analysis

The data were checked manually for completeness during their collection, and then coded and entered into Epi Info version 3.1 statistical software (Centers for Disease Control and Prevention, Atlanta, GA, USA). Then, it was analyzed by SPSS version 17 software application (SPSS Inc., Chicago, IL, USA). Inferential analysis was done by logistic regression.

Ethical consideration

The ethical approval for this study was granted by the Institutional Review Board of the College of Health Sciences, Addis Ababa University. All participants provided verbal consent. Written consent was not required, as confidentiality and anonymity were strictly maintained, and the study could cause no harm to the study participants.

Results

Sociodemographic characteristics and respondents’ BMI

In all, 98% of the respondents were involved in the study. The mean ages of respondents were 20.57±1.36 (standard deviation). Christianity was the major (89.56%) religion of the respondents. The majority (90.7%) of the respondents were single, and 28.1% had an average monthly income <7 USD, 50.1% received 7–17 USD, and the remainder received >17 USD. Regarding their family income, the majority (50.1%) earned between 88.25 and 176.47 USD (Table 1).

Table 1.

Sociodemographic characteristics

Variable Category Participants (n) Participants (%)
Age ≤20 years 220 51.0
21–22 years 180 41.8
>23 years 31 7.2
Religion Christian 386 89.6
Muslim 45 10.4
Ethnicity Amhara 316 73.3
Oromo 41 9.5
Tigrie 40 9.3
Guragie 19 4.4
Others 15 3.5
Marital status Single 391 90.7
Ever married 40 9.3
Educational level First year 115 26.7
Second year 136 31.6
Third year 160 37.1
Fourth year 20 4.6
Monthly income <150 ETB 121 28.1
150–300 ETB 216 50.1
>300 ETB 94 21.8
Family income <1,500 ETB 121 28.1
1,500–3,000 ETB 216 50.1
>3,000 ETB 94 21.8
Parity Nullipara 372 86.3
Multipara 59 13.7

Note: 1 ETB is equivalent to 0.06 USD.

Abbreviation: ETB, Ethiopian Birr.

The majority of respondents’ (347 [80.5%]) BMI value rested on the normal range (18.00–24.99 kg/m2), whereas the rest (49 [11.4%]) were malnourished (<18.00 kg/m2) and 35 (8.1%) were overweight (25.00–29.99 kg/m2) (Figure 1).

Figure 1.

Figure 1

BMI of students.

Abbreviation: BMI, body mass index.

Prevalence of PD and its effect on students’ academic performance

The prevalence of PD accounted for 85.4% and 88.3% of the respondents with PD reported that the disorder interferes with their academic performance. The most commonly reported effect of menstrual pain on students’ academic performance was: school absence (260 [80%]), loss of class concentration (217 [66.8%]), class absence (183 [56.3%]), loss of class participation (154 [47.4%]), limited sport participation (123 [37.8%]), limited going out with friends (103 [31.7%]), inability to do homework (68 [21%]), and reduced test taking skill (50 [15.4%]) (Table 2).

Table 2.

Prevalence and effect of primary dysmenorrhea on academic performance

Variable Category Participants (n) Participants (%)
Menstruation associated with pain Yes 368 85.4
No 63 14.6
Menstrual problems interfere with school performance Yes 325 88.3
No 43 11.7
Effects of menstrual pain on school performance School absence
 Yes 260 80.0
 No 65 20.0
Class absence
 Yes 183 56.3
 No 142 43.7
Inability to do homework
 Yes 68 21.0
 No 257 79.0
Loss of class participation
 Yes 154 47.4
 No 171 52.6
Loss of class concentration
 Yes 217 66.8
 No 108 33.2
Reduced test taking skill
 Yes 50 15.4
 No 275 84.6
Limited sport participation
 Yes 123 37.8
 No 202 62.2
Limitation in going out with friends
 Yes 103 31.7
 No 222 68.3

PD pain characterization

According to the verbal multidimensional scoring system and visual analog scale for assessment of PD pain, out of 368 (85.4%) students who had menstrual pain, 123 (28.5%) students’ menstruation was painful but seldom inhibits normal activity and analgesics are seldom required (mild pain). The majority of students’ (164 [38.1%]) daily activity was affected; analgesics were required and gave sufficient relief so that absence from school was unusual (moderate pain). Additionally, in 81 (18.8%) of students, daily activity was clearly inhibited by PD, the effect of analgesics to give relief of the pain was insignificant, and they experienced vegetative symptoms such as headache, fatigue, vomiting, and diarrhea (severe pain).

Logistic regression analysis of significant variables related to PD

Students’ sociodemographic characteristics versus PD

Table 3 shows the results of the multivariate analysis using significant bivariate variables for student’s sociodemographic characteristics. The analysis showed that students in the third and fourth years of university had a lower risk of PD. The risk of PD was 0.046 times less in the second year (adjusted odds ratio [AOR] =0.046, 95% confidence interval [CI] [0.014–0.288], P≤0.001), 1.08 times higher in first year, though it was not statistically significant when adjusted for possible confounders (crude odds ratio =2.242, 95% CI [1.141–4.406], P=0.019) and (crude odds ratio =1.080, 95% CI [0.204–5.721], P=0.019). The risk of PD was 6.671 times higher in students whose monthly income was <150 ETB compared with students whose monthly income was above 300 ETB (AOR =6.671, 95% CI [1.427–31.180], P=0.016).

Table 3.

Student’s sociodemographic variables versus primary dysmenorrhea

Variable Primary dysmenorrhea, n (%)
Adjusted OR (95% CI) P-value
Yes (n=368) No (n=63)
Educational level
 1st year 102 (27.7) 13 (20.6) 1.080 (0.204–5.721) 0.927
 2nd year 126 (34.2) 10 (15.9) 0.064 (0.014–0.288)* <0.001
 3rd and 4th year 140 (38.0) 40 (63.5) 1
Students’ monthly income**
 <150 ETB 103 (28.0) 7 (11.1) 6.671 (1.427–31.180)* 0.016
 150–200 ETB 95 (25.8) 20 (31.7) 0.572 (0.162–2.025) 0.386
 201–300 ETB 99 (26.9) 12 (19.0) 0.269 (0.062–1.169) 0.08
 >300 ETB 71 (19.3) 24 (38.1) 1
History of attempt to lose weight
 Yes 226 (61.4) 13 (20.6) 6.085 (1.998–18.529)* 0.001
 No 142 (38.6) 50 (79.4) 1
History of depression or anxiety
 Yes 314 (85.3) 26 (41.3) 13.607 (4.542–40.767)* <0.001
 No 54 (14.7) 37 (58.7) 1
Disruption of social networks, eg, family, friends or people they love
 Yes 260 (70.7) 26 (41.3) 3.218 (1.261–8.212)* 0.014
 No 108 (29.3) 37 (58.7) 1

Notes:

*

Statistically significant variables,

**

1 ETB is equivalent to 0.06 USD.

Abbreviations: CI, confidence interval; ETB, Ethiopian Birr; OR, odds ratio.

The risk of PD in students who had a history of attempt to lose weight was approximately six times higher than students with no prior history of attempt to lose weight (AOR =6.085, 95% CI [1.998–18.529], P=0.001). Other risk factors for PD were ~14 times higher risk in students who had a previous history of depression or anxiety compared with those who had no prior history of depression or anxiety (AOR =13.607, 95% CI [4.542–40.767], P≤0.001); an approximately three times higher risk in students who had a previous history of disruption of social network, such as with family, friends, or people they love compared with students who had no prior history of disruption of social network (AOR =3.218, 95% CI [1.261–8.212], P=0.014).

Students’ behavioral and gynecologic factors versus PD

Table 4 demonstrates the result of logistic regression of behavioral and gynecologic factors versus PD. The risk of PD was ~19 times higher in students consuming more than four glasses of tea per day compared with students who did not consume tea at all (AOR =18.938, 95% CI [2.190–163.730], P=0.008), whereas students who consume less than four glasses of tea per day had 0.093 times less risk for PD when compared to that of nonconsumers (AOR =0.093, 95% CI [0.023–0.376], P≤0.001). Concerning Coca-Cola or Pepsi consumption, the risk of PD was approximately seven times higher in students consuming one and more than one Coca-Cola or Pepsi per day compared with that of nonconsumers (AOR =6.786, 95% CI [1.881–24.476], P=0.003). On the other hand, the risk of PD was found to be 0.186 times less in students who ate two or more chocolates per day compared with nonconsumers (AOR =0.186, 95% CI [0.042–0.815], P=0.026).

Table 4.

Behavioral and gynecologic factors versus primary dysmenorrhea

Variable Primary dysmenorrhea, n (%)
Crude OR (95% CI) Adjusted OR (95% CI) P-value
Yes No Crude Adjusted
Tea consumption per day
 Not at all 38 (10.3) 14 (22.2) 1.00
 <4 glasses per day 292 (79.3) 46 (73.0) 8.01 (3.49–18.39) 0.09 (0.02–0.38)* <0.001 <0.001
 >4 glasses per day 38 (10.3) 3 (4.8) 15.56 (3.82–63.33) 18.94 (2.19–163.73)* <0.001 0.008
Coca-Cola or Pepsi consumption per day
 Not at all 244 (66.5) 52 (82.5) 1.00
 One Coca-Cola per day 124 (33.7) 11 (17.5) 2.40 (1.21–4.77) 6.79 (1.88–24.47)* 0.012 0.003
Chocolate consumption per day
 Not at all 339 (92.1) 55 (87.3) 1.00
 Two bars of chocolate per day 29 (7.9) 8 (12.7) 0.59 (0.26–1.35) 0.19 (0.04–0.82)* 0.212 0.026
Parity
 Nullipara 337 (91.6) 35 (55.6) 8.7 (4.69–16.14) 47.32 (11.04–202.86)* <0.001 <0.001
 Multipara 31 (8.4) 28 (44.4) 1.00
Family history of dysmenorrhea
 Yes 242 (65.8) 10 (15.9) 10.18 (5.01–20.69) 27.23 (8.03–92.35)* <0.001 <0.001
 No 126 (34.2) 53 (84.1) 1.00

Note:

*

Statistically significant.

Abbreviations: CI, confidence interval; OR, odds ratio.

Concerning gynecologic factors, the risk of PD was 47 times higher in students who are nullipara compared with students who are multipara. The risk of PD in students who had a family history of dysmenorrhea was ~27 times higher than students with no prior family history.

Discussion

This study shows a high prevalence of PD (85.4%), which is slightly higher than a study done in Dumlupinar University in Kutahya Health High School, Western Turkey (72.7%);17 a study done in three medical colleges of India (73.83%);10 a study conducted in Dabat and Kola Diba North West Ethiopia among secondary school adolescent students (72%),16 but more higher than a study done among Nigeria college students (62.5%);15 a study done in Turkish University (55.5%);10 and a study done among Mexican university students (64%).11 A difference among these studies could be due to the dissimilarity in the selected groups of students, age variation, and the absence of universally accepted methods of defining PD because many studies use the definition of dysmenorrhea. The variations in sociocultural, ethnic, and lifestyle factors among university students could also be due to other pertinent reasons. But the prevalence of PD in this study was similar with a study done among Thai secondary school students in KhonKaen province which was ~85%.12

The mean age of this study was 20.57 years, which is similar to a study done among Nigeria college students (21.1 years)15 and students from Turkey University (21.47 years).6 This study shows the age at menarche was 14.96 years, which is concurrent with a study done among Nigeria college students (14.2 years)15 but slightly higher than with a study done at Turkey University (13.08 years).6 The possible justification for this variation could be the difference of the study groups in socioeconomic status and the studies were carried out among different age groups.

This study shows that more than half of the female students (56.9%) had moderate and severe types of PD, and 28.5% of the students had mild PD, which is slightly lower than that (66.2% of students had moderate and severe dysmenorrhea) in another study.17 On the contrary, this study had a higher (38.1% of moderate and 18.8% of severe) PD compared with a study,10 which revealed 30.37% with moderate dysmenorrhea and 6.32% severe dysmenorrhea. The possible explanation for this variation could be the study participants’ variance in menstrual pain characterization with differences of social, lifestyle, or cultural backgrounds among the students. Despite the observed percentage variation among studies, overall, PD in female students from different areas experience severe or moderate pain, which would impair their quality of life and have a negative effect on their academic performance.

Common symptoms mentioned in this study for PD were back pain or abdominal pain (88.3%), mood change – irritability and depression (57.8%), menstrual irregularity (49.5%), headache (29.3%), pain at the groin (27.2%), and sleeplessness (17.3%), which are almost similar to a study done among Mexican university students, which indicated cramping lower abdominal pain (93%), backache (43%), irritability (50%), depression (48%), and headache (24%),25 and a study done among Thai secondary school students in KhonKaen in which the major symptoms were mood change (84.8%), headache (37.5%), and backache (63.7%).12

This study showed that among participants with PD, 88.3% reported that PD had an effect on academic performance. Some of its effects were school absence (80%), class absence (56.3%), loss of class participation (47.4%), loss of class concentration (66.8%), limited sport participation (37.8%), limited going out with friends (31.7%), inability to do homework (21%), and reduced test taking skill (15.4%), which are somehow different with studies done among Hispanic female students in which there was a loss of class concentration (59%), limited sport participation (51%), loss of class participation (50%), homework (35%), and test taking skill (36%).13 The finding from this study is also different from a study done in KhonKaen, Thailand,12 which indicated poor class concentration (73.9%), limited sport activity (59.8%), and absence from school (18.2%). In one of the effects, absence from school, a study done among Northwest Ethiopia secondary school adolescents revealed that 48.8% of students had suffered with PD and reported to be absent from school, which was also slightly lower compared with results of this study. This variation could be because of the difference in the operational definition of terms, severity of dysmenorrhea pain, and sociodemographic variables. Nevertheless, in all the studies, we can understand that PD interferes with their academic performance due to the intensity of the symptoms instead of the stigma related to it.

In addition, a finding from this study revealed that among students with PD, 47% reported 1 day school absence, 23.4% reported 2 days school absence, and 5.7% of students reported 3 days school absence, which is comparable with a study done among Hispanic female adolescents with 46% with a half to 1 day of school absence, 36% 2 to 3 days school absence, and 18% more than four school days’ absence.13 Based on this finding, one can learn that PD is an important public health problem in school female attendees and brings a negative effect on their academic performance.

First year and second year students were mostly affected by PD than third and fourth year students though it was not statistically significant when adjusted. This might be because the first and second year female students are younger and they are in a new environment full of stress than the senior female students.

Regarding multivariate analyses, a history of an attempt to lose weight was an important risk factor for PD, which is comparable with findings from Dumlupinar University,17 and likewise a history of depression or anxiety and disruption of social networks with family, friends, or people they love was an important risk factor for PD. This is analogous with other studies.21,23,24

A study done in Turkish university showed that PD was ~1.5 times higher in females with satisfactory stipend allowance,6 which is completely different from this study that shows PD is seven times higher in students with less monthly income than those with relatively large monthly income. From this study, one can imply that other factors, such as sociocultural and personal factors, had significant contributions to PD rather than individual’s monthly income but it is suggested to have further research.

The prevalence of PD was higher among students who had a higher intake of tea and Coca-Cola or Pepsi, which is also represented in Turkish university students6 in whom dysmenorrhea was higher in women with an excessive sugar intake. The possible explanation for this relationship could be that vitamins and mineral absorption and metabolism are compromised by sugar intake. It then leads to muscle spasm, which can be manifested by menstrual pain.

In this study, those students with a family history of dysmenorrhea had a higher risk of developing PD. This finding is also confirmed by other studies from Turkish University6 and Dumlupinar University.17 To explain more, daughters of mothers with dysmenorrhea might experience and learn the same behaviors18 and evidently family history is basically associated with gynecologic problems.31

Parity was also found to be an important risk factor for PD in which being nullipara has more risk than being multipara. This could be explained by the presence of excessive release of prostaglandins by the endometrium and presence of large circulating prostaglandin hormones during menstruation with dysmenorrhea than women with no dysmenorrhea. This is again more frequent in nullipara than multipara.6

Many studies revealed that having a low BMI was an important risk factor for PD21,23,24 but in this study BMI was not an important risk factor for PD (P=0.732). The possible explanation for this could be many of the study participants had normal BMI (80.5%) as well as the presence of difference in the measuring instrument among studies could also be valuable.

Other studies showed that early age at menarche was an important risk factor for PD, which is <13 years.21,23,24 But, in this study, students’ age at menarche was not significantly associated with PD. Possibly, this discrepancy can be explained that in this study many of the respondents’ age at menarche was above 13 years (82.6%). Additionally, studies showed that having heavy menstrual blood flow had a significant association with PD;21,23,24 however, in this study, duration of menstruation was not significantly associated with PD (P=0.116). The possible explanation might be due to the majority of the respondents (68.2%) in this study having a normal duration of menstruation than the others.

Limitations of the study

This study included only one university, which may not be representative though students are enrolled from the whole regions of the country and show up as representative in terms of participants. It was also hard to compare results with local studies due to lack of research in the area. Besides, as the study design was cross-sectional, temporal relations could not be assessed. Lastly, from the participants’ perspectives, there could be a recall bias and over-reporting of the condition as the students were asked for events within the last years prior to the study, such as a question about the age at menarche.

Conclusion

PD is prevalent in higher institutions and has a marked effect on students’ academic performance. PD has a significant association with their educational level, monthly income, history of attempt to lose weight, depression or anxiety, and disruption of social network, tea drinking, Coca-Cola or Pepsi and chocolate intake, being nullipara, having menstrual irregularity, and having a family history of PD.

Acknowledgments

The authors are very thankful to Addis Ababa University for financial support. The authors also appreciate the support and cooperation offered by Debre Berhan University during data collection. Lastly, the study participants need to be acknowledged for their valuable information and involvement in the study.

Footnotes

Author contributions

All authors contributed toward data analysis, drafting and critically revising the paper, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.

Disclosure

The authors report no conflicts of interest in this work.

References

  • 1.Davis AR, Westhoff CL. Primary dysmenorrhea in adolescent girls and treatment with oral contraceptives. J Pediatr Adolesc Gynecol. 2001;14(1):3–8. doi: 10.1016/s1083-3188(00)00076-0. [DOI] [PubMed] [Google Scholar]
  • 2.Callejo J, Diaz J, Ruiz A, Garci RM. Effect of a low-dose oral contraceptive containing 20 μg ethinylestradiol and 150 μg desogestrel on dysmenorrhea. Contraception. 2003;68:183–188. doi: 10.1016/s0010-7824(03)00132-x. [DOI] [PubMed] [Google Scholar]
  • 3.Cunningham AS, Muneyyirci-Delale O. The association between primary dysmenorrhea and hyperemesis gravidarum. Medical Hypotheses. 2009;73(1):90–91. doi: 10.1016/j.mehy.2008.12.048. [DOI] [PubMed] [Google Scholar]
  • 4.Li N, Liu H, Chen C, et al. CYP1A1 gene polymorphisms in modifying the association between passive smoking and primary dysmenorrhea. Ann Epidemiol. 2007;17(11):882–888. doi: 10.1016/j.annepidem.2007.05.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Mannix KL. Menstrual-related pain conditions: dysmenorrhea and migraine. J Womens Health. 2008;17(5):879–891. doi: 10.1089/jwh.2007.0440. [DOI] [PubMed] [Google Scholar]
  • 6.Ozerdogan N, Sayiner D, Ayranci U, Unsal A, Giray S. Prevalence and predictors of dysmenorrhea among students at a university in Turkey. Int J Gynaecol Obstet. 2009;107(1):39–43. doi: 10.1016/j.ijgo.2009.05.010. [DOI] [PubMed] [Google Scholar]
  • 7.Ylikorkala O, Dawood MY. New concepts in dysmenorrhea. Am J Obstet Gynecol. 1978;130(7):833–847. doi: 10.1016/0002-9378(78)90019-4. [DOI] [PubMed] [Google Scholar]
  • 8.Dawood MY. Dysmenorrhea. J Reprod Med. 1985;30:154–167. [PubMed] [Google Scholar]
  • 9.Klein JR, Litt IF. Epidemiology of adolescent dysmenorrhea. Pediatrics. 1981;68(5):661–664. [PubMed] [Google Scholar]
  • 10.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):389–397. [PubMed] [Google Scholar]
  • 11.Mario I, Ortiz IM. Primary dysmenorrhea among Mexican university students: prevalence, impact and treatment. Eur J Obstet Gynecol Reprod Biol. 2010;152(1):73–77. doi: 10.1016/j.ejogrb.2010.04.015. [DOI] [PubMed] [Google Scholar]
  • 12.Chongpensuklert Y, Kaewrudee S, Soontrapa S, Sakondhavut C. Dysmenorrhea in Thai Secondary School students in KhonKaen, Thailand. Thailand J Obstet Gynaecol. 2008;16(1):47–53. [Google Scholar]
  • 13.Banikarim C, Chacko MR, Kelder SH. Prevalence and impact of dysmenorrhea on Hispanic female adolescents. Arch Pediatr Adolesc Med. 2000;154(12):1226–1229. doi: 10.1001/archpedi.154.12.1226. [DOI] [PubMed] [Google Scholar]
  • 14.Balbi C, Musone R, Menditto A, et al. Influence of menstrual factors and dietary habits on menstrual pain in adolescence age. Eur J Obstet Gynecol Reprod Biol. 2000;91(2):143–148. doi: 10.1016/s0301-2115(99)00277-8. [DOI] [PubMed] [Google Scholar]
  • 15.Esimie OA, Esan OGO. Awareness of menstrual abnormality amongst college students in urban area of Ile-Ife, Osun state, Nigeria. 2010. [Accessed March 17, 2016]. Available from: http://www.ijcm.org. [DOI] [PMC free article] [PubMed]
  • 16.Zegeye DT, Megabiaw B, Mulu A. Age at menarche and the menstrual pattern of secondary school adolescents in northwest Ethiopia. BMC Womens Health. 2009;9:29. doi: 10.1186/1472-6874-9-29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Unsa 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. Ups J Med Sci. 2010;115(2):138–145. doi: 10.3109/03009730903457218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Dorn LD, Negriff S, Huang B, et al. Menstrual symptoms in adolescent girls: association with smoking, depressive symptoms, and anxiety. Journal of Adolescent Health. 2009;44:237–243. doi: 10.1016/j.jadohealth.2008.07.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Juang CM, Yen MS, Twu NF, Horng HC, Yu HC, Chen CY. Impact of pregnancy on primary dysmenorrhea review. Int J Gynaecol Obstet. 2006;92(3):221–227. doi: 10.1016/j.ijgo.2005.12.006. [DOI] [PubMed] [Google Scholar]
  • 20.Dawood YM. Dysmenorrhea. Clin Obstet Gynecol. 1990;33(1):168–178. doi: 10.1097/00003081-199003000-00023. [DOI] [PubMed] [Google Scholar]
  • 21.French L. Dysmenorrhea in adolescents: diagnosis and treatment. Paediatr Drugs. 2008;10(1):1–7. doi: 10.2165/00148581-200810010-00001. [DOI] [PubMed] [Google Scholar]
  • 22.Burnett MA, Antao V, Black A, et al. Prevalence of primary dysmenorrhea in Canada. J Obstet Gynaecol Can. 2005;27(8):765–770. doi: 10.1016/s1701-2163(16)30728-9. [DOI] [PubMed] [Google Scholar]
  • 23.Latthe P, Mignini L, Gray R, Hills R, Khan K. Factors predisposing women to chronic pelvic pain: systematic review. Br Med J. 2006;332(7544):749–755. doi: 10.1136/bmj.38748.697465.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Tonini G. Dysmenorrhea, endometriosis and premenstrual syndrome. Minerva Pediatrics. 2002;54:525–538. [PubMed] [Google Scholar]
  • 25.Ortiz MI. Primary dysmenorrhea among Mexican university students: prevalence, impact and treatment. Eur J Obstet Gynecol Reprod Biol. 2010;152(1):73–77. doi: 10.1016/j.ejogrb.2010.04.015. [DOI] [PubMed] [Google Scholar]
  • 26.Strinic T, Bukovic D, Pavelic L, et al. Anthropological and clinical characteristics in adolescent women with dysmenorrhea. Coll Antropol. 2003;27(2):707–711. [PubMed] [Google Scholar]
  • 27.Baranowski AP, Abrams P, Fall M. Urogenital Pain in Clinical Practice. New York: Information Healthcare USA, Inc; 2007. [Google Scholar]
  • 28.Dawood MY. Nonsteroidal anti-inflammatory drugs and changing attitudes toward dysmenorrhea. Am J Med. 1988;84(5A):23–29. doi: 10.1016/0002-9343(88)90473-1. [DOI] [PubMed] [Google Scholar]
  • 29.Andersch B, Milsom I. An epidemiologic study of young women with dysmenorrhea. Am J Obstet Gynecol. 1982;144(6):655–660. doi: 10.1016/0002-9378(82)90433-1. [DOI] [PubMed] [Google Scholar]
  • 30.Wewers ME, Lowe NK. A critical review of visual analogue scales in the measurement of clinical phenomena. Res Nurs Health. 1990;13(4):227–236. doi: 10.1002/nur.4770130405. [DOI] [PubMed] [Google Scholar]
  • 31.Patel V, Tanksale V, Sahasrabhojanee M, Gupte S, Nevrekar P. The burden and determinants of dysmenorrhoea: a population-based survey of 2262 women in Goa, India. BJOG. 2006;113(4):453–463. doi: 10.1111/j.1471-0528.2006.00874.x. [DOI] [PubMed] [Google Scholar]

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