Obstetrics and Gynecology International

Obstetrics and Gynecology International / 2015 / Article

Clinical Study | Open Access

Volume 2015 |Article ID 902426 | https://doi.org/10.1155/2015/902426

Feras Sendy, Eman AlShehri, Amani AlAjmi, Elham Bamanie, Surekha Appani, Taghreed Shams, "Failure Rate of Single Dose Methotrexate in Managment of Ectopic Pregnancy", Obstetrics and Gynecology International, vol. 2015, Article ID 902426, 5 pages, 2015. https://doi.org/10.1155/2015/902426

Failure Rate of Single Dose Methotrexate in Managment of Ectopic Pregnancy

Academic Editor: Robert Coleman
Received13 Jan 2015
Revised11 Feb 2015
Accepted23 Feb 2015
Published12 Mar 2015


Background. One of the treatment modalities for ectopic pregnancy is methotrexate. The purpose of this study is to identify the failure rate of methotrexate in treating patients with ectopic pregnancy as well as the risk factors leading to treatment failure. Methods. A retrospective chart review of 225 patients who received methotrexate as a primary management option for ectopic pregnancy. Failure of single dose of methotrexate was defined as drop of BHCG level less than or equal to 14% in the seventh day after administration of methotrexate. Results. 225 patients had methotrexate. Most of the patients (151 (67%)) received methotrexate based on the following formula: f 50 mg X body surface area. Single dose of methotrexate was successful in 72% (162/225) of the patients. 28% (63/225) were labeled as failure of single dose of methotrexate because of suboptimal drop in BhCG. 63% (40/63) of failure received a second dose of methotrexate, and 37% (23/63) underwent surgical treatment. Among patient who received initial dose of methotrexate, 71% had moderate or severe pain, and 58% had ectopic mass size of more than 4 cm on ultrasound. Conclusion. Liberal use of medical treatment of ectopic pregnancy results in 71% success rate.

1. Introduction

Implantation of a fertilized ovum outside the uterine cavity is known as ectopic pregnancy (EP) [13]. It is a medical emergency due to the high morbidity and mortality in the reproductive age [47]. The incidence of ectopic pregnancies is 1-2% in the developed countries [8]. Ninety-eight percent of the implants are in the fallopian tube but also can be implanted at various sites such as ampulla, isthmus, ovaries, abdomen, and broad ligament [9, 10].

The etiology is uncertain but there are various risk factors, such as infertility, previous tubal surgery, contraceptive failure, cigarette smoking, and previous ectopic pregnancy [11]. Patients usually come with lower abdominal pain and vaginal bleeding from the 6th to 10th week of gestation [1]. It has been reported that one-third of patients have no clinical symptoms [12, 13]. If a patient came with syncope and signs of shock with a positive pregnancy test ruptured ectopic pregnancy should be suspected [11].

When the patient is pregnant, the physician should perform a work-up to detect possible ectopic or ruptured EP. Prompt ultrasound evaluation is the key in diagnosing ectopic pregnancy. Equivocal ultrasound results should be combined with quantitative beta subunit of human chorionic gonadotropin (BhCG) levels [14, 15]. If a patient has a BhCG level of 1,500 MIU per mL or greater, but the transvaginal ultrasonography does not show an intrauterine gestational sac, EP should be suspected [16].

While surgical approaches are the mainstay of treatment, advances in early diagnosis facilitated the introduction of medical therapy with methotrexate (MTX) in the 1980 [1719]. Approximately 35% of women with EP are eligible for medical treatment [20]. The use of methotrexate (MTX) to treat early unruptured EP has been shown to be a safe and effective alternative to surgery in properly selected cases [2123].

A Cochrane systemic review concluded that MTX treatment of EP had the highest success rate when plasma BhCG levels were below 3,000 IU/mL. It was stated that side effects from multiple-dose MTX treatment impaired quality of life [24]. In addition, MTX treatment was more expensive than laparoscopic salpingotomy when initial plasma-BhCG levels were above 3,000 IU/L [25]. Treatment with a single dose of MTX had fewer side effects, but the success rate was less than following a multiple-dose regimen [26].

Due to the routine use of early ultrasound among infertile patients who conceive, diagnosis of EP can be established early and medical treatment can be administered in most cases. The overall success rate of medical treatment in properly selected women is nearly 90% [2729].

Our rational in this study was to review the cases that were diagnosed with EP and treated medically with MTX and observe the failure rate among them.

2. Methodology

Medical records of patients admitted to KAMC with a diagnosis of ectopic pregnancy which were retrospectively reviewed in the period between 2005 and 2011 were screened. Patients who had methotrexate as medical treatment of ectopic pregnancy were identified and included in this review. Patients who underwent surgical treatment as the first option of management were excluded.

The primary outcome measure of this review was the failure of first dose of methotrexate. Failure is defined in two ways: firstly, as suboptimal drop in BHCG level to 14% or less that necessitate second dose of methotrexate or surgical treatment; secondly, as the need for emergency laparoscopy or laparotomy in case of hemodynamic instability or severe abdominal pain. The following data were collected: demographic data including age, weight, and height, presenting symptoms, methotrexate dose given, ultrasound finding including ectopic size, fluid in pouch of Douglas, and BhCG level on day one and day 7 of methotrexate administration. BhCG level on the day of 1 at the time of methotrexate administration was called day 1. Some variation might be noted in the numbers of patients and that is due to some missing data. Bivariate associations were evaluated with use of odds ratio (OR) and Pearson’s #2. Logistic regression was used to create an explanatory model for MTX failure. All analyses were performed with use of SPSS software (version 17).

3. Results

371 charts were reviewed. 146 subjects were excluded, 140 subjects were excluded because patients had surgery as primary mode of treatment, and 6 subjects were excluded because of the need for emergency surgery due to suspension of ruptured ectopic data after admission. 225 charts were included in the study and analyzed. The diagnosis of EP was based on the admitting physician assessment note. Dosing of methotrexate was based on body surface area (50 mg X BSA) in 151/225 (67%) of the patients; the rest received dose based on 1mg per kg body weight.

The average age was 30 years old. Before receiving methotrexate, most of the patients (68%) quantified their pain as moderate, only 29% were asymptomatic (Figure 3). Size of ectopic pregnancy on ultrasound was more than 4 cm in 58% of cases (Table 1).

VariableMean (SD)

Age 30.3 (5.7)
Body weight (in kg)72.7 (15.7)
Height (in centimeter)154.2 (12.6)
Methotrexate dose (mg)85.9 (12.7)

Clinical presentation
Before starting treatment
Asymptomatic65 (28.9%)
Moderate pain153 (68%)
Severe pain7 (3.1%)

After receiving the 1st dose of methotrexate
Asymptomatic182 (80.8%)
Symptomatic43 (19.1%)

Ectopic size on U/S
Less than 4 cm86 (42%)
More than 4 cm119 (58%)

BHCG level
Day 1Mean 2219
Day 7Mean 1802

In 72% of the patients (162/225), single dose of methotrexate was successful; that is, BhCG decreased by more than 15% in the seventh day after administration. 28% (63/225) were labeled as failure of single dose of methotrexate because of suboptimal drop in BhCG (Figure 1).

63% (40/63) of failure received a second dose of methotrexate, and 37% (23/63) underwent surgical treatment (Figure 2).

The indication for surgical treatment were patient choice in 39%. Presence of pain 7 days after medical treatment 35% and rupture of ectopic 26% (Table 2).

IndicationsNumber 23Percentage

Patient refusal of second dose of MTX939
Presence of pain on day 7 after medical treatment835
Rupture of ectopic626

Predictors for failure of single dose of methotrexate is Figure 4.

(i) Initial Level of BhCG (Table 3). The higher the BHCG on day one, the lower is the failure rate (odds ratio of failure 0.3 95% CI (0.1–0.7); value 0.004). In another term, with every increase log of beta HCG milli-international units per milliliter (mIU/mL) on day one, there is 60% chance of reducing likelihood of medical treatment failure.

VariableOR95% OR CI value

BhCG day 10.30.1–0.70.004
Fluid in pouch of Douglas0.40.1–1.10.1
Size of ectopic ≥4 cm1.30.5–3.30.4
BhCG day 73.662.0–6.40.0001

(ii) BHCG Day 7. The higher is the levels of BhCG on day seven, the higher is the failure rate. (OR 3.66 95% CI 2.0–6.4; value = 0.0001). With every increase log of beta HCG milli-international units per milliliter (mIU/mL) at day 7, there are 3.6 times higher odds of medical treatment failure. Mass size of ectopic pregnancy being ≥4 cm on U/S has not been shown to be statistically significant predictor of failure in our review.

4. Discussion

Methotrexate was first introduced as a successful treatment option for EP in the 1980’s by Tanaka et al. [29]. Numerous published literatures have presented different success rates of medical management in resolving an EP; these rates were ranging from 85% to 95% [30, 31]. A study in Scandinavia showed a success rate of medical treatment in EP 76.2% [32]. Nguyen et al., 2010, described an outstandingly success rate of 100% (). In 2013, a similar cohort study presented a success rate of 89% [33]. Another study conducted in Makkah showed that all patients given methotrexate were successfully treated [34].

In this study the success rate of the medical management of ectopic pregnancy with methotrexate was found to be 72%. It appears to be relativity lower than international rates, an average of 90%; however our study had a remarkably higher success rate than a study conducted in Nigeria, which presented a success rate of only 3.8% [35]. This lower success rate in our study compared to the majority of equivalent studies may be attributed to the lack of a careful selection of patients as candidates for medical therapy and confining to a strict selection criterion. Among patient who received medical treatment, 71% had moderate or severe pain, and 58% had ectopic mass size of more than 4 cm.

As it has been established in a similar study conducted in Oman, following strict selection criteria raised the success rate of methotrexate therapy up to 20% more than their previous average success rate 40% [36].

Of those 28% who had failed medical treatment, 63% received a second dose of MTX, which is comparable to around 15–20% of women receiving a single dose of methotrexate who required a repeat dose of this chemotherapeutic agent in related studies [33–38], while the rest (37%) underwent surgical management either due to rupture of the EP, patient preference, or new onset of severe pain.

One of the risk factors of developing EP is being of age 40 years or older [27]. In this study, the mean age was 30 years, which is comparable to former studies [35–37]. Maternal age is not a predictor of MTX treatment in our study. It did however appear in a similar study that an increased maternal age will lead to a decrease in the in the success rate of MTX [36]. There were no mortalities in this study compared to the to a mortality report in the UK (issued in December 2007), showing a total of 10 deaths. These fatalities occurred during the nonsurgical management of an accurately established diagnosis of EP rather than because of an overlooked diagnosis or delayed surgical management, as these were the most common reasons for EP mortality during the previous four years [37, 38].

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


This study was done as part of research summer school program of King Abdullah International Medical Research Center (KAIMRC).


  1. J. J. Walker, “Ectopic pregnancy,” Clinical Obstetrics and Gynecology, vol. 50, no. 1, pp. 89–99, 2007. View at: Google Scholar
  2. D. Della-Giustina and M. Denny, “Ectopic pregnancy,” Emergency Medicine Clinics of North America, vol. 21, no. 3, pp. 565–584, 2003. View at: Publisher Site | Google Scholar
  3. R. Varma and J. Gupta, “Tubal ectopic pregnancy,” Clinical Evidence, vol. 2009, p. 1406, 2009. View at: Google Scholar
  4. C. J. Berg, J. Chang, W. M. Callaghan, and S. J. Whitehead, “Pregnancy-related mortality in the United States, 1991–1997,” Obstetrics and Gynecology, vol. 101, no. 2, pp. 289–296, 2003. View at: Publisher Site | Google Scholar
  5. A. K. Majhi, N. Roy, K. S. Karmakar, and P. K. Banerjee, “Ectopic pregnancy—an analysis of 180 cases,” Journal of the Indian Medical Association, vol. 105, no. 6, pp. 308–314, 2007. View at: Google Scholar
  6. J. L. V. Shaw, S. K. Dey, H. O. D. Critchley, and A. W. Horne, “Current knowledge of the aetiology of human tubal ectopic pregnancy,” Human Reproduction Update, vol. 16, no. 4, Article ID dmp057, pp. 432–444, 2010. View at: Google Scholar
  7. G. O. Udigwe, O. S. Umeonihu, and I. I. Mbachu, “Ectopic pregnancy: a 5 year review of cases at nnamdi azikiwe university teaching hospital (NAUTH) Nnewi,” Nigerian Medical Journal, vol. 51, no. 4, pp. 160–163, 2010. View at: Google Scholar
  8. T. E. Goldner, H. W. Lawson, Z. Xia et al., “Surveillance for ectopic pregnancy—United States, 1970–1989,” MMWR CDC Surveillance Summaries, vol. 42, pp. 73–85, 1993. View at: Google Scholar
  9. J. A. Wong and J. F. Clark, “Correlation of symptoms with age and location of gestation in tubal pregnancy,” Journal of the National Medical Association, vol. 60, no. 3, pp. 221–223, 1968. View at: Google Scholar
  10. A. Kellogg, “Intratubalmethotrextate versus laproscopicsalpingotomy,” World Journal of Laparoscopic Surgery, vol. 2, no. 2, pp. 18–21, 2009. View at: Google Scholar
  11. V. Sivalingam, W. Duncan, E. Kirk, L. Shephard, and A. Horne, “Diagnosis and management of ectopic pregnancy,” Journal of Family Planning and Reproductive Health Care, vol. 37, pp. 231–240, 2011. View at: Publisher Site | Google Scholar
  12. J. I. Tay, J. Moore, and J. J. Walker, “Ectopic pregnancy,” British Medical Journal, vol. 320, no. 7239, pp. 916–919, 2000. View at: Publisher Site | Google Scholar
  13. B. C. Kaplan, R. G. Dart, M. Moskos et al., “Ectopic pregnancy: prospective study with improved diagnostic accuracy,” Annals of Emergency Medicine, vol. 28, no. 1, pp. 10–17, 1996. View at: Publisher Site | Google Scholar
  14. K. Barnhart, M. T. Mennuti, I. Benjamin, S. Jacobson, D. Goodman, and C. Coutifaris, “Prompt diagnosis of ectopic pregnancy in an emergency department setting,” Obstetrics and Gynecology, vol. 84, no. 6, pp. 1010–1015, 1994. View at: Google Scholar
  15. C. R. Gracia and K. T. Barnhart, “Diagnosing ectopic pregnancy: decision analysis comparing six strategies,” Obstetrics and Gynecology, vol. 97, no. 3, pp. 464–470, 2001. View at: Publisher Site | Google Scholar
  16. A.-M. Lozeau and B. Potter, “Diagnosis and management of ectopic pregnancy,” American Family Physician, vol. 72, no. 9, pp. 1707–1714, 2005. View at: Google Scholar
  17. I. A. Rodi, M. V. Sauer, M. J. Gorrill et al., “The medical treatment of unruptured ectopic pregnancy with methotrexate and citrovorum rescue: preliminary experience,” Fertility and Sterility, vol. 46, no. 5, pp. 811–813, 1986. View at: Google Scholar
  18. T. G. Stovall, F. W. Ling, and J. E. Buster, “Outpatient chemotherapy of unruptured ectopic pregnancy,” Fertility and Sterility, vol. 51, no. 3, pp. 435–438, 1989. View at: Google Scholar
  19. M. D. Pisarska, S. A. Carson, and J. E. Buster, “Ectopic pregnancy,” The Lancet, vol. 351, no. 9109, pp. 1115–1120, 1998. View at: Publisher Site | Google Scholar
  20. S. K. van den Eeden, J. Shan, C. Bruce, and M. Glasser, “Ectopic pregnancy rate and treatment utilization in a large managed care organization,” Obstetrics & Gynecology, vol. 105, no. 5, part 1, pp. 1052–1057, 2005. View at: Publisher Site | Google Scholar
  21. P. J. Hajenius, S. Engelsbel, B. W. J. Mol et al., “Randomised trial of systemic methotrexate versus laparoscopic salpingostomy in tubal pregnancy,” The Lancet, vol. 350, no. 9080, pp. 774–779, 1997. View at: Publisher Site | Google Scholar
  22. S. J. Ory, A. L. Villanueva, P. K. Sand, and R. K. Tamura, “Conservative treatment of ectopic pregnancy with methotrexate,” The American Journal of Obstetrics and Gynecology, vol. 154, no. 6, pp. 1299–1306, 1986. View at: Publisher Site | Google Scholar
  23. T. G. Stovall and F. W. Ling, “Single-dose methotrexate: an expanded clinical trial,” The American Journal of Obstetrics and Gynecology, vol. 168, no. 6, pp. 1759–1765, 1993. View at: Publisher Site | Google Scholar
  24. P. J. Hajenius, F. Mol, B. W. Mol, P. M. Bossuyt, W. M. Ankum, and F. van der Veen, “Interventions for tubal ectopic pregnancy,” Cochrane Database of Systematic Reviews, no. 1, Article ID CD000324, 2007. View at: Google Scholar
  25. B. W. J. Mol, P. J. Hajenius, S. Engelsbel et al., “Treatment of tubal pregnancy in the Netherlands: an economic comparison of systemic methotrexate administration and laparoscopic salpingostomy,” The American Journal of Obstetrics and Gynecology, vol. 181, no. 4, pp. 945–951, 1999. View at: Publisher Site | Google Scholar
  26. M. C. Sowter, C. M. Farquhar, K. J. Petrie, and G. Gudex, “A randomised trial comparing single dose systemic methotrexate and laparoscopic surgery for the treatment of unruptured tubal pregnancy,” British Journal of Obstetrics and Gynaecology, vol. 108, no. 2, pp. 192–203, 2001. View at: Publisher Site | Google Scholar
  27. K. T. Barnhart, G. Gosman, R. Ashby, and M. Sammel, “The medical management of ectopic pregnancy: a meta-analysis comparing ‘single dose’ and ‘multidose’ regimens,” Obstetrics and Gynecology, vol. 101, no. 4, pp. 778–784, 2003. View at: Publisher Site | Google Scholar
  28. C. M. Farquhar, “Ectopic pregnancy,” The Lancet, vol. 366, no. 9485, pp. 583–591, 2005. View at: Publisher Site | Google Scholar
  29. R. J. Morlock, J. E. Lafata, and D. Eisenstein, “Cost-effectiveness of single-dose methotrexate compared with laparoscopic treatment of ectopic pregnancy,” Obstetrics and Gynecology, vol. 95, no. 3, pp. 407–412, 2000. View at: Publisher Site | Google Scholar
  30. T. Tanaka, H. Hayashi, T. Kutsuzawa, S. Fujimoto, and K. Ichinoe, “Treatment of interstitial ectopic pregnancy with methotrexate: report of a successful case,” Fertility and Sterility, vol. 37, no. 6, pp. 851–852, 1982. View at: Google Scholar
  31. G. H. Lipscomb, V. M. Givens, N. L. Meyer, D. Bran, and S. Zinberg, “Comparison of multidose and single-dose methotrexate protocols for the treatment of ectopic pregnancy,” The American Journal of Obstetrics and Gynecology, vol. 192, no. 6, pp. 1844–1847, 2005. View at: Publisher Site | Google Scholar
  32. M. B. Potter, L. A. Lepine, and D. J. Jamieson, “Predictors of success with methotrexate treatment of tubal ectopic pregnancy at Grady Memorial Hospital,” The American Journal of Obstetrics and Gynecology, vol. 188, no. 5, pp. 1192–1194, 2003. View at: Publisher Site | Google Scholar
  33. D. T. Westaby, O. Wu, W. C. Duncan, H. O. D. Critchley, S. Tong, and A. W. Horne, “Has increased clinical experience with methotrexate reduced the direct costs of medical management of ectopic pregnancy compared to surgery?” BMC Pregnancy and Childbirth, vol. 12, article 98, 2012. View at: Publisher Site | Google Scholar
  34. M. Skubisz, P. Dutton, W. C. Duncan, A. W. Horne, and S. Tong, “Using a decline in serum hCG between days 0–4 to predict ectopic pregnancy treatment success after single-dose methotrexate: a retrospective cohort study,” BMC Pregnancy and Childbirth, vol. 13, article 30, 2013. View at: Publisher Site | Google Scholar
  35. A. Ayaz, S. Emam, and M. U. Farooq, “Clinical course of ectopic pregnancy: a single-center experience,” Journal of Human Reproductive Sciences, vol. 6, no. 1, pp. 70–73, 2013. View at: Publisher Site | Google Scholar
  36. A. Panti, N. E. Ikechukwu, O. lukman, E. Yakubu, S. Egondu, and B. A. Tanko, “Ectopic pregnancy at Usmanu Danfodiyo University Teaching Hospital Sokoto: a ten year review,” Annals of Nigerian Medicine, vol. 6, no. 2, pp. 87–91, 2012. View at: Publisher Site | Google Scholar
  37. U. Mahboob and S. B. Mazhar, “Management of ectopic pregnancy: a two-year study,” Journal of Ayub Medical College, Abbottabad, vol. 18, no. 4, pp. 34–37, 2006. View at: Google Scholar
  38. L. C. Edozien, “Non-surgical management of ectopic pregnancy: appropriate risk management must be in place,” Archives of Gynecology and Obstetrics, vol. 283, no. 5, pp. 925–927, 2011. View at: Publisher Site | Google Scholar

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