* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download References
Reproductive health wikipedia , lookup
Compartmental models in epidemiology wikipedia , lookup
Transmission (medicine) wikipedia , lookup
Race and health wikipedia , lookup
Eradication of infectious diseases wikipedia , lookup
Preventive healthcare wikipedia , lookup
Infection control wikipedia , lookup
Hygiene hypothesis wikipedia , lookup
Epidemiology wikipedia , lookup
Fetal origins hypothesis wikipedia , lookup
Running head: PELVIC INFLAMMATORY DISEASE Pelvic Inflammatory Disease Irene Zasa-Willett, FNP-s SUNYIT 1 PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 2 Pelvic inflammatory disease (PID) commonly known as PID is an infection of the female reproductive organs. The CDC reports that approximately 750,000 women are affected by this disease each year in the United States and possibly more due to misdiagnosis (CDC, 2013). Women who are sexually active and between the ages of 15-29 are at a much higher risk most likely due to the number of sexual partners than any other reason and poor use of condoms (Schuiling & Likis, 2013). Any female who is sexually active can get this disease, but certain behaviors can increase the risk substantially such as multiple sex partners in a short period of time and substance abuse (PubMedHealth, 2011). Among other risk factors for PID is an existing sexually transmitted disease, a sex partner who has multiple sex partners, a past history of PID, IUD insertion within 2 months, other recent gynecological procedure, or frequent douching (Shuiling & Likis, 2013). Gradison (2012) reports that the cost of treatment is approximately 1.5 billion dollars a year to treat PID. This cost includes treatment for complications of this disease. PID is a preventable disease and often misdiagnosed. According to Domino (2013), 30% of PID has been misdiagnosed in the past, leading to increased risks for infertility, chronic pelvic pain, and pelvic organ scarring (Shephard, 2010). There have been multiple organisms documented to cause PID such as N. Gonorrhea, C. Trachomatis, anaerobes, G. Vaginalis, H. Influenza, Streptococcus Agalactaie, enteric gram negative rods, cytomegalovirus, M. Hominis, urealyticum and M. Genitalium. The most common being gonorrhea and chlamydia (Gradison, 2012). These microorganisms are thought to spread in three different ways: intra-abdominally—the bacteria travels from the cervix to the endometrium, through the salpinx and into the peritoneal cavity causing endometritis, salpingitis, and tubal-ovarian abscesses. This complication is the most serious (Gradison, 2012). Another PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 3 way this infection is spread is through the lymphatic system from an infection of the parametrium from an IUD or gyn procedure. This can also cause peritonitis. The most rare transmission is hematogenous route such as TB. However this is very rare (Gradison, 2012). In a report released by PubMedHealth (2011) and also cited in an article by Taylor-Robinson (2012), it was noted that the main cause of PID is gonorrhea and chlamydia. According to the New York State Department of Health (NYSDOH) in 2011 the Oneida county rates for gonorrhea and chlamydia (the most common organisms for PID) were 60.2 and 453.2 respectively (per 100,000). These organisms or any of the above cited organisms upset the vaginal flora. Once an organism is introduced into the vagina it can take anywhere from a few days to months before the infection travels up to the pelvic organs (PubMedHealth, 2011). Symptomatology is varied among women. Some women experience very mild symptoms and other women can experience intolerable pain and discomfort. For this reason the diagnosis of PID for many years was difficult to ascertain. The symptoms of PID can be all or some of the following: abnormal vaginal foul-smelling discharge, lower abdominal or back pain or aching, pain in the upper right abdomen, abnormal menstrual bleeding, spotting, painful periods, painful intercourse, burning when urinating, nausea, vomiting, fever, chills, rebound tenderness and guarding (CDC, 2011). United States Preventive Services Task Force (USPST, 2012) recommends screening for chlamydia and gonorrhea if sexually active and under 25, pregnant or any woman who is at an increased risk due to multiple sex partners or a partner who has multiple sex partners. The diagnosis of PID can often be difficult. Delayed diagnosis can lead to life-altering complications that may affect fertility and quality of life due to chronic pelvic floor pain. The reasons for delayed diagnosis is from the imprecise nature of the disease but also include mild PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 4 symptomology, varied levels of pain threshold among women, lack of recognition of mild symptoms that are PID, health care providers stereotypical picture of women who may have PID or any sexually transmitted disease, failure of the health care provider to see young teens as sexual beings, failure to obtain accurate history from women overlooking recent IUD insertion (CDC, 2010). The medical community has recognized the life-altering consequences due to failure of early diagnosis of PID. For this reason CDC recommendations have been set to help health care providers recognize and treat symptoms of PID (Sexually Transmitted Disease (STD) Treatment Guidelines, 2010). The diagnostic criterion that has been recommended by the CDC is also cited in the multiple articles reviewed including an article in The American Family Physician (2008). These articles do not overlook the importance of a precise history of the women’s symptoms, sexual history and pelvic examination necessary in order to identify the criteria that must be met. The diagnostic criteria is as follows: cervical motion tenderness, uterine tenderness and/or adnexal tenderness, signs of lower genital tract inflammation such as cervical exudates or friability, and/or increased leukocytes in vaginal secretions, and/or fever, foul-smelling discharge, elevated sed. rate and c-reactive protein, and/or laboratory diagnosis of gonorrhea or chlamydia (STD Treatment Guidelines, 2010). Further and more specific criteria for diagnosing PID may be necessary for women with complaints of pain but have no other signs or risk factors. Doppler study, sonograms and laparoscopy may show abnormalities consistent with PID. Endometrial biopsy may need to be done as endometriosis may be the only sign of PID in some women (Healey, Priya & Quinn, 2010). The criteria helps health care providers better diagnose and treat this disease. The need for these criteria is because the symptoms of PID may mimic the signs/symptoms of other disease PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 5 entities. Some of the differential diagnoses are adnexal mass, malignancy, fibroid tumors, appendicitis, ectopic pregnancy, endometriosis, interstitial cystitis, ovarian cysts, ovarian torsion, and irritable bowel disease (Shephard, 2010). In order to provide optimal treatment for women with PID it is advised that the health practitioner be aware of the most common organism that is being found in their area of practice. This does not change the treatment in as much to ensure sensitivity to the medication that is prescribed (Rotblatt, Montoya, Plant, Guerry, & Kerndt, 2013). Empiric treatment for PID should be started immediately in sexually active young women or any women at high risk for STI if they are experiencing unexplained lower abdominal pain. In an article that reviewed studies for unexplained pelvic pain by Abatangelo, Okereke, ParhamFoster, et al. (2010) there has been no harm done to patients treated empirically when no other source for pelvic pain can be found. Treatment for PID must be effective against N. gonorrhea and C. trachomatis (Gradison, 2012). The guidelines recommend medications to target anaerobic microorganisms as well since some women have been found to have these organisms (Gradison, 2012). Mycoplasma genitalium infection has been found to be associated with treatment failure in some women. The guidelines are not suggestive to include treatment of this as of yet. More studies need to be done to determine routine treatment for this organism (Gradison, 2012). Recommended treatment guidelines from CDC include both oral and IV therapy for mild to moderate PID. For severe PID it is suggested that the patient be hospitalized 24-48 hours for IV therapy and then may switch to oral therapy. Noncompliance issues with the patient need to be determined by the provider with regards to hospitalization. Hospitalization is recommended for any woman who is pregnant, has tubo-ovarian abscess or underlying comorbidity (CDC, 2010). PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 6 Various studies have shown that compliant woman with mild to moderate disease have had similar clinical outcomes as those on IV therapy (AHRQ, 2002). The consideration for outpatient treatment should be provider judgment (Evans, Jaleel, Kinsella, Aggarwal, 2008). Women who have not shown clinical improvement within 72 hours of oral treatment should be re-evaluated and given IV therapy as an outpatient or inpatient (Evans, Jaleel, et al., 2008). Regimen A is suggested for mild to moderate disease. This consists of Cefotetan IV every 12 hours or Cefoxitin IV every 6 hours plus Doxycycline PO or IV every 12 hours. If there is tuboovarian involvement add metronidazole to provide more anaerobic coverage (CDC, 2010). Regimen B can be followed instead which includes Clindomycin IV every 8 hours plus Gentamycin every 8 hours or as a loading dose. With clinical improvement in 24 hours may switch to Doxycycline twice a day for 14 days or Clindamycin four times a day for 14 days. Clindamycin provides better anaerobic coverage (CDC, 2010). There are alternative regimens by there is limited data to support the use of other parenteral medications. These alternative drugs are Ampicillin/Sulbactam plus Doxycycline or Azithromycin or combined with a 12 day course of metronidazole (CDC, 2010 and AHRQ, 2010). For very severe disease, combined treatments are suggested, but varied according to the severity and length of illness. Oral treatment for PID can be utilized if the infection does not include tubo-ovarian abscess or the patient is not pregnant or have a serious underlying disease (CDC, 2010). Oral medication is followed after an IM injection of antibiotics. Ceftriaxone or Cefoxitin IM + Probenicid by mouth is given IM for one dose along with Doxycycline with or without metronidazole for 14 days. Other parenteral 3rd generation cephalosporin such as Cefexime plus Doxycycline twice a day with or without metronidazole twice a day for 14 days can also be used. The addition of metronidazole should be considered because of the anaerobic organisms suspected in PID (CDC PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 7 2010). PID is a serious disease and can lead to fulminating infection affecting all vital organs if left untreated. There are no known safe alternative or natural treatments for PID. Although most cases of PID can be treated successfully as an outpatient there are some reasons where outpatient treatment is not indicated and inpatient care is necessary. Women who present with acute abdomen, severe nausea and vomiting due to treatment, pregnancy, poor improvement noted, tubo-ovarian abscess, poor compliance with treatment, Severe intolerable upper abdominal pain suggestive of hepatic involvement or immunocompromise disease (Abatangelo, et al. 2010). Care for women with PID in the emergency room unless hospitalized provides for poor follow up. It is recommended that women seen in the emergency room (ER) be followed by their primary physician (Abatangelo et al. 2010). ER physicians are encouraged to provide counseling to patients with PID to follow up with their primary care provider. Unfortunately, some women may not have a provider. ER providers should stress the importance of obtaining a primary provider and know the resources in the area if the patient needs help in accessing health care services. Education and counseling on prevention of PID is crucial for patients to understand the risks and practice prevention. Education and counseling can be in pamphlet form that is printed in large print and using language on 5th grade reading level. It should never be assumed a patient can read. Therefore, verbal information should also be provided. This education should include practicing safe sex, limit the number of partners, get tested as often as you need to, don’t routinely douche, and after toileting wipe from front to back. It is also important for the patient to understand their partner should be tested for any STD. PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 8 Health providers should be well informed of resources in their community available to the patient for help and support. Referrals to reduce high risk behavior should be done after discussing this with the patient. Despite multiple advances in medicine and health promotion over the century preventable disease continues to exist and adversely affect the future of young people. Strong motivational factors sometimes exist in patients that affect the ability to change their behavior. Clinicians are too often pressed for time, which does not allow for meaningful discussion with their patients. Recognition of barriers to care for out patients is a necessary facet for positive outcomes. Wolff, Kaplan, & Liss (2010) have identified some of these barriers. These barriers include assumptions of a women’s sexuality, educational level, understanding, and poor knowledge of community resources. In conclusion, PID is a serious infection that can lead to serious complications. As health care providers understanding the disease process and presentation as well as understanding incidence rates of certain diseases in your community is necessary in order to provide optimal care and improving outcomes for patients. PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 9 References Agency for Healthcare Research and Quality. (2002). Women with pelvic inflammatory disease treated as outpatients have long-term outcomes comparable to those treated as inpatients; U.S. Department of Health and Human Services. http://archive.ahrq.gov/news/press/pr2002/pelvicpr.htm. Agency for Healthcare Research and Quality. (2010). Pelvic inflammatory disease: Sexually transmitted diseases treatment guidelines. Retrieved from Health and Human Services website: http://www.guideline.gov/content.aspx?id=25586. Abatangelo, L., Okereke, L., Parham-Foster, C., Parrish, C., Scaglione, L., Zotte, D., & Taub, L. (2010). If pelvic inflammatory disease is suspected empiric treatment should be initiated. Journal of the American Academy f Nurse Practitioners, 22(Feb.), 117-22. doi: http://dx.doi.org/10.1111/J.1745-7599.2009.00478.x Center for Disease Control, (2011). Sexually transmitted diseases: Factsheet. Pelvic inflammatory disease. Retrieved from Center for Disease Control and Prevention. Retrieved from website: http://www.cdc.gov/std/PID/STDfact-PID.htm Center for Disease Control and Prevention. National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention , Division of STD Prevention. (2010). Sexually transmitted diseases: Treatment guidelines, 2010. Retrieved from website: http://www.cdc.gov/std/treatment/2010/pid.htm Domino, F. (2013). Pelvic inflammatory disease. The 5-minute Clinical Consult (21 ed., pp. 961-2). Philadelphia, Penn.: Wolters Kluwer Health/Lippincott Williams & Wilkins PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 10 Evans, D., Jaleel, H., Kinsella, M., & Aggarwal, V. (2008). A retrospect audit of the management and complications of pelvic inflammatory disease. International Jounal of STD & AIDS, 19(2), 123-4. doi: 10.1258/ija.2007.007157 Healey, P., & Quinn, D. (2010). Review: imaging pelvic inflammatory disease. Ultrasound 2010, 18(3), 119-24. doi: http://dx.doi.org/10.1258/ult.2010.010025 Gradison, M. (2012). Pelvic inflammatory disease. American Family Physician, 85(8), 791-6. Retrieved from www.aafp.org/afp Mayo Clinic Staff. (2011). Pelvic inflammatory disease. In Mayo Clinic (Ed.), Retrieved from http://www.mayoclinic.com/health/pelvic-inflammatorydisease/DS00402 MedicineNet.com. Pelvic inflammatory Disease, 2013. Retrieved from http://www.medicinenet.com/script/main/art.asp?articlekey 64165&pf=3&page=2 Medicine net. (2013). Pelvic inflammatory disease. In Retrieved 9/24/2013 from http://www.medicinenet.com/script/main/art.asp?articlekey=64165&pf=3&page=2 Meyers, D., Wolff, T., Gregory, K., Nelson, H., Marion, L., Petitti, D. & Moyer, V. (2008, March 15). Uspstf recommendations for sti screening. American Family Physician, 77(6), 819-24. Retrieved from http://www.aafp.org/afp/2008/0315/p819.html PubMed Health. (2011). Pelvic inflammatory disease. A.D.A.M. Medical Encyclopedia(internet), Retrieved from http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001890/ Rottblatt, H., Montoya, J., Plant, A., & Kerndt, P. (2013). There's no place like home: First year use of the home testing program for chlamydia and gonorrhea. American Journal of Public Health, 103(8), 1376-80. doi: ISSN:0002838X NLM ISO PELVIC INFLAMMATORY DISEASEPELVIC INFLAMMATORY DISEASE 11 Schuiling, K., & Likis, F. (2013). Women's gynecologic health. (2nd. ed.). Burlington, Mass.: Jones & Bartlett Learning. Shephard, S. (2013, April 10). Pelvic inflammatory disease differential diagnosis. Medscape, Retrieved from http://emedicine.medscape.com/article/256448-differential Taylor-Robinson, D., Jensen, J., Svenstrup, H., & Stacey, C. (2012). Difficulties experienced in defining the microbial cause of pelvic inflammatory disease. International Journal of STD & AIDS, 23(1), 18-24. doi: 10.1258/ijsa.2011.011066