
Pelvic Inflammatory Disease: Diagnosis and Treatment Strategies
Pelvic Inflammatory Disease (PID) is a sneaky infection that affects the upper female reproductive tract – uterus, fallopian tubes and ovaries – and is classified as an upper genital tract infection. Often linked to untreated sexually transmitted infections (STIs), most cases of PID are caused by sexually transmitted bacteria.
PID can have serious reproductive consequences such as chronic pelvic pain, ectopic pregnancy and infertility. If left untreated PID can cause permanent damage to reproductive organs which can impact fertility and overall reproductive health.
The challenge for clinicians is not only the subtle or non specific symptoms but also the expanding list of causative pathogens and shifting resistance patterns. Risk factors for PID are unprotected sex and having multiple partners which increases the risk of PID especially in young women. Fortunately recent research is changing how we approach diagnosis, treatment and prevention – offering hope for better outcomes with early comprehensive care.
Diagnosing a PID isn't as simple as ordering one test. Most clinicians rely on a combination of clinical signs: lower abdominal pain, cervical motion tenderness and uterine or adnexal tenderness. Clinical diagnosis is key with pelvic examination playing a big role in evaluating cervical discharge, uterine tenderness and lower genital tract inflammation.
The classic 2008 study on PID management advises to have a 'low threshold' for diagnosis especially since delayed treatment can cause permanent reproductive damage [1]. Early diagnosis is essential to prevent complications and long term sequelae.
But the microbial picture is more complicated than that. While Chlamydia trachomatis and Neisseria gonorrhoeae are still the well known culprits, they're not the only ones. A 2021 review in The Journal of Infectious Diseases points to pathogens like Mycoplasma genitalium as emerging players in PID [7]. These atypical bacteria often evade traditional STI tests making diagnosis harder and highlighting the need for broader microbial screening.
Subclinical PID often resulting from less symptomatic infections like chlamydia can still cause long term consequences even in the absence of symptoms. Another 2021 study 'Etiology and Diagnosis of Pelvic Inflammatory Disease' goes even further by suggesting diagnostic strategies that go beyond gonorrhea and chlamydia [8]. This broader approach reduces misdiagnosis and ensures treatment addresses the full range of potential infections – a key to better long term outcomes.
When evaluating severe pain in the pelvic region or lower abdomen, clinicians must consider alternative diagnoses like ovarian torsion and tubo ovarian abscess. Diagnostic tools may include pelvic ultrasound and in uncertain cases endometrial biopsy to clarify the diagnosis. Comprehensive evaluation is key and clinicians must diagnose PID accurately to avoid missing cases with atypical presentations.
When PID is suspected the standard advice is to treat immediately before test results confirm a specific pathogen. That's because empiric therapy which uses broad spectrum antibiotics covers the wide range of bacteria associated with PID. Empiric treatment and prompt treatment is crucial to prevent complications like chronic pelvic pain, infertility and ectopic pregnancy.
The 2019 American Family Physician review outlines best practices for outpatient and inpatient settings and emphasizes early treatment especially in high risk women [2]. Outpatient treatment is an option for most patients with mild to moderate symptoms and allows them to manage the infection without hospitalization.
Emergency medicine literature reinforces this point. Studies in Emergency Medicine Practice (2016 and 2022) stress the importance of prompt intervention especially in emergency departments where many PID cases present first [5] [6]. These papers also emphasize clear discharge instructions and the need for close follow up especially for women whose symptoms don't resolve fully within the first few days. It's essential to treat PID promptly and make sure patients receive treatment to avoid long term complications from pelvic infection.
Choosing the right antibiotic combination matters too. A 2013 BMJ review using GRADE scoring to assess evidence strength suggests regimens with doxycycline, cefoxitin or ceftriaxone and metronidazole are most effective [9]. The same review also highlights the benefit of prophylactic antibiotics before IUD insertion especially in high risk patients. Birth control methods like IUDs can increase the risk of pelvic infection especially in the presence of bacterial vaginosis which disrupts the vaginal flora and may contribute to ascending infections.
While most PID can be managed with outpatient antibiotics some scenarios require more intensive management. Hospitalization is recommended for patients who are pregnant, have severe symptoms, have an abscess or aren't responding to oral medications. Infections of the upper female genital tract and pelvic organs can cause long term complications including damage to the reproductive organs like the uterus, fallopian tubes and ovaries.
A 2023 article in Therapeutics and Clinical Risk Management advises clinicians to stratify care based on illness severity and risk factors [3]. This includes considering polymicrobial infections and resistance trends when choosing treatment regimens. Presence of anaerobes or treatment resistant bacteria may require intravenous antibiotics or surgical intervention. There is also potential for scar tissue formation in the fallopian tube and other reproductive organs which can cause chronic pain and infertility.
A 2010 review in Obstetrics and Gynecology echoes this message. It states most women recover well with outpatient care but clinicians must be aware of microbial diversity especially in populations where STI prevalence is high or access to care is limited [4].
As our understanding of PID evolves so do the tools to diagnose and treat it. Traditional STI panels may miss important pathogens which is why there's growing interest in non-invasive tests and molecular diagnostics. These technologies including nucleic acid amplification tests (NAATs) can detect low abundance microbes like Mycoplasma genitalium that traditional methods miss [3] [7].
Looking ahead experts recommend a multipronged approach:
Some public health campaigns are already incorporating these principles. For example the CDC's updated STI guidelines now include emerging pathogens and detailed follow up protocols. Planned Parenthood's PID awareness campaign stresses education, partner treatment and timely care – all key to stopping the cycle of reinfection. Comprehensive testing for other STIs like HIV and syphilis is also recommended for sexually active individuals.
When discussing partner notification and public health education all sexual partners should be treated and advised to abstain from sexual intercourse or sexual contact until treatment is complete to prevent reinfection and further spread among sexually active individuals.
Pelvic Inflammatory Disease is one of the most common and most misunderstood gynecological emergencies. The infection's polymicrobial nature, subtle presentation and potential for long term harm make it a unique challenge in women's health. But the tide is turning.
With growing awareness, better diagnostic tools and research based treatment strategies there is a clear path forward. Clinicians must stay up to date with evolving recommendations especially as we discover new pathogens and confront antibiotic resistance. The goal is no longer just treatment – it's prevention, precision and protecting reproductive futures.
[1] Haggerty, C. L., & Ness, R. B. (2008). Diagnosis and treatment of pelvic inflammatory disease. Women's health (London, England), 4(4), 383–397. https://doi.org/10.2217/17455057.4.4.383
[2] Curry, A., Williams, T., & Penny, M. L. (2019). Pelvic Inflammatory Disease: Diagnosis, Management, and Prevention. American family physician, 100(6), 357–364. https://pubmed.ncbi.nlm.nih.gov/31524362/
[3] Yusuf, H., & Trent, M. (2023). Management of Pelvic Inflammatory Disease in Clinical Practice. Therapeutics and clinical risk management, 19, 183–192. https://doi.org/10.2147/TCRM.S350750
[4] Soper D. E. (2010). Pelvic inflammatory disease. Obstetrics and gynecology, 116(2 Pt 1), 419–428. https://doi.org/10.1097/AOG.0b013e3181e92c54
[5] Bugg, C. W., & Taira, T. (2016). Pelvic Inflammatory Disease: Diagnosis And Treatment In The Emergency Department. Emergency medicine practice, 18(12), 1–24. https://pubmed.ncbi.nlm.nih.gov/27879197/
[6] Taira, T., Broussard, N., & Bugg, C. (2022). Pelvic inflammatory disease: diagnosis and treatment in the emergency department. Emergency medicine practice, 24(12), 1–24. https://pubmed.ncbi.nlm.nih.gov/36378827/
[7] Hillier, S. L., Bernstein, K. T., & Aral, S. (2021). A Review of the Challenges and Complexities in the Diagnosis, Etiology, Epidemiology, and Pathogenesis of Pelvic Inflammatory Disease. The Journal of infectious diseases, 224(12 Suppl 2), S23–S28. https://doi.org/10.1093/infdis/jiab116
[8] Mitchell, C. M., Anyalechi, G. E., Cohen, C. R., Haggerty, C. L., Manhart, L. E., & Hillier, S. L. (2021). Etiology and Diagnosis of Pelvic Inflammatory Disease: Looking Beyond Gonorrhea and Chlamydia. The Journal of infectious diseases, 224(12 Suppl 2), S29–S35. https://doi.org/10.1093/infdis/jiab067
[9] Ross J. D. (2013). Pelvic inflammatory disease. BMJ clinical evidence, 2013, 1606. https://pubmed.ncbi.nlm.nih.gov/24330771/
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Los Angeles Times
2 days ago
- Los Angeles Times
Pelvic Inflammatory Disease: Diagnosis and Treatment Strategies
Pelvic Inflammatory Disease (PID) is a sneaky infection that affects the upper female reproductive tract – uterus, fallopian tubes and ovaries – and is classified as an upper genital tract infection. Often linked to untreated sexually transmitted infections (STIs), most cases of PID are caused by sexually transmitted bacteria. PID can have serious reproductive consequences such as chronic pelvic pain, ectopic pregnancy and infertility. If left untreated PID can cause permanent damage to reproductive organs which can impact fertility and overall reproductive health. The challenge for clinicians is not only the subtle or non specific symptoms but also the expanding list of causative pathogens and shifting resistance patterns. Risk factors for PID are unprotected sex and having multiple partners which increases the risk of PID especially in young women. Fortunately recent research is changing how we approach diagnosis, treatment and prevention – offering hope for better outcomes with early comprehensive care. Diagnosing a PID isn't as simple as ordering one test. Most clinicians rely on a combination of clinical signs: lower abdominal pain, cervical motion tenderness and uterine or adnexal tenderness. Clinical diagnosis is key with pelvic examination playing a big role in evaluating cervical discharge, uterine tenderness and lower genital tract inflammation. The classic 2008 study on PID management advises to have a 'low threshold' for diagnosis especially since delayed treatment can cause permanent reproductive damage [1]. Early diagnosis is essential to prevent complications and long term sequelae. But the microbial picture is more complicated than that. While Chlamydia trachomatis and Neisseria gonorrhoeae are still the well known culprits, they're not the only ones. A 2021 review in The Journal of Infectious Diseases points to pathogens like Mycoplasma genitalium as emerging players in PID [7]. These atypical bacteria often evade traditional STI tests making diagnosis harder and highlighting the need for broader microbial screening. Subclinical PID often resulting from less symptomatic infections like chlamydia can still cause long term consequences even in the absence of symptoms. Another 2021 study 'Etiology and Diagnosis of Pelvic Inflammatory Disease' goes even further by suggesting diagnostic strategies that go beyond gonorrhea and chlamydia [8]. This broader approach reduces misdiagnosis and ensures treatment addresses the full range of potential infections – a key to better long term outcomes. When evaluating severe pain in the pelvic region or lower abdomen, clinicians must consider alternative diagnoses like ovarian torsion and tubo ovarian abscess. Diagnostic tools may include pelvic ultrasound and in uncertain cases endometrial biopsy to clarify the diagnosis. Comprehensive evaluation is key and clinicians must diagnose PID accurately to avoid missing cases with atypical presentations. When PID is suspected the standard advice is to treat immediately before test results confirm a specific pathogen. That's because empiric therapy which uses broad spectrum antibiotics covers the wide range of bacteria associated with PID. Empiric treatment and prompt treatment is crucial to prevent complications like chronic pelvic pain, infertility and ectopic pregnancy. The 2019 American Family Physician review outlines best practices for outpatient and inpatient settings and emphasizes early treatment especially in high risk women [2]. Outpatient treatment is an option for most patients with mild to moderate symptoms and allows them to manage the infection without hospitalization. Emergency medicine literature reinforces this point. Studies in Emergency Medicine Practice (2016 and 2022) stress the importance of prompt intervention especially in emergency departments where many PID cases present first [5] [6]. These papers also emphasize clear discharge instructions and the need for close follow up especially for women whose symptoms don't resolve fully within the first few days. It's essential to treat PID promptly and make sure patients receive treatment to avoid long term complications from pelvic infection. Choosing the right antibiotic combination matters too. A 2013 BMJ review using GRADE scoring to assess evidence strength suggests regimens with doxycycline, cefoxitin or ceftriaxone and metronidazole are most effective [9]. The same review also highlights the benefit of prophylactic antibiotics before IUD insertion especially in high risk patients. Birth control methods like IUDs can increase the risk of pelvic infection especially in the presence of bacterial vaginosis which disrupts the vaginal flora and may contribute to ascending infections. While most PID can be managed with outpatient antibiotics some scenarios require more intensive management. Hospitalization is recommended for patients who are pregnant, have severe symptoms, have an abscess or aren't responding to oral medications. Infections of the upper female genital tract and pelvic organs can cause long term complications including damage to the reproductive organs like the uterus, fallopian tubes and ovaries. A 2023 article in Therapeutics and Clinical Risk Management advises clinicians to stratify care based on illness severity and risk factors [3]. This includes considering polymicrobial infections and resistance trends when choosing treatment regimens. Presence of anaerobes or treatment resistant bacteria may require intravenous antibiotics or surgical intervention. There is also potential for scar tissue formation in the fallopian tube and other reproductive organs which can cause chronic pain and infertility. A 2010 review in Obstetrics and Gynecology echoes this message. It states most women recover well with outpatient care but clinicians must be aware of microbial diversity especially in populations where STI prevalence is high or access to care is limited [4]. As our understanding of PID evolves so do the tools to diagnose and treat it. Traditional STI panels may miss important pathogens which is why there's growing interest in non-invasive tests and molecular diagnostics. These technologies including nucleic acid amplification tests (NAATs) can detect low abundance microbes like Mycoplasma genitalium that traditional methods miss [3] [7]. Looking ahead experts recommend a multipronged approach: Some public health campaigns are already incorporating these principles. For example the CDC's updated STI guidelines now include emerging pathogens and detailed follow up protocols. Planned Parenthood's PID awareness campaign stresses education, partner treatment and timely care – all key to stopping the cycle of reinfection. Comprehensive testing for other STIs like HIV and syphilis is also recommended for sexually active individuals. When discussing partner notification and public health education all sexual partners should be treated and advised to abstain from sexual intercourse or sexual contact until treatment is complete to prevent reinfection and further spread among sexually active individuals. Pelvic Inflammatory Disease is one of the most common and most misunderstood gynecological emergencies. The infection's polymicrobial nature, subtle presentation and potential for long term harm make it a unique challenge in women's health. But the tide is turning. With growing awareness, better diagnostic tools and research based treatment strategies there is a clear path forward. Clinicians must stay up to date with evolving recommendations especially as we discover new pathogens and confront antibiotic resistance. The goal is no longer just treatment – it's prevention, precision and protecting reproductive futures. [1] Haggerty, C. L., & Ness, R. B. (2008). Diagnosis and treatment of pelvic inflammatory disease. Women's health (London, England), 4(4), 383–397. [2] Curry, A., Williams, T., & Penny, M. L. (2019). Pelvic Inflammatory Disease: Diagnosis, Management, and Prevention. American family physician, 100(6), 357–364. [3] Yusuf, H., & Trent, M. (2023). Management of Pelvic Inflammatory Disease in Clinical Practice. Therapeutics and clinical risk management, 19, 183–192. [4] Soper D. E. (2010). Pelvic inflammatory disease. Obstetrics and gynecology, 116(2 Pt 1), 419–428. [5] Bugg, C. W., & Taira, T. (2016). Pelvic Inflammatory Disease: Diagnosis And Treatment In The Emergency Department. Emergency medicine practice, 18(12), 1–24. [6] Taira, T., Broussard, N., & Bugg, C. (2022). Pelvic inflammatory disease: diagnosis and treatment in the emergency department. Emergency medicine practice, 24(12), 1–24. [7] Hillier, S. L., Bernstein, K. T., & Aral, S. (2021). A Review of the Challenges and Complexities in the Diagnosis, Etiology, Epidemiology, and Pathogenesis of Pelvic Inflammatory Disease. The Journal of infectious diseases, 224(12 Suppl 2), S23–S28. [8] Mitchell, C. M., Anyalechi, G. E., Cohen, C. R., Haggerty, C. L., Manhart, L. E., & Hillier, S. L. (2021). Etiology and Diagnosis of Pelvic Inflammatory Disease: Looking Beyond Gonorrhea and Chlamydia. The Journal of infectious diseases, 224(12 Suppl 2), S29–S35. [9] Ross J. D. (2013). Pelvic inflammatory disease. BMJ clinical evidence, 2013, 1606.
Yahoo
4 days ago
- Yahoo
Innoviva Specialty Therapeutics Receives FDA New Drug Application Acceptance for Zoliflodacin, a First-in-Class Oral Antibiotic for Uncomplicated Gonorrhea in Adults
In laboratory studies, zoliflodacin has been shown to be active against Neisseria gonorrhoeae including multidrug-resistant strains. If approved, zoliflodacin could become the first new antibiotic treatment for gonorrhea in decades. WALTHAM, Mass. & GENEVA, Switzerland, June 10, 2025--(BUSINESS WIRE)--Innoviva Specialty Therapeutics, Inc., a subsidiary of Innoviva, Inc. (NASDAQ: INVA), in collaboration with the Global Antibiotic Research & Development Partnership (GARDP), today announced that the U.S. Food and Drug Administration (FDA) has accepted its New Drug Application (NDA) for zoliflodacin, the investigational first-in-class, single dose, spiropyrimidinetrione oral antibiotic for the treatment of uncomplicated gonorrhea in adults and pediatric patients 12 years and older. If approved, zoliflodacin would be the first new antibiotic for treating gonorrhea in decades. With more than 82 million new gonorrhea infections occurring globally each year, gonorrhea is the second most common bacterial sexually transmitted infection (STI), affecting both men and women, which, if left untreated, can result in serious and permanent health consequences. With the rise and spread of drug-resistant infections and the World Health Organization (WHO) identifying antimicrobial resistance (AMR) as one of the ten most critical global threats to public health, the bacterium Neisseria gonorrhoeae has progressively developed resistance to many classes of antibiotics used to treat these infections, including ceftriaxone, a widely used intramuscular injection that was first made available in 1984. "Today's acceptance of the zoliflodacin NDA marks significant progress toward delivering health care providers with a potential new oral treatment option for uncomplicated gonorrhea, including infections caused by drug-resistant strains," said David Altarac, M.D., Chief Medical Officer, Innoviva Specialty Therapeutics. "We look forward to working closely with the FDA during its review and, if approved, we are committed to expediting the availability of zoliflodacin to patients in the U.S." Recent reports (The Lancet Infectious Diseases) of emergent ceftriaxone-resistant infections have heightened the urgency for new antibiotics. Effective treatment options are essential to reducing the burden of disease for individuals and preventing the spread of highly drug-resistant gonorrhea globally. If left untreated, gonorrhea can also cause infertility in women, life-threatening ectopic pregnancies, and pelvic inflammatory disease.2 The FDA's acceptance of the zoliflodacin NDA is based on the totality of data collected from several clinical trials as part of an innovative public-private partnership with GARDP. These trials include a pivotal Phase 3 clinical trial which demonstrated non-inferiority in achieving microbiological cure at the urogenital site of infection of a single oral dose of zoliflodacin compared to a treatment regimen of a single intramuscular injection of ceftriaxone followed by 1 week of oral azithromycin. The Phase 3 study found that zoliflodacin was generally well-tolerated, with no serious adverse events or deaths reported during the trial. "This important milestone demonstrates the crucial role that public-private partnerships can play in tackling the escalating global antimicrobial resistance crisis," said Dr. Manica Balasegaram, Executive Director, Global Antibiotic Research Development Partnership (GARDP). "If zoliflodacin is approved, this collaboration paves the way for millions of people across the world to get access to a potentially powerful new drug to treat multidrug-resistant gonorrhea." Zoliflodacin has a unique mechanism of action, inhibiting a crucial bacterial enzyme called type II topoisomerase, which is essential for bacterial function and reproduction. In vitro studies have demonstrated its activity against multidrug-resistant strains of Neisseria gonorrhoeae, including those resistant to ceftriaxone and azithromycin, with no cross-resistance to other antibiotics. This investigational antibacterial is administered in a single, oral dose, simplifying treatment by providing a convenient option for patients unable to receive an intramuscular injection. The U.S. FDA has granted zoliflodacin a Qualified Infectious Disease Product (QIDP) designation. This designation allows it to benefit from FDA Priority Review, and Extended Market Exclusivity. Innoviva Specialty Therapeutics, Inc., anticipates that the NDA review will proceed according to the standard process for drugs with this designation. Entasis Therapeutics, Inc., the legal NDA holder and affiliate of Innoviva Specialty Therapeutics, Inc., retains the commercial rights for zoliflodacin in the major markets in North America, Europe, and Asia-Pacific. GARDP retains the right to register and commercialize the product in more than three-quarters of the world's countries, including all low-income countries, most middle-income countries, and several high-income countries. GARDP is committed to working with its partners and local health authorities in markets where zoliflodacin receives regulatory approval to help remove access barriers to ensure treatment is available to address unmet medical needs while ensuring appropriate and sustainable use. About GARDP The Global Antibiotic Research & Development Partnership (GARDP) is a not-for-profit global health organization driven to protect people from the rise and spread of drug-resistant infections, one of the biggest threats to us all. By forging the public and private partnerships that matter, we develop and make accessible antibiotic treatments for people who need them. Vital support for our work comes from the governments of Canada, Germany, Japan, Monaco, the Netherlands, Switzerland, the United Kingdom, the Canton of Geneva, the European Union, as well as the Gates Foundation, Global Health EDCTP3, GSK, the RIGHT Foundation, the South African Medical Research Council (SAMRC) and Wellcome. About Innoviva Innoviva is a diversified holding company with a core royalties portfolio, a leading critical care and infectious disease platform known as Innoviva Specialty Therapeutics ("IST"), and a portfolio of strategic investments in healthcare assets. Innoviva's royalty portfolio includes respiratory assets partnered with Glaxo Group Limited ("GSK"). Innoviva is entitled to receive royalties from GSK on sales of RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®. Innoviva's other innovative healthcare assets include infectious disease and critical care assets stemming from acquisitions of Entasis Therapeutics, including XACDURO® (sulbactam for injection; durlobactam for injection), co-packaged for intravenous use approved for the treatment of adults with hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia caused by susceptible strains of Acinetobacter baumannii-calcoaceticus complex and the investigational zoliflodacin currently being developed for the treatment of uncomplicated gonorrhea, and La Jolla Pharmaceutical Company, including GIAPREZA® (angiotensin II), approved to increase blood pressure in adults with septic or other distributive shock and XERAVA® (eravacycline) for the treatment of complicated intra-abdominal infections in adults. On December 14, 2024, Innoviva entered into an exclusive distribution and license agreement with Basilea Pharmaceutica Ltd, Allschwil for the commercialization of ZEVTERA® (ceftobiprole), an advanced-generation cephalosporin antibiotic, in the U.S. For more information about Innoviva, go to For information about Innoviva Specialty Therapeutics, go to View source version on Contacts Media Contacts:Innoviva Specialty TherapeuticsDavid +1.908.421.5971GARDPDuncan Graham-Rowedgrahamrowe@ +44 7966 413623 Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data
Yahoo
5 days ago
- Yahoo
New test could transform diagnosis and treatment of STIs
A new rapid test for sexually transmitted infections could soon transform on-the-spot diagnosis and treatment. Birmingham-based Linear Diagnostics has secured £1 million in funding to develop the technology, which could deliver results in less than 20 minutes. The funding comes from the NIHR Invention for Innovation programme and will support a three-year project to finalise the test and prepare it for clinical trials. Dr Jean-Louis Duprey, head of research and development at Linear Diagnostics, said: "We are developing a near patient device that will overcome this conundrum." The company is working with the NIHR HealthTech Research Centre and the North East Innovation Lab to deliver the project. Dr Jana Suklan, senior methodologist at the HRC, said: "The NIHR HRC in Diagnostic and Technology Evaluation is delighted to be collaborating with the North East Innovation Lab to support Linear Diagnostics with their exciting technology. "Our research involves analysing unmet needs, examining current practice and identifying the most promising point in the patient pathway for implementing the technology." The test uses Linear's Exponential Amplification (EXPAR) technology, which detects bacterial DNA within minutes. The company has focused on STIs such as Neisseria gonorrhoeae and Chlamydia trachomatis, where rapid diagnosis is essential to prevent further transmission and begin treatment immediately.