The document discusses various causes of bleeding in early pregnancy including abortion, ectopic pregnancy, and hydatidiform mole. Abortion is described as spontaneous or induced expulsion of products of conception before viability. Ectopic pregnancy is implantation outside the uterus, most commonly in the fallopian tubes. Hydatidiform mole is an abnormal placenta with cyst formation due to genetic abnormalities preventing embryo development. Signs of these conditions include vaginal bleeding, abdominal pain, and elevated beta-hCG levels. Diagnosis involves ultrasound and beta-hCG testing. Treatment depends on factors like severity but may include medication, surgery, or monitoring.
Please find the power point on Vacuum delivery. I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
Please find the power point on Vacuum delivery. I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
This slide presents some Gynecologic diseases and disorders in females and their proper management. It is a third-year course for those wishing to major PA or Nursing.
Demographic characteristics of a country provide an overview of its population size, composition, territorial distribution, changes therein and the components of changes such as natality, mortality and social mobility
A decentralized system of disease surveillance for timely and effective public health action with a focus on functional integration of surveillance components of various vertical programmes.
An initiative of Ministry of Health & Family Welfare to leverage information technology for ensuring delivery of full spectrum of healthcare and immunization services to pregnant women and children up to 5 years of age.
Launched by the ministry of health & family welfare, government of India, under the national health mission.
It envisages Child Health Screening and Early Intervention Services
Roles and responsibilities of MIDDLE LEVEL HEALTHCARE PROVIDERSharon Treesa Antony
Mid-level health worker can be defined as ‘Front-line health workers in the community who are not doctors but who have been trained to diagnose and treat common health problems, to manage emergencies, to refer appropriately and to transfer the seriously ill or injured for further care.
Launched as recommended by the national health policy 2017
To achieve the vision of universal health coverage (UHC).
This initiative has been designed to meet Sustainable Development Goals (SDGs) and its underlining commitment, which is to "leave no one behind.“
Health economics is a branch of economics concerned with issues related to efficiency, effectiveness, value and behaviour in the production and consumption of health and health care.
In broad terms, health economists study the functioning of health care systems and health- affecting behaviour such as smoking.
It is the discipline of economics applied to the health care.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
16. GRADE 1
Antibiotics
• Gram positive
• Penicillin G 5 million units Q6H
• Ampicillin 0.5-1g IV Q6h
• Gram negative
• Genta 15mg/kg IV Q8H
• Ceftriaxone 1g IV Q12H
17. • Anaerobes
• Metronidazole 500mg IV Q8H
• Clindamycin 600mg IV Q8H
• AGS 8000 units IM
• ATS 3000 units IM
• Analgesics and sedatives
• blood transfusion
• evacuation
21. ETIOLOGY
FIRST TRIMESTER
Genetic factors
Endocrine and metabolic factors
Infection
Inherited thrombophilia
Immunological causes
SECOND TRIMESTER
Chronic maternal illness
Infection
Unexplained
22. NURSING CARE
Physiologic stabilization
Preparation for manual or surgical evacuation
Oxytocin
Management of bleeding
Antibiotics
Analgesics
Transfusion therapy
Anti D
Psychosocial care
Home care
Discharge teaching
23. ECTOPIC PREGNANCY
An ectopic pregnancy is one in which
the zygote is implanted and develops
outside the normal endometrial cavity.
26. ETIOLOGY
MECHANICAL FACTORS
Salpingitis
Peritubal adhesions
Developmental abnormalities
Previous ectopic pregnancy
Previous operations on the tube
Multiple previous induced aabortions
Tumors that distort the tube
Previous caesarean section
Previous pelvic surgery
27. FUNCTIONAL FACTORS
External migration of the ovum
Menstrual reflux
Altered tubal motility
Cigarette smoking
28. Increased receptivity of tubal mucosa to fertilized
ovum
Assisted reproduction
Failed contraception
29. TUBAL PREGNANCY
Anatomical considerations
Ampulla is the most frequent site
Zygote implantation
Burrows through the epithelium
Lies in the muscular wall
Maternal blood vessels open into the space
between trophoblast
embryo or foetus is usually absent
30. UTERINE CHANGES
Under the influence of corpus luteum
Softening of cervix
Increase in size
Increased vascularity
Decidua develops but no villi
Decidual cast
31. CHANGES IN THE TUBE
Implant in inter columnar fashion
Stretching of muscles
Engorged blood vessels
May burrow through the mucous membrane
Intra muscular implantation
Blood in between blastocyst and serous coat
Distended tube
Blood spillage from fimbrial end
Stretching of peritoneum
Hemoperitoneum
32. NATURAL HISTORY OF TUBAL PREGNANCY
Tubal abortion: ampulla
Hemorrhage
Disrupt connection between the placenta and
membranes and tubal wall
May expel through fimbrial end forming
hematosalpinx
Incomplete abortion placental polyp
33. TUBAL RUPTURE
Isthmic : early rupture
Interstitial : late rupture
Signs of collapse
If expelled into peritoneal cavity may survive or
absorbed
May become lithopedion in cul-de-sac
Abdominal pregnancy
Broad ligament pregnancy
35. BROAD LIGAMENT PREGNANCY
When implantation is towards mesosalpinx, rupture
may occur at a site not immediately covered by
peritoneum
Extrusion of gestational sac into a space between
the folds of broad ligament
37. TUBAL MOLE
Multiple small hemorrhage in chorio-capsular space
Villi separate from attachment
Complete absorption
Tubal abortion
Pelvic hematocele
38. ARIAS STELLA REACTION
Benign change in the endometrium associated with
presence of chorionic tissue
May be misdiagnosed as malignancy
39. CLINICAL AND LABORATORY FEATURES OF
TUBAL PREGNANCY
Spotting
Severe lower abdominal pain
Vertigo to syncope
Amenorrhea/ delayed menstruation
ABDOMINAL PALPATION
Tenderness
VAGINAL EXAMINATION
Cervix excitation positive
Bulged posterior fornix
40. SYMPTOMS OF DIAPHRAGMATIC IRRITATION
Pain in neck or shoulder especially on inspiration
49. DOSAGE
50mg/ m2 IM
MONITORING
S. Beta HCG on D4 and D7
Weekly follow up until <10 mIU/ ml
If the decline is< 15%, a second dose of Mtx is
given on D7
50. VARIABLE DOSE OF METHOTREXATE
Methotrexate 1 mg/ kg IM on D 1,3,5,7
Folinic acid 0.1 mg/ kg IM on D 2,4,6,8
51. FOR ACUTE CASES
Resuscitation with preparation for laparotomy
RL IV
Blood transfusion after clamping
Colloids
Anti D
53. SYMPTOMS
History suggestive of disturbed tubal pregnancy
Exaggerated minor ailments
SIGNS
Absent Braxtonhick’s contraction
Ill defined uterine contour
Fetal parts felt easily
Persistent abnormal attitude and position
54. Internal examination
Difficult to separate uterus from abdominal mass
USG
Absent uterine wall around fetus
Abnormally high position with abnormal atttitude
Fetal parts in close approximation to abdominal wall
Separate visualisation of uterus
Intraperitoneal
Intra ligamentary
55. MRI
X ray
Abnormally high position of fetus with absence of
outline of uterine shadow
Superimposition of gas shadow on the fetal
skeleton
Lateral X ray on standing position shows
superimposition of fetal skeleton shadow with the
maternal spine shadow
57. OVARIAN PREGNANCY
Criteria for diagnosis
Intact tube on affected side
Gestational sac must be in the position of ovary
The gestation sac is connected to the uterus by the
ovarian ligament
The ovarian tissue must be present on its wall on
histological examination
58. SIGNS AND SYMPTOMS
Similar to tubal pregnancy or bleeding corpus
luteum
MANAGEMENT
Ovarian wedge resection/ cystectomy
Ovariectomy
Unruptured: methotrexate
59. CERVICAL PREGNANCY
Implantation at or below the internal os
Diagnostic criteria
soft, enlarged cervix equal to or larger than the
fundus
Uterine bleeding following amenorrhea without
cramping pain
Products of conception entirely confined within and
firmly attached to endocervix
A closed cervical internal os and a partially opened
external os
60. SIGNS AND SYMPTOMS
Painless bleeding appearing shortly after
implantation
Distended thin walled cervix with the external os
partially dialated
64. CORNUAL PREGNANCY
In rudimentary horn of a bicornuate uterus
Rupture by 12-20 weeks with massive
intraperitoneal hemorrhage
65. NURSING MANAGEMENT
Monitor for active bleeding
Single PV examination
Preop preparation
V/s Q15 min before surgery
Preop lab tests
Blood replacement
Support
Monitor beta hcg in Mtx therapy
66. DURING MTX THERAPY
Avoid tampons and intercourse
No alcohol and folic acid containing tablets
Avoid sun exposure
70. HYDATIDIFORM MOLE
It is an abnormal condition of the placenta where
there are partly degenerative and partly proliferative
changes in the young chorionic villi.these result in
formation of clusters of small cysts of varying sizes.
71. ETIOLOGY
Teenage pregnancy
Age> 35 years
Inadequate intake of protein, animal fat
low intake of carotene
Disturbed maternal immune system
Cytogenetic abnormality
prior hydatidiform mole
72.
73. PATHOLOGY
Death of ovum/ failure of embryo growth is needed
for Complete mole
Secretion from cells
Substances from maternal blood
Edema
Liquefaction of stroma
Distension of
vesicles with hcg
rich fluid
74.
75. OVARIAN CHANGES
Bilateral lutein cysts
Due to excessive production of chorionic
gonadotropin
Regress within 2 months of expulsion
78. PARTIAL MOLE
Changes are focal and less advanced
There may be a fetus or at least an amniotic sac
79. CLINICAL FEATURES
Amenorrhea of 8-12 weeks
Vaginal bleeding
WHITE CURRANT IN RED CURRANT JUICE
Lower abdominal pain
Hyperemesis
Breathlessness
Thyrotoxic features
Grape like vesicles PV
No quickening
81. CLASSICAL CLINICAL FEATURES OF COMPLETE
MOLE
Abnormal vaginal bleeding
Lower abdominal pain
Hyperemesis gravidarum
Features of early onset pre- eclampsia<20 weeks
Uterus> 20 weeks
Absent fetal pulse and FHS
Expulsion of vesicular tissue
Theca lutein cyst of ovaries
Hyperthyroidism
Serum hcg>100,000mIU/ml
USG: snow storm appearance
82. PER ABDOMEN
Size more than gestational age
Doughy feel of uterus
No fetal parts and movements
No external ballotment
No FHS
83. VAGINAL EXAMINATION
No internal ballottment
Unilateral or bilateral enlargement of ovary
Finding of vesicles in vaginal discharge
If cervical is open, blood clots or vesicles may be
felt
85. QUANTITATIVE ESTIMATION OF CHORIONIC
GONADOTROPIN
High hcg titre in urine
Rapidly increasing serum hcg (> 100,000 mIU/ml)
Hcg value > 2 MoM for corresponding gestational
age
86. PLAIN X RAY ABDOMEN
If uterine size> 16 weeks, absent fetal shadow
CXR : for pulmonary embolization
Histological examination
87. MANAGEMENT
Group A: mole in process of expulsion
Group B: inert uterus
Supportive therapy for anemia and infection
89. GROUP A
Cervix is favourable
Sution evacuation(200-250 mmHg)
D&C
Digital exploration followed by removal of mole by
ovum forceps
Post procedure
Inj. Methergin 0.2 mg IM
90. GROUP B
Cervix tubular and closed
Laminaria tent/
misoprostol PG E1 400 microgram, 3 hours before
surgery
Hysterotomy
Anti D
Vaginal curettage 5-7 days after evacuation in
persistent bleeding
91. FOLLOW UP
For at least 1 year
Hcg should regress to normal level within 3 months
INTERVAL
Weekly till hcg becomes negative ( within 56 days)
Then every one month for 6 months
Those undergone chemotherapy, followed up for 1
year
93. METHODS EMPLOYED IN EACH VISIT
Symptoms
Abdomino vaginal examination
Detection of hcg in urine or serum
CXR
94. PROPHYLATIC CHEMOTHERAPY
High hcg after 10-12 weeks / re elevation
hemorrhage
Inadequate follow up
Evidences of metastasis
Risk for malignancy
95. REGIMES
Methotrexate 1mg/kg on D1,3,5,7 IM/IV
Folinic acid 0.1mg/kg on D2,4,6,8 IM
Repeated every 7 days
MONITOR HCG
Contraceptive advise
For 1 year
96. COMPLICATIONS
Immediate
Hemorrhage, shock
Sepsis
Perforation of uterus
Pre eclampsia
Acute pulmonary insufficiency
Coagulation failure
Late
Chorio carcinoma
97. RISK FACTORS OF MALIGNANT CHANGE
Age> 40or <20
Parity>3
S. Hcg100,000 mIU/ml
Uterine size> 20 weeks
Previous history of molar pregnancy
Theca lutein cyst> 6 cm
98. NURSING MANAGEMENT
Monitor for signs in 1st 24 weeks
Anti D
Help to cope with pregnancy loss
Follow up
Advise contraception
V/S
Fowl smelling discharge