PPIUCD Reference Manual
PPIUCD Reference Manual
PPIUCD Reference Manual
Reference Manual
November 2010
November, 2010
Any part of this document may be reproduced and excerpts from it may be quoted without
permission provided the material is distributed free of cost and the source is acknowledged.
This manual was developed through technical assistance from USAID under the ACCESS-FP
program and printed with support from Bill and Melinda Gates Foundation: content of this
document do not necessarily reflect the Foundation’s views.
TABLE OF CONTENTS
Background
Postpartum period is one of the critical times when both woman and newborn need a special and integrated
package of health services as morbidity and mortality rates are quite high during this period and also the
women are vulnerable to unintended pregnancy. Studies show that pregnancies taking place within 24
months of a previous birth have a higher risk of adverse outcomes like abortions, premature labor,
postpartum hemorrhage, low birth weight babies, fetal loss and maternal death.
Postpartum Period
The postpartum period has traditionally been understood as the first six weeks after the birth of a child, as
by then, the woman’s body has largely returned to its pre-pregnancy state. However there is a need to focus
on the “extended postpartum period;” i.e., the first 12 months after birth.
Programmatically it is convenient to further define the time periods as the interventions and issues vary
during the period of first 6 weeks and beyond up to one year after childbirth.
Women are highly motivated and receptive to accept Family Planning (FP) methods during the postpartum
period. Demographic and Health Survey show that 40 percent of women in the first year postpartum intend
to use a family planning (FP) method but are not doing so.
Institutional deliveries have increased significantly all across the country, thereby creating opportunities for
providing quality postpartum family planning services. The postpartum services need to be strengthened by
integrating maternal and child health (MCH) and FP services at each level of health facility from the district
hospital to the sub-centre.
Figure 1.2 Factors Related to Return to Fertility and Risk of Pregnancy in the First Year after Birth
100%
90%
80%
Percent of Postpartum Women
70%
Sexually active
60%
50% Return to menses
40%
30% Exclusively
breastfeeding
20%
10%
0%
0-3 4-6 7-9 10-12
Postpartum Months
Source: USAID/ACCESS. 2009. Family Planning Needs during the Extended Postpartum Period in Asia
Return to sexual activity-As in figure 1.2,during the first year postpartum, approximately 40%
women return to sexual activity within the first three months and by 10-12 months postpartum
90% have resumed sexual activity which exposes the woman to risk of having an unintended
pregnancy.
The period after three months, when exclusive breastfeeding is falling, menses is returning and couples
resume sexual activity, can be considered a period of high–yet unperceived–risk of an unintended
pregnancy. Couples will not necessarily see themselves at risk of pregnancy at this time and will not
fully recognize the need for family planning.
Following an abortion, a woman’s fertility returns within 10–11 days. Women who have
experienced a spontaneous or induced abortion should begin use of a contraceptive method within
48 hours to prevent an unintended pregnancy.
Approximately 27% of births in India occur in less than 24 months after a previous birth. Another 34% of
births occur between 24 and 35 months. 61% of births in India occur at intervals that are shorter than the
recommended birth-to-birth interval of approximately 36 months.
Helping couples understand their risk of unplanned pregnancy and ensuring high quality postpartum
family planning services.
Information about optimal birth spacing—including the benefits of spacing births—should be provided
to the woman /couple at various points of contact like in family planning clinics; antenatal clinics; labor
wards/rooms; postpartum and postnatal care facilities; immunization and child health services; and any
service or facility where mothers and children receive routine health care.
Linkage of maternal and newborn health and family planning services at all levels.
Background
Intrauterine contraceptive devices (IUCDs) have been used by women in India for decades for spacing
pregnancies. In some of the health facilities, it has also been provided to women in the immediate
postpartum period. Returning to health facilities for postpartum services after delivery is challenging to
mothers who have competing demands.
Taking advantage of the immediate postpartum period for counseling on family planning and IUCD
insertion, overcomes multiple barriers to service provision. The increased institutional deliveries are the
opportunity to provide women easy access to immediate PPIUCD services.
Policy
The CuT-380A is approved for immediate postpartum insertion as a method of contraception.
The PPIUCD must only be placed after the woman is counseled and gives informed consent.
Counseling should take place in the antenatal period, in early labor or immediately postpartum.
Counseling for informed consent should not take place during the active phase of labor.
The PPIUCD can be placed immediately following delivery of the placenta, during cesarean section or
within 48 hours following childbirth.
The IUCD must be inserted only by a service provider who has been trained to competency in
Immediate PPIUCD service provision according to national standards.
PPIUCD insertion must be done in a healthcare facility that provides delivery services and has
acceptable standards of infection prevention.
Standards
The following standards of care must be maintained.
1. Woman must be counseled regarding advantages, limitations, effectiveness, side effects and problems
related to IUCD.
2. The provider must explain the procedure for insertion and/or removal of the immediate PPIUCD.
3. Woman must be screened for clinical situations as per WHO Medical Eligibility Criteria (MEC).
Screening should take place in the antenatal period, as well as immediately prior to insertion, immediate
postpartum.
4. The woman must be counseled and offered another suitable postpartum family planning method if her
clinical situation does not allow for insertion of the immediate PPIUCD.
5. The provider must insert the IUCD by following all recommended clinical and infection prevention
measures for successful insertion.
The IUCD should NOT be inserted from 48 hours to 6 weeks following delivery
because there is an increased risk of infection and expulsion.
Overview of IUCDs
There are 2 types of IUCDs available in India –
Copper-bearing IUCDs, made of a small inert plastic frame covered with copper sleeves and/or copper wire
Progestin-releasing IUCDs which continuously release a small amount of levonorgestrel.
Among the copper-bearing IUCDs, the CuT-380A is available in the government program and it is used for
immediate postpartum insertion. Cu-375 (popular commercial name Multi Load) has been approved for use in
the private sector, with planned introduction into the government program (Refer IUCD Reference Manual,
Ministry of Health and Family Welfare, Government of India 2006 for details).
Mode of Action
The IUCD interferes with the ability of sperm to survive and to ascend the fallopian tubes where
fertilization occurs. It alters or inhibits sperm migration, ovum transport and fertilization. It stimulates a
sterile foreign body reaction in endometrium potentiated by copper.
Advantages
The specific advantages of an IUCD placed in the immediate postpartum period include:
Advantages for the woman:
Convenience; saves time and additional visit.
Safe because it is certain that she is not pregnant at the time of insertion.
High motivation (woman and family) for a reliable birth spacing method.
Has no risk of uterine perforation because of the thick wall of the uterus.
Reduced perception of initial side effects (bleeding and cramping).
Reduced chance of heavy bleeding, especially among lactational amenorrhea method (LAM) users, since
they are experiencing amenorrhea.
No effect on amount or quality of breast milk.
The woman has an effective method for contraception before discharge from hospital.
Advantages for the service provider or the service delivery site:
Certainty that the woman is not pregnant.
Saves time as performed on the same delivery table for postplacental/intracesarean insertions. Additional
evaluations and separate clinical procedure is not required.
Limitations
The specific limitations of an IUCD placed in the immediate postpartum period include:
Increased risk of spontaneous expulsion. The skilled clinicians with right technique of insertion are
associated with lower expulsion rates.
Perforation of the uterus while placing a PPIUCD immediately after delivery of placenta or during
cesarean section or during the first 48 hours postpartum is unlikely because of the thickness of the
uterine wall in the postpartum period. No such cases are reported in the literature.
The other limitations of the immediate PPIUCD are the same as the interval IUCD.
Counseling should be done with the woman, and if she prefers, with her husband and/or
mother-in-law.
Women should be ideally counseled in the antenatal period for immediate PPIUCD insertion. The
provider may use the Job-aid for counseling (Annexure C) to address the woman’s and her family’s
concerns and clarify their doubts. Fig 3.1 Prototype of Stamp
to be put on ANC Card
A woman’s choice of Family Planning method should be noted clearly on
her antenatal card or record. This stamp or specific notation in the ANC
record (figure 3.1) will enable the delivery room staff, to be prepared for
providing the method immediately following delivery of the placenta.
The labor room staff should check the ANC card for this information
when the woman presents for delivery.
A woman should NOT be counseled for the first time about immediate PPIUCD during
active labor as she may not be able to make an informed choice due to stress of labor.
Following insertion of the IUCD, the provider who has done the insertion should reinforce the key messages
related to PPIUCD and inform the woman regarding follow-up visits. A follow up card providing all relevant
instructions may be given to her on discharge from the facility.
Points to be stressed are importance of exclusive breastfeeding and assurance that the IUCD does not affect
breastfeeding.
To return after six weeks for IUCD/Postnatal Care (PNC)/newborn check-up.
To come back any time if she has any concern or experiences any warning sign or if the IUCD is expelled.
Follow-up care of the immediate PPIUCD acceptor is very important to ensure client satisfaction and
continuation of the accepted method. It allows the provider to know if the counseling messages were clearly
understood by the woman and also to confirm that the IUCD is in place. A woman should come for check-
up at 6 weeks and thereafter as and when necessary. If the woman lives far from the facility where the
immediate PPIUCD was inserted, ANM/ASHAs, can provide appropriate follow-up counseling.
If the woman does not have any concerns or complaints, she need not have additional follow-up solely
related to the IUCD.
Ensure that the woman knows that she can come any time if there is a problem.
If large numbers of women are not returning for follow-up to the site where the IUCD was inserted,
consider following-up those women by community health workers through their out-reach services.
While counseling clients, the provider may use Annexure B and C as Counseling Guide.
Infection prevention practices are an integral part of all clinical procedures to ensure the quality of services. It is
mandatory to practice appropriate infection prevention procedures at all times with all clients to decrease the
risk of transmissison of infection including HIV, Hepatitis B and Hepatitis C to the acceptor and protect the
health workers and other clients from exposure to infection.
1. Hand washing:
Wash hands with soap and water or an appropriate alcohol-based hand rub before performing
immediate PPIUCD insertions and after the procedure.
Hands should be dried with a clean personal towel or air-dried. Towel should not be shared.
Step 1: Decontamination
This step helps prevent transmission of Hepatitis B virus (HBV), Hepatitis C virus (HCV) and HIV. It
should be done before the staff is allowed to handle or clean instruments.
Immediately after use, fully immerse all instruments in a plastic container filled with 0.5% chlorine
solution, for 10 minutes. If the instruments are not to be cleaned (refer to Step 2: Cleaning and
Rinsing) immediately after decontamination, rinse them with water and dry them with a clean towel
to minimize possible corrosion of the instruments due to chlorine. Refer to Annexure D for steps in
processing instruments.
Briefly immerse both gloved hands in the bucket containing the 0.5% chlorine solution and then
carefully remove them by turning them inside out. Leave them in the 0.5% chlorine solution for 10
minutes.
Remove items using high-level disinfected forceps, and place in a high-level disinfected container.
Allow items to cool and air dry.
Use objects immediately or store them in a covered airtight, dry high level disinfected container for
up to 7 days. If stored in an ordinary covered HLD container, it should be used only up to 24 hours.
Sterilized packs can be used up to one week if kept dry and intact and drum is not opened.
Once drum is opened, use instruments within 24 hours.
Items such as scissors and forceps should be put into the solution in an open position.
Do not add or remove any items once timing starts.
Items should be rinsed well with sterile water (not boiled water), air-dried and stored in a covered
sterile container for up to seven days. (Sterile water can be prepared by autoclaving water for 20
minutes at 15 lb/sq inches in an autoclave).
Refer to Annexure E for additional information on chemicals used for infection prevention processes.
Step 4: Storage:
Use high-level disinfected or sterilized instruments and gloves immediately, or store them for up to 1
week in a high-level disinfected or sterilized container accordingly with a tight-fitting cover.
If lid is opened then repeat the procedure after 24 hours
Refer to Annexure D and E for details.
6. Waste disposal:
After completing a procedure (e.g., IUCD insertion), and while still wearing gloves, dispose off
contaminated waste (e.g., gauze, cotton, disposable gloves) in a properly marked leak-proof waste
container (with a tight-fitting lid) or plastic bag.
Segregate the waste in proper container. Safely dispose of waste materials as per protocol.
The waste should be disposed off properly either by burial or burning. Burning should preferably be
done in an incinerator or steel drum as opposed to open burning. If burning is not possible, waste
should be put in a pit and buried but never be thrown out side or left in open pits.
For waste that is to be picked up by the municipalities, these should be contained in closed
containers prior to removal.
Before insertion
Ensure that HLD /sterilized instruments and supplies are available and ready for use. Open all required
HLD/sterile instruments and supplies onto a dry, HLD/sterile surface. IUCD should be placed close by
in its sterile unopened packet.
Ensure that the IUCD package is unopened and undamaged and check the expiry date.
For immediate postpartum insertion within 48 hours of delivery, wash or have the woman wash her
perineal area with water before preparing the vagina and cervix. If immediately after delivery, in the
Sterile or HLD gloves are used to stabilize the IUCD in its packet when trying to hold it by the
placental forceps while the IUCD is still in its packet.
Throughout the procedure, use “no-touch” technique to reduce the risk of infection. If successful
fundal placement is not achieved and the IUCD is dislodged, it may be removed and reinserted once
more with all aseptic precautions.
After insertion
Before removing gloves follow all the steps of decontamination (Refer to Annexure D) and waste
management as per health facility protocol.
The WHO Medical Eligibility Criteria form the scientific foundation for client assessment regarding family
planning methods. It gives detailed guidance regarding whether a woman with a certain condition can safely
use a given method of family planning. The MEC has four categories:
Category 1: A condition for which there is no restriction for the use of the contraceptive method.
Safely use.
Category 2: A condition where the advantages of using the method generally outweigh the theoretical
or proven risks. Generally use.
Category 3: A condition where the theoretical or proven risks usually outweigh the advantages of
using the method. Generally do not use.
Category 4: A condition which represents an unacceptable health risk if the contraceptive method is
used. Do not use.
In general, therefore, medical eligibility criteria for the immediate PPIUCD services can be grouped as follows:
Category 1:
Diagnosis of Chorioamnionitis
Immediate postplacental, immediate postpartum<48
hours or during cesarean section Chorioamnionitis is an intra-amniotic
infection of the fetal membranes and
> six weeks postpartum
amniotic liquor prior to or during labor
Category 2: no conditions which is characterized by:
Temperature of 38°c
Category 3: Abdominal pain
Between 48 hours and six weeks postpartum PLUS one of the following:
Chorioamnionitis Tender uterus
Prolonged rupture of membranes (ROM)> 18 hours Leaking of foul-smelling amniotic
fluid
Category 4: Fetal tachycardia (>160 BPM)
Puerperal sepsis
Unresolved postpartum haemorrhage
The attention and priority should be on addressing the cause of the bleeding and achieving
hemodynamic stability rather than inserting the IUCD.
Client Assessment
Assessment of women for provision of immediate PPIUCD services should be done in two phases. The first
assessment is a general review of the woman’s medical history and eligibility for the method. A second
assessment is done immediately prior to insertion (during cesarean, following delivery of the placenta or within
48 hours after birth) to assess those criteria which may have changed as a result of the delivery.
First
First Assessment
A first assessment should be carried out with the pregnant woman during antenatal care and it must include
assessment for the following conditions, listed in the Medical Eligibility Criteria and relevant to immediate
PPIUCD services,
Known distorted uterine cavity (uterine septum, fibroid uterus, etc.)
Acute purulent discharge
High individual likelihood of exposure to Gonorrhoea or Chlamydia
Malignant or benign trophoblastic disease
Suffering from AIDS and neither clinically well nor on antiretroviral therapy
For those women who present to the facility for delivery care, and who have not had a prior assessment, the
clinician must use her/his clinical judgement about the likelihood of contraindications to use. In the situation
where a woman has just experienced a normal, vertex, full-term vaginal delivery, it is reasonable to assume that
she is eligible for PPIUCD.
Refer to the Medical Eligibility Criteria table in Annexure F for details.
A second assessment should be done immediately prior to insertion by the person who will insert the IUCD.
The purpose of the second assessment is to ensure that the process of labor has not created any clinical situation
which may be a contraindication for insertion of the immediate PPIUCD and to rule out the following
conditions:
Chorioamnionitis
Postpartum endometritis/metritis or puerperal sepsis
More than 18 hours from rupture of membranes to delivery of the baby
Unresolved postpartum haemorrhage
Extensive genital trauma
If her clinical condition makes the IUCD unsuitable for her at this time, the reason should be explained to her
and she should be offered another method of postpartum family planning. If she prefers IUCD, she may be
informed that it can be provided to her after six weeks when she comes for post natal visit.
Immediate PPIUCD services are intended to be fully integrated with intrapartum and postpartum care.
This chapter describes the changes in the cervix and uterus after birth which influence both the timing as
well as the technique for successful IUCD placement in the immediate postpartum period. The timing
of insertion in relation to active management of the third stage of labor will also be discussed.
Figure 6.1: Anatomy of Postpartum Uterus
Uterine
fundus
Vagina
Postpartum
uterus
Cervix
Uterine
cavity
Immediately after expulsion of the placenta, the fundus or top of the the uterus is just below the
umbilicus. It weighs about 1 kg and is approximately the size of a five month pregnancy. It can be
palpated easily through the abdominal wall.
The anterior and posterior walls of the body of the uterus are close together, each wall is about four to
five centimeters in thickness.
The lower part of the uterus (also called the lower uterine segment) is stretched thin and is extremely
floppy adding to the marked mobility of the body of the uterus which is usually tilted forward.
This disparity in consistency and weight between the heavy and thickened body of the uterus and the
stretched and folded lower uterine segment contributes to the extreme curvature that can be noted upon
manual exploration or bimanual examination. (See Figure 6.1).
Immediately following delivery and active management of third stage of labor, the uterus contracts and
is slightly tilted forwards in the lower abdominal cavity.
Over the next 48 hours, the uterus remains approximately the same size and consistency.
Within two weeks however the uterus cannot be felt above the pubic bone as it has almost completely
descended into the pelvis. The lower uterine segment can no longer be appreciated, and the uterine
cavity straightens and shrinks.
During the process of involution, the uterus normally regains its previous nonpregnant size within five
to six weeks postpartum.
Immediately after completion of the third stage of labor, the cervix and lower uterine segment are thin,
collapsed and flabby.
The outer margins of the cervix are often lacerated, and the cervix is extremely soft.
The cervical opening contracts slowly and for a few days after delivery, it readily admits at least two fingers.
By the end of the first week however the cervical canal has re-formed with progressive narrowing of the
cervical opening and thickening of the cervical walls.
At the completion of involution, the cervix is firm and tightly closed while retaining permanent changes
that characterize a parous cervix.
For the first 48 hours after birth, the length of the uterus is almost 30 cm. This makes successful fundal
placement of the IUCD with a typical interval IUCD inserter tube difficult, as the length of the tube is not
sufficient. Instead, either hand or a long placental forceps with a fenestrated end is used for insertion of the
immediate PPIUCD to ensure the placement of IUCD at the fundus. Negotiation of the “bend” where the
uterine body flops over the lower uterine segment is a common challenge during insertion.
A common error in insertion technique is to mistake the back or posterior wall of the uterus for the fundus.
Careful confirmation of fundal placement by manual palpation minimizes the risk of this error which
can lead to an increased risk of expulsion.
Between 48 hours and six weeks after birth, perhaps because the uterus is softer and more vascular than in
its non-pregnant state, an increase in the perforation and overall complication rate like infection, has been
observed. IUCD insertion therefore is not recommended during this period.
Interval insertion using no-touch technique and the traditional inserter tube assembly is recommended for
all insertions starting at six weeks after birth when the uterus has returned to its pre-pregnant state.
1. Postplacental: Postplacental insertion of the IUCD is done immediately following delivery of the
placenta, typically within 10 minutes.
The woman is not yet shifted from the delivery table. The insertion takes place immediately following active
management of third stage labor and the delivery of the placenta.
Postplacental insertion can be done by two techniques:
A. Instrumental insertion (Using forceps): the IUCD is held
in a suitably long forceps without a lock (eg. long placental
forceps). The instrument is inserted upto the fundus of the
uterus, and the IUCD is released.
B. Manual postplacental insertion: the IUCD is held in the provider’s hand as shown in
Fig. and inserted to the uterine fundus. The provider should use long gloves that reach
midway up the arm for the protection of both the provider and the woman.
2. Intracesarean: the IUCD is introduced through the uterine incision during a caesaren section and placed
at the uterine fundus. This is done manually or using a regular ring forceps, since it is not necessary to use a
long instrument to reach the fundus.
After the placenta is removed, the provider inserts the IUCD, and then closes the uterine incision. It is
important NOT to attempt to pass the strings of the IUCD through the cervical os before closure of the
uterus as this will displace the IUCD and leave it lower down in the uterine cavity. There is no need to fix
the IUCD with a ligature.
3. Immediate postpartum: the IUCD is inserted within 48 hours following the birth of the baby. The
trained provider can insert the IUCD in a procedure or examination room in the postpartum ward even
with a regular ring forceps.
4. Extended postpartum/Interval IUCD: women who return for postpartum care at six weeks or
later, can receive the IUCD. The technique of insertion and the related precautions are the same as for
regular IUCD insertion.
Immediate PPIUCD Insertion and Active Management of Third Stage Labor (AMTSL)
Insertion of an IUCD immediately postpartum should not interfere with the routine intrapartum and
postpartum management protocol.
Life-threatening medical conditions such as postpartum hemorrhage and pre-eclampsia/eclampsia should
be treated as per national guidelines on priority. Sound clinical judgment should always prevail.
Administration of a uterotonic, controlled cord traction, and uterine massage for active manangement of
third stage of labor does not increase the subsequent risk of expulsion of the PPIUCD nor does it make
the PPIUCD insertion more difficult.
No aspect of AMTSL should be modified to accommodate immediate PPIUCD insertion.
The steps described below follow the ‘Clinical Skills Checklist for Postplacental Insertion of the IUCD Using
Forceps’. The following table gives greater detail about each step of the insertion process. The differences in
technique for immediate postpartum insertion and for intracesarean insertion are then explained.
5. Inspect perineum, labia and vaginal walls for lacerations. If lacerations are not bleeding heavily,
insert the IUCD and repair if needed.
6. Gently visualize cervix by inserting a Sims speculum in the vagina
and depressing the posterior wall of the vagina.
8. Gently grasp the anterior lip of the cervix with the ring forceps
upto the first lock.
(The same ring forceps that was used to clean the cervix can be
used).
10. Apply gentle traction on the anterior lip of the cervix using the ring
forceps and insert IUCD into lower uterine cavity. Avoid touching
the walls of vagina.
The provider passes the placental forceps with the IUCD carefully
into the lower uterine cavity.
11. Once the placental forceps is in the lower uterine cavity, lower the
ring forceps that is holding the anterior lip of the cervix. Move the
left hand to the woman’s abdomen and push the entire uterus
superiorly (upward). This is to straighten out the angle between the
vagina and the uterus, so that the instrument can easily move
upward toward the uterine fundus.
The provider should take care not to apply excessive force. If the
uterus is not pushed upward, the angle between the cervix and
the uterus may not allow the instrument to advance smoothly.
The provider should always keep the instrument closed so that
the IUCD is not dropped accidentally in the mid-portion of the
uterine cavity.
13. Confirm that the end of placental forceps has reached the fundus and tilt the forceps slightly
inwards. When it reaches the uterine fundus, the provider will feel resistance and will also feel the
thrust of the instrument at the fundus of the uterus with her left hand which is placed on the
abdomen.
14. Open placental forceps and release the IUCD at the fundus.
Sweep placental forceps to side wall of the uterus.
Stabilize uterus (using base of hand against lower part of body of
uterus).
Slowly remove placental forceps from uterine cavity, keeping it
slightly open. Take particular care not to dislodge the IUCD as
placental forceps are removed.
insertion.
Inform her about the IUCD side effects and normal
postpartum symptoms.
Tell the woman when to return for IUCD follow-up/PNC/
newborn checkup.
Emphasize that she should come back any time she has a
These instructions should be reinforced again by the staff of the postpartum unit and repeated to
the woman, and if possible with her family.
20. Record information regarding the PPIUCD insertion in the woman’s chart or record and in the
Immediate PPIUCD register kept at the facility.
There are few notable differences between immediate postplacental insertion and immediate postpartum
insertion of the IUCD. Refer to Annexure I for checklist for immediate postpartum insertion of the IUCD.
The provider should ensure that the woman’s understanding about the immediate PPIUCD is adequate.
Make sure that there is adequate hygiene and her bladder is empty.
Once the woman is on the procedure table the provider should do an abdominal examination to check
the level of the uterus and to be certain there is good uterine tone.
Perform appropriate hand hygiene and use a new pair of sterile or high level disinfected gloves.
Insert the IUCD using the placental forceps or the ring forceps. Using the ring forceps may require some
modification in the technique to bring the uterus a little down and may require slightly more pressure
close to the cervix to allow the ring forceps with the IUCD to reach the fundus.
The provider must ensure that the IUCD is placed at the uterine fundus and should visually examine the
cervix following insertion. In some cases the strings may be visible within the cervical canal due to the
rapid involution of the uterus. If the strings seem inappropriately long, the provider should consider
whether the IUCD has actually rested at the uterine fundus. If there is doubt, it is better to remove the
IUCD and reinsert it.
Women who present to the hospital for scheduled cesarean section, or who require a cesarean section prior to
the onset of labor, can be counseled about the insertion of the PPIUCD. Because they are not in active labor,
they may be able to clearly consider the decision to use an IUCD.
The insertion of the IUCD during a cesarean is straightforward. However some factors should be considered.
Refer to Annexure J for checklist for intracesarean insertion of the IUCD.
Insertion can be done either manually or using a ring forceps since the provider can easily see and reach
the uterine fundus. The provider should hold the IUCD between the middle and index fingers of the
Postpartum IUCD Reference Manual 26
hand and pass it through the uterine incision. Once it is placed at the fundus, the hand should be slowly
withdrawn, noting whether the IUCD remains properly placed.
The strings can be pointed towards the cervix but should NOT be pushed through the cervical canal.
This is to prevent uterine infection by contamination of the uterine cavity with vaginal flora, and to
prevent displacement of the IUCD from the fundus by drawing the strings downward toward the
cervical canal.
Care should be taken during closure of the uterine incision that the strings of the IUCD do not get
included into the suture.
Right technique
Elevate the uterus.
Place IUCD at the fundus.
Sweep instrument to the side of the uterine cavity.
Keep placental forceps closed while going in and open while coming out of the uterine cavity.
Right instrument
Use an instrument that is long enough to reach the fundus.
Right time
Postplacental and intracesarean insertions have lowest expulsion rates.
Management
o Reassure the client that a moderate amount of discomfort is associated with insertion and continue
communicating with the client during the procedure.
o Perform the procedure as gently and as quickly as possible.
Possible Signs/Symptoms
o IUCD can be visualized in the cervix or upper vagina after placement.
o The woman has discomfort or pain.
o Length of the string visible in the vagina is not consistent with fundal positioning in an immediate
postpartum uterus.
Management
o Using an HLD or sterile forceps, remove the IUCD and reinsert the same IUCD if not
contaminated, with all aseptic precautions. If the IUCD has been contaminated, discard it and use
a new IUCD.
3. Cervical Laceration
Possible Signs/Symptoms
Excessive vaginal bleeding
Management
If laceration is seen, repair as needed depending on size of laceration and amount of bleeding.
Follow-up care after immediate PPIUCD is a vital component for ensuring client satisfaction and quality of
care. It is the responsibility of the service provider to provide regular and need based follow-up care and
manage any problems experienced by the client or observed during assessment.
Key Objectives
Assess the woman’s overall satisfaction with the IUCD and address any questions or concerns she may
have.
Identify and manage potential problems
Reinforce key messages
After immediate PPIUCD insertion, a woman should be advised to return to the clinic for routine postpartum
care at 6th week as per guidelines, unless she has serious problems which require emergency services. Routine
immediate PPIUCD followup care should be integrated with standard postpartum services.
The woman is also encouraged to return anytime if she is experiencing problems, if she wants the IUCD
removed, or for any reason she feels that she needs to consult a health provider.
If the woman lives far from the health facility where the Immediate postpartum IUCD was inserted, she should
be counseled and supported by ANM, ASHA to attend the nearby health facility for follow-up care.
In addition to the usual elements of the postpartum check-up, the following activities are to be performed:
Improving the quality of IUCD services includes ensuring providers’ performance as per standards, creating
a supportive work environment, meeting clients’ needs effectively and acknowledging the achievements of
the providers and sustaining the progress made.
Provision of quality postpartum IUCD clinical services require adequate Provision of PPIUCD
infrastructure, supplies and trained personnel. services requires careful
coordination and
It is important to ensure that all personnel of the obstetrics/maternity care team collaboration of
are oriented to immediate PPIUCD service provision and that counseling antenatal, intrapartum
messages are uniform and consistent right from the antenatal care clinic to the and postnatal care
labor room, postpartum ward and family planning clinic. services in the facility.
The minimum criteria for safe provision of immediate PPIUCD services include:
Infrastructure: an outpatient care area for both antenatal screening and counseling as well as
postpartum follow-up and evaluation; an intrapartum care area, where deliveries are conducted and
postplacental insertions can take place; and an examination/treatment room in or near the postpartum
ward where immediate postpartum insertions can take place.
Supplies: Uninterrupted supply of consumables and appropriate instruments should be ensured.
Personnel: Training of service providers in the standard technique and protocol
Coordination of care: a system of communication and sharing of information between the antenatal
care service, the labor/delivery unit, the postpartum ward and the outpatient postpartum care unit.
Infection prevention practices: Ensuring the availability of materials and clean running water for
infection prevention.
IEC/BCC: Availability of posters or panels and Flip charts on the family planning services offered and
information related to clinic timing.
Record maintenance: The clinic has a simple FP client record system. The records are reviewed and
analyzed regularly. It is very important to maintain careful records of immediate PPIUCD services to
monitor the acceptance and continuation rate of IUCD .
Refer to Annexure N for supplies and equipment for postpartum IUCD clinical services.
These performance standards are meant to serve as a guide to the establishment and maintenance of high
quality clinical services. Refer to Annexure N for the performance standards for provision of immediate
PPIUCD services
Written routine protocols and efficient record keeping are mandatory to ensure quality in services
Very few women come to the health facility Figure 6.3 Public Health Approach PPIUCD
for postpartum care. Postpartum care rates,
counseling and provision of family
planning services during postpartum care
are low.
Assuming that women will return later
often can leave women with no option at
all.
While the expulsion rate may be as high as
8-10%, this implies that the retention rate
is still 90-92%. (With good technique
expulsion rate is reduced to <3%). Thus,
despite the potentially higher expulsion
rates for immediate PPIUCDs, the public
health benefit of the service is high Source: Adapted from Mohamed SA, Kamel MA, Shaaban OM, Salem
In situations of limited access to care and HT. Acceptability for the Use of Postpartum Intrauterine
Contraceptive Devices: Assiut Experience. Med Prine Pract
infrequent postpartum care, this level of
2003;12:170-175
programmatic achievement can be
considered a success.
Providing correct information about the IUCD and its insertion immediately postpartum is a very
important component of counseling to potential immediate PPIUCD clients, especially in regions
where awareness about the method is low or misinformation about the method is prevalent.
What it is The IUCD is a small plastic device that is inserted into the uterus.
When is it inserted It is inserted either immediately after the placenta comes out, during a cesarean
section or in the first two days after delivery, while the client is still in the
healthcare facility. This makes it very convenient for her, because by the time
she leaves the hospital, she will have her family planning method active and
effective.
Who can use it Most postpartum women can safely use the IUCD, including those who are
young, breastfeeding, or do hard work. It is especially good for women who
think they do not want any more children, but want to delay sterilization until
they are certain.
Some women should not use the IUCD, including women who have an
abnormal shaped uterus or have a high personal risk of sexually transmitted
infection.
Sometimes women develop an infection during the time of birth. They should
wait until after the infection has been treated to have the IUCD inserted.
Effectiveness The IUCD is more than 99% effective in preventing pregnancy, making it one
of the most effective, reversible contraceptive methods currently available.
Mechanism of The IUCD prevents pregnancy by preventing the sperm from fertilizing the egg.
action
Breastfeeding Using an IUCD immediately postpartum will not affect breastfeeding adversely
and will not change the amount or quality of breastmilk.
Course of The IUCD begins to work immediately and the Copper T 380A is effective for
protection up to 10 years.
Health benefits The IUCD is very safe at preventing pregnancy. When it is inserted immediately
and possible risks postpartum, about 5–10 women out of 100 will find that the IUCD has fallen
out during the first three months. If this happens, she should return to the
health facility and have another IUCD inserted to continue protection against
pregnancy.
Protection from The IUCD offers no protection against HIV or other STIs. Only barrier
HIV and other methods (e.g., the condom) help protect against exposure to HIV and other
STIs.
STIs If the woman thinks that she has a “very high personal risk” for certain STIs she
should not use the IUCD.
Cost and Getting an PPIUCD is inexpensive and very convenient. The IUCD will be
Convenience placed before the woman leaves the healthcare facility after delivery.
In most cases, only one follow-up visit after 6 weeks postpartum to the clinic is
required.
Additional Action Once the IUCD is inserted, no additional actions are needed by the woman. She
and Removal must come to the health facility to have it removed whenever she wants to get
pregnant, otherwise, at the end of the recommended period. She will be able to
get pregnant soon after IUCD is removed.
The woman can get the IUCD removed any time she desires for a pregnancy or
to change to another method. If she wants to continue to use the IUCD for a
longer time, she can use it for 10 years and then have it replaced with another
one.
IUCD IUCD
MALE STERILIZATION
fdfdf
* This is to be used only in emergency. For a regular contraceptive use, take advice from ANM/Doctor at government health centre.
** This is available in private sector.
1
Adapted from: Perkins 1983
This annexure is intended to supplement Chapter 4. It contains guidance on the following topics:
Making dilute chlorine solutions for decontamination and HLD
Choosing appropriate chemicals for HLD
Storing chemicals and processing chemical containers
Preparing and using chemical disinfectants
The WHO recommends 0.5% chlorine solution for decontaminating instruments before cleaning or when
potable water is not available for making the solution (WHO 1989). For HLD, a 0.1% solution is satisfactory,
provided boiled water is used for dilution.
The approximate amounts (in grams) needed to make 0.5% and 0.1% chlorine-releasing solutions from several
commercially available compounds (dry powders) are listed in Table E.1. The formula for making a dilute
solution from a powder of any % available chlorine is listed in Textbox E.1.
A
Use boiled water when preparing a 0.1% chlorine solution for HLD because tap water contains microscopic organic matter that
inactivates chlorine.
B
For dry powders, read x grams per liter (example: Calcium hypochlorite—7.1 grams mixed with 1 liter water).
C
Chloramine releases chlorine at a slower rate than does hypochlorite. Before using the solution, be sure the tablet is completely
dissolved.
2
Adapted from: WHO 1989
The two most commonly used chemicals approved for use as high-level disinfectants are chlorine (0.1%) and
glutaraldehyde (2%). The major advantages and disadvantages of these chemicals are presented in Table E.2.
Note that although alcohols and iodophors are disinfectants, they are no longer classified as high-level
disinfectants. They should be used only when chlorine (0.1%) and glutaraldehyde (2%) are not available or
appropriate.
Table E.2 Advantages and Disadvantages of Commonly Used Chemicals Approved for Use in HLD
Chlorine solutions Fast-acting Concentrated chlorine solutions (≥ 0.5%) can discolor and
(0.1%) Very effective corrode metals. Stainless steel instruments can be soaked
against HBV and safely in a 0.1% chlorine solution (using a plastic container)
HIV for up to 20 minutes. Discoloration is a problem only when
Inexpensive calcium (not sodium) hypochlorite powders are used (Wiping
instruments with vinegar, which is weakly acidic, will quickly
Readily available
remove the discoloration). Also, corrosion will not be a
problem if items are rinsed with boiled water and dried
promptly.
Because chlorine solutions break down rapidly and can lose
their effectiveness, fresh solutions should be made at least
daily or more often if the solution is visibly cloudy.
Glutaraldehyde (2%) Can be used for Although less irritating than formaldehyde, glutaraldehyde
HLD and should be used in well-ventilated areas following
sterilization recommended precautions.
Because glutaraldehyde leaves a residue, instruments must be
rinsed thoroughly with boiled water three times after HLD to
remove any residue and prevent skin irritation.
Disinfectants should be stored in a cool, dark area. Never store chemicals in direct sunlight or in
excessive heat (e.g., upper shelves in a tin-roofed building).
Glass containers used for toxic substances (e.g., glutaraldehyde, formaldehyde) may be washed with soap
and water, rinsed, dried, and reused. Alternatively, they should be thoroughly rinsed with water (at least
three times) and disposed of by burying.
Plastic containers used for toxic substances should be thoroughly rinsed (at least two times) with water,
punctured (so that they cannot be used to carry water or other liquids), and disposed of by burning or
burial.
Information on preparing solutions and using for high-level disinfection and simple disinfection is provided in Table E.3.
3
Table E.3 Preparing and Using Chemical Disinfectants
CHEMICALS FOR STERILIZATION AND/OR HIGH-LEVEL DISINFECTION
Disinfectant
Time Time
(common Effective How to Skin Eye Respiratory Leaves Activated Shelf
Corrosive Needed for Needed for A
solution or Concentration Dilute Irritant Irritant Irritant Residue Life
HLD Sterilization
brand)
Chlorine 0.1% Dilution Yes (with Yes Yes YesC Yes 20 minutes Do not use Change every 24
procedures prolonged hours, sooner if
varyB contact) cloudy.
Glutaraldehyde Varies (2–4%) Add activator Yes Yes Yes No Yes 20 minutes 10 hours for Change every 14–28
(Cidex7) (vapors) at 25°CD Cidex days, sooner if
cloudy.
(See manufacturer’s
instructions)
CHEMICALS FOR DISINFECTION (Note: alcohols and iodophors are not high-level disinfectants.)
Alcohol (ethyl 60–90% Use full Yes (can Yes No No No Do not use Do not use If container (bottle)
or isopropyl) strength dry skin) kept closed, use until
empty.
Lodophors Approximately 1 part 10% No Yes No Yes Yes Do not use Do not use If container (bottle)
(10% povidone- 2.5% PVI to 3 parts kept closed, use until
iodine [PVI]) water empty.
A
All chemical disinfectants are heat- and light-sensitive and should be stored away from direct sunlight and in a cool place (< 40°C).
B
See Table E.1 and Textbox E.1 for instructions on preparing chlorine solutions.
C
Corrosive with prolonged (> 20 minutes) contact at concentrations > 0.5% if not rinsed immediately with boiled water.
D
Different commercial preparations of Cidex and other glutaraldehydes are effective at lower temperatures (20C) and for longer activated shelf life. Always check
manufacturers’ instruction.
3
Adapted from: Rutala 1996
Characteristics and conditions listed below are in WHO Eligibility Criteria Category one. Women
with characteristics and conditions in WHO category 2 also can use this method. With proper
counseling, women of any age or number of children can use IUCD. (Age less than 20 and having
no children are characteristics in WHO Eligibility Criteria Category 2).
Review the course of her labor and delivery and ensure that none of the following
conditions are present:
If planning an im m ed iate po st placen tal in sertio n ,
check whether any of the following conditions are
present:
C horioamnionitis (during labor) Yes No
More than 18 hours from rupture of
Yes No
membranes to delivery of baby
U nresolved postpartum hemorrhage Yes No
If planning a im m ed iate po stpartum in sertio n , check
whether any of the following conditions are
present:
Puerperal sepsis Yes No
Postpartum endometritis/metritis Yes No
C ontinued excessive postpartum bleeding Yes No
Extensive genital trauma where the repair
would be disrupted by immediate postpartum Yes No
placement of an IU CD
Chorioamnionitis
Puerperal sepsis
Post-Insertion Tasks (refer to steps 32 to 35 of Skills Checklist for Postplacental Insertion of the IUCD
using forceps)
13. Tells the client that IUCD has been successfully placed. Reassure her
and answers any questions she may have. Tells the post-insertion
instructions to the client:
Reviews IUCD side effects and normal postpartum symptoms.
Tells the client when to return for IUCD/PNC/ newborn
checkup.
Emphasizes that she should come back any time she has a concern
or experiences warning signs.
Informs about the warning signs for IUCD
Explains how to check for expulsion and what to do in case of
expulsion.
Assures the woman that the IUCD will not affect breastfeeding
and breast milk.
Ensures that the woman understands the post insertion
instructions.
Gives written post-insertion instructions, if possible.
Provides card showing type of IUCD and date of insertion.
Tells her that detailed instructions will be provided prior to
discharge.
14. Records information in the client’s chart or record.
15. Records information in the procedure room register.
Chorioamnionitis
NOTE: IUCD is inserted manually through uterine incision, this takes place after delivery of the
placenta and evaluation for any postpartum bleeding, but prior to repair of uterine incision.
7. Inspects uterine cavity for malformations which would limit use of
IUCD.
8. Ensures that the nurse has opened IUCD on the sterile field.
9. Stabilizes uterus by grasping it at fundus.
10. Holds IUCD at end of fingers, between middle and index finger
(alternatively, use ring forceps to hold the IUCD. Be certain to hold
IUCD by the edge and not entangle strings in the forceps).
11. Inserts IUCD through uterine incision at the fundus of the uterus.
12. Releases IUCD at fundus of uterus.
1. Be sure the woman has been 2. Be sure your supplies/equipment 3. Complete Active Management 4. Ask the woman if she is still
consented. are ready. 3 rd Stage. willing for IUD insertion.
5. Inspect the perineum for 6. Visualize cervix using retractor. 7. Clean cervix and vagina TWICE. 8. Grasp anterior lip of cervix
lacerations. with forceps.
9. Hold the IUCD with forceps 10. Insert forceps with IUCD through 11. Move hand to abdomen; 12. Move IUCD + forceps upward
in a sterile packet. cervix to lower uterine cavity. place it on top of sterile towel until it can be felt at fundus.
Avoid touching vagina. over the fundus of uterus. Follow contour of uterine cavity.
13. Open forceps and release IUD at 14. Sweep forceps to side wall of 15. Slowly remove forceps— 16. Stabilize uterus until forceps are
fundus uterus keep slightly open out.
Allow the woman to rest. Perform infection prevention steps Be sure she gets complete postpartum
Complete records. to process instruments. care. Provide post insertion instructions.
Postpartum
PostpartumIUCD Reference
IUCD Manual
Reference Manual 62 62
Annexure L
PROTOCOL FOR MISSING STRINGS
Case #__________
Date #__________
Protocol for Management of Missing PPIUCD Strings
Situation: Use this protocol when you do not find the strings of the IUCD protruding from the cervix on
P/S exam of a woman who has returned following postpartum placement of IUCD
5 6 5 Yes No 6
9 10 Yes 9 No 10
Follow-up at 12 weeks
11 12 and record result* IUCD seen 11
4
Other standard supplies for delivery are not mentioned here
Remarks
No. of Date of Name of Provider
Indoor
Antenatal Care
(within 10 min)
Forceps (Kelly)
(within 48 hrs.)
Long Placental
Immediate PP
Post placental
Sponge/ Ring
S. No Name Age Postal Address Phone No Living PPIUCD who inserted
Early Labor
Postpartum
Caesarean
Reg No
Children insertion PPIUCD
Forceps
Manual
Period
Intra
Postpartum IUCD Reference Manual 68
Annexure O (ii)
POSTPARTUM IUCD FOLLOW-UP REGISTER FORMAT
Type of
PPIUCD Type of FU
Time of FU
insertion (Tick Finding of FU
(Tick
(Tick appropriate (Tick appropriate column)
appropriate
appropriate column)
column)
column) Name of Action
Indoor Due Reason
S. Phone Date of provider who Actual taken for
Other Complaints
Reg Name Age date of for Remarks
(within 10 min.)
Missing Strings
(within 48 hrs.)
No No insertion inserted date of FU complica-
Immediate PP
Intracesarean
Up to 6 weeks
After 6 weeks
No complaint
No FU removal
Postpartum
Clinic Visit
Telephonic
Expulsion
PPIUCD tions
Infection
(Specify)
Postpartum IUCD Reference Manual 69
Annexure P
MONTHLY PPFP/PPIUCD SERVICES REPORT
Name of the Facility _________________________________________________________
Type of Facility- Medical college District Hospital FRU CHC 24x7 PHC
Pvt Hospital Pvt Clinic
District ____________________________ State_________________________________
Item Number
1) No. of women attending the ANC clinic
2) No of clients counseled for PPFP at ANC clinic
3) No. of deliveries conducted in the facility
a) Normal Deliveries
b) Caesarean
c) Assisted
TOTAL
4) No. of women counseled for PPFP during early labor (EL) and postpartum(PP) period
5) No. of deliveries with use of utero-tonic drug for AMTSL
a) Oxytocin
b) Misoprostol
c) Other (Specify)
TOTAL
6) No. of postpartum female sterilization performed
7) No. of PPIUCD Insertion
a) Postplacental (within 10 min)
b) Postpartum (within 48 hrs)
c) Intracesarean
TOTAL
8) No. of PPIUCD clients followed up
a) At Clinic
b) By Telephone
TOTAL
9) No of clients coming for follow-up
a) Upto 6 weeks
b) After 6 weeks